Vol.:(0123456789)1 3 Histochemistry and Cell Biology (2023) 160:63–77 https://doi.org/10.1007/s00418-023-02193-6 ORIGINAL PAPER Effect of muscle fibre types and carnosine levels on the expression of carnosine‑related genes in pig skeletal muscle Claudia Kalbe1 · Katharina Metzger2 · Claude Gariépy3 · Marie‑France Palin4 Accepted: 21 March 2023 / Published online: 12 May 2023 © His Majesty the King in Right of Canada, as represented by the Minister of Agriculture and Agri-Food Canada 2023 Abstract It is generally accepted that carnosine (β-alanyl-l-histidine) content is higher in glycolytic than in oxidative muscle fibres, but the underlying mechanisms responsible for this difference remain to be elucidated. A first study to better understand potential mechanisms involved was undertaken (1) to determine whether differences in the expression of carnosine-related enzymes (CARNS1, CNDP2) and transporters (SLC6A6, SLC15A3, SLC15A4, SLC36A1) exist between oxidative and glycolytic myofibres and (2) to study the effect of carnosine on myoblast proliferative growth and on carnosine-related gene expres- sion in cultured myoblasts isolated from glycolytic and oxidative muscles. Immunohistochemistry analyses were conducted to determine the cellular localization of carnosine-related proteins. Laser-capture microdissection and qPCR analyses were performed to measure the expression of carnosine-related genes in different myofibres isolated from the longissimus dorsi muscle of ten crossbred pigs. Myogenic cells originating from glycolytic and oxidative muscles were cultured to assess the effect of carnosine (0, 10, 25 and 50 mM) on their proliferative growth and on carnosine-related gene expression. The mRNA abundance of CNDP2 and of the studied carnosine transporters was higher in oxidative than in glycolytic myofibres. Since carnosine synthase (CARNS1) mRNA abundance was not affected by either the fibre type or the addition of carnosine to myoblasts, its transcriptional regulation would not be the main process by which carnosine content differences are determined in oxidative and glycolytic muscles. The addition of carnosine to myoblasts leading to a dose-dependent increase in SLC15A3 transcripts, however, suggests a role for this transporter in carnosine uptake and/or efflux to maintain cellular homeostasis. Keywords Carnosine-related genes · Gene expression · Immunohistochemistry · Muscle fibres · Myoblasts · Pig Introduction Carnosine is a histidine-containing dipeptide (β-alanyl-l- histidine) present in several mammalian organs and tissues, where it exerts multiple biochemical functions (Boldyrev et al. 2013). Carnosine is abundant in skeletal muscle (Man- nion et al. 1992), and diet, gender, age, fibre type compo- sition and the genetic background are major determinants that can modulate its muscle content (Harris et al. 2012; D’Astous-Pagé et al. 2017). In this tissue, carnosine acts as an antioxidant, a pH-buffering molecule (Baguet et al. 2010) and a regulator of calcium homeostasis (Dutka et al. 2012). Carnosine’s ability to increase skeletal muscle growth has also been suggested based on the observed increase in aver- age daily gain values in pigs supplemented with l-carnosine (Bao et al. 2015) and on its capacity to increase the prolifera- tion of porcine myogenic cells in vitro (Palin et al. 2020). Carnosine is synthesized from β-alanine and l-histidine by the carnosine synthase (CARNS1) enzyme, and its deg- radation is performed by carnosine dipeptidases (serum car- nosinase [CNDP1] and cytosolic non-specific dipeptidase [CNDP2]) (Boldyrev et al. 2013). Intracellular carnosine levels are also determined by β-alanine (proton-coupled amino acid transporter [PAT1/SLC36A6] and β-alanine/ taurine transporter [TAUT/SLC6A6]) and carnosine/l-his- tidine (peptide/histidine transporters 1 [PHT1/SLC15A4] and 2 [PHT2/SLC15A3]) transmembrane transporters (Liu * Marie-France Palin Mariefrance.palin@agr.gc.ca 1 Research Institute for Farm Animal Biology, Institute of Muscle Biology and Growth, Dummerstorf, Germany 2 Research Institute for Farm Animal Biology, Institute of Behavioural Physiology, Dummerstorf, Germany 3 Agriculture and Agri-Food Canada, St-Hyacinthe Research and Development Centre, St-Hyacinthe, QC, Canada 4 Agriculture and Agri-Food Canada, Sherbrooke Research and Development Centre, Sherbrooke, QC, Canada http://crossmark.crossref.org/dialog/?doi=10.1007/s00418-023-02193-6&domain=pdf 64 Histochemistry and Cell Biology (2023) 160:63–77 1 3 et al. 1992; Thwaites and Anderson 2011; Oppermann et al. 2019), all of which were previously detected in the porcine longissimus muscle (D’Astous-Pagé et al. 2017). Mainte- nance of carnosine homeostasis therefore depends on the gene expression and activity of the aforementioned enzymes and transporters, which can be modulated according to intra- cellular carnosine levels. A possible retro-control effect of carnosine on CARNS1 messenger RNA (mRNA) levels has been suggested in the longissimus muscle of Duroc pigs having high muscle carnosine content (D’Astous-Pagé et al. 2017), and modulation of CARNS1 mRNA expression in conditions of decreased or increased carnosine content in the mouse tibialis anterior muscle was reported by Everaert et al. (2013). However, evidence for a direct effect of carno- sine on the expression of carnosine-related genes has never been demonstrated in muscle cells. It is generally accepted that carnosine content increases with muscle glycolytic activity (Mora et  al. 2008) and, when looking at individual muscle fibres, the ratio of type II (glycolytic) to type I (oxidative) carnosine content varies from 3.5 in the horse gluteus medius (Dunnett and Harris 1997) to 2.2 in the human vastus lateralis (Harris et al. 1998) and 2.1 in the camel gluteus medius (Dunnett and Harris 1997). Although carnosine content has never been inves- tigated in pig individual muscle fibres, greater concentra- tions of carnosine were reported in skeletal muscles classi- fied as predominantly glycolytic (e.g. longissimus dorsi and semimembranosus) than in oxidative muscles such as the masseter (Reig et al. 2013). On the other hand, the higher carnosine content found in the Duroc longissimus muscle, when compared with Landrace and Yorkshire pigs, could not be explained by differences in fibre type composition (D’Astous-Pagé et al. 2017). The gene expression and activity of carnosine-related enzymes and transporters may account for some of the observed differences in carnosine content in glycolytic and oxidative muscle fibres, and variations in muscle fibre carno- sine content may in turn affect these carnosine-related genes. However, no one has yet investigated whether glycolytic and oxidative muscle fibres present differences in the expression of carnosine synthase, carnosine dipeptidase and β-alanine, histidine and carnosine transporters. Moreover, it remains to be established whether the effect of carnosine on the expres- sion of these genes differs according to the metabolic origin of the myogenic cells (e.g. glycolytic or oxidative muscles). The present study was therefore undertaken (1) to deter- mine whether there are differences in the expression (mRNA and protein) of carnosine-related genes in red (oxidative) and white (glycolytic) muscle fibres and (2) to study the effect of carnosine on proliferative growth and carnosine-related gene expression in primary myogenic cell cultures originat- ing from predominantly glycolytic (longissimus dorsi [LD]) and oxidative (rhomboideus [RH]) muscles. Materials and methods Animals and tissue collection A total of ten crossbred barrows (Duroc × Landrace-York- shire) were used for immunohistochemistry (IHC) and laser-capture microdissection (LCM) followed by quanti- tative polymerase chain reaction (qPCR) analyses. These pigs entered the Sherbrooke Research and Development Centre (SRDC, Agriculture and Agri-Food Canada, QC, Canada) at 20.5 ± 2.38 kg body weight (BW) and were sacrificed upon reaching 152.7 ± 11.90 kg BW. Pigs were fed ad libitum following a three-phase feeding program and had free access to water. Pigs were stunned with a captive bolt pistol prior to slaughter by exsanguination to ensure that the animals were killed humanely. The LD muscle was excised immediately after slaughter, and tissue samples were snap-frozen in liquid nitrogen and stored at −80 °C until IHC, LCM and gene expression analyses. Animal husbandry and slaughter procedures were con- ducted according to the recommended guidelines of the Canadian Council on Animal Care (2009) and approved by the local animal care committee of the SRDC. For myogenic cell culture-related experiments (BrdU, DNA content and gene expression analyses), a total of five German Landrace female piglets from the experimental pig unit of the Research Institute for Farm Animal Biology (FBN, Dummerstorf, Germany) were used and slaughtered at 4–5 days of age. Four- to 5-day-old piglets were selected because they provide a better yield of satellite cells, in accordance with previous studies reporting a decline in the abundance of satellite cells with advancing age (Campion et al. 1981; Mesires and Doumit 2002). Piglets were sac- rificed using exsanguination after stunning with a captive bolt pistol. The entire LD and RH muscles were rapidly collected and used for the isolation of satellite cells. The RH muscle is used as an oxidative (red) reference muscle with a high proportion of oxidative fibres (approximately 75%) and the LD is used as a glycolytic (white) reference muscle with a low proportion of oxidative fibres (approxi- mately 35%) (Lösel et al. 2013). Experimental procedures were approved by the institutional Animal Protection Board at FBN. Laser‑capture microdissection and qPCR analyses of carnosine‑related genes in oxidative and glycolytic muscle fibres The LCM (MicroBeam, PALM, Bernried, Germany) was performed as described by Albrecht et al. (2011) and Revs- kij et al. (2022), with some modifications. Briefly, frozen 65Histochemistry and Cell Biology (2023) 160:63–77 1 3 LD muscle tissue samples were cut into 10-µm-thick sec- tions with a cryostat microtome (Leica CM 1950; Leica, Bensheim, Germany) at −20 °C. Membrane slides (Mem- braneSlide NF 1.0 PEN; Carl Zeiss, Göttingen, Germany) were activated with UV light for 60 min. Three serial sec- tions were transferred to a membrane slide and air-dried before performing the dehydration procedure. The slide was then placed in 96% ethanol (−20 °C) and twice in absolute ethanol at room temperature (RT) for 30 s each. Thereafter, it was gently washed in xylene and placed in a second xylene container for 5 min before air-drying under a fume hood. The slide was immediately used for LCM. Red and white muscle fibres can be distinguished in microscopic cross section without specific staining, as demonstrated in Fig. 1, where two adjacent sections are shown, one without staining and the other one stained with NADH-tetrazolium reductase as described below. Some adjacent fibres of the same metabolic type (red or white) were marked, cut and collected in an adhesive cap (AdhesiveCap 500 opaque; Carl Zeiss). For each of the 10 animals, five slides were freshly prepared and processed, resulting in a total of 2500 red and 2500 white fibre cross sections, wherein the order of red and white fibre extrac- tion was changed from slide to slide. The collected fibre cross sections per tube (500) were lysed in 100 µl RLT buffer (Qiagen, Hilden, Germany) containing 1 µl mer- captoethanol, shaken overhead and incubated for 30 min at RT before being stored at −80 °C. Total RNA isola- tion was performed with an RNeasy Micro Kit (Qiagen) according to the manufacturer’s instructions. For each animal, total RNA was isolated from white and red myofi- bres, resulting in five pooled tubes each. Total RNA was resuspended in 14 µl RNase free water. Complementary DNA (cDNA) synthesis was carried out with 7.5 µl of total RNA, a mixture (1:1) of random p(dN)6 and anchored- oligo (dT)18 primers (Roche, Mannheim, Germany) and 200 units of Moloney mouse leukaemia virus reverse transcriptase (M-MLV RT RNase H Minus Point Mutant, Promega, Mannheim, Germany) in 25 µl of the incubation buffer provided by the supplier, supplemented with 25 mM deoxy-NTPs (Roche) and 40 units of RNasin ribonucle- ase inhibitor (Promega). This mixture was incubated for 60 min at 42 °C. The cDNA was aliquoted and stored at −80 °C. For qPCR analyses, the diluted cDNA (1:4) was amplified in duplicate with the LightCycler FastStart DNA MasterPLUS SYBR Green I kit (Roche) in a 10 µl reaction volume. Primer information for the CARNS1, CNDP2, SLC6A6, SLC15A3, SLC15A4 and SLC36A1 genes is described in D’Astous-Pagé et al. (2017). Amplification and quantification of amplified products were performed in a LightCycler 2.0 instrument (Roche) under the following cycling conditions: pre-incubation at 95 °C for 10 min, followed by 40 cycles of denaturation at 95 °C for 15 s, annealing for 10 s at 60 °C, extension at 72 °C for 10 s and single-point fluorescence acquisition for 6 s to avoid quan- tification of primer artefacts. The melting peaks of all sam- ples were routinely determined by melting curve analysis to ensure that only the expected products were generated. The quantification was performed with LightCycler soft- ware version 4.5 using the quantification module Absolute Quantification. To calculate the PCR efficiency, routine dilutions of gene-specific external standards (cloned PCR products) of known concentrations covering five orders of magnitude (5 × 10–16 to 5 × 10–12 g DNA) were co-ampli- fied during each run. Detection and localization of carnosine‑related proteins in oxidative and glycolytic muscle fibres Histochemistry and IHC analyses were carried out to ena- ble the identification of individual muscle fibre types and to detect the CARNS1, CNDP2, PHT2/SLC15A3 and PHT1/ SLC15A4 proteins in red oxidative, intermediate and white glycolytic fibres. For these analyses, the LD muscle of Fig. 1 Representative sections of the longissimus dorsi (LD) mus- cle used for laser-capture microdissection (LCM). a Unstained sec- tion used to collect individual white glycolytic (W) and red oxidative (R) muscle fibres by LCM. b Adjacent section stained with NADH- tetrazolium reductase to allow the identification of different metabolic muscle fibre types (R, W and I [intermediate]), scale bar = 200 µm 66 Histochemistry and Cell Biology (2023) 160:63–77 1 3 crossbred barrows (Duroc × Landrace-Yorkshire; n = 10) described above were used. In addition, the semitendinosus (ST) muscles of two randomly selected 3-month-old domes- tic pigs (German Landrace females) were simultaneously stained as a reference for a mixed muscle with around 50% oxidative and 50% glycolytic fibres. Detailed information for housing, feeding management and muscle sample collection procedures for the 3-month-old domestic pigs are described in Lösel et al. (2013). For the histochemistry analyses, serial transverse sec- tions of both muscles (8 µm) were cut at −20 °C using a cryostat microtome (Leica CM 1950; Leica). One section was exposed to the reaction for NADH-tetrazolium reduc- tase (Novikoff et al. 1961), which enables classification into metabolic fibre types (red oxidative, intermediate and white glycolytic) (Rehfeldt et al. 2008). Images were taken with an Olympus BX43 microscope (Olympus GmbH, Hamburg, Germany) equipped with an Olympus DP23 digital camera and using a 10× objective. Cell^D 5.1 software was used for image analysis (Olympus). Image acquisition details are as follows: image dimensions of 2080 (width) × 1544 (height) pixels and 24-bit depth, detector gain set at 1×, time and space resolution data 552.169 nm/pixel (X) and 552.169 nm/ pixel (Y) with 96 pixels per inch. Exposure time for NADH- tetrazolium reductase was set at 33 ms. For IHC analyses, the transverse frozen sections were mounted on poly-l-lysine-coated glass slides (Thermo Fisher Scientific, Darmstadt, Germany) and stored at −80 °C until staining. After thawing, sections were fixed in 4% for- maldehyde (CNDP2, PHT2/SLC15A3) and/or in 0.3% H2O2 in methanol (CARNS1, PHT1/SLC15A4, CNDP2) and then washed with phosphate-buffered saline (PBS). Sections were pretreated with 10% bovine serum albumin (Sigma–Aldrich, Taufkirchen, Germany; PHT2/SLC15A3, PHT1/SLC15A4), 10% normal goat serum (Sigma–Aldrich; CARNS1) or Roti® Block (Carl Roth, Karlsruhe, Germany; CNDP2) for 1 h to block unspecific binding of the secondary antibodies. The primary antibodies to PHT2/SLC15A3 (rabbit polyclonal to mouse SLC15A3, 1:50, ab113819, Abcam, Amsterdam, Netherlands), PHT1/SLC15A4 (chicken polyclonal to pig SLC15A4, 1:100, Immune Biosolutions, Sherbrooke, QC, Canada), CARNS1 (chicken polyclonal to pig CARNS1, 1:100, Immune Biosolutions) or CNDP2 (rabbit polyclonal to human CNDP2, 1:250, ab204351, Abcam) were added and sections were incubated in a humidified chamber over- night at 4 °C. More detail on primary and secondary anti- bodies is provided in Supplemental Table 1 (Supplemental Information file). Negative controls were incubated in PBS in place of primary antibody (Supplemental Fig. 1), and anti- body specificity is presented in Supplemental Figs. 2, 3, 4 and 5. After washing with PBS, the sections were incubated with the secondary antibody Atto 488 goat anti-chicken immunoglobulin Y (IgY; VWR International, Mississauga, ON, Canada) for PHT1/SLC15A4 and CARNS1 staining at a dilution of 1:1000 for 1 h at RT. For PHT2/SLC15A3 and CNDP2 staining, the secondary antibody Alexa 488 goat anti-rabbit IgG (Abcam) at a dilution of 1:500 was used for 1 h at RT. Following washing in PBS (three times for 5 min each in the dark), slides were covered with Roti® Fluor Care DAPI (Carl Roth) and a coverslip. Images were taken by the same experienced technician using a Leica DM 4000B microscope equipped with a DFC450 3.3 megapixel digital camera (Leica Microsystems, Wetzlar, Germany) and using a 10× objective. The band pass filter for excitation was set at BP450-490 nm (blue) and the long pass filter for emis- sion was set at LP515 nm (green). QWin software (3.5.1) was used for image analysis (Leica Microsystems). Image acquisition was performed with the following parameters: image dimensions of 2088 (width) × 1550 (height) pixels and 24-bit depth, detector gain set at 48.86×, time and space Table 1 Effect of fibre type on the mRNA abundance (quantity units) of carnosine-related genes in the longissimus dorsi muscle a CARNS1 carnosine synthase 1, CNDP2 carnosine dipeptidase 2, SLC6A6 solute carrier family 6, member 6, SLC15A3 solute carrier family 15, member 3, SLC15A4 solute carrier family 15, member 4, SLC36A1 solute carrier family 36, member A1 b Data represent mean values of ten pigs with their corresponding SEM. Red and white fibres were isolated from the longissimus dorsi muscle using laser-capture microdissection c Statistical analyses followed the usual verification of the normality of the residuals (Shapiro–Wilk tests), and the ANOVA was performed with heterogeneous variances. A non-parametric Friedman’s test was also used as confirmatory test Genea Fibre typeb Red oxidative White glycolytic SEMc red SEMc white Fibre type p value CARNS1 6.68 7.73 0.873 1.411 0.426 CNDP2 55.36 23.33 3.222 2.708 ≤ 0.001 SLC6A6 3.66 0.75 0.853 0.026 0.007 SLC15A3 11.58 4.32 1.431 0.720 ≤ 0.001 SLC15A4 3.19 1.26 0.311 0.225 ≤ 0.001 SLC36A1 8.15 3.38 0.726 0.531 ≤ 0.001 67Histochemistry and Cell Biology (2023) 160:63–77 1 3 resolution data 539.567 nm/pixel (X) and 539.567 nm/pixel (Y) with 96 pixels per inch. Exposure time was set at 1.0 s for CARNS1, 1.2 s for CNDP2, 986 ms for PHT2/SLC15A3 and 1.4 s for PHT1/SLC15A4. We did not conduct IHC analy- ses for the TAUT/SLC6A6 and PAT1/SLC36A1 proteins, as none of the commercially available antibodies raised against the human and rodent SLC6A6 and SLC36A1 proteins were suitable for detecting the porcine proteins. Western blot analyses were also performed to confirm antibody speci- ficity in pig skeletal muscle and negative tissues. Detailed information on primary and secondary antibody character- istics (Supplemental Table S1) and western blot methods used are included in the Supplemental Information file. The CARNS1, SLC15A3 and SLC15A4 antibodies were used in a previous study, where we observed strong positive correla- tions between mRNA and protein abundance of CARNS1 (r = 0.98, p < 0.0001), SLC15A3 (r = 0.96, p < 0.0001) and SLC15A4 (r = 0.96, p < 0.0001) in pig skeletal muscle and where antibody specificity was confirmed in the longissimus muscle (D’Astous-Pagé et al. 2017). Myogenic cell culture and carnosine treatments Isolation and characterization of porcine satellite cells from the LD and RH muscles was performed as reported previ- ously (Metzger et al. 2020). The isolated myogenic cells were aliquoted, stored in liquid nitrogen and used as pas- sage 3 for the experiments. Previous studies have shown that satellite cells isolated from different muscle types pos- sess preprogrammed characteristics of their muscle of origin (Ono et al. 2010; Zhang et al. 2022; Zhu et al. 2013). For each experiment, the myogenic cells were seeded in gelatin- coated plates at a density of 3000 cells per well for 96-well plates for proliferative responses (BrdU and DNA content analyses) or 150,000 cells in 6-mm cell culture dishes for RNA isolation (gene expression analyses). Cells were grown for 48 h in growth medium (GM: DMEM (Biochrom, Ber- lin Germany) containing 10% foetal bovine serum and 10% horse serum (Sigma–Aldrich), 1% glutamine (Carl Roth) and 1% penicillin/streptomycin (Biochrom)/amphotericin B (Sigma-Aldrich)) and treated with carnosine (0, 10, 25 and 50 mM; Sigma-Aldrich) for an additional 48 h. Selected carnosine concentrations and cell exposure time were chosen based on a previous study indicating similar cell prolifera- tion curves up to 48 h for the 0, 10 and 50 mM carnosine doses (Palin et al. 2020). The 10 and 25 mM concentrations correspond to the physiological range for carnosine in pig skeletal muscle (Boldyrev et al. 2013), whereas the 50 mM carnosine represents a supra-physiological concentration. We recently demonstrated that these carnosine concentra- tions had no toxic effect in porcine myoblasts that were cul- tured up to 48 h (Palin et al. 2020). Myogenic cell proliferation assays and DNA content The effect of carnosine and muscle type (LD vs RH) on the porcine myoblast proliferative response was measured by a BrdU colorimetric immunoassay (Cell Proliferation ELISA BrdU, colorimetric, Roche) allowing measurements of BrdU incorporation into newly synthesized DNA. After 48 h of cell growth in GM supplemented with carnosine (0, 10, 25 and 50 mM), myoblasts were incubated with 10 µM of the BrdU labelling solution for an additional 5 h. The culture medium was then removed by suction and cells were fixed using the provided FixDenat solution (Roche). Cells were incubated at RT for 2 h with the anti-BrdU-POD solu- tion, allowing the formation of an immune complex, which was detected at an absorbance of 450 nm (reference wave- length 690 nm) after addition of the substrate solution. The stop solution option (H2SO4) was used before detection in order to stop the reaction. Absorbance was measured with a Synergy™ MX plate reader (BioTek, Bad Friedrichshall, Germany). The DNA content was used as an equivalent for myogenic cell number and was measured as previously reported for piglet myoblasts (Mau et al. 2008a). For the BrdU assay and DNA content analyses, three independent experiments were conducted for each muscle (LD and RH), with n = 5 piglets used in each experiment (2 muscles × 3 experiments × 5 pig- lets) and carnosine concentrations in duplicate. The plate scheme was changed from experiment to experiment. qPCR analyses of carnosine‑related genes in myogenic cells The relative mRNA abundance of carnosine-related genes (CARNS1, CNDP2, SLC6A6, SLC15A3, SLC15A4, SLC36A1) was investigated in myoblasts after 48 h of cell growth with 0, 10, 25 and 50 mM carnosine. RNA isola- tion, cDNA synthesis and qPCR analyses were carried out and analysed as described previously (Kalbe et al. 2008, 2018) using the primers of D’Astous-Pagé et al. (2017). Data are expressed as arbitrary units after normalization with the endogenous reference gene RPL32 (ribosomal protein L32, Wang et al. 2018). The RPL32 mRNA expression was unaf- fected by carnosine, muscle type or the interaction of both (p > 0.10). Statistical analyses Statistical analyses were performed with the MIXED proce- dure of SAS (2012; SAS Institute Inc., Cary, NC, USA). To analyse the effect of fibre type (red and white fibres) on the expression of carnosine-related genes (LCM + qPCR), an analysis of variance (ANOVA) was carried out. Statistical analyses followed the usual verification of the normality of 68 Histochemistry and Cell Biology (2023) 160:63–77 1 3 the residuals (Shapiro–Wilk tests) to validate the ANOVA, and the analysis was also performed using a Friedman test as a confirmatory test. For the BrdU, DNA content and qPCR analyses per- formed in myogenic cell cultures treated or not with carno- sine, statistical analyses were undertaken using a 2 × 4 fac- torial analysis (2 muscles × 4 carnosine levels) randomized complete block design (3 experiments × 5 piglets = 15 blocks) that allowed comparisons between the LD and RH muscles (muscle effect) and the muscle × carnosine interac- tion. Partitioned analyses were performed for each muscle separately where the effect of carnosine was carried out, followed by Dunnett’s correction for comparing the 10, 25 and 50 mM carnosine treatments to the 0 mM control. Statistical significance was set at p ≤ 0.05 and tendencies at 0.05 < p ≤ 0.10. Results Expression of carnosine‑related genes in oxidative and glycolytic muscle fibres The qPCR analyses of carnosine-related genes in red oxida- tive and white glycolytic muscle fibres isolated from the LD muscle by LCM are presented in Table 1. A fibre type effect was observed for the CNDP2, SLC6A6, SLC15A3, SLC15A4 and SLC36A1 genes (p ≤ 0.01), with higher mRNA levels found in red oxidative than in the white glycolytic fibres. The red and white muscle fibres had similar CARNS1 mRNA levels (p > 0.10). Immunohistochemical detection of carnosine‑related proteins in porcine skeletal muscle fibres Detection and localization of the CARNS1, CNDP2, PHT2/ SLC15A3 and PHT1/SLC15A4 proteins was performed by IHC in cross sections of the LD and ST muscles (Figs. 2 and 3). For the CARNS1 enzyme, a strong signal was detected at the periphery of white glycolytic (W) and red oxidative (R) fibres (Fig. 2). Diffuse cytosolic staining was also observed for CARNS1 in all fibre types (intermediate [I], R and W), with slightly stronger intensity found in red oxidative fibres. A strong CNDP2 signal was observed at the periphery of muscle fibres, with a stronger intensity found in R fibres. Diffuse and weaker CNDP2 cytosolic staining was found in all fibre types (Fig. 2). Again, slightly stronger cytosolic CNDP2 staining was observed in R fibres when compared to the I and W fibres of both muscles. For the PHT2/SLC15A3 and PHT1/SLC15A4 carnosine/histidine transporters, a strong signal was detected at the periphery of R fibres in LD and ST muscles (Fig. 3). For these two proteins, diffuse cytosolic staining was also present in all fibre types, with stronger intensity observed in R fibres (Fig. 3). Effect of carnosine on the proliferation of myoblasts isolated from the longissimus dorsi and rhomboideus muscles The effect of carnosine and muscle type on myoblast pro- liferation was evaluated by measuring the incorporation of BrdU into newly synthesized DNA after 48 h of carnosine treatment. This analysis revealed a significant overall car- nosine effect on myoblast proliferation in the LD and RH muscles (p < 0.0001; Fig. 4a, b) and, in both muscles, the addition of 10 mM, 25 mM and 50 mM carnosine to the culture media significantly increased the myoblast prolif- eration when compared with the 0 mM carnosine treatment (p ≤ 0.0001). In addition, there was a muscle type effect, with higher absorbance values (450 mm) being observed in myoblasts isolated from RH (0.84) when compared with the LD (0.78) muscle (p < 0.001, SEM 0.032). There was no muscle × carnosine interaction. The effect of carnosine on cell number (DNA content) was also investigated after 48 h of carnosine treatment (Fig. 4c, d). An overall carnosine effect was observed for myoblasts isolated from the LD and RH muscles (p < 0.05). For the LD muscle (Fig. 4c), the addition of 10 mM, 25 mM and 50 mM carnosine to the culture media decreased the DNA content values when compared with the 0 mM carno- sine treatment (p < 0.05 for 10 mM and 50 mM carnosine; p < 0.01 for 25 mM carnosine). Lower DNA content values were also observed with the addition of 25 mM (tendency, p = 0.10) and 50 mM (p < 0.01) carnosine for myoblasts isolated from the RH muscle (Fig. 4d). Similar DNA con- tent values were found between LD (0.433 µg/well) and RH (0.431 µg/well) muscles (muscle effect > 0.10, SEM 0.072) and there was no muscle × carnosine interaction. Effect of carnosine on carnosine‑related gene mRNA abundance in cultured myoblasts isolated from the longissimus dorsi and rhomboideus muscles Results for the mRNA abundance of carnosine-related genes in myoblast cell cultures from the LD and RH mus- cles are presented in Table 2. The qPCR analyses were performed after 48 h of cell growth in the presence of dif- ferent doses of carnosine (0, 10, 25 and 50 mM). There was an overall effect of carnosine on the SLC15A3 mRNA abundance in myoblasts isolated from LD and RH muscles (p < 0.001). For the LD muscle, higher SLC15A3 mRNA levels were found in myoblasts that were exposed to 10 mM (p < 0.01), 25 mM (p < 0.0001) and 50 mM (p < 0.0001) carnosine when compared with the 0 mM treatment. For 69Histochemistry and Cell Biology (2023) 160:63–77 1 3 the RH muscle, increases in SLC15A3 mRNA abundance were observed with the addition of 25 mM (p < 0.01) and 50 mM (p < 0.0001) carnosine. There was a muscle type effect on SLC15A3 mRNA abundance, with higher abun- dance in LD than in the RH muscle (1.44 vs 1.30, p < 0.001, SEM = 0.150). There was a tendency for an overall car- nosine effect on CNDP2 mRNA abundance (p = 0.092) in the LD muscle. In addition, there was a muscle type effect (p < 0.01), with higher CNDP2 mRNA abundance found in LD than in the RH muscle (1.12 vs 1.04, SEM = 0.037). A muscle type effect was also observed for the SLC36A1 gene (p < 0.05), with higher mRNA abundance found in RH than in the LD muscle (1.17 vs 1.12, SEM = 0.077). There was no muscle × carnosine interaction for any of the studied genes. Discussion Several studies performed in different species have reported that muscle carnosine content is higher in white glycolytic than in red oxidative muscles (Baldi et al. 2021; Dunnett and Harris 1997; Mora et al. 2008). This finding is possibly linked with the higher pH buffering capacity of carnosine required in glycolytic fibres, which produce more lactic acid Fig. 2 Immunohistochemical detection of carnosine synthase (CARNS1) and carnosine dipeptidase 2 (CNDP2) enzymes in serial cross sec- tions of the longissimus dorsi (LD) and semitendinosus (ST) muscles. Serial sections were stained with anti-CARNS1 and anti-CNDP2 antibodies (left panels, green staining) or with a histochemical reaction based on NADH-tetrazolium reductase activity (right panels) to identify white glycolytic (W), intermediate (I) and red oxida- tive (R) muscle fibres. CARNS1 staining is mainly found at the periphery of W and R muscle fibres. A strong CNDP2 signal is also observed at the periphery of muscle fibres, with stronger intensity found in red oxida- tive fibres. Diffuse cytosolic CARNS1 and CNDP2 staining is also present in all fibre types, with slightly stronger intensity found in red oxidative fibres. Scale bar = 200 µm 70 Histochemistry and Cell Biology (2023) 160:63–77 1 3 than oxidative fibres. The higher carnosine content generally observed in glycolytic fibres may also be associated with differences in the regulation of the abundance and/or activ- ity of carnosine-related enzymes and transporters. To better understand the underlying mechanisms leading to the greater accumulation of carnosine in glycolytic fibres, we first inves- tigated the mRNA abundance of carnosine-related genes in white glycolytic and red oxidative muscle fibres isolated with LCM. Study results showed similar mRNA abundance of CARNS1 in red and white muscle fibres, a finding that was also confirmed at the protein level with IHC analyses. This may suggest that red and white fibres have similar capacity to synthesize carnosine from its precursors. This was indeed demonstrated by Hill et al. (2007), who reported a similar increase in carnosine content in type I (oxidative) and type II (glycolytic) muscle fibres after 10 weeks of β-alanine supplementation. The greater abundance of the CNDP2 transcript and its protein found in red oxidative fibres could lead to an increase in carnosine hydrolysis that would explain, at least in part, the lower carnosine content generally observed in these fibres. However, the importance of muscle carnosi- nase in controlling carnosine homeostasis has been ques- tioned by indirect evidence of low carnosinase activity in Fig. 3 Immunohistochemical detection of PHT2/SLC15A3 and PHT1/SLC15A4 transport- ers in serial cross sections of the longissimus dorsi (LD) and semitendinosus (ST) muscles. Serial sections were stained with anti-SLC15A3 and anti-SLC15A4 antibodies (left panels, green staining) or with a histochemical reaction based on the NADH-tetrazolium reductase activity (right panels) to identify white glycolytic (W), intermediate (I) and red oxidative (R) muscle fibres. SLC15A3 and SLC15A4 sig- nals are found at the periphery of muscle fibres, with a much stronger signal intensity present in red oxidative fibres for both muscles. A diffuse cytosolic staining is also present in all fibre types of the LD and RH muscles, with a stronger intensity found in red oxidative fibres. Scale bar = 200 µm 71Histochemistry and Cell Biology (2023) 160:63–77 1 3 Fig. 4 Effect of carnosine on myoblast proliferation (a, b) and cell number (c, d) after 48  h of growth. The effect of carnosine treat- ment on myoblast proliferation was assessed with the BrdU assay using myogenic cells isolated from the longissimus dorsi (LD; a) and rhomboideus (RH; b) muscles. The effect of carnosine on cellular DNA content (equivalent for myogenic cell number) was measured in myoblasts isolated from LD (c) and RH (d) muscles. Data represent mean values of n = 15 observations (5 pigs × 3 experiments) ± SEM. For both assays, the effect of carnosine was determined by comparing each dose of carnosine (10, 25 and 50 mM) to the 0 mM carnosine treatment on which a Dunnett’s correction was applied. BrdU SEM in LD = 0.046 and in RH = 0.036. DNA content SEM in LD = 0.074 and in RH = 0.073. †0.05 < p ≤ 0.10; *p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001 Table 2 Effect of carnosine and muscle type on the relative mRNA abundance of carnosine-related genes in cultured myoblasts from the longis- simus dorsi and rhomboideus muscles a CARNS1 carnosine synthase 1, CNDP2 carnosine dipeptidase 2, SLC6A6 solute carrier family 6, member 6; SLC15A3 solute carrier family 15, member 3; SLC15A4 solute carrier family 15, member 4; SLC36A1 solute carrier family 36, member A1 b LD longissimus dorsi, RH rhomboideus c Data represent mean values of n = 15 observations (5 pigs × 3 experiments). The mRNA abundance was normalized with the ribosomal protein L32 (RPL32) reference gene that was not affected by carnosine (p > 0.10) or the muscle type (p > 0.10). **p < 0.01; ***p < 0.0001 Genesa Muscleb Carnosine (mM)c SEM Carn p value Muscle p value Carn × Mus- cle p value 0 10 25 50 CARNS1 LD 1.02 1.10 1.03 1.01 0.177 0.549 0.905 0.885 RH 1.07 1.07 0.99 1.00 0.189 0.527 CNDP2 LD 1.13 1.16 1.13 1.06 0.068 0.092 0.006 0.990 RH 1.07 1.07 1.04 0.98 0.050 0.283 SLC6A6 LD 1.08 1.02 0.98 1.01 0.120 0.296 0.426 0.829 RH 1.11 1.09 1.01 0.99 0.107 0.113 SLC15A3 LD 1.17 1.40** 1.49*** 1.70*** 0.173 < 0.001 < 0.001 0.844 RH 1.08 1.21 1.35** 1.55*** 0.129 < 0.001 SLC15A4 LD 1.05 1.04 1.01 1.01 0.057 0.357 0.835 0.694 RH 1.02 1.04 1.04 1.03 0.078 0.891 SLC36A1 LD 1.08 1.10 1.12 1.15 0.083 0.175 0.041 0.895 RH 1.16 1.18 1.18 1.18 0.097 0.945 72 Histochemistry and Cell Biology (2023) 160:63–77 1 3 skeletal muscle. This was indeed suggested by the slow washout profile (9 weeks) of muscle carnosine after cessa- tion of β-alanine supplementation (Baguet et al. 2009) and by the optimal pH for CNDP2 activity that peaks at 9.5, whereas that of the skeletal muscle is at 7.1 (Lenney et al. 1985). Although these studies report important findings, fur- ther work assessing the CNDP2 activity in isolated muscle fibres is needed in order to obtain more direct evidence of increased carnosine hydrolysis in oxidative fibres (vs gly- colytic fibres). In the present study, the mRNA abundance of carnosine/l- histidine (SLC15A3 and SLC15A4) and β-alanine (SLC6A6 and SLC36A1) transporters was greater in red oxidative than in white glycolytic fibres, and this was also confirmed at the protein level when performing the IHC analyses. Since these transporters are involved in the cellular uptake of car- nosine (Oppermann et al. 2019) and its constituents l-histi- dine (Yamashita et al. 1997) and β-alanine (Liu et al. 1992; Metzner et al. 2006), a higher mRNA abundance was rather expected in white glycolytic fibres, reported to accumulate more carnosine. A possible explanation may be that these transporters are also responsible for the release of carnosine, l-histidine and β-alanine from the cells (efflux) in order to maintain cellular homeostasis. This was suggested by Lind- ley et al. (2011), reporting on a potential efflux mechanism of PHT1/SLC15A4 for the histidine and Gly-Sar substrates in a transfected hPHT1-COS-7 cell model. Carnosine release was also demonstrated in primary cultures of glial cells (Bauer et al. 1982) and from the skeletal muscle of rats that had access to running wheels compared with sedentary rats (Nagai et al. 2003). Although it is tempting to hypothesize that red oxidative fibres present lower carnosine content because of greater carnosine and/or histidine cellular efflux, additional experiments are needed to determine whether such an active transporter-mediated process is involved. Although the CARNS1, CNDP2, PHT2/SLC15A3 and PHT1/SLC15A4 proteins were previously detected in pig (D’Astous-Pagé et al. 2017), mice (Everaert et al. 2013) and human (Hoetker et al. 2018) skeletal muscle, their cellular localization has never been reported for this tissue. Moreo- ver, very few studies have investigated their localization in other cell types. The CARNS1 enzyme has been observed in the cytosol and plasma membranes of neurons in the mice olfactory bulb (Wang-Eckhardt et al. 2020) and in intracel- lular, membranous and nuclear locations in human kidney, glial, neuronal and testis cells (www. prote inatl as. org). These results are in accordance with the observed localization of CARNS1 protein at the periphery of muscle fibres where myonuclei are located and in the cytosolic compartment of pig LD and ST muscles (current study). A similar cellu- lar localization was found for CNDP2, with signals being observed in the cytosol and at the periphery of muscle fibres, with stronger staining intensities being observed in the red oxidative fibres of the LD and ST muscles. Cytosolic CNDP2 staining has been reported in human dopaminergic neurons (Licker et al. 2012) and in the cytoplasm and nucleus of Drosophila melanogaster S2 cells (Andreyeva et al. 2019), but the present study is the first to report staining at the periphery of muscle fibres. Accordingly, the Human Protein Atlas databank reported weak CNDP2 signals in the cyto- solic, membranous and nuclear compartments of neuronal, kidney and testis cells (www. prote inatl as. org). The presence of CARNS1 and CNDP2 proteins in or in close proximity to the plasma membrane is quite surprising since both proteins lack transmembrane and secretion signal sequences and were predicted to be cytosolic enzymes (Drozak et al. 2010; Otani et al. 2005). The membrane-proximal staining in the muscle fibre cross section may suggest nucleus-associated expres- sion due to the peripheral location of the nuclei in muscle fibres. Additional analyses using co-localization experiments with membrane-specific markers should help in determining the exact subcellular localization of these two proteins. Carnosine is transported across cellular membranes through proton-coupled oligopeptide transporters (POTs) such as PEPT1/SLC15A1, PEPT2/SLC15A2, PHT2/ SLC15A3 and PHT1/SLC15A4 (Kamal et  al. 2009; Oppermann et al. 2019) and, in addition to carnosine, the PHT2/SLC15A3 and PHT1/SLC15A4 transporters are also involved in the cellular uptake of histidine (Bhardwaj et al. 2006; Sakata et al. 2001). The PEPT1/SLC15A1 and PEPT2/SLC15A2 transporters were not included in the pre- sent study because of undetectable transcripts (SLC15A1) or very low transcript levels (SCL15A2) in mouse, human and pig skeletal muscles (Everaert et al. 2013; D’Astous-Pagé et al. 2017). Intracellular lysosomal localization has been reported for PHT1/SLC15A4 (Sasawatari et al. 2011) and PHT2/SLC15A3 (Sakata et al. 2001) proteins in a number of cell lines (HEK-293 T, BHK, COS-7 and RAW264.7). However, ectopic overexpression of PHT1/SLC15A4 and PHT2/SLC15A3 was conducted for all of these cell lines, which may not reflect the cellular localization found in vivo. In fact, the human PHT1/SLC15A4 protein was found in the plasma membrane of villous epithelial cells from the small intestine (Bhardwaj et al. 2006) and in the nuclei of nasal epithelial cells (Agu et al. 2011) and, to our knowledge, no one has yet reported the presence of PHT1/SLC15A4 and PHT2/SLC15A3 in the lysosomal compartment of human, mouse or pig skeletal muscle tissues. The only report of PHT1/SLC15A4 and PHT2/SLC15A3 protein localization in skeletal muscle comes from the Human Protein Atlas databank (www. prote inatl as. org), with cytoplasmic and membranous localization being observed in myocytes. In the present study, the strong PHT2/SLC15A3 and PHT1/ SLC15A4 signals observed at the periphery of red oxida- tive muscle fibres suggest implications for these proteins in the trans-sarcolemma transport of carnosine and histidine. http://www.proteinatlas.org http://www.proteinatlas.org http://www.proteinatlas.org 73Histochemistry and Cell Biology (2023) 160:63–77 1 3 The presence of a weak and more diffuse signal for PHT2/ SLC15A3 and PHT1/SLC15A4 in the cytosol of pig muscle fibres may also suggest intracellular membrane-bound local- ization. As previously reported for the rat PHT1/SLC15A4 and PHT2/SLC15A3 proteins (Sakata et  al. 2001), the presence of a di-leucine-based motif at the N-terminus of the porcine PHT2/SLC15A3 (GERRPLLA) and PHT1/ SLC15A4 (GERAPLLG) proteins may allow protein sorting to the endosomes and lysosomes. However, additional IHC experiments with lysosomal-specific markers are needed to elucidate the exact subcellular localization of the porcine PHT2/SLC15A3 and PHT1/SLC15A4 proteins in the cyto- solic compartment of muscle fibres. The addition of 10, 25 and 50 mM carnosine to cul- tured myoblasts led to a decline in cell number, as indi- cated by lower DNA content values (vs 0 mM carnosine) in the LD and RH muscles. A similar observation has been reported when using the 3-(4,5-dimethyl-thiazol-2-yl)-5-(3- carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay as a surrogate for porcine myoblast viability and, in both studies, this was accompanied by an increase in cell proliferation (at 10, 25 and 50 mM carnosine in the current study and at 10 and 25 mM carnosine in Palin et al. 2020). Seidel et al. (2022) recently reported that the effect of carnosine on cell viability differs between malignant and non-malignant cells, with a minor effect of carnosine in human fibroblasts and significant reduction of cell viabil- ity when carnosine is added to glioblastoma cell cultures. The anti-neoplastic effect of carnosine was also confirmed in gastric and colon cancer cells (Shen et al. 2014; Iovine et al. 2012). The similar reduction in cell viability found in cancer cells and satellite-derived myoblast cells (cur- rent study) when exposed to carnosine may be explained, at least in part, by common features shared by these two cell types. Indeed, satellite cells are considered as adult mus- cle stem cells that, just like cancer cells, have the capacity to proliferate and the potential to differentiate (Yin et al. 2013). The dose-dependent stimulation of myoblast prolif- eration with the addition of carnosine, while observing a concomitant decrease in cell viability/DNA content, may be caused by DNA repair mechanisms. Such compensatory DNA synthesis has already been described after the addi- tion of high concentrations of the phytoestrogens genistein (from 10 µM) and daidzein (100 µM) in porcine myoblasts (Mau et al. 2008b). Alternatively, proliferative growth of the remaining healthy myoblasts in the carnosine-supplemented cell culture may be an explanation. The addition of carno- sine may also increase the cellular lifespan as previously observed in human senescent myoblasts showing increased replicative potential after carnosine supplementation to the culture media (Maier et al 2012). The gene expression analyses of carnosine-related genes in cultured myoblasts treated with different concentrations of carnosine revealed a clear dose-dependent increase in SLC15A3 mRNA abundance in both muscles (LD and RH), whereas there was no carnosine effect on the SLC15A4 gene. The lack of effect of carnosine on SLC15A4 mRNA abundance was unexpected, since small interfering RNA (SiRNA)-mediated knockdown of both receptors (SLC15A3 and SLC15A4) was found to significantly reduce carnosine transport in human glioblastoma cells (Oppermann et al. 2019). On the other hand, oral supplementation of carno- sine to mice for 8 weeks reduced SLC15A3 mRNA expres- sion levels by 34% in the tibialis anterior muscle and had no effect on SLC15A4 mRNA abundance (Everaert et al. 2013). Discrepancies among studies may be explained by species (human, mice and pig) and/or tissue (glioblastoma, skeletal muscle) specific effects. Exposure time to carnos- ine may also affect the transporter transcriptional response, with a possible retro-control effect of carnosine on SLC15A3 mRNA abundance after 8 weeks of carnosine supplementa- tion (Everaert et al. 2013) and an upregulation of SLC15A3 transcript abundance in short-term experiments (48 h in current study) where carnosine levels would remain within the limits of cellular homeostasis. The above studies also suggest that SLC15A3 would be the main receptor involved in the trans-sarcolemma transport of carnosine in muscle cells, since SLC15A4 was unaffected by either long-term (Everaert et al. 2013) or short-term (current study) exposure to carnosine. A possible retro-control effect of carnosine on its own synthesis has been suggested in previous studies. This was first proposed by Everaert et al. (2013), who reported lower CARNS1 mRNA abundance in conditions of high muscle carnosine content and, on the contrary, higher CARNS1 gene expression with reduced carnosine content. A similar observation was made in the pig skeletal muscle, with lower CARNS1 mRNA abundance found in pigs having high mus- cle carnosine content (D’Astous-Pagé et al. 2017). However, this was only observed in the Duroc breed, which had the highest concentrations of muscle carnosine, and not in Lan- drace or Yorkshire pigs, which presented lower carnosine values. This has led to the hypothesis that a certain threshold of muscle carnosine must be reached before triggering a carnosine-inhibitory effect on CARNS1 transcription. Cur- rent results indicate that CARNS1 mRNA abundance is not affected by the addition of carnosine to cultured myoblasts isolated from LD or RH muscles. A similar observation was made in mice skeletal muscle, where oral supplementation of carnosine for 8 weeks increased muscle carnosine content by 48%, but had no effect on CARNS1 mRNA abundance (Everaert et al. 2013). However, an increase in CARNS1 mRNA abundance was observed (tendency) in the skeletal muscle when these mice were instead supplemented with β-alanine over the same period of time (Everaert et al. 2013). An increase in CARNS1 mRNA abundance was also reported 74 Histochemistry and Cell Biology (2023) 160:63–77 1 3 in skeletal muscle of broilers that were supplemented with β-alanine for 42 days (Qi et al. 2018). Together, these results suggest that carnosine synthase substrates such as β-alanine, but not its product carnosine, can modulate the abundance of CARNS1 transcript levels. Results from Barca et al. (2019) further suggest that the regulation of CARNS1 transcript abundance may vary according to the tissue analysed, since an increase in CARNS1 mRNA abundance was observed in the brain of mice supplemented with carnosine. Lastly, the absence of carnosine effect on CARNS1 mRNA abundance in cultured myoblasts could be because carnosine doses used in the current study were not high enough to cause a retro- control effect. The CNDP2 transcript is present in human, mouse and pig skeletal muscle, whereas that of the serum carnosinase CNDP1 is undetectable or barely detectable (D’Astous- Pagé et al. 2017). Although an overall effect of carnosine (tendency) is observed on CNDP2 mRNA abundance in cultured myoblasts isolated from the LD muscle only, the comparison of each carnosine dose to the control (0 mM carnosine) did not reach statistical significance. Very few studies have investigated the effect of carnosine on CNDP2 transcript abundance. In accordance with our findings, there was no significant change in CNDP2 mRNA abundance in the mouse brain after 2 weeks of carnosine supplementation (Barca et al. 2019). Intriguingly, mice supplemented with β-alanine for 8 weeks showed a 27% increase in CNDP2 mRNA levels in the skeletal muscle, while supplementation with carnosine resulted in a 39% decrease (Everaert et al. 2013). Although discrepancies among the abovementioned studies may be explained by species (mice vs pigs), tissue (skeletal muscle vs brain) and/or time (48 h, 2 weeks and 8 weeks) effects, the importance of CNDP2 in controlling intramuscular carnosine homeostasis remains to be demon- strated. According to Everaert et al. (2013), the ability of CNDP2 to hydrolyse carnosine in skeletal muscle would be quite limited due to its optimal activity being reached at pH 9.5 and the slow carnosine washout in skeletal muscle upon cessation of β-alanine supplementation (Baguet et al. 2009; Lenney et al. 1985). The lack of effect of carnosine on SLC6A6 and SLC36A1 mRNA abundance in cultured myoblasts from both muscles (LD and RH) was expected, as these two transporters are rather involved in β-alanine and histidine cellular uptake (Yamashita et al. 1997; Liu et al. 1992; Metzner et al. 2006). Oral supplementation of β-alanine for 8 weeks significantly increased the expression of SLC6A6 in mice skeletal muscle and had no effect on SLC36A1, thus suggesting a dominant role for SLC6A6 in the cellular uptake of β-alanine (Ever- aert et al. 2013). Surprisingly, a 21% increase in SLC6A6 mRNA abundance (tendency) was also observed in the skel- etal muscle of mice supplemented with carnosine (Everaert et al. 2013). Since PAT1/SLC6A6 has never been shown to be involved in carnosine transport, it can be hypothesized that the observed increase in its transcript abundance is related to an increase in cellular efflux of β-alanine and/or histidine in order to maintain carnosine homeostasis during long-term supplementation. We were unable to observe such an increase in SLC6A6 mRNA abundance in cultured myo- blasts, possibly due to the short-term exposure to carnosine (48 h) or its limited effect on carnosine cellular homeostasis in pig skeletal muscle. Conclusions The present study identifies for the first time the cellular localization of carnosine-related proteins in white glyco- lytic and red oxidative muscle fibres and presents a clear fibre type effect with higher mRNA abundance of CNDP2, SLC6A6, SLC15A3, SLC15A4 and SLC36A1 in red com- pared with white myofibres. Carnosine synthase mRNA abundance was not affected by either fibre type or the addi- tion of carnosine to myoblast culture, which serve as an in vitro model for metabolic fibre types, thus suggesting that its transcriptional regulation would not be the main process by which carnosine content differences are determined in oxidative and glycolytic muscles. The dose-dependent effect of carnosine on the mRNA abundance of SLC15A3 in myo- blasts and its higher expression in oxidative fibres suggest a role for this transporter in carnosine uptake and/or efflux in order to maintain cellular homeostasis. The unexpected increase in SLC6A6, SLC15A3, SLC15A4 and SLC36A1 transcripts (LCM) and proteins (IHC) in red oxidative fibres that present lower carnosine content further suggests that cellular efflux mechanisms should be considered as impor- tant points of regulation in controlling carnosine homeo- stasis. It is also important to mention that other alternative mechanisms, such as the enzymes involved in β-alanine synthesis (GADL1) or degradation (ABAT and AGXT2), may also affect carnosine homeostasis in the skeletal muscle (Mahootchi et al. 2020; Blancquaert et al. 2016), although this has not yet been demonstrated in pigs. Although the present study has allowed us to better understand fibre type- specific carnosine-related gene expression and protein local- ization, additional information is needed on the mechanisms controlling the synthesis and degradation, as well as the cel- lular uptake and release of carnosine, histidine and β-alanine in white and red muscle fibres. Supplementary Information The online version contains supplemen- tary material available at https:// doi. org/ 10. 1007/ s00418- 023- 02193-6. Acknowledgements The authors are grateful to S. Méthot for statisti- cal analyses, A. Berndt, K. Niemann, M. Jugert-Lund, B. Jentz and G. Bernatchez for technical assistance, and the staff of the Swine Complex https://doi.org/10.1007/s00418-023-02193-6 75Histochemistry and Cell Biology (2023) 160:63–77 1 3 at the Sherbrooke Research and Development Center and at the experi- mental pig unit of FBN Dummerstorf for care of the animals. Author contributions CK and MFP designed and conceptualized the research. Longissimus muscle samples used for the determination of carnosine-related genes and proteins originated from a prior experi- ment on carnosine in pigs designed and conceptualized by CG and MFP CK, KM and MFP conducted the experiments and acquired and analysed the data. CK and MFP wrote the first version of the manu- script. All authors critically revised the manuscript and approved the published version. Funding Open access funding provided by Agriculture & Agri-Food Canada. The present study was funded by Agriculture and Agri- Food Canada and by the Leibniz Institute of Farm Animal Biology (Zukunftsfonds). Data availability All data supporting the findings of this study are included in the published article. Additional information is available from the corresponding author upon reasonable request. Declarations Conflict of interest The authors declare that they have no conflicts of interest in relation to this paper. Ethical approval Animal husbandry and slaughter procedures were conducted according to the recommended guidelines of the Canadian Council on Animal Care (2009) and approved by the local animal care committee of the Sherbrooke Research and Development Centre (Sherbrooke, QC, Canada) and by the institutional Animal Protection Board of the Research Institute for Farm Animal Biology (FBN, Dum- merstorf, Germany). 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