The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.
Fibrosis and adipogenesis originate from a common mesenchymal progenitor in skeletal muscle
Abstract
Accumulation of adipocytes and collagen type-I-producing cells (fibrosis) is observed in muscular dystrophies. The origin of these cells had been largely unknown, but recently we identified mesenchymal progenitors positive for platelet-derived growth factor receptor alpha (PDGFRα) as the origin of adipocytes in skeletal muscle. However, the origin of muscle fibrosis remains largely unknown. In this study, clonal analyses show that PDGFRα+ cells also differentiate into collagen type-I-producing cells. In fact, PDGFRα+ cells accumulated in fibrotic areas of the diaphragm in the mdx mouse, a model of Duchenne muscular dystrophy. Furthermore, mRNA of fibrosis markers was expressed exclusively in the PDGFRα+ cell fraction in the mdx diaphragm. Importantly, TGF-β isoforms, known as potent profibrotic cytokines, induced expression of markers of fibrosis in PDGFRα+ cells but not in myogenic cells. Transplantation studies revealed that fibrogenic PDGFRα+ cells mainly derived from pre-existing PDGFRα+ cells and that the contribution of PDGFRα− cells and circulating cells was limited. These results indicate that mesenchymal progenitors are the main origin of not only fat accumulation but also fibrosis in skeletal muscle.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In muscle disuse or pathological conditions, such as Duchenne muscular dystrophy, FAPs proliferate and differentiate into adipose and fibrous tissue.[ 41 ]”
From Pathogenesis of sarcopenia and the relationship with fat mass: descriptive review (2022) · cites this paper as [41]
Citations
Cites
Multilineage potential of adult human mesenchymal stem cells
Pittenger, M. F., Mackay, A. M., Beck, S. C., Jaiswal, R. K., Douglas, R., Mosca, J. D., Moorman, M. A., Simonetti, D. W., Craig, S., & Marshak, D. R. (1999) · Science · doi:10.1126/science.284.5411.143 · Cited by 21,052
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
‘Green mice’ as a source of ubiquitous green cells
Okabe, M., Ikawa, M., Kominami, K., Nakanishi, T., & Nishimune, Y. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)00313-x · Cited by 2,581
Role of platelet-derived growth factors in physiology and medicinePreprint
Andræ, J., Gallini, R., & Betsholtz, C. (2008) · Genes & Development · doi:10.1101/gad.1653708 · Cited by 2,534
Endothelial-to-mesenchymal transition contributes to cardiac fibrosis
Zeisberg, E. M., Tarnavski, O., Zeisberg, M., Dorfman, A. L., McMullen, J. R., Gustafsson, E., Chandraker, A. K., Yuan, X., Pu, W. T., Roberts, A. B., et al. (2007) · Nature Medicine · doi:10.1038/nm1613 · Cited by 2,251
Molecular Regulation of Hepatic Fibrosis, an Integrated Cellular Response to Tissue Injury
Friedman, S. L. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.4.2247 · Cited by 2,067
Evidence that fibroblasts derive from epithelium during tissue fibrosis
Iwano, M., Plieth, D., Danoff, T. M., Xue, C., Okada, H., & Neilson, E. G. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15518 · Cited by 1,809
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
Evidence that fibroblasts derive from epithelium during tissue fibrosis
Iwano, M., Plieth, D., Danoff, T. M., Xue, C., Okada, H., & Neilson, E. G. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215518 · Cited by 1,589
Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis
Brack, A. S., Conboy, M. J., Roy, S., Lee, M., Kuo, C. J., Keller, C., & Rando, T. A. (2007) · Science · doi:10.1126/science.1144090 · Cited by 1,564
Research works printed but not linked: 1
- Carpenter, 2001, Disease of skeletal muscle, 373
Cited by
Sorted by citations
Adipose-tissue plasticity in health and disease
Sakers, A. P., Siqueira, M. K. D., Seale, P., & Villanueva, C. J. (2022) · Cell · doi:10.1016/j.cell.2021.12.016 · Cited by 1,124
Lemos, D. R., Babaeijandaghi, F., Low, M., Chang, C.-K., Lee, S. T., Fiore, D., Zhang, R.-H., Natarajan, A., Nedospasov, S. A., & Rossi, F. M. V. (2015) · Nature Medicine · doi:10.1038/nm.3869 · Cited by 740
Regulation of Muscle Growth and Regeneration by the Immune System
Tidball, J. G. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2016.150 · Cited by 740
Pathogenesis of sarcopenia and the relationship with fat mass: descriptive review
Li, C., Yu, K., Shyh‐Chang, N., Jiang, Z., Liu, T., Ma, S., Luo, L., Guang, L., Liang, K., Ma, W., et al. (2022) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12901 · Cited by 626
Role of Inflammation in Muscle Homeostasis and Myogenesis
Costamagna, D., Costelli, P., Sampaolesi, M., & Penna, F. (2015) · Mediators of Inflammation · doi:10.1155/2015/805172 · Cited by 554
Control of satellite cell function in muscle regeneration and its disruption in ageing
Sousa-Victor, P., García-Prat, L., & Muñoz-Cánoves, P. (2022) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-021-00421-2 · Cited by 476
Cellular dynamics in the muscle satellite cell niche
Bentzinger, C. F., Wang, Y. X., Dumont, N. A., & Rudnicki, M. A. (2013) · The EMBO Reports · doi:10.1038/embor.2013.182 · Cited by 398
High-Dimensional Single-Cell Cartography Reveals Novel Skeletal Muscle-Resident Cell Populations
Giordani, L., He, G. J., Négroni, E., Sakai, H., Law, J., Siu, M. M., Wan, R., Corneau, A., Tajbakhsh, S., Cheung, T. H., et al. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.02.026 · Cited by 406
Bao, H., Cao, J., Chen, M., Min, C., Chen, W., Chen, X., Chen, Y., Chen, Y., Chen, Y., Chen, Z., et al. (2023) · Science China Life Sciences · doi:10.1007/s11427-023-2305-0 · Cited by 402
De Micheli, A. J., Laurilliard, E. J., Heinke, C. L., Ravichandran, H., Fraczek, P., Soueid-Baumgarten, S., De Vlaminck, I., Elemento, O., & Cosgrove, B. D. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.02.067 · Cited by 373
Skeletal muscle fibrosis: an overview
Mahdy, M. A. A. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2955-2 · Cited by 320
A Muscle Stem Cell Support Group: Coordinated Cellular Responses in Muscle Regeneration
Wosczyna, M. N., & Rando, T. A. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.06.018 · Cited by 363
Single-cell transcriptional profiles in human skeletal muscle
Rubenstein, A. B., Smith, G. R., Raue, U., Begue, G., Minchev, K., Ruf-Zamojski, F., Nair, V. D., Wang, X., Zhou, L., Zaslavsky, E., et al. (2020) · Scientific Reports · doi:10.1038/s41598-019-57110-6 · Cited by 323
Park, S. J., Beak, S.-H., Jung, D. J. S., Kim, S. Y., Jeong, I. H., Piao, M. Y., Kang, H. J., Fassah, D. M., Na, S. W., Yoo, S. P., et al. (2018) · Asian-Australasian Journal of Animal Sciences · doi:10.5713/ajas.18.0310 · Cited by 321
Adult stem cells at work: regenerating skeletal muscle
Schmidt, M., Schüler, S. C., Hüttner, S. S., von Eyß, B., & von Maltzahn, J. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03093-6 · Cited by 337
Lieber, R. L., & Ward, S. R. (2013) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00173.2013 · Cited by 315
Role of Pericytes in Skeletal Muscle Regeneration and Fat Accumulation
Birbrair, A., Zhang, T., Wang, Z., Messi, M. L., Enikolopov, G., Mintz, A., & Delbono, O. (2013) · Stem Cells and Development · doi:10.1089/scd.2012.0647 · Cited by 319
Identification and characterization of PDGFRα+ mesenchymal progenitors in human skeletal muscle
Uezumi, A., Fukada, S., Yamamoto, N., Ikemoto‐Uezumi, M., Nakatani, M., Morita, M., Yamaguchi, A., Yamada, H., Nishino, I., Hamada, Y., et al. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.161 · Cited by 304
Self-citationIntradermal adipocytes mediate fibroblast recruitment during skin wound healing
Schmidt, B. A., & Horsley, V. (2013) · Development · doi:10.1242/dev.087593 · Cited by 318
Marcelin, G., Ferreira, A. V. M., Liu, Y., Atlan, M., Aron‐Wisnewsky, J., Pelloux, V., Botbol, Y. M., Ambrosini, M., Fradet, M., Rouault, C., et al. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.01.010 · Cited by 295
Deciphering the cellular interplays underlying obesity-induced adipose tissue fibrosis
Marcelin, G., Silveira, A. L. M., Martins, L. B., Ferreira, A. V. M., & Clément, K. (2019) · Journal of Clinical Investigation · doi:10.1172/jci129192 · Cited by 291
Ciliary Hedgehog Signaling Restricts Injury-Induced Adipogenesis
Kopinke, D., Roberson, E. C., & Reiter, J. F. (2017) · Cell · doi:10.1016/j.cell.2017.06.035 · Cited by 260
Regulation of the muscle fiber micro environment by activated satellite cells during hypertrophy
Fry, C. S., Lee, J. D., Jackson, J. R., Kirby, T. J., Stasko, S. A., Liu, H., Dupont‐Versteegden, E. E., McCarthy, J. J., & Peterson, C. A. (2014) · The FASEB Journal · doi:10.1096/fj.13-239426 · Cited by 273
Du, ., Huang, Y., Das, A. K., Yang, Q., Duarte, M. D. S., Dodson, M. V., & Zhu, M. J. (2012) · Journal of Animal Science · doi:10.2527/jas.2012-5670 · Cited by 262
Mozzetta, C., Consalvi, S., Saccone, V., Tierney, M. T., Diamantini, A., Mitchell, K. J., Marazzi, G., Borsellino, G., Battistini, L., Sassoon, D. A., et al. (2013) · EMBO Molecular Medicine · doi:10.1002/emmm.201202096 · Cited by 261
Understanding the Process of Fibrosis in Duchenne Muscular Dystrophy
Kharraz, Y., Guerra, J., Pessina, P., Serrano, A. L., & Muñoz‐Cánoves, P. (2014) · BioMed Research International · doi:10.1155/2014/965631 · Cited by 270
Fibro–Adipogenic Progenitors Cross-Talk in Skeletal Muscle: The Social Network
Biferali, B., Proietti, D., Mozzetta, C., & Madaro, L. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01074 · Cited by 257
Lees‐Shepard, J. B., Yamamoto, M., Biswas, A. A., Stoessel, S. J., Nicholas, S.-A. E., Cogswell, C. A., Devarakonda, P. M., Schneider, M. J., Cummins, S. M., Legendre, N. P., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-02872-2 · Cited by 228
Cell Sources for Cultivated Meat: Applications and Considerations throughout the Production Workflow
Reiss, J. F., Robertson, S., & Suzuki, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147513 · Cited by 235
Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy
Malecová, B., Gatto, S., Etxaniz, U., Passafaro, M., Cortez, A., Nicoletti, C., Giordani, L., Torcinaro, A., Bardi, M. D., Bicciato, S., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06068-6 · Cited by 221
Adipose tissue plasticity from WAT to BAT and in between
Lee, Y., Mottillo, E. P., & Granneman, J. G. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.05.011 · Cited by 236
Inflammaging: Implications in Sarcopenia
Antuña, E., Cachán-Vega, C., Bermejo-Millo, J. C., Potes, Y., Caballero, B., Vega‐Naredo, I., Coto‐Montes, A. M., & García-González, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315039 · Cited by 234
Scott, R. W., Arostegui, M., Schweitzer, R., Rossi, F. M. V., & Underhill, T. M. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.11.004 · Cited by 214
Bedi, A., Bishop, J. Y., Keener, J. D., Lansdown, D. A., Levy, O., MacDonald, P. B., Maffulli, N., Oh, J. H., Sabesan, V. J., Sánchez‐Sotelo, J., et al. (2024) · Nature Reviews Disease Primers · doi:10.1038/s41572-024-00492-3 · Cited by 227
Intermuscular and intramuscular adipose tissues: Bad vs. good adipose tissues
Hausman, G. J., Basu, U., Du, ., Fernyhough, M. E., & Dodson, M. V. (2014) · Adipocyte · doi:10.4161/adip.28546 · Cited by 218
Saito, Y., Chikenji, T. S., Matsumura, T., Nakano, M., & Fujimiya, M. (2020) · Nature Communications · doi:10.1038/s41467-020-14734-x · Cited by 196
Two tissue-resident progenitor lineages drive distinct phenotypes of heterotopic ossification
Dey, D., Bagarova, J., Hatsell, S. J., Armstrong, K. A., Huang, L., Ermann, J., Vonner, A. J., Shen, Y., Mohedas, A. H., Lee, A. M., et al. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf1090 · Cited by 195
Fibro-adipogenic progenitors in skeletal muscle homeostasis, regeneration and diseases
Molina, T., Fabre, P., & Dumont, N. A. (2021) · Open Biology · doi:10.1098/rsob.210110 · Cited by 205
Fetal programming in meat production
Du, ., Wang, B., Fu, X., Yang, Q., & Zhu, M. J. (2015) · Meat Science · doi:10.1016/j.meatsci.2015.04.010 · Cited by 186
Stem Cell Aging in Skeletal Muscle Regeneration and Disease
Yamakawa, H., Kusumoto, D., Hashimoto, H., & Yuasa, S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21051830 · Cited by 187
Roles of nonmyogenic mesenchymal progenitors in pathogenesis and regeneration of skeletal muscle
Uezumi, A., Ikemoto‐Uezumi, M., & Tsuchida, K. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00068 · Cited by 171
Self-citationUezumi, A., Ikemoto‐Uezumi, M., Zhou, H., Kurosawa, T., Yoshimoto, Y., Nakatani, M., Hitachi, K., Yamaguchi, H., Wakatsuki, S., Araki, T., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci139617 · Cited by 166
Self-citationThe perivascular origin of pathological fibroblasts
Di Carlo, S. E., & Peduto, L. (2018) · Journal of Clinical Investigation · doi:10.1172/jci93558 · Cited by 164
Saccone, V., Consalvi, S., Giordani, L., Mozzetta, C., Barozzi, I., Sandonà, M., Ryan, T. L., Rojas‐Muñoz, A., Madaro, L., Fasanaro, P., et al. (2014) · Genes & Development · doi:10.1101/gad.234468.113 · Cited by 164
Farup, J., Madaro, L., Puri, P., & Mikkelsen, U. R. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.198 · Cited by 162
Fiore, D., Judson, R. N., Low, M., Lee, S., Erica, Z., Hopkins, C. I., Xu, P., Lenzi, A., Rossi, F. M. V., & Lemos, D. R. (2016) · Stem Cell Research · doi:10.1016/j.scr.2016.06.007 · Cited by 156
Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle
Waisman, A., Norris, A. M., Costa, M. E., & Kopinke, D. (2021) · Scientific Reports · doi:10.1038/s41598-021-91191-6 · Cited by 158
Obesity Impairs Skeletal Muscle Regeneration Through Inhibition of AMPK
Fu, X., Zhu, M., Zhang, S., Foretz, M., Viollet, B., & Du, M. (2016) · Diabetes · doi:10.2337/db15-0647 · Cited by 155
“To explore whether AMPKa1 KO affects fibrogenesis, we isolated Lin(2)/Sca-1 fibro/adipogenic progenitor cells (10,32).”
BackgroundContreras, O., Rossi, F. M. V., & Théret, M. (2021) · Skeletal Muscle · doi:10.1186/s13395-021-00265-6 · Cited by 163
Santa, F. D., Vitiello, L., Torcinaro, A., & Ferraro, E. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7420 · Cited by 157
An Overview About the Biology of Skeletal Muscle Satellite Cells
Forcina, L., Miano, C., Pelosi, L., & Musarò, A. (2019) · Current Genomics · doi:10.2174/1389202920666190116094736 · Cited by 155
Defining skeletal muscle resident progenitors and their cell fate potentials
Pannérec, A., Formicola, L., Besson, V., Marazzi, G., & Sassoon, D. A. (2013) · Development · doi:10.1242/dev.089326 · Cited by 151
Reggio, A., Rosina, M., Palma, A., Perpetuini, A. C., Petrilli, L. L., Gargioli, C., Fuoco, C., Micarelli, E., Giuliani, G., Cerretani, M., et al. (2020) · Cell Death and Differentiation · doi:10.1038/s41418-020-0551-y · Cited by 160
Coulis, G., Jaime, D., Guerrero-Juarez, C., Kastenschmidt, J. M., Farahat, P. K., Nguyen, Q., Pervolarakis, N., McLinden, K., Thurlow, L., Movahedi, S., et al. (2023) · Science Advances · doi:10.1126/sciadv.add9984 · Cited by 150
Fat infiltration in skeletal muscle: Influential triggers and regulatory mechanism
Wang, L., Valencak, T. G., & Shan, T. (2024) · iScience · doi:10.1016/j.isci.2024.109221 · Cited by 149
Contreras, O., Rebolledo, D. L., Oyarzún, J. E., Olguín, H. C., & Brandan, E. (2016) · Cell and Tissue Research · doi:10.1007/s00441-015-2343-0 · Cited by 154
Chen, L., Acciani, T. H., Cras, T. D. L., Lutzko, C., & Perl, A. T. (2012) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2012-0030oc · Cited by 145
A Wnt-TGFβ2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice
Biressi, S., Miyabara, E. H., Gopinath, S. D., Carlig, P. M. M., & Rando, T. A. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3008411 · Cited by 152
Vallecillo-García, P., Orgeur, M., vom Hofe-Schneider, S., Stumm, J., Kappert, V., Ibrahim, D. M., Börno, S. T., Hayashi, S., Relaix, F., Hildebrandt, K., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-01120-3 · Cited by 126
Théret, M., Rossi, F. M. V., & Contreras, O. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.673404 · Cited by 154
Pericytes: multitasking cells in the regeneration of injured, diseased, and aged skeletal muscle
Birbrair, A., Zhang, T., Wang, Z., Messi, M. L., Mintz, A., & Delbono, O. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00245 · Cited by 145
Giuliani, G., Rosina, M., & Reggio, A. (2021) · FEBS Journal · doi:10.1111/febs.16080 · Cited by 144
The Basis of Muscle Regeneration
Musarò, A. (2014) · Advances in Biology · doi:10.1155/2014/612471 · Cited by 149
Skeletal muscle fibroblasts in health and disease
Chapman, M., Meza, R. C., & Lieber, R. L. (2016) · Differentiation · doi:10.1016/j.diff.2016.05.007 · Cited by 143
TGF-β–driven muscle degeneration and failed regeneration underlie disease onset in a DMD mouse model
Mázala, D. A. G., Novak, J. S., Hogarth, M. W., Nearing, M., Adusumalli, P., Tully, C., Habib, N. F., Gordish‐Dressman, H., Chen, Y.-W., Jaiswal, J. K., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.135703 · Cited by 137
Regulation of fibrosis in muscular dystrophy
Smith, L., & Barton, E. R. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.01.014 · Cited by 138
Arrighi, N., Moratal, C., Clément, N., Giorgetti‐Peraldi, S., Peraldi, P., Loubat, A., Kurzenne, J.-Y., Dani, C., Chopard, A., & Dechesne, C. A. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.79 · Cited by 143
Contreras, O., Cruz-Soca, M., Théret, M., Soliman, H. S., Tung, L. W., Groppa, E., Rossi, F. M. V., & Brandan, E. (2019) · Journal of Cell Science · doi:10.1242/jcs.232157 · Cited by 143
Intronic polyadenylation of PDGFRα in resident stem cells attenuates muscle fibrosis
Mueller, A. A., van Velthoven, C. T. J., Fukumoto, K. D., Cheung, T. H., & Rando, T. A. (2016) · Nature · doi:10.1038/nature20160 · Cited by 130
Muscle wasting and aging: Experimental models, fatty infiltrations, and prevention
Brioche, T., Pagano, A. F., Py, G., & Chopard, A. (2016) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2016.04.006 · Cited by 129
González, D., Contreras, O., Rebolledo, D. L., Espinoza, J. P., van Zundert, B., & Brandan, E. (2017) · PLoS ONE · doi:10.1371/journal.pone.0177649 · Cited by 128
Li, X., Fu, X., Yang, G., & Du, . (2019) · animal · doi:10.1017/s175173111900209x · Cited by 131
Espino-González, E., Dalbram, E., Mounier, R., Gondin, J., Farup, J., Jessen, N., & Treebak, J. T. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2024.02.014 · Cited by 141
Direct contribution of skeletal muscle mesenchymal progenitors to bone repair
Julien, A., Kanagalingam, A., Martínez‐Sarrà, E., Megret, J., Luka, M., Ménager, M. M., Relaix, F., & Colnot, C. (2021) · Nature Communications · doi:10.1038/s41467-021-22842-5 · Cited by 128
Cardiac fibroblasts: from development to heart failure
Moore‐Morris, T., Guimarães‐Camboa, N., Yutzey, K. E., Pucéat, M., & Evans, S. Μ. (2015) · Journal of Molecular Medicine · doi:10.1007/s00109-015-1314-y · Cited by 125
Agley, C. C., Rowlerson, A. M., Velloso, C. P., Lazarus, N. R., & Harridge, S. D. R. (2013) · Journal of Cell Science · doi:10.1242/jcs.132563 · Cited by 133
Uezumi, A., Nakatani, M., Ikemoto‐Uezumi, M., Yamamoto, N., Morita, M., Yamaguchi, A., Yamada, H., Kasai, T., Masuda, S., Narita, A., et al. (2016) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.07.004 · Cited by 118
Self-citationBidirectional roles of skeletal muscle fibro-adipogenic progenitors in homeostasis and disease
Chen, W., You, W., Valencak, T. G., & Shan, T. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101682 · Cited by 120
Molecular mechanisms of skeletal muscle development, regeneration, and osteogenic conversion
Endo, T. (2015) · Bone · doi:10.1016/j.bone.2015.02.028 · Cited by 117
Short‐term disuse promotes fatty acid infiltration into skeletal muscle
Pagano, A. F., Brioche, T., Arc-Chagnaud, C., Demangel, R., Chopard, A., & Py, G. (2017) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12259 · Cited by 99
Tissue‐resident mesenchymal stem/progenitor cells in skeletal muscle: collaborators or saboteurs?
Judson, R. N., Zhang, R., & Rossi, F. M. V. (2013) · FEBS Journal · doi:10.1111/febs.12370 · Cited by 113
Adipocytes in Skin Health and DiseasePreprint
Rivera-Gonzalez, G. C., Shook, B., & Horsley, V. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a015271 · Cited by 117
Nutrigenomics and Beef Quality: A Review about Lipogenesis
Ladeira, M. M., Schoonmaker, J. P., Gionbelli, M. P., Dias, J. C. O., Gionbelli, T. R. S., de Carvalho, J. R. R., & Teixeira, P. D. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17060918 · Cited by 121
Non-myogenic Contribution to Muscle Development and Homeostasis: The Role of Connective Tissues
Nassari, S., Duprez, D., & Fournier‐Thibault, C. (2017) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2017.00022 · Cited by 111
Dietary alpha‐ketoglutarate promotes beige adipogenesis and prevents obesity in middle‐aged mice
Tian, Q., Zhao, J., Yang, Q., Wang, B., de Avila, J. M., Zhu, M. J., & Du, . (2019) · Aging Cell · doi:10.1111/acel.13059 · Cited by 108
Sandonà, M., Pietro, L. D., Esposito, F., Ventura, A., Silini, A. R., Parolini, O., & Saccone, V. (2021) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2021.652970 · Cited by 108
αv integrins on mesenchymal cells regulate skeletal and cardiac muscle fibrosis
Murray, I. R., Gonzalez-Galofre, Z. N., Baily, J., Dobie, R., Wallace, R. J., MacKinnon, A. C., Smith, J. R., Greenhalgh, S. N., Thompson, A., Conroy, K. P., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-01097-z · Cited by 108
Muscle injury: review of experimental models.
de Souza, J. B., & Gottfried, C. (2013) · Journal of Electromyography & Kinesiology · doi:10.1016/j.jelekin.2013.07.009 · Cited by 115
Skeletal and cardiac muscle pericytes: Functions and therapeutic potential
Murray, I. R., Baily, J. E., Chen, W. C. W., Dar, A., Gonzalez-Galofre, Z. N., Jensen, A. R., Petrigliano, F. A., Deb, A., & Henderson, N. C. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.09.005 · Cited by 107
Stem cell-based therapies for Duchenne muscular dystrophy
Sun, C., Serra, C., Lee, G., & Wagner, K. R. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113086 · Cited by 109
Fibrogenic Cell Plasticity Blunts Tissue Regeneration and Aggravates Muscular Dystrophy
Pessina, P., Kharraz, Y., Jardı́, M., Fukada, S., Serrano, A. L., Perdiguero, E., & Muñoz‐Cánoves, P. (2015) · Stem Cell Reports · doi:10.1016/j.stemcr.2015.04.007 · Cited by 101
Self-citationExon-Skipping in Duchenne Muscular Dystrophy
Takeda, S., Clemens, P. R., & Hoffman, E. P. (2021) · Journal of Neuromuscular Diseases · doi:10.3233/jnd-210682 · Cited by 99
Self-citationEnhancement of adipogenesis and fibrogenesis in skeletal muscle of Wagyu compared with Angus cattle
Duarte, M. D. S., Paulino, P. V. R., Das, A. K., Wei, S., Serão, N. V. L., Fu, X., Harris, S. M., Dodson, M. V., & Du, . (2013) · Journal of Animal Science · doi:10.2527/jas.2012-5892 · Cited by 99
Skeletal muscle tissue engineering: strategies for volumetric constructs
Cittadella, G., & Mantero, S. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00362 · Cited by 97
Skeletal muscle in health and disease
Morgan, J. E., & Partridge, T. A. (2020) · Disease Models & Mechanisms · doi:10.1242/dmm.042192 · Cited by 98
Sastourné-Arrey, Q., Mathieu, M., Contreras, X., Monferran, S., Bourlier, V., Gil‐Ortega, M., Murphy, E. E., Laurens, C., Varin, A., Guissard, C., et al. (2023) · Nature Communications · doi:10.1038/s41467-022-35524-7 · Cited by 96
Ieronimakis, N. M., Hays, A. L., Prasad, A., Janebodin, K., Duffield, J. S., & Reyes, M. (2016) · The Journal of Pathology · doi:10.1002/path.4801 · Cited by 96
Soglia, F., Petracci, M., Davoli, R., & Zappaterra, M. (2021) · Poultry Science · doi:10.1016/j.psj.2021.101180 · Cited by 96
Angiotensins as therapeutic targets beyond heart disease
Passos-Silva, D. G., Brandan, E., & Santos, R. A. S. (2015) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2015.03.001 · Cited by 97
Sandonà, M., Consalvi, S., Tucciarone, L., Bardi, M. D., Scimeca, M., Angelini, D. F., Buffa, V., D’Amico, A., Bertini, E., Cazzaniga, S., et al. (2020) · EMBO Reports · doi:10.15252/embr.202050863 · Cited by 94
Metadata
- Authors
- Uezumi, A., Ito, T., Morikawa, D., Shimizu, N., Yoneda, T., Segawa, M., Yamaguchi, M., Ogawa, R., Matev, M. M., Miyagoe-Suzuki, Y., Takeda, S., Tsujikawa, K., Tsuchida, K., Yamamoto, H., & Fukada, S.-I.
- Affiliations
- Fujita Health University (JP)
- The University of Osaka (JP)
- Department of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1 Ogawa-higashi, Kodaira, Tokyo 187-8502, Japan
- National Center of Neurology and Psychiatry (JP)
- Corresponding author
- Fukada, So-ichiro
- ORCID
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2011-11-01
- Volume
- 124
- Issue
- 21
- Pages
- 3654-3664
- ISSN
- 0021-9533 (ISSN-L)
- 1477-9137
- OpenAlex
- W1964124818
- Cited by
- 680
- References
- 38
- Citations by year
- 2026: 47 · 2025: 54 · 2024: 57 · 2023: 52 · 2022: 58 · 2021: 61 · 2020: 69 · 2019: 55 · 2018: 46 · 2017: 36 · 2016: 42 · 2015: 34 · 2014: 28 · 2013: 28 · 2012: 13
- FWCI
- 8.97
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Cell Science (publishedVersion)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Japan Society for the Promotion of Science (21590320, 21300149, 21790884)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Genetics (clinical) › Neurogenetic and Muscular Disorders Research
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
- Keywords
- muscle fibrosis, adipogenesis, mesenchymal progenitor cells, PDGFRA, Duchenne muscular dystrophy, mdx mice, diaphragm, TGF-beta, type I collagen, fat deposition, cell of origin, clonal analysis, transplantation
- MeSH terms
- Animals, Cell Differentiation, Disease Models, Animal, Fibrosis, Humans, Mice, Inbred C57BL, Muscular Dystrophies, Adipocytes, Mice, Inbred mdx, Muscle, Skeletal, Receptor, Platelet-Derived Growth Factor alpha, Adipogenesis, Mice, Mesenchymal Stem Cells
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 ›
Are you an author, or do you see a problem with this page? Request a review