Introduction

Meat is one of the most important sources of animal protein for humans, and its quality is associated with human health. Recently, due to the development of economic levels and the improvement of living standards, people are seeking for ‘less but better’ meat (Sahlin & Trewern, 2022). Intramuscular fat (IMF) deposition is a key factor positively related to meat quality traits and lipo-nutritional values of meat, such as flavor, tenderness, and juiciness(Hausman, Basu, Du, Fernyhough-Culver, & Dodson, 2014; W. Yi, Huang, Wang, & Shan, 2023). Besides, fat infiltration in skeletal muscle (also known as myosteatosis) is the pathologic fat accumulation in skeletal muscle with poor metabolic and musculoskeletal health, it always accompanied by the decline of muscle quality and function(Biltz et al., 2020; Jiang, Marriott, & Maly, 2019). Myosteatosis is now considered as a common feature of ageing and is also related to some diseases(Wang, Valencak, & Shan, 2024). However, the occurrence mechanism and cell sources of fat accumulation in skeletal muscle is very complicated. Recently, with the rapid development of multi-omics including single-cell RNA sequencing (scRNA-seq)(Tabula Muris et al., 2018), single-nucleus RNA-seq (snRNA-seq)(Petrany et al., 2020), and spatial transcriptomics (ST)(Jin et al., 2021), more and more cell types have been found to contribute to lipid deposition in skeletal muscle including myogenic cells (e.g., satellite cells (SCs)(Asakura, Komaki, & Rudnicki, 2001) and myogenic factor 5 (Myf5)⁺ mesenchymal stem cells (MSCs)(Yin et al., 2013)) and non-myogenic cells (e.g., fibro/adipogenic progenitors (FAPs)(Uezumi, Fukada, Yamamoto, Takeda, & Tsuchida, 2010), fibroblasts, myeloid-derived cells(Z. Xu et al., 2020), pericytes(Farrington-Rock et al., 2004), endothelial cells (ECs)(Lang et al., 2008), PW1⁺/Pax7^- interstitial cells (PICs)(Mitchell et al., 2010), and side population cells (SPs)(Tamaki et al., 2002)) based on animal models. Hence, more and more researches have been focusing on exploring the regulatory mechanism of myosteatosis at the cytological levels. Besides, fat infiltration in skeletal muscle is regulated by many influential triggers, including ageing, metabolic and nonmetabolic diseases, disuse and inactivity, and muscle injury(Wang et al., 2024). Many genes and signaling pathways participate in the formation and regulation of fat infiltration in skeletal muscle (Biferali et al., 2021; Wosczyna et al., 2021). However, the specific mechanism of nutrients regulates fat infiltration in muscle is still unknown.

Nutritional regulation strategy is one of the most vital strategies to regulate lipid accumulation in skeletal muscle based on some animal models and clinic trials, including vitamins(Gilsanz, Kremer, Mo, Wren, & Kremer, 2010; L. Zhao et al., 2020), conjugated linoleic acid (CLAs)(van Vliet, Fappi, Reeds, & Mittendorfer, 2020), linseed(Wei et al., 2016), plant extract(You et al., 2023), and so on. Hence, exploring the potential nutritional strategies to regulate fat accumulation in skeletal muscle is valuable for animal production and human health. Pigs are not only an important source of animal protein in the human diet but also serve as a valuable model for human medical biology due to their similar physiological structure in terms of size, metabolic characteristics, and cardiovascular system (Groenen et al., 2012; Lunney et al., 2021). Chinese local pig species could be used as excellent animal models to study the mechanism of lipid deposition due to they have better meat quality and high IMF content. There are different myogenesis potential in neonatal skeletal muscle between Laiwu pigs and Duroc pigs(D. D. Xu et al., 2023). Our previous study has revealed the cell heterogeneity and transcriptional dynamics of lipid deposition in skeletal muscle of Laiwu pigs(Wang, Zhao, et al., 2023). Heigai pig is a model of Chinese indigenous pig breeds, which has advantages including high farrowing rate, good pork quality, and strong disease resistance(Liyi Wang et al., 2022). Specially, we have found CLAs can improve IMF content both in lean type pig breeds and fat type pig breeds(Wang, Huang, Wang, & Shan, 2021; L. Wang et al., 2022). However, although many studies have discussed the effects of CLA on IMF deposition, there are still gaps in the cytological mechanism of CLAs in regulating lipid deposition in skeletal muscle.

Here, we present a snRNA-seq dataset collected from longissimus dorsi muscle (LDM) of Heigai pigs after feeding CLAs supplement to allow for analysing heterogeneity of transcriptional states in muscles. We investigated the regulatory effects of CLAs on the muscle fiber type transformation and IMF deposition. We also identified the differentiation trajectories of three subclusters in adipocytes based on Heigai pig models and high IMF content Laiwu pig models. Based on the pseudotemporal trajectories analysis, we found CLAs could promote FAPs differentiate into SCD⁺/DGAT2⁺ adipocytes via regulating mitogen-activated protein kinase (MAPK) signalling pathway. This study paves a way to regulate lipid accumulation in muscles by using nutritional strategies and provides theoretical basis on using pig as an animal model to study human muscle-related diseases.

Results

CLAs changed cell populations and transcriptional dynamics in LDM

Our previous study discovered CLAs improved IMF content in LDM of Heigai pigs(L. Wang et al., 2022), here, we also found CLAs significantly increased TG content but significantly decreased TC content in LDM of pigs (Figure. 1A). Meanwhile, immunofluorescence staining results showed more lipid droplets in the LDM of the CLAs group (Figure. 1B). To investigate the changes of cell heterogeneity in pig muscles after CLAs treatment at the cellular level, we performed snRNA-seq from LDM tissue of Heigai pigs using the 10× Genomics Chromium platform (Figure. 1C). First, after Cell Ranger analyses, the estimated number of cells, fraction of reads in cells, mean reads per cell, median genes per cell and median UMI counts per cell in LDM were showed in Supplementary Fig. S1a. We obtained 25507 cells from 2 individual libraries, comprising 10835 cells from CON group and 11705 cells from CLA group for the downstream analysis after the quality control of snRNA-seq data (Figure. S1B). Based on the Seurat package, we used Uniform Manifold Approximation and Projection (UMAP) plots to show the different subclusters (Figure. 1D). We identified 8 different clusters in two groups of pig muscles, including myofibers (CAPN3), FAPs/fibroblasts (PDGFRA), ECs (CD34), adipocytes (PPARG), immune cells (PTPRC), muscle satellite cells (MuSCs) (PAX7), myeloid derived cells (MRC1) and pericytes (RGS5) using the expression of marker genes (Figure. 1E). Next, the percentage of these cell types showed differences in different group (Figure. 1F). Compared with the CON group, the FAPs/fibroblasts (3.39% vs. 8.31%), ECs (1.26% vs. 2.94%), adipocytes (1.74% vs. 2.37%), myeloid derived cells (0.93% vs. 2.17%) and pericytes (0.45% vs. 0.7%) had a higher proportion in the CLA group. However, CLA decreased the proportion of myofibers (90.46% vs. 81.1%). The top 10 most differentially expressed genes (DEGs) were showed in the heatmap and the bar plot showed the top 3 KEGG enrichment of DEGs between the 8 different cell types in LDM (Figure. 1G). Besides, violin plots displayed CLAs upregulated the expression of mature adipocyte master genes including ADIPOQ, FABP4, PLIN1, and LIPE, adipogenic marker genes including PPARG, PPARA, CEBPA, and CEBPB, and lipid metabolism-related genes including LPL, ELOVL4, ACAA2 and HACD2 in pig muscles (Figures. S1C-E). These results indicated the cell types in LDM of Heigai pigs had significant differences after feeding CLAs which might induce the alterations in lipid deposition.

Figure. 1.

Characterization of myofibers after CLAs treatment through clustering analysis

To explore the changes of myofibers after CLA treatment, we next carried out a subcluster analysis and investigated the cell heterogeneity of myofibers. UMAP plots displayed the distribution in different subsets of myofibers (Figure. 2A). Based on our previous study(Wang, Zhao, et al., 2023) and different gene expression in myofibers, we also characterized 6 different cell types in myofibers, including I myofibers (MYH7), IIA myofibers (MYH2), IIX myofibers (MYH1), IIB myofibers (MYH4), myotendinous junctions (MTJ, ANKRD1), and neuromuscular junction (NMJ, ABLIM2) (Figure. 2B). The bar plot showed the proportion of type I myofibers (17.54% vs. 22.01%) and IIA myofibers (3.64% vs. 7.52%) had an increased tendency while the proportion of IIX myofibers (10.09% vs. 3.87%), IIB myofibers (63.88% vs. 59.35%), MTJ (6.41% vs. 0.28%) and NMJ (5.32% vs. 0.09%) had a reduced tendency in CLA group (Figure. 2C). Besides, violin plot displayed CLAs increased the expression of myofiber type marker genes (MYH7, MYH2, MYH1, and MYH4), myofiber type transformation-related genes (PPARGC1A, STK11, and HDAC1) and oxidation-related genes (COX5A, COX5B, and COX8A) but decreased glycolysis-related genes (PFKM, HK2, and LDHC) (Figure. 2D). Additionally, the expression of MYHCI and COX5B in LDM of Heigai pigs was also significantly increased after CLA treatment (Figure. 2E). The top 10 DEGs between the 6 cell types in myofibers were showed in heatmap (Figure. 2F). Functional enrichment analyses revealed the enrichment of metabolic pathways, oxidative phosphorylation, and thermogenesis in I myofibers and calcium, cGMP-PKG, and MAPK signalling pathway in IIB myofibers by using KEGG pathways (Figure. 2G). These data discovered the significantly heterogeneity in myofibers between two groups and CLAs could promote slow oxidative myofibers switch into fast glycolic myofibers in pig muscles.

Figure. 2.

Clustering and RNA velocity analysis revealed subpopulations and cellular dynamics of adipocytes after CLAs treatment

To investigate the regulatory mechanism of CLAs in IMF deposition, we next performed a subset analysis on adipocytes. Our previous study had discovered there are three subclusters in adipocytes nuclei of Laiwu pigs(Wang, Zhao, et al., 2023). In this study, we also characterized 3 subpopulations including SCD⁺/DGAT2⁺ adipocytes, FABP5⁺/SIAH1⁺ adipocytes, and PDE4D⁺/PDE7B⁺ adipocytes according to the most DEGs (Figures. 3A and S2A). Interestingly, we discovered CLAs increased the amounts of SCD⁺/DGAT2⁺ adipocytes (Figure. 3B) and the proportion of SCD⁺/DGAT2⁺ adipocytes (79.37% vs. 82.31%) but decreased the proportion of PDE4D⁺/PDE7B⁺ adipocytes (14.81% vs. 11.19%) (Figure. S2B). We also found CLAs increased the expression of SCD⁺/DGAT2⁺ adipocytes marker genes (SCD and ARHGAP31) and FABP5⁺/SIAH1⁺ adipocytes marker genes (SIAH1 and COX1) but decreased the expression of PDE4D⁺/PDE7B⁺ adipocytes marker genes (PDE4D) in adipocytes (Figure. 3C). Similarly, we also discovered SCD and DGAT2 expression was remarkably increased in LDM after feeding with CLAs (Figure. 3D). Meanwhile, immunofluorescence results showed more SCD1⁺ adipocytes in the LDM of the CLAs group (Figure. 3E). The top 10 most DEGs were displayed in the heatmap and the bar plot showed the top 3 KEGG enrichment of DEGs between the 3 subclusters in LDM (Figure. 3F). To explore the effects of CLAs on differentiated trajectory of adipocytes, we carried out the RNA velocity analysis of adipocytes (Figure. S2C). RNA velocity results showed the differentiated trajectory of mature adipocytes in muscles of Heigai pigs (Figure. 3G). Transcriptional dynamics of PDE4D and CAPN3 were showed in Figure. S2D based on RNA velocity analysis. These results indicated in mature adipocytes, PDE4D⁺/PDE7B⁺ adipocytes and FABP5⁺/SIAH1⁺ adipocytes could differentiate into SCD⁺/DGAT2⁺ adipocytes (Figure. 3H).

Figure. 3.

The verification of differentiated trajectories of adipocytes by using Laiwu pig models

To further verify the differentiated trajectory of adipocytes, we next carried out a pseudotemporal trajectory analysis and RNA velocity analysis of adipocytes by using our previous high IMF content pig models based on Monocle 2 and scVelo (Wang, Zhao, et al., 2023) (Figure. 4A). In adipocytes of Laiwu pigs, HLW group had the higher proportion of SCD⁺ /DGAT2⁺ adipocytes but the lower proportion of PDE4D⁺/PDE7B⁺ adipocytes (Figure. 4B). Meanwhile, immunofluorescence staining results also showed the more SCD1⁺ adipocytes in HLW group (Figure. 4C). The pseudotemporal trajectory and RNA velocity analysis verified that PDE4D⁺/PDE7B⁺ subclusters could differentiate in two different directions, SCD⁺/DGAT2⁺ and FABP5⁺/SIAH1⁺ subclusters with two bifurcations (Figures. 4D-F). The pseudotemporal heatmap showed gene expression dynamics including COX1, ANO4, PPARG, ADIPOQ, ACACA, and ELOVL6 at Point 2 (Figure. S3A). UMAP plots also showed transcriptional dynamics of marker genes such as FABP4, ADIPOQ, MYBPC1, and EYV4 (Figures. S3B-D). Also, we discovered the expression of preadipocytes related genes including PDGFRA, CD34, CD38, and WT1 was enriched in PDE4D⁺/PDE7B⁺ adipocytes and mature adipocytes related genes including FABP4, ADIPOQ, LIPE, PLIN1, PPARG, and AGT were enriched in SCD⁺/DGAT2⁺ and FABP5⁺/SIAH1⁺ adipocytes (Figure. 4G). Hence, the differentiated trajectory of mature adipocytes in muscles was displayed in Figure. 4H based on above results, which showed that PDE4D⁺/PDE7B⁺ adipocytes could differentiate into SCD⁺/DGAT2⁺ and FABP5⁺/SIAH1⁺ adipocytes, and FABP5⁺/SIAH1⁺ adipocytes also can differentiate into SCD⁺/DGAT2⁺ adipocytes. Additionally, the expression of SCD, DGAT2, FABP5, and SIAH1 was upregulated but PDE4D and PDE7B expression were downregulated in HLW group (Figure. 4I). These data indicated the differentiated trajectory of mature adipocytes in muscle of pigs and the percentage of SCD⁺/DGAT2⁺ and FABP5⁺/SIAH1⁺ subclusters was higher in HLW group.

Figure. 4.

Transcriptional dynamics of glycerophospholipid metabolism in high IMF deposition pigs

Our previous studies have discovered the changes of glycerophospholipid metabolism in muscles after CLA treatment(L. Wang et al., 2022) and in high IMF content Laiwu pigs(Wang, Zhao, et al., 2023). To further investigate the transcriptional dynamics of glycerophospholipid metabolism in high IMF deposition pigs, we then compare the gene program in Heigai pigs and Laiwu pigs. After CLA treatment, the snRNA-seq dataset the expression of genes involved in the glycerophospholipid metabolism in different groups and subclusters was displayed slight differences in (Figures. S4A-C). Also, in Laiwu pigs, there are differences in gene program involved in the glycerophospholipid metabolism between two groups (Figures. S4D-F). Interestingly, we found LCLAT1 was enriched in PDE4D⁺/PDE7B⁺ subcluster and AGPAT3 and AGPAT5 was enriched in SCD⁺/DGAT2⁺ subcluster (Figures. S5B and S5E). We also discovered the increase of diglycerides and phosphatidylinositols and the decrease of phosphatidic acids and phosphatidylethanolamines in high IMF deposition pigs might due to the changes of AGPAT3, AGPAT4, AGPAT5, CEPT1, and CDIPT1 (Figures. S5C and S5F). These data revealed the significant differences in lipid composition and distribution in LDM of high IMF deposition pigs might be due to the different expression levels of glycerophospholipid metabolism-related genes.

Cell-cell communication analysis showed the interaction between adipocytes and FAPs/fibroblasts

To further explore the association between adipocytes nuclei and other cell clusters, we applied cell-cell communication analysis by using CellPhoneDB on 8 cell types in muscles of Heigai pigs and found adipocytes mainly interacted with ECs, FAPs/fibroblasts, MuSCs, and pericytes (Figure. 5A). In addition, dot plot represented stronger communication from adipocytes to other subclusters through LRP6, FGFR1, and COL4A2 pathways in LDM of Heigai pigs (Figure. 5C). Next, we also applied cell-cell communication analysis by using CellPhoneDB on 9 cell types in muscles of Laiwu pigs and found adipocytes mainly interacted with SPs, FAPs/fibroblasts, ECs, and pericytes (Figure. 5B). Also, dot plot showed stronger communication from adipocytes to other subclusters through COL6A3, LAMC1, and THBS1 pathways in LDM of Laiwu pigs (Figure. 5D). These results suggested adipocytes has tight association with FAPs/fibroblasts.

Figure. 5.

Characterization of FAPs after CLAs treatment through clustering and pseudotime analysis

Previous studies have demonstrated that FAPs could differentiate into mature adipocytes and are the main cell sources of IMF cells(Joe et al., 2010; Uezumi et al., 2010). To further investigate the effects of CLAs on occurrence mechanism of IMF deposition, we then performed subcluster and pseudotemporal trajectory analysis on FAPs/fibroblasts. First, UMAP plots displayed the cell distribution in different subpopulations of FAPs/fibroblasts (Figure. 6A) and we identified 3 subpopulations in FAPs/fibroblasts based on the expression of marker genes, including FAPs (PDGFRA), Fibroblasts (COL1A1), and PDE4D⁺/PDE7B⁺ subclusters (PDE4D and PDE7B) (Figure. 6B). In CLA group, we found the proportion of FAPs (70.40% vs. 37.06%) and PDE4D⁺/PDE7B⁺ (4.11% vs. 2.18%) was higher than that in CON group but the proportion of in Fibroblasts (60. 76% vs. 25.49%) was lower (Figure. 6C). The top 10 most DEGs between the 3 subpopulations were showed in the heatmap and the bar plot displayed the significant enrichment of the signalling pathways in muscles by using KEGG enrichment analyses and we also found calcium and cGMP-PKG signalling pathway were enriched in PDE4D⁺/PDE7B⁺ subclusters (Figure. 6D). Besides, dot plot showed CLAs upregulated the expression of preadipocytes-related genes including CD38 and CD34, adipogenic master genes including ADIPOQ, FABP4, PLIN1, and LIPE, mature adipocyte marker genes including CEBPA, and lipid metabolism-related genes including LPL, ELOVL4, ACAA2 and HACD2 in FAPs/Fibroblasts (Figure. S5A). To further explore FAPs’ differentiated trajectory, we applied a pseudotemporal trajectory analysis and RNA velocity analysis of FAPs/Fibroblasts. According to the results, we found FAPs could differentiate into PDE4D⁺/PDE7B⁺ and Fibroblasts subpopulations (Figures. 6E and S5C). The pseudotemporal heatmap also displayed transcriptional dynamics including TIMP3 and THBS1 at Point 1 (Figure. 6F). UMAP plots also showed transcriptional dynamics of marker genes in three subpopulations such as ITGA5, HSPH1, and ETF1 (Figures. S5B-E). To further identify the differentiated trajectory of IMF cells, we isolated primary FAPs from pigs and found the expression of FABP4, ADIPOQ, SCD, and DGAT2 was significantly increased but PDE4D expression was significantly downregulated during adipogenic differentiation in vitro (Figure. 6G). Besides, the expression of FABP5 and SIAH1 was first significantly increased then significantly decreased during adipogenic differentiation (Figure. 6G). Hence, FAPs may first differentiate into PDE4D⁺/PDE7B⁺ preadipocytes and then differentiate into PDE4D⁺/PDE7B⁺ adipocytes (Figure. 6H). These results displayed the differentiated trajectory of preadipocytes into mature adipocytes in pig muscles and CLAs might influence this process then affect IMF deposition.

Figure. 6.

CLAs promoted FAPs directed differentiation into SCD⁺/DGAT2⁺ subclusters

To further explore the cytological mechanism of CLAs regulating IMF deposition, we next investigated the regulatory effects of CLAs on the differentiation trajectory of FAPs differentiate into adipocytes. First, to explore the role of CLAs in the adipogenic differentiation of FAPs, we isolated primary FAPs from piglets and induced these adipogenic differentiation. Nile Red staining and OD490 results revealed CLAs can promote the adipogenic differentiation of FAPs after adipogenic differentiation for 8 days in vitro (Figures. 7A-B). Besides, the mRNA expression of SCD, SIAH1 and adipogenic genes, including FABP4, PPARG, and FASN were significantly upregulated but PDE4D was significantly downregulated (Figure. 7C). The protein levels of FABP4 and SCD1 were significantly upregulated and PDE4D were significantly downregulated (Figure. 7D). In addition, the marker genes’ expression at key points of adipogenic differentiation such as ADIPOQ, ELOVL6, ACACA, ARBB1, NEB, and MYBPC1 were significantly upregulated and THBS1 and TIMP3 were significantly downregulated (Figure. S6A). Interestingly, we next found MAPK signaling pathway were enriched in adipocytes nuclei especially SCD⁺/DGAT2⁺ subcluster (Figure. 7E). The expression of MAPK signaling pathway including ERK, c-Jun N-terminal kinase (JNK), and p38 signaling pathway related genes were changed in muscle nuclei (Figures. 7F and S6B-C). Furthermore, we observed that the protein levels of JNK phosphorylation were significantly decreased after CLA treatment during FAPs adipogenic differentiation (Figure. 7G). Hence, we next used JNK activator Anisomysin to explore the regulatory mechanism (Figure. 7H). Oil Red O staining result showed that after 24h 20 nM Anisomysin treatment, the increased adipogenic differentiation of FAPs by CLA were significantly inhibited (Figure. 7I). Also, CLA + Anisomysin group had the lower OD 490 value compared with CLA group (Figure. 7J). Nile Red staining result also showed that Anisomysin significantly inhibited the enhanced lipid droplets in FAPs after CLA treatment (Figure. 7K). MAP2K4 expression significantly upregulated and the expression of FABP4 and SCD significantly decrease after Anisomysin treatment (Figure. 7L). These data indicated that CLAs may promote the directed differentiation of FAPs into SCD⁺/DGAT2⁺ subclusters via inhibiting JNK signaling pathway.

Figure. 7.

Discussion

CLAs can serve as a nutritional intervention to regulate lipid deposition in skeletal muscle of human according to clinic trials(van Vliet et al., 2020). In animal production, CLAs could regulate meat quality in pigs and cattle, especially improve IMF content (L. Wang et al., 2022; Zhang et al., 2016). These studies pointed out that the CLAs plays a vital role in regulating fat infiltration in skeletal muscle. However, to date, the cellular mechanism of CLAs regulates lipid deposition has not been studied. Here, we utilized the 10x Genomics platform to identify the cell heterogeneity and transcriptional changes in muscles after CLAs treatment based on pig models. This study revealed the effects of CLAs on cell populations and molecular characteristics of muscles and highlighted the cytological mechanism of CLAs regulates pork quality in skeletal muscle.

CLAs is always found in ruminant animals and dairy products, it is a class of positional and geometric isomers of linoleic acids with a conjugated double bond. CLAs not only has anti-cancer, anti-hypertension, anti-adipogenic, and anti-diabetic effects, but also can improve muscle function and decrease body fat percentage. For example, adding 3.2 g/day CLAs significantly increased muscle mass in higher body fat percentage Chinese adults (Chang et al., 2020). After 0.9 g/day CLAs supplementation, body weight variation and muscle mass significantly increased and body fat percentage variation decreased in student athletes (Terasawa, Okamoto, Nakada, & Masuda, 2017). LC-MS metabolomics results discovered CLAs changed 57 metabolites which enriched in lipids/lipid-like molecules in plasma of humans (He et al., 2022). However, another study found that for sedentary older adults, CLAs had no significant influence on muscle anabolic effects (van Vliet et al., 2020). Therefore, the specific influences of CLAs on skeletal muscle is still disputed and the function on lipid deposition in human skeletal muscle needs further investigation. In animal models, many studies have demonstrated the important effects of CLAs on regulating fat accumulation in skeletal muscles. In porcine models, our foregoing studies have discovered that adding CLAs into the pig diet could significantly increase IMF contents in LDM of lean pig breeds and Heigai pigs(Wang et al., 2021; L. Wang et al., 2022). Zhang et al (Zhang et al., 2016)found 2% dietary CLAs significantly increased IMF deposition and reduced subcutaneous fat deposition in cattle. However, in mouse model, 0.5% mixed isomer CLAs did not lead to lipid accumulation in muscle of mice(M, S, & M, 2013). Hence, CLAs supplementation positively affect IMF deposition in muscles of pigs and ruminants but the effects of CLAs may have species-specific. In our study, we found CLAs improved TG content and increased the percentage of adipocytes nuclei in LDM. Previous study demonstrated there are three subclusters in adipocytes and the formation and deposition of IMF mainly relied on DGAT2⁺/SCD⁺ adipocytes and FABP5⁺/SIAH1⁺ adipocytes(Wang, Zhao, et al., 2023). Specially, we found CLAs enhanced the percentage of SCD⁺/DGAT2⁺ subclusters. These indicated CLAs improve IMF deposition might through increasing SCD⁺/DGAT2⁺subpopulations of adipocytes. However, the specific function of CLAs on fat infiltration and deposition of skeletal muscle in people and rodents needs further study.

Skeletal muscle contains slow and fast muscle fibers and there are four major muscle fiber types in mice, including slow muscle fibers with type I muscle fibers (Myh7), fast muscle fibers with type IIA muscle fibers (Myh2), type IIX muscle fibers (Myh1), and type IIB muscle fibers (Myh4)(Dos Santos et al., 2020; Petrany et al., 2020). In pigs, illustrated there are three myofiber composition including type I, type IIA, and type IIB in skeletal muscles by ST technology(Jin et al., 2021). In this study, we identified six different subpopulations in myofibers including I myofibers, IIA myofibers, IIX myofibers, IIB myofibers, MTJ, and NMJ and IIB myofibers had the highest percentage in pig muscles. Besides, slow muscle fibers always called slow-twitch oxidative muscle fibers like I myofibers have higher activities in mitochondrial oxidative metabolic enzymes and myoglobin while fast muscle fibers always called fast-twitch glycolytic muscle fibers like II myofibers have higher levels of glycolytic enzymes and glycogen (Schiaffino & Reggiani, 2011). Similarly, we also found I myofibers enriched in metabolic pathways, oxidative phosphorylation, and thermogenesis. In recent years, studies have focused on exploring the influences of CLAs on regulating muscle fiber type. In commercial pigs, the MyHC I mRNA abundance were improved in LDM of the CLAs group (Men, Deng, Xu, Tao, & Qi, 2013). In mice, t10, c12-CLAs, but not c9, t11-CLAs can increase oxidative skeletal muscle fiber type in gastrocnemius muscle and C2C12 myoblasts (Duan et al., 2021). CLAs have been found to prevent sarcopenia by maintaining redox balance during aging, actively regulating mitochondrial adaptation, improve muscle metabolism, and inducing hypertrophy of type IIX myofibers after endurance exercise(Barone et al., 2017; Chen, Yang, & Park, 2018). Also, we discovered CLAs enhanced the percentage of I and IIA myofibers but reduced the percentage of IIB myofibers. Previous study has found PPARγ coactivator-1α (PGC1α) serves a valuable role in skeletal muscle metabolism and is a master regulator of oxidative phosphorylation genes and could regulate muscle fiber type transformation(Handschin & Spiegelman, 2011). In our study, the PGC1α expression was also increased after CLA treatment in myofiber. These results suggested CLAs can promote glycolytic skeletal muscle fiber types switching into oxidative skeletal muscle fiber types through upregulating PGC1α expression.

Numerous studies have discovered that the cell sources of IMF cells and found several cell subsets lead to the ectopic IMF formation and deposition including SCs, Myf5⁺ MSCs, FAPs, ECs, pericytes, Fibroblasts, myeloid-derived cells, SPs, and PICs (Sciorati, Clementi, Manfredi, & Rovere-Querini, 2015; Z. Xu et al., 2020). In this study, we found CLAs increased the percentage of preadipocytes such as FAPs, ECs, myeloid-derived cells, and pericytes. Importantly, FAPs are the major source of IMF cells(Joe et al., 2010; Uezumi et al., 2010) and our previous study also verified the adipogenic capacity of FAPs in 2D and 3D culture models(Wang, Zhao, et al., 2023). Xu et al. found that FAPs serve as a cellular interaction hub in skeletal muscle of pigs(D. D. Xu et al., 2023). We used pseudotemporal trajectory and RNA velocity analysis combined with in vitro study to investigate that FAPs could first differentiate into PDE4D⁺/PDE7B⁺ adipocytes and then differentiate into DGAT2⁺/ SCD⁺ and FABP5⁺/SIAH1⁺ adipocytes. However, the regulatory mechanism of FAPs directional differentiation still needs to be further explored. In vitro studies demonstrated trans-10, cis-12 CLAs inhibited skeletal muscle differentiation in C2C12 cells and inhibited 3T3-L1 adipocyte adipogenesis (Hommelberg et al., 2010; Yeganeh, Taylor, Poole, Tworek, & Zahradka, 2016). However, the influences of CLAs on regulating the adipogenic differentiation of FAPs are still unclear. In this study, we found CLAs facilitated FAPs differentiating into SCD⁺/DGAT2⁺ adipocytes. Previous studies have found mice orally treated with CLAs mixture upregulated Scd1 expression in muscle(Parra, Serra, & Palou, 2012). Besides, SCD1 expression is modulated by mTOR signaling pathway in cancer cells(J. M. Yi, Zhu, Wu, Thompson, & Jiang, 2020; S. H. Zhao et al., 2021). Moreover, MAPK signaling pathway were enriched in adipogenic differentiation of FAPs after CLAs treatment. Previous studies have discovered JNK had negative effects on regulating the adipogenic differentiation of human mesenchymal stem cells(Jang et al., 2015) and FAPs could prevent skeletal muscle regeneration after muscle injury by ST2/JNK signaling pathways(Yamakawa et al., 2023). In this study, we found CLAs may promote FAPs directed differentiation into SCD⁺/DGAT2⁺ adipocytes via inhibiting JNK signaling pathway. However, the downstream transcriptional regulators need further discovery.

In a word, we provide detailed insights into the cytological mechanism of CLAs regulates fat infiltration in skeletal muscles based on pig models via using snRNA-seq. We analysed the effects of CLAs on the cell heterogeneity and transcriptional dynamics in pig muscles and discovered CLAs could promote glycolytic muscle fiber types switching into oxidative muscle fiber types through regulating PGC1α. We also identified the differentiation trajectories of adipocytes and FAPs. Our data also demonstrated CLAs could promote FAPs differentiate into DGAT2⁺/SCD⁺ adipocytes via inhibiting JNK signalling pathway. This study provides a new way of developing nutritional strategies to combat myosteatosis and other muscle-related diseases and also offers potential opportunities to promote the utilization of pigs as animal models to study human diseases.

Materials and methods

Animals and samples

The Zhejiang University Animal Care and Use Committee approved all procedures and housing (ZJU20170466). 56 Heigai pigs (average body weight: 85.58 ± 10.39 kg) were divided randomly into CON group (added 1% soyabean oil) and CLA group (added 1% CLAs) and the nutritional levels and the feeding process as we previously reported(L. Wang et al., 2022; Wang, Zhang, Huang, Zhou, & Shan, 2023). At the end of experiment, we collected LDM from the right side of the carcass for subsequent immunofluorescence staining, biochemical assay, and snRNA-seq analyses.

Triglycerides (TG) and total cholesterol (TC) determination

The contents of TG and TC in LDM were determined by commercial kits (TG, E1025-105; TC, E1015-50) bought from Beijing APPLYGEN Gene Technology Co., LTD.

Immunofluorescence staining

The paraffin section was dewaxed and immersed in pre-heated sodium citrate, then placed in a microwave oven and heated for 15 min to perform antigen retrieval. Fixed the sections that cooled to room temperature in 4% paraformaldehyde for 10 min, followed by 10 min permeated with 0.5% Triton-X100and 1 h blocked with blocking buffer (5% goat serum and 2% BSA). Sections were then incubated overnight at 4 °C with Perilipin (Abcam, ab16667, 1:500), MF20 (Developmental Studies Hybridoma Bank, 1:50), and SCD1 (HuaBio, ER1916-26, 1:500) primary antibodies. Then the primary antibody was discarded and the sections were washed three times with PBS for 5 min each time. Incubated the sections with secondary antibodies for 1h and DAPI for 5 min, then washed with PBS. Sealed cell with glycerol and used fluorescent microscope to capture images.

LDM nuclei isolation and 10X Genomics Chromium library and sequencing

LDM nuclei isolation and 10X Genomics Chromium library and sequencing were performed by LC-Bio Technology Co., Ltd. (Hangzhou, China) as previous published paper(Wang, Zhao, et al., 2023). Briefly, nuclei of LDM samples were isolated, then homogenized and incubated for 5 min on ice. The homogenate was then filtered, centrifuged and collected. The pellet was then resuspended, washed by the buffer, incubated and centrifuged. After centrifugation, the pellet was resuspended, filtered, and counted. Single-cell suspensions were loaded onto 10X Genomics Chromium for capturing 5000 single cells, followed by cDNA amplification and library construction steps were performed. Libraries were sequenced using the Illumina NovaSeq 6000 sequencing system.

Bioinformatics analysis

SnRNA-seq results were demultiplexed and converted to FASTQ format by using Illumina bcl2fastq software and followingly processed by the Cell Ranger. Then, the Seurat packages was used to analysis the cell Ranger output. After the quality control, 22540 cells were obtained. DoubletFinder package was used to remove doublets and Harmony package was used to performed batch correction of data integration between samples. We further used Seurat, UMAP, the FindAllMarkers function to visualize the data, find clusters, and select marker genes. Monocle 2 package was used to perform trajectory analysis and model differentiation trajectories. RNA velocity analysis was independently performed in FAPs by SAMTools and the Velocyto (Bergen, Lange, Peidli, Wolf, & Theis, 2020). CellPhoneDB package was used to cell communication analysis and make further speculations about potential cellular interaction mechanisms.

Primary FAPs isolation, magnetic cell sorting and cell culture

Primary FAPs isolation were performed as previously described (Wang, Zhao, et al., 2023). Briefly, a piece of muscle from a 3-day-old piglet was minced, and added 5 times the volume of 0.2% collagenase type I, then digested at 37 °C for 1 hour., After filtering and centrifuging, adding red blood cell lysate to split for 5 min at 4 °C followed by incubated with a Dead Cell Removal Kit at room temperature for 15 min. Then adding CD140a antibody, incubating and centrifugating. Next, added 20 μL antibiotin microbeads, incubation and centrifugation. After passing through the magnetic column, the cells on the adsorption column were PDGFRα⁺ cells. For FAPs adipogenic differentiation, when the cells confluence reached 90%, the10% FBS growth medium was replaced with induction medium after 4 days, the medium was changed to differentiation mediumand cultured for another 4 days until the adipocytes were mature.

Nile Red staining

Rinse cultured FAPs with 1 x PBS 3 times, discard PBS, fix FAPs with 4% formaldehyde for 15 min, repeat the rinsing step, and then add Nile Red solution (1:500 for lipid droplet staining) and DAPI (1:500 for nuclei staining) for 5 min. Sealed cell with glycerol and used fluorescent microscope to capture images.

Total RNA extraction and quantitative real-time PCR (qPCR)

Total RNA extraction and qPCR were conducted as described before (Shan et al., 2016). Briefly, total RNA of FAPs were extracted by using TRIzol and the Spectrophotometer and a ReverAid First Strand cDNA Synthesis Kit were used to measure the purity and concentration of total RNA and reversed RNA samples. qPCR was performed by using Applied Biosystems StepOnePlus Real-Time PCR System with Hieff qPCR SYBR® Green Master Mix and gene-specific primers (Supplementary Table 1). Relative changes in gene expression were analysed using the 2^-ΔΔCT method and normalized using 18S ribosomal RNA as an internal control.

Protein extraction and western blotting

Protein extraction and western blotting were carried out as mentioned previously (Shan et al., 2016). In brief, total proteins were isolated from cells or tissues with RIPA buffer. After measuring the concentrations, proteins were separated using SDS-PAGE and subsequently transferred to a polyvinylidene fluoride membrane (PVDF, Millipore Corporation). Then blocked PVDF membrane with blocking buffer (5% fat-free milk) for 1 h and incubated with primary antibodies overnight at 4 °C. The peroxisome proliferator-activated receptorγ (PPARγ) (C26H12, 1:1000) were purchased from Cell Signaling Technology (CST). The β-actin (M1210-2, 1:10000), FABP4 (E71703-98, 1:2000), SCD1 (ER1916-26, 1:1000), PDE4D (ER1916-26, 1:500), p-JNK1/2/3(T183+T183+T221) (ET1609-42, 1:2000), and JNK1/2/3 (ET1601-28, 1:2000) antibody were from HuaBio. Dilution of the secondary antibody was 500-fold. The ChemiScope3500 Mini-System was used for protein detected.

Statistical analysis

GraphPad (Prism 8.3.0) was used for data analyses and R software (version 4.3.2) was used for data visualization. Data comparisons were made by unpaired two-tailed Student’s t tests and one-way ANOVA analysis. Differences were considered significant at P < 0.05.

Author contribution

Liyi Wang: conceptualization, data curation, formal analysis, investigation, methodology, software, validation, visualization, writing-original draft. Shiqi Liu: investigation, methodology, writing-review & editing. Shu Zhang: investigation. Yizhen Wang: resources, supervision. Yanbing Zhou: conceptualization, investigation, methodology, supervision. Tizhong Shan: conceptualization, funding acquisition, project administration, resources, supervision, writing-review & editing.

Acknowledgements

We thank members of the Shan Laboratory for comments and this work was partially supported by the National Natural Science Foundation of China (32272887), the Natural Science Foundation of Zhejiang Province (LZ22C170003), and the “Hundred Talents Program” funding from Zhejiang University to TZS.

Data availability

Data will be made available on reasonable request.

Conflict of interest

The authors declare no conflict of interest with the contents of this article.