Myotube formation is affected by adipogenic lineage cells in a cell-to-Cell contact-independent manner
Abstract
Intramuscular adipose tissue (IMAT) formation is observed in some pathological conditions such as Duchenne muscular dystrophy (DMD) and sarcopenia. Several studies have suggested that IMAT formation is not only negatively correlated with skeletal muscle mass but also causes decreased muscle contraction in sarcopenia. In the present study, we examined w hether adipocytes affect myogenesis. For this purpose, skeletal muscle progenitor cells were transfected with siRNA of PPARγ (siPPARγ) in an attempt to inhibit adipogenesis. Myosin heavy chain (MHC)-positive myotube formation was promoted in cells transfected with siPPARγ compared to that of cells transfected with control siRNA. To determine whether direct cell-to-cell contact between adipocytes and myoblasts is a prerequisite for adipocytes to affect myogenesis, skeletal muscle progenitor cells were cocultured with pre- or mature adipocytes in a Transwell coculture system. MHC-positive myotube formation was inhibited when skeletal muscle progenitor cells were cocultured with mature adipocytes, but was promoted when they were cocultured with preadipocytes. Similar effects were observed when pre- or mature adipocyte-conditioned medium was used. These results indicate that preadipocytes play an important role in maintaining skeletal muscle mass by promoting myogenesis; once differentiated, the resulting mature adipocytes negatively affect myogenesis, leading to the muscle deterioration observed in skeletal muscle pathologies.
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In-vitro studies showed that the coculture of mature adipocytes and skeletal muscle progenitor cells led to a reduction of nuclei number in myosin heavy chain (MHC)-positive myotubes.
“In-vitro studies showed that the coculture of mature adipocytes and skeletal muscle progenitor cells led to a reduction of nuclei number in myosin heavy chain (MHC)-positive myotubes (29).”
From The role of obesity in sarcopenia and the optimal body composition to prevent against sarcopenia and obesity (2023) · cites this paper as [29]
Cites
SATELLITE CELL OF SKELETAL MUSCLE FIBERS
Mauro, A. (1961) · The Journal of Cell Biology · doi:10.1083/jcb.9.2.493 · Cited by 3,683 · see citing works
Cellular and Molecular Regulation of Muscle Regeneration
CHARGÉ, S. B. P., & Rudnicki, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00019.2003 · Cited by 2,691 · see citing works
Satellite Cells and the Muscle Stem Cell Niche
Yin, H., Price, F., & Rudnicki, M. A. (2013) · Physiological Reviews · doi:10.1152/physrev.00043.2011 · Cited by 2,166 · see citing works
What is the cause of the ageing atrophy?
Lexell, J. E., Taylor, C. C., & Sjöstróm, M. (1988) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(88)90132-3 · Cited by 2,080 · see citing works
Dystrophin expression in the mdx mouse restored by stem cell transplantation
Gussoni, E., Soneoka, Y., Strickland, C. D., Buzney, E. A., Khan, M. K., Flint, A., Kunkel, L. M., & Mulligan, R. C. (1999) · Nature · doi:10.1038/43919 · Cited by 1,800 · see citing works
MyoD or Myf-5 is required for the formation of skeletal muscle
Rudnicki, M. A., Schnegelsberg, P. N. J., Stead, R. H., Braun, T. W., Arnold, H.-H., & Jaenisch, R. (1993) · Cell · doi:10.1016/0092-8674(93)90621-v · Cited by 1,731 · see citing works
Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis
Joe, A. W. B., Yi, L., Natarajan, A., Le Grand, F., So, L., Wang, J., Rudnicki, M. A., & Rossi, F. M. V. (2010) · Nature Cell Biology · doi:10.1038/ncb2015 · Cited by 1,690 · see citing works
CCAAT/enhancer-binding proteins: structure, function and regulation
Ramji, D. P., & Foka, P. (2002) · Biochemical Journal · doi:10.1042/bj20020508 · Cited by 1,401 · see citing works
Uezumi, A., Fukada, S., Yamamoto, N., Takeda, S., & Tsuchida, K. (2010) · Nature Cell Biology · doi:10.1038/ncb2014 · Cited by 1,315 · see citing works
Myogenin, a factor regulating myogenesis, has a domain homologous to MyoD
Wright, W. E., Sassoon, D. A., & Lin, V. K. (1989) · Cell · doi:10.1016/0092-8674(89)90583-7 · Cited by 1,309 · see citing works
Visser, M., Pahor, M., Taaffe, D. R., Goodpaster, B. H., Simonsick, E. M., Newman, A. B., Nevitt, M., & Harris, T. B. (2002) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/57.5.m326 · Cited by 1,294 · see citing works
McDonald, C. M., Abresch, R. T., Carter, G. T., Fowler, W. M., Johnson, E. R., Kilmer, D. D., & Sigford, B. J. (1995) · American Journal of Physical Medicine & Rehabilitation · doi:10.1097/00002060-199509001-00003 · Cited by 1,070 · see citing works
Fibrosis and adipogenesis originate from a common mesenchymal progenitor in skeletal muscle
Uezumi, A., Ito, T., Morikawa, D., Shimizu, N., Yoneda, T., Segawa, M., Yamaguchi, M., Ogawa, R., Matev, M. M., Miyagoe-Suzuki, Y., et al. (2011) · Journal of Cell Science · doi:10.1242/jcs.086629 · Cited by 680 · see citing works
Insulin Resistance in Morbid Obesity
Greco, A. V., Mingrone, G., Giancaterini, A., Manco, M., Morroni, M., Cinti, S., Granzotto, M., Vettor, R., Camastra, S., & Ferrannini, E. (2002) · Diabetes · doi:10.2337/diabetes.51.1.144 · Cited by 442 · see citing works
Sarcopenia and increased adipose tissue infiltration of muscle in elderly African American women
Song, M.-Y., Ruts, E., Kim, J., Janumala, I., Heymsfield, S., & Gallagher, D. (2004) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/79.5.874 · Cited by 324 · see citing works
The Potential of Muscle Stem Cells
Seale, P., Asakura, A., & Rudnicki, M. A. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00049-1 · Cited by 258 · see citing works
Adipose tissue distribution is different in type 2 diabetes
Gallagher, D., Kelley, D. E., Yim, J., Spence, N., Albu, J., Boxt, L. M., Pi‐Sunyer, F. X., & Heshka, S. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2008.26955 · Cited by 201 · see citing works
Ervinna, N., Mita, T., Yasunari, E., Azuma, K., Tanaka, R., Fujimura, S., Sukmawati, D., Nomiyama, T., Kanazawa, A., Kawamori, R., et al. (2013) · Endocrinology · doi:10.1210/en.2012-1855 · Cited by 167 · see citing works
Compositional analysis of muscle in boys with Duchenne muscular dystrophy using MR imaging
Marden, F. A., Connolly, A. M., Siegel, M. J., & Rubin, D. A. (2004) · Skeletal Radiology · doi:10.1007/s00256-004-0825-3 · Cited by 145 · see citing works
Two Patterns of Adipokine and Other Biomarker Dynamics in a Long-Term Weight Loss Intervention
Blüher, M., Rudich, A., Klöting, N., Golan, R., Henkin, Y., Rubin, E., Schwarzfuchs, D., Gepner, Y., Stampfer, M. J., Fiedler, M., et al. (2011) · Diabetes Care · doi:10.2337/dc11-1267 · Cited by 135 · see citing works
Functional heterogeneity of side population cells in skeletal muscle
Uezumi, A., Ojima, K., Fukada, S., Ikemoto‐Uezumi, M., Masuda, S., Miyagoe‐Suzuki, Y., & Takeda, S. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.01.037 · Cited by 122 · see citing works
Origins and early descriptions of “Duchenne muscular dystrophy”
Tyler, K. L. (2003) · Muscle & Nerve · doi:10.1002/mus.10435 · Cited by 102 · see citing works
Osteogenic Differentiation Capacity of Human Skeletal Muscle-Derived Progenitor Cells
Oishi, T., Uezumi, A., Kanaji, A., Yamamoto, N., Yamaguchi, A., Yamada, H., & Tsuchida, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056641 · Cited by 89 · see citing works
Machida, S., & Booth, F. W. (2004) · Experimental Gerontology · doi:10.1016/j.exger.2004.08.009 · Cited by 87 · see citing works
Motohashi, N., Uezumi, A., Yada, E., Fukada, S., Fukushima, K., Imaizumi, K., Miyagoe‐Suzuki, Y., & Takeda, S. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.070902 · Cited by 86 · see citing works
Denervation Hypertrophy of Muscle
Petersilge, C. A., Pathria, M. N., Gentili, A., Recht, M. P., & RESNICK, D. L. (1995) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199507000-00017 · Cited by 82 · see citing works
Yang, H., Li, F., Kong, X., Yuan, X., Wang, W., Huang, R., Li, T., Geng, M., Wu, G., & Yin, Y. (2012) · Cytokine · doi:10.1016/j.cyto.2012.07.033 · Cited by 56 · see citing works
Phalitakul, S., Okada, M., Hara, Y., & Yamawaki, H. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.06.052 · Cited by 50 · see citing works
The MRF4 Activation Domain Is Required To Induce Muscle-Specific Gene Expression
Mak, K.-L., To, R. Q., Kong, Y., & Konieczny, S. F. (1992) · Molecular and Cellular Biology · doi:10.1128/mcb.12.10.4334 · Cited by 48 · see citing works
Myostatin regulates preadipocyte differentiation and lipid metabolism of adipocyte via ERK1/2
Li, F., Yang, H., Duan, Y., & Yin, Y. (2011) · Cell Biology International · doi:10.1042/cbi20110112 · Cited by 47 · see citing works
Nakamura, S. K., Nakano, S., Miyoshi, T., Yamanouchi, K., Matsuwaki, T., & Nishihara, M. (2012) · Aging · doi:10.18632/aging.100426 · Cited by 44 · see citing works
Self-citationTherapeutic Strategies for Duchenne and Becker Dystrophies
Voisin, V., & de la Porte, S. (2004) · International review of cytology · doi:10.1016/s0074-7696(04)40001-1 · Cited by 32 · see citing works
Increased adipogenicity of cells from regenerating skeletal muscle
Yamanouchi, K., Yada, E., Ishiguro, N., Hosoyama, T., & Nishihara, M. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.04.014 · Cited by 28 · see citing works
Self-citation18α-Glycyrrhetinic Acid Induces Phenotypic Changes of Skeletal Muscle Cells to Enter Adipogenesis
Yamanouchi, K., Yada, E., Ishiguro, N., & Nishihara, M. (2007) · Cellular Physiology and Biochemistry · doi:10.1159/000110438 · Cited by 27 · see citing works
Self-citationYang, H., Li, F., Kong, X., Yuan, X., Lian, G., Geng, M., Li, T., Yin, J., & Yin, Y. (2011) · Molecular Biology Reports · doi:10.1007/s11033-011-0934-8 · Cited by 20 · see citing works
Fibrous-adipose replacement in skeletal muscle biopsy
Mora, M. (1989) · European Heart Journal · doi:10.1093/eurheartj/10.suppl_d.103 · Cited by 18 · see citing works
Wang, S., Liang, C., Wu, J., Huang, J.-J., Chien, H., Tsai, J., Yen, Y.-S., Tseng, Y.-C., Lue, J., & Chen, Y. (2011) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2011.10.023 · Cited by 17 · see citing works
Establishment of bipotent progenitor cell clone from rat skeletal muscle
MURAKAMI, Y., Yada, E., Nakano, S., Miyagoe‐Suzuki, Y., Hosoyama, T., Matsuwaki, T., Yamanouchi, K., & Nishihara, M. (2011) · Animal Science Journal · doi:10.1111/j.1740-0929.2011.00907.x · Cited by 10 · see citing works
Self-citationEx vivo bupivacaine treatment results in increased adipogenesis of skeletal muscle cells in the rat
Yamanouchi, K., Nakamura, K., Takegahara, Y., Nakano, S., & Nishihara, M. (2013) · Animal Science Journal · doi:10.1111/asj.12112 · Cited by 6 · see citing works
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Infiltration of intramuscular adipose tissue impairs skeletal muscle contraction
Biltz, N. K., Collins, K. H., Shen, K. C., Schwartz, K., Harris, C. A., & Meyer, G. A. (2020) · The Journal of Physiology · doi:10.1113/jp279595 · Cited by 214 · see citing works
Human Adipocytes Induce Inflammation and Atrophy in Muscle Cells During Obesity
Pellegrinelli, V., Rouault, C., Rodríguez‐Cuenca, S., Albert, V., Edom‐Vovard, F., Vidal‐Puig, A., Clément, K., Butler-Browne, G. S., & Lacasa, D. (2015) · Diabetes · doi:10.2337/db14-0796 · Cited by 197 · see citing works
Engineered marble-like bovine fat tissue for cultured meat
Zagury, Y., Ianovici, I., Landau, S., Lavon, N., & Levenberg, S. (2022) · Communications Biology · doi:10.1038/s42003-022-03852-5 · Cited by 112 · see citing works
Fatty Infiltration Is a Prognostic Marker of Muscle Function After Rotator Cuff Tear
Valencia, A. P., Lai, J. K., Iyer, S. R., Mistretta, K. L., Spangenburg, E. E., Davis, D. L., Lovering, R. M., & Gilotra, M. N. (2018) · The American Journal of Sports Medicine · doi:10.1177/0363546518769267 · Cited by 92 · see citing works
Liu, C., Cheng, K. Y.-K., Tong, X., Cheung, W.-H., Chow, S. K.-H., Law, S. W., & Wong, R. M. Y. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1077255 · Cited by 88 · see citing works
“In-vitro studies showed that the coculture of mature adipocytes and skeletal muscle progenitor cells led to a reduction of nuclei number in myosin heavy chain (MHC)-positive myotubes (29).”
BackgroundO’Leary, M. F., Wallace, G. R., Davis, E. T., Murphy, D. P., Nicholson, T. A., Bennett, A. J., Tsintzas, K., & Jones, S. W. (2018) · Scientific Reports · doi:10.1038/s41598-018-33840-x · Cited by 69 · see citing works
The increasingly complex regulation of adipocyte differentiation
Poulos, S. P., Dodson, M. V., Culver, M. F., & Hausman, G. J. (2015) · Experimental Biology and Medicine · doi:10.1177/1535370215619041 · Cited by 55 · see citing works
Adipocytes suppress differentiation of muscle cells in a co‐culture system
Seo, K., Suzuki, T., Kobayashi, K., & Nishimura, T. (2018) · Animal Science Journal · doi:10.1111/asj.13145 · Cited by 54 · see citing works
Sugihara, H., Teramoto, N., Yamanouchi, K., Matsuwaki, T., & Nishihara, M. (2018) · Aging · doi:10.18632/aging.101425 · Cited by 40 · see citing works
Self-citationPagano, A. F., Demangel, R., Brioche, T., Jublanc, É., Bertrand‐Gaday, C., Candau, R. B., Dechesne, C. A., Dani, C., Bonnieu, A., Py, G., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144230 · Cited by 39 · see citing works
Zhang, X., Wang, L., Qiu, K., Xu, D., & Yin, J. (2019) · The FASEB Journal · doi:10.1096/fj.201801907r · Cited by 38 · see citing works
Martel‐Duguech, L., Alonso‐Jiménez, A., Bascuñana, H., Díaz‐Manera, J., Llauger, J., Nuñez‐Peralta, C., Biagetti, B., Montesinos, P., Webb, S. M., & Valassi, E. (2020) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgz329 · Cited by 31 · see citing works
Rossi, A. P., Gottin, L., Donadello, K., Schweiger, V., Brandimarte, P., Zamboni, G. A., Florio, A., BOETTI, R. P., Pavan, G., Zamboni, M. M., et al. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.651167 · Cited by 28 · see citing works
Ma, T., Ren, R., Lv, J., Yang, R., Zheng, X., Hu, Y., Zhu, G., & Wang, H. (2024) · eLife · doi:10.7554/elife.93220 · Cited by 26 · see citing works
Intramuscular adipose tissue restricts functional muscle recovery
Norris, A. M., Palzkill, V. R., Appu, A. B., Fierman, K. E., Noble, C. D., RYAN, T. E., & Kopinke, D. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116021 · Cited by 25 · see citing works
Takeuchi, S., Nakano, S.-I., Nakamura, K., Ozoe, A., Chien, P., Yoshihara, H., Hakuno, F., Matsuwaki, T., Saeki, Y., Takahashi, S., et al. (2016) · Experimental Cell Research · doi:10.1016/j.yexcr.2016.08.023 · Cited by 26 · see citing works
Self-citationTowards a More Realistic In Vitro Meat: The Cross Talk between Adipose and Muscle Cells
Pallaoro, M., Modina, S., Fiorati, A., Altomare, L., Mirra, G., Scocco, P., & Giancamillo, A. D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076630 · Cited by 20 · see citing works
Ma, T., Ren, R., Lv, J., Yang, R., Zheng, X., Hu, Y., Zhu, G., & Wang, H. (2024) · eLife · doi:10.7554/elife.93220.3 · Cited by 23 · see citing works
Wáng, Y., Gao, J., Fan, B., Hu, Y., Yang, Y., Wu, Y., Li, F., & Ju, H. (2023) · Scientific Reports · doi:10.1038/s41598-023-40350-y · Cited by 22 · see citing works
Body Composition and Falls Risk in Older Adults
Xu, C. L. H., Ebeling, P. R., & Scott, D. S. (2019) · Current Geriatrics Reports · doi:10.1007/s13670-019-00294-6 · Cited by 15 · see citing works
Suppression of MyoD induces spontaneous adipogenesis in skeletal muscle progenitor cell culture
Yamanouchi, K., Nakamura, K., Takeuchi, S., Hosoyama, T., Matsuwaki, T., & Nishihara, M. (2021) · Animal Science Journal · doi:10.1111/asj.13573 · Cited by 15 · see citing works
Self-citationRouaud, T., Siami, N., Dupas, T., Gervier, P., Gardahaut, M.-F., Auda-Boucher, G., & Thiriet, C. (2017) · Scientific Reports · doi:10.1038/s41598-017-00099-7 · Cited by 14 · see citing works
Xu, X., Zhao, R., Ma, W., Zhao, Q., & Zhang, G. (2021) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.13599 · Cited by 13 · see citing works
Vepkhvadze, T. F., Vorotnikov, A. V., & Викторович, П. Д. (2021) · Biochemistry (Moscow) · doi:10.1134/s0006297921050084 · Cited by 12 · see citing works
Grau-Monge, C., Delcroix, G. J.-R., Bonnin-Marquez, A., Valdes, M., Awadallah, E. L. M., Quevedo, D. F., Armour, M. R., Montero, R. B., Schiller, P. C., Andreopoulos, F. M., et al. (2017) · Biomedical Materials · doi:10.1088/1748-605x/aa5a74 · Cited by 13 · see citing works
Gautam, J., & Yao, Y. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-11093-2_4 · Cited by 9 · see citing works
Adipogenic Differentiation Alters Properties of Vascularized Tissue-Engineered Skeletal Muscle
Acosta, F. M., Howland, K. K., Stojkova, K., Hernandez, E., Brey, E. M., & Rathbone, C. R. (2021) · Tissue Engineering Part A · doi:10.1089/ten.tea.2021.0064 · Cited by 9 · see citing works
Acosta, F. M., Jia, U.-T. A., Stojkova, K., Pacelli, S., Brey, E. M., & Rathbone, C. R. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.03.025 · Cited by 9 · see citing works
Development of a 3D Tissue‐Engineered Skeletal Muscle and Bone Co‐culture System
Wragg, N. M., Mosqueira, D., Blokpeol‐Ferreras, L., Capel, A. J., Player, D. J., Martin, N. R. W., Liu, Y., & Lewis, M. P. (2019) · Biotechnology Journal · doi:10.1002/biot.201900106 · Cited by 8 · see citing works
Wang, L., He, T., Zhang, X., Wang, Y., Qiu, K., Jiao, N., He, L., & Yin, J. (2021) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-020-00524-4 · Cited by 7 · see citing works
Goffette, V., Sabin, N., Bugeon, J., Jagot, S., Hue, I., & Gabillard, J. (2024) · Scientific Reports · doi:10.1038/s41598-024-67152-0 · Cited by 7 · see citing works
Song, C., Wu, Z., Liu, G., Xu, Y., Deng, Z., Xiu, Y., Zhang, R., Yang, L., Zhang, Y., Yu, G., et al. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103467 · Cited by 3 · see citing works
Yoshida, K., Kobatake, Y., Takashima, S., & NISHII, N. (2024) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.17065 · Cited by 3 · see citing works
Nakamura, K., Kanou, M., Fujii, W., Kouzaki, K., Jimbo, T., Yamanouchi, K., Nakazato, K., Ueda, H., Hirata, J., & Yamana, K. (2025) · Human Molecular Genetics · doi:10.1093/hmg/ddaf028 · Cited by 3 · see citing works
Self-citationMa, T., Ren, R., Lv, J., Yang, R., Zheng, X., Hu, Y., Zhu, G., & Wang, H. (2024) · eLife · doi:10.7554/elife.93220.2 · Cited by 2 · see citing works
Mehmood, W., Abraham, A., Rabinovich‐Toidman, P., Lavon, N., Therkildsen, M., Young, J. F., & Rasmussen, M. K. (2025) · Sustainable Food Technology · doi:10.1039/d5fb00506j · Cited by 1 · see citing works
Ma, T., Ren, R., Lv, J., Yang, R., Zheng, X., Hu, Y., Zhu, G., & Wang, H. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.26.564179 · Cited by 1 · see citing works
Abraham, A., Auguet-Lara, M., Skrivergaard, S., Therkildsen, M., Rasmussen, M. K., & Young, J. F. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4872912 · Cited by 1 · see citing works
Development of a 3D tissue engineered skeletal muscle and bone pre-clinical co-culture platform
Wragg, N. M. (2016) · Loughborough University Institutional Repository (Loughborough University)
Vepkhvadze, T. F., Vorotnikov, A. V., & Викторович, П. Д. (2021) · Biochemistry (Moscow) · doi:10.31857/s0320972521050080
Ke, S., Feng, Y., Luo, L., Qin, W., Liu, H., Nie, J., Liang, B., Ma, H., Xie, M., Li, J., et al. (2023) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-023-00836-5
Ma, T., Ren, R., Yang, R., Zheng, X., Hu, Y., Zhu, G., & Wang, H. (2024) · eLife · doi:10.7554/elife.93220.1
Wang, L., He, T., Zhang, X., Wang, Y., Qiu, K., Jiao, N., He, L., & Yin, J. (2021) · Figshare · doi:10.6084/m9.figshare.13684763
Intramuscular adipose tissue physically restricts functional muscle recoveryPreprint
Norris, A. M., Palzkill, V. R., Appu, A. B., RYAN, T. E., & Kopinke, D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.17.628009
Wang, L., He, T., Zhang, X., Wang, Y., Qiu, K., Jiao, N., He, L., & Yin, J. (2021) · Figshare · doi:10.6084/m9.figshare.13684757
Wang, L., He, T., Zhang, X., Wang, Y., Qiu, K., Jiao, N., He, L., & Yin, J. (2021) · Figshare · doi:10.6084/m9.figshare.13684748
Wang, L., He, T., Zhang, X., Wang, Y., Qiu, K., Jiao, N., He, L., & Yin, J. (2021) · Figshare · doi:10.6084/m9.figshare.13684766
Wang, L., He, T., Zhang, X., Wang, Y., Qiu, K., Jiao, N., He, L., & Yin, J. (2021) · Figshare · doi:10.6084/m9.figshare.13684760
Wang, L., He, T., Zhang, X., Wang, Y., Qiu, K., Jiao, N., He, L., & Yin, J. (2021) · Figshare · doi:10.6084/m9.figshare.13684751
Serum-free media drive lipid accumulation in porcine satellite cells intended for cultivated meat
Abraham, A., Auguet-Lara, M., Skrivergaard, S., Therkildsen, M., Rasmussen, M. K., & Young, J. F. (2026) · Sustainable Food Technology · doi:10.1039/d5fb00572h
Modeling intramuscular fat infiltration in the engineered skeletal muscle myobundles
Wang, D., Liu, Q., Han, S., Zhong, W., Yin, B., Zou, J., Liu, H., Zhang, X., Zhang, X., Qin, J., et al. (2026) · Materials & Design · doi:10.1016/j.matdes.2026.116301
Targeting nuclear receptors in muscular dystrophies and regenerative myogenesis
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- Authors
- Takegahara, Y., Yamanouchi, K., Nakamura, K., Nakano, S.-I., & Nishihara, M.
- Affiliations
- The University of Tokyo (JP)
- Corresponding author
- Yamanouchi, Keitaro
- Venue
- Experimental Cell Research
- Publisher
- Elsevier BV
- Published
- 2014-05
- Volume
- 324
- Issue
- 1
- Pages
- 105-114
- ISSN
- 0014-4827 (ISSN-L)
- OpenAlex
- W2066125811
- Cited by
- 53
- References
- 39
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 9 · 2023: 5 · 2022: 1 · 2021: 12 · 2020: 4 · 2019: 4 · 2018: 4 · 2017: 2 · 2016: 3 · 2015: 3
- FWCI
- 1.09
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Experimental Cell Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (23228004, 25292185)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Keywords
- intramuscular fat, myotube formation, myogenesis, adipocytes, preadipocytes, PPARγ, skeletal muscle progenitor cells, cell-cell contact, Duchenne muscular dystrophy, sarcopenia, myosin heavy chain, conditioned medium, skeletal muscle mass
- MeSH terms
- Animals, Cell Communication, Cells, Cultured, Male, Stem Cells, Rats, Wistar, Adipocytes, Muscle Fibers, Skeletal, Coculture Techniques, Cell Lineage, Muscle Development, RNA, Small Interfering, PPAR gamma, Adipogenesis, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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