Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis

Myofibroblasts and mechano-regulation of connective tissue remodelling

Tomasek, J. J., Gabbiani, G., Hinz, B., Chaponnier, C., & Brown, R. A. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm809 · Cited by 4,290 · see citing works

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

Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus

Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121 · see citing works

Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo

Bodine, S. C., Stitt, T. N., Gonzalez, M., Kline, W. O., Stover, G. L., Bauerlein, R., Zlotchenko, E., Scrimgeour, A., Lawrence, J. C., Glass, D. J., et al. (2001) · Nature Cell Biology · doi:10.1038/ncb1101-1014 · Cited by 2,752 · 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

PRDM16 controls a brown fat/skeletal muscle switch

Seale, P., Bjork, B., Yang, W., Kajimura, S., Chin, S., Kuang, S., Scimè, A., Devarakonda, S., Conroe, H. M., Erdjument-Bromage, H., et al. (2008) · Nature · doi:10.1038/nature07182 · Cited by 2,347 · cited 1× · see citing works

Generation of a functional mammary gland from a single stem cell

Shackleton, M., Vaillant, F., Simpson, K. J., Stingl, J., Smyth, G. K., Asselin-Labat, M.-L., Wu, L., Lindeman, G. J., & Visvader, J. E. (2006) · Nature · doi:10.1038/nature04372 · Cited by 2,005 · see citing works

Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis

Arnold, L., Henry, A., Poron, F., Baba-Amer, Y., van Rooijen, N., Plonquet, A., Gherardi, R. K., & Chazaud, B. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070075 · Cited by 2,002 · see citing works

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 · see citing works

Asymmetric self-renewal and commitment of satellite stem cells in muscle

Kuang, S., Kuroda, K., Le Grand, F., & Rudnicki, M. A. (2007) · Cell · doi:10.1016/j.cell.2007.03.044 · Cited by 1,449 · see citing works

Stem Cell Function, Self-Renewal, and Behavioral Heterogeneity of Cells from the Adult Muscle Satellite Cell Niche

Collins, C. A., Olsen, I., Zammit, P. S., Heslop, L., Petrie, A., Partridge, T. A., & Morgan, J. E. (2005) · Cell · doi:10.1016/j.cell.2005.05.010 · Cited by 1,445 · see citing works

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

Shore, E. M., Xu, M., Feldman, G. J., Fenstermacher, D., Cho, T., Choi, I. H., Connor, J. M., Delai, P. L. R., Glaser, D. L., Merrer, M. F. L., et al. (2006) · Nature Genetics · doi:10.1038/ng1783 · Cited by 1,215 · see citing works

White Fat Progenitor Cells Reside in the Adipose Vasculature

Tang, W., Zeve, D., Suh, J. M., Bosnakovski, D., Kyba, M., Hammer, R. E., Tallquist, M. D., & Graff, J. M. (2008) · Science · doi:10.1126/science.1156232 · Cited by 1,113 · see citing works

Direct Isolation of Satellite Cells for Skeletal Muscle Regeneration

Montarras, D., Morgan, J., Collins, C., Relaix, F., Zaffran, S., Cumano, A., Partridge, T., & Buckingham, M. (2005) · Science · doi:10.1126/science.1114758 · Cited by 1,100 · see citing works

Identification and characterization of a fibroblast marker: FSP1.

Strutz, F. M., Okada, H., Lo, C. W., Danoff, T. M., Carone, R. L., Tomaszewski, J. E., & Neilson, E. G. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.130.2.393 · Cited by 1,075 · see citing works

Identification of White Adipocyte Progenitor Cells In Vivo

Rodeheffer, M. S., Birsoy, K., & Friedman, J. M. (2008) · Cell · doi:10.1016/j.cell.2008.09.036 · Cited by 945 · see citing works

Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy.

Rando, T. A., & Blau, H. M. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.125.6.1275 · Cited by 944 · see citing works

Expression of Cd34 and Myf5 Defines the Majority of Quiescent Adult Skeletal Muscle Satellite Cells

Beauchamp, J. R., Heslop, L., Yu, D. S., Tajbakhsh, S., Kelly, R. G., Wernig, A., BUCKINGHAM, M. E., Partridge, T. A., & Zammit, P. S. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.6.1221 · Cited by 917 · see citing works

The Regulation of Notch Signaling Controls Satellite Cell Activation and Cell Fate Determination in Postnatal Myogenesis

Conboy, I. M., & Rando, T. A. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00254-x · Cited by 905 · see citing works

Self-renewal and expansion of single transplanted muscle stem cells

Sacco, A., Doyonnas, R., Kraft, P., Vitorovic, S., & Blau, H. M. (2008) · Nature · doi:10.1038/nature07384 · Cited by 901 · see citing works

Interleukin-6 Is an Essential Regulator of Satellite Cell-Mediated Skeletal Muscle Hypertrophy

Serrano, A. L., Baeza-Raja, B., Perdiguero, E., Jardí, M., & Muñoz-Cánoves, P. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2007.11.011 · Cited by 873 · see citing works

Wound Healing: Biochemical and Clinical Aspects

Clay, R. P. (1993) · Mayo Clinic Proceedings · doi:10.1016/s0025-6196(12)60711-3 · Cited by 535 · see citing works

Wnt Signaling Induces the Myogenic Specification of Resident CD45+ Adult Stem Cells during Muscle Regeneration

Polesskaya, A., Seale, P., & Rudnicki, M. A. (2003) · Cell · doi:10.1016/s0092-8674(03)00437-9 · Cited by 515 · see citing works

Isolation of Adult Mouse Myogenic Progenitors

Sherwood, R. I., Christensen, J. L., Conboy, I. M., Conboy, M. J., Rando, T. A., Weissman, I. L., & Wagers, A. J. (2004) · Cell · doi:10.1016/j.cell.2004.10.021 · Cited by 491 · see citing works

Stem cells in postnatal myogenesis: molecular mechanisms of satellite cell quiescence, activation and replenishment

Dhawan, J., & Rando, T. A. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.10.007 · Cited by 466 · see citing works

Transforming Growth Factor-β1 Induces the Differentiation of Myogenic Cells into Fibrotic Cells in Injured Skeletal Muscle

Li, Y., Foster, W. H., Deasy, B. M., Chan, Y., Prisk, V. R., Tang, Y., Cummins, J. H., & Huard, J. (2004) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63188-4 · Cited by 454 · see citing works

Myogenic progenitor cells and skeletal myogenesis in vertebrates

BUCKINGHAM, M. E. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.08.008 · Cited by 452 · see citing works

Muscle satellite cells

Morgan, J. E., & Partridge, T. A. (2003) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(03)00042-6 · Cited by 438 · see citing works

Skeletal Myogenic Progenitors Originating from Embryonic Dorsal Aorta Coexpress Endothelial and Myogenic Markers and Contribute to Postnatal Muscle Growth and Regeneration

Angelis, L. D., Berghella, L., Coletta, M., Lattanzi, L., Zanchi, M., Gabriella, M., Ponzetto, C., & Cossu, G. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.4.869 · Cited by 421 · see citing works

Vascular endothelial growth factor stimulates skeletal muscle regeneration in Vivo

Arsic, N., Zacchigna, S., Zentilin, L., Ramirez‐Correa, G. A., Pattarini, L., Salvi, A., Sinagra, G., & Giacca, M. (2004) · Molecular Therapy · doi:10.1016/j.ymthe.2004.08.007 · Cited by 349 · see citing works

Mechanisms of Muscle Degeneration, Regeneration, and Repair in the Muscular Dystrophies

Wallace, G. Q., & McNally, E. M. (2008) · Annual Review of Physiology · doi:10.1146/annurev.physiol.010908.163216 · Cited by 343 · see citing works

Skeletal muscle satellite cells can spontaneously enter an alternative mesenchymal pathway

Shefer, G., Wleklinski‐Lee, M., & Yablonka‐Reuveni, Z. (2004) · Journal of Cell Science · doi:10.1242/jcs.01419 · Cited by 290 · see citing works

Canonical Wnt signalling induces satellite-cell proliferation during adult skeletal muscle regeneration

Otto, A., Schmidt, C., Luke, G. N., Allen, S., Valášek, P., Francesco Muntoni, A., Lawrence‐Watt, D. J., & Patel, K. (2008) · Journal of Cell Science · doi:10.1242/jcs.026534 · Cited by 282 · see citing works

Depot-Specific Differences in Adipogenic Progenitor Abundance and Proliferative Response to High-Fat Diet

Joe, A. W., Yi, L., Even, Y., Vogl, A. W., & Rossi, F. M. V. (2009) · Stem Cells · doi:10.1002/stem.190 · Cited by 278 · see citing works

Increased PDGFRα Activation Disrupts Connective Tissue Development and Drives Systemic Fibrosis

Olson, L. E., & Soriano, P. (2009) · Developmental Cell · doi:10.1016/j.devcel.2008.12.003 · Cited by 264 · see citing works

Differentiation of Muscle-Derived Cells into Myofibroblasts in Injured Skeletal Muscle

Li, Y., & Huard, J. (2002) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64250-2 · Cited by 243 · see citing works

Human macrophages rescue myoblasts and myotubes from apoptosis through a set of adhesion molecular systems

Sonnet, C., Lafuste, P., Arnold, L., Brigitte, M., Poron, F., Authier, F., Chrétien, F. C., Gherardi, R. K., & Chazaud, B. (2006) · Journal of Cell Science · doi:10.1242/jcs.02988 · Cited by 169 · see citing works

Purification of Mouse Primary Myoblasts Based on α7 Integrin Expression

Blanco-Bose, W. E., Yao, C. J., Kramer, R. H., & Blau, H. M. (2001) · Experimental Cell Research · doi:10.1006/excr.2001.5191 · Cited by 165 · see citing works

Thymic microenvironments for T cell differentiation and selection

Ladi, E., Yin, X., Chtanova, T., & Robey, E. A. (2006) · Nature Immunology · doi:10.1038/ni1323 · Cited by 164 · see citing works

Fat accumulation with altered inflammation and regeneration in skeletal muscle of CCR2−/− mice following ischemic injury

Contreras‐Shannon, V., Ochoa, O., Reyna, S. M., Sun, D., Michalek, J. E., Kuziel, W. A., McManus, L. M., & Shireman, P. K. (2006) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00154.2006 · Cited by 161 · see citing works

Myotoxic phospholipases A2 and the regeneration of skeletal muscles

Harris, J. B. (2003) · Toxicon · doi:10.1016/j.toxicon.2003.11.011 · Cited by 150 · see citing works

Optimizing Techniques for Tracking Transplanted Stem Cells In Vivo

Brazelton, T. R., & Blau, H. M. (2005) · Stem Cells · doi:10.1634/stemcells.2005-0149 · Cited by 127 · see citing works

Sca-1 negatively regulates proliferation and differentiation of muscle cells

Mitchell, P. O., Mills, T., O’Connor, R. S., Graubert, T. A., Dzierzak, E. A., & Pavlath, G. K. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.04.016 · Cited by 107 · see citing works

Sca-1 expression is required for efficient remodeling of the extracellular matrix during skeletal muscle regeneration

Kafadar, K. A., Yi, L., Ahmad, Y., So, L., Rossi, F. M. V., & Pavlath, G. K. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.10.036 · Cited by 61 · see citing works

Muscle fibre breakdown in venom‐induced muscle degeneration

Harris, J. B., Vater, R., Wilson, M., & Cullen, M. J. (2003) · Journal of Anatomy · doi:10.1046/j.1469-7580.2003.00171.x · Cited by 38 · see citing works

The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells

Trapnell, C., Cacchiarelli, D., Grimsby, J., Pokharel, P., Li, S., Morse, M., Lennon, N. J., Livak, K. J., Mikkelsen, T. S., & Rinn, J. L. (2014) · Nature Biotechnology · doi:10.1038/nbt.2859 · Cited by 7,314 · see citing works

Beige Adipocytes Are a Distinct Type of Thermogenic Fat Cell in Mouse and Human

Wu, J., Boström, P., Sparks, L. M., Li, Y., Choi, J. H., Giang, A.-H., Khandekar, M. J., Virtanen, K. A., Nuutila, P., Schaart, G., et al. (2012) · Cell · doi:10.1016/j.cell.2012.05.016 · Cited by 3,299 · see citing works

What we talk about when we talk about fat

Rosen, E. D., & Spiegelman, B. M. (2014) · Cell · doi:10.1016/j.cell.2013.12.012 · Cited by 2,373 · 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

Nrf2-Keap1 signaling in oxidative and reductive stress

Bellezza, I., Giambanco, I., Minelli, A., & Donato, R. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2018.02.010 · Cited by 2,093 · see citing works

Extracellular matrix: A dynamic microenvironment for stem cell niche

Gattazzo, F., Urciuolo, A., & Bonaldo, P. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.01.010 · Cited by 1,304 · see citing works

Satellite cells, connective tissue fibroblasts and their interactions are crucial for muscle regeneration

Murphy, M. M., Lawson, J. A., Mathew, S. J., Hutcheson, D. A., & Kardon, G. (2011) · Development · doi:10.1242/dev.064162 · Cited by 1,249 · see citing works

Molecular regulation of stem cell quiescence

Cheung, T. H., & Rando, T. A. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3591 · Cited by 1,148 · see citing works

Fibroblasts: Origins, definitions, and functions in health and disease

Plikus, M. V., Wang, X., Sinha, S., Forte, E., Thompson, S. M., Herzog, E. L., Driskell, R. R., Rosenthal, N. A., Biernaskie, J. A., & Horsley, V. (2021) · Cell · doi:10.1016/j.cell.2021.06.024 · Cited by 1,162 · see citing works

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 1,061 · see citing works

Pax7-expressing satellite cells are indispensable for adult skeletal muscle regeneration

Sambasivan, R., Yao, R., Kissenpfennig, A., Van Wittenberghe, L., Paldi, A., Gayraud-Morel, B., Guenou, H., Malissen, B., Tajbakhsh, S., & Galy, A. (2011) · Development · doi:10.1242/dev.067587 · Cited by 939 · see citing works

Aberrant repair and fibrosis development in skeletal muscle

Mann, C. J., Perdiguero, E., Kharraz, Y., Aguilar, S., Pessina, P., Serrano, A. L., & Muñoz-Cánoves, P. (2011) · Skeletal Muscle · doi:10.1186/2044-5040-1-21 · Cited by 853 · see citing works

Type 2 Innate Signals Stimulate Fibro/Adipogenic Progenitors to Facilitate Muscle Regeneration

Heredia, J. E., Mukundan, L., Chen, F. M., Mueller, A. A., Deo, R. C., Locksley, R. M., Rando, T. A., & Chawla, A. (2013) · Cell · doi:10.1016/j.cell.2013.02.053 · Cited by 818 · see citing works

Adaptive thermogenesis in adipocytes: Is beige the new brown?

Wu, J., Cohen, P., & Spiegelman, B. M. (2013) · Genes & Development · doi:10.1101/gad.211649.112 · Cited by 828 · see citing works

Stem cell aging: mechanisms, regulators and therapeutic opportunities

Oh, J., Lee, Y. D., & Wagers, A. J. (2014) · Nature Medicine · doi:10.1038/nm.3651 · Cited by 796 · see citing works

Interleukin‐6 myokine signaling in skeletal muscle: a double‐edged sword?

Muñoz‐Cánoves, P., Scheele, C., Pedersen, B. K., & Serrano, A. L. (2013) · The FEBS Journal · doi:10.1111/febs.12338 · Cited by 774 · see citing works

mTORC1 controls the adaptive transition of quiescent stem cells from G0 to GAlert

Rodgers, J. T., King, K. Y., Brett, J. O., Cromie, M. J., Charville, G. W., Maguire, K. K., Brunson, C., Mastey, N., Liu, L., Tsai, C.-R., et al. (2014) · Nature · doi:10.1038/nature13255 · Cited by 776 · see citing works

Satellite Cells and Skeletal Muscle Regeneration

Dumont, N. A., Bentzinger, C. F., Sincennes, M., & Rudnicki, M. A. (2015) · Comprehensive Physiology · doi:10.1002/cphy.c140068 · Cited by 719 · see citing works

Nilotinib reduces muscle fibrosis in chronic muscle injury by promoting TNF-mediated apoptosis of fibro/adipogenic progenitors

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 · see citing works

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 · see citing works

Macrophages in inflammation, repair and regeneration

Oishi, Y., & Manabe, I. (2018) · International Immunology · doi:10.1093/intimm/dxy054 · Cited by 645 · see citing works

Identification and isolation of a dermal lineage with intrinsic fibrogenic potential

Rinkevich, Y., Walmsley, G. G., Hu, M. S.-M., Maan, Z. N., Newman, A. M., Drukker, M., Januszyk, M., Krampitz, G. W., Gurtner, G. C., Lorenz, H. P., et al. (2015) · Science · doi:10.1126/science.aaa2151 · Cited by 695 · see citing works

In Vivo Identification of Bipotential Adipocyte Progenitors Recruited by β3-Adrenoceptor Activation and High-Fat Feeding

Lee, Y., Petkova, A. P., Mottillo, E. P., & Granneman, J. G. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.03.009 · Cited by 676 · 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

Skeletal muscle: A review of molecular structure and function, in health and disease

Mukund, K., & Subramaniam, S. (2019) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1462 · Cited by 680 · see citing works

Specialized fibroblast differentiated states underlie scar formation in the infarcted mouse heart

Fu, X., Khalil, H., Kanisicak, O., Boyer, J. G., Vagnozzi, R. J., Maliken, B. D., Sargent, M. A., Prasad, V., Valiente-Alandi, I., Blaxall, B. C., et al. (2018) · Journal of Clinical Investigation · doi:10.1172/jci98215 · Cited by 636 · see citing works

Identification of a mesenchymal progenitor cell hierarchy in adipose tissue

Merrick, D., Sakers, A., Irgebay, Z., Okada, C., Calvert, C., Morley, M. P., Percec, I., & Seale, P. (2019) · Science · doi:10.1126/science.aav2501 · Cited by 664 · see citing works

Adipocyte Lineage Cells Contribute to the Skin Stem Cell Niche to Drive Hair Cycling

Festa, E., Fretz, J. A., Berry, R., Schmidt, B., Rodeheffer, M. S., Horowitz, M. C., & Horsley, V. (2011) · Cell · doi:10.1016/j.cell.2011.07.019 · Cited by 616 · see citing works

Chromatin modifications as determinants of muscle stem cell quiescence and chronological aging

Liu, L., Cheung, T. H., Charville, G. W., Hurgo, B. M. C., Leavitt, T., Shih, J., Brunet, A., & Rando, T. A. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.05.043 · Cited by 544 · see citing works

Characterization of the adipocyte cellular lineage in vivo

Berry, R., & Rodeheffer, M. S. (2013) · Nature Cell Biology · doi:10.1038/ncb2696 · Cited by 542 · see citing works

Mesenchymal Cell Contributions to the Stem Cell Niche

Kfoury, Y. S., & Scadden, D. T. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.02.019 · Cited by 548 · see citing works

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 390 · see citing works

A Critical Requirement for Notch Signaling in Maintenance of the Quiescent Skeletal Muscle Stem Cell State

Mourikis, P., Sambasivan, R., Castel, D., Rocheteau, P., Bizzarro, V., & Tajbakhsh, S. (2012) · Stem Cells · doi:10.1002/stem.775 · Cited by 526 · see citing works

Poor Repair of Skeletal Muscle in Aging Mice Reflects a Defect in Local, Interleukin-33-Dependent Accumulation of Regulatory T Cells

Kuswanto, W. F., Burzyn, D., Panduro, M., Wang, K. K., Jang, Y. C., Wagers, A. J., Benoist, C. O., & Mathis, D. J. (2016) · Immunity · doi:10.1016/j.immuni.2016.01.009 · Cited by 509 · see citing works

eRNAs Promote Transcription by Establishing Chromatin Accessibility at Defined Genomic Loci

Mousavi, K., Zare, H., Dell’Orso, S., Grøntved, L., Gutierrez-Cruz, G., Derfoul, A., Hager, G. L., & Sartorelli, V. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.07.022 · Cited by 503 · see citing works

Satellite cells, the engines of muscle repair

Wang, Y. X., & Rudnicki, M. A. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3265 · Cited by 493 · see citing works

Functions of tissue-resident eosinophils

Weller, P. F., & Spencer, L. A. (2017) · Nature reviews. Immunology · doi:10.1038/nri.2017.95 · Cited by 480 · see citing works

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 · see citing works

AMPKα1 Regulates Macrophage Skewing at the Time of Resolution of Inflammation during Skeletal Muscle Regeneration

Mounier, R., Théret, M., Arnold, L., Cuvellier, S., Bultot, L., Göransson, O., Sanz, N., Ferry, A., Sakamoto, K., Foretz, M., et al. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.06.017 · Cited by 464 · see citing works

Identification of inducible brown adipocyte progenitors residing in skeletal muscle and white fat

Schulz, T. J., Huang, T. L., Tran, T. T., Zhang, H., Townsend, K. L., Shadrach, J. L., Cerletti, M., McDougall, L. E., Giorgadze, N., Tchkonia, T., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010929108 · Cited by 459 · see citing works

The central role of muscle stem cells in regenerative failure with aging

Blau, H. M., Cosgrove, B. D., & Ho, A. T. V. (2015) · Nature Medicine · doi:10.1038/nm.3918 · Cited by 437 · see citing works

Arrhythmogenic Cardiomyopathy

Corrado, D., Basso, C., & Judge, D. P. (2017) · Circulation Research · doi:10.1161/circresaha.117.309345 · Cited by 462 · see citing works

Adipose tissue stem cells meet preadipocyte commitment: going back to the future

Cawthorn, W. P., Scheller, E. L., & MacDougald, O. A. (2011) · Journal of Lipid Research · doi:10.1194/jlr.r021089 · Cited by 440 · see citing works

No Identical “Mesenchymal Stem Cells” at Different Times and Sites: Human Committed Progenitors of Distinct Origin and Differentiation Potential Are Incorporated as Adventitial Cells in Microvessels

Sacchetti, B., Funari, A., Remoli, C., Giannicola, G., Kogler, G., Liedtke, S., Cossu, G., Serafini, M., Sampaolesi, M., Tagliafico, E., et al. (2016) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.05.011 · Cited by 428 · see citing works

Mesenchymal Stromal Cells Are Required for Regeneration and Homeostatic Maintenance of Skeletal Muscle

Wosczyna, M. N., Konishi, C. T., Carbajal, E. E. P., Wang, T. T., Walsh, R. A., Gan, Q., Wagner, M. W., & Rando, T. A. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.04.074 · Cited by 438 · see citing works

Zfp423 Expression Identifies Committed Preadipocytes and Localizes to Adipose Endothelial and Perivascular Cells

Gupta, R. K., Mepani, R. J., Kleiner, S., Lo, J. C., Khandekar, M. J., Cohen, P., Frontini, A., Bhowmick, D. C., Ye, L., Cinti, S., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.01.010 · Cited by 426 · see citing works

Lineage tracing and genetic ablation of ADAM12(+) perivascular cells identify a major source of profibrotic cells during acute tissue injury

Dulauroy, S., Di Carlo, S. E., Langa, F., Eberl, G., & Peduto, L. (2012) · Nature Medicine · doi:10.1038/nm.2848 · Cited by 418 · see citing works

Tissue-specific stem cells: Lessons from the skeletal muscle satellite cell

Brack, A. S., & Rando, T. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2012.04.001 · Cited by 409 · see citing works

Oxytocin is an age-specific circulating hormone that is necessary for muscle maintenance and regeneration

Elabd, C., Cousin, W., Upadhyayula, P., Chen, R. Y., Chooljian, M. S., Li, J., Kung, S., Jiang, K. P., & Conboy, I. M. (2014) · Nature Communications · doi:10.1038/ncomms5082 · Cited by 411 · see citing works

Isolation of skeletal muscle stem cells by fluorescence-activated cell sorting

Liu, L. A., Cheung, T. H., Charville, G. W., & Rando, T. A. (2015) · Nature Protocols · doi:10.1038/nprot.2015.110 · Cited by 396 · see citing works

Short-Term Calorie Restriction Enhances Skeletal Muscle Stem Cell Function

Cerletti, M., Jang, Y. C., Finley, L. W. S., Haigis, M. C., & Wagers, A. J. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.04.002 · Cited by 397 · see citing works

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 · see citing works

High-Dimensional Single-Cell Cartography Reveals Novel Skeletal Muscle-Resident Cell Populations

Giordani, L., He, G. J., Négroni, E., Sakai, H., Law, J. Y. C., 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 389 · see citing works

Fibronectin Regulates Wnt7a Signaling and Satellite Cell Expansion

Bentzinger, C. F., Wang, Y. X., von Maltzahn, J., Soleimani, V. D., Yin, H., & Rudnicki, M. A. (2013) · Cell Stem Cell · doi:10.1016/j.stem.2012.09.015 · Cited by 386 · see citing works

Biomarkers of aging

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 389 · see citing works

Single-cell analysis of the muscle stem cell hierarchy identifies heterotypic communication signals involved in skeletal muscle regeneration

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 · see citing works

Aging disrupts muscle stem cell function by impairing matricellular WISP1 secretion from fibro-adipogenic progenitors

Lukjanenko, L., Karaz, S., Stuelsatz, P., Gurriaran-Rodriguez, U., Michaud, J., Dammone, G., Sizzano, F., Mashinchian, O., Ancel, S., Migliavacca, E., et al. (2019) · Cell stem cell · doi:10.1016/j.stem.2018.12.014 · Cited by 374 · see citing works

NF-κB–mediated Pax7 dysregulation in the muscle microenvironment promotes cancer cachexia

He, W. A., Berardi, E., Cardillo, V. M., Acharyya, S., Aulino, P., Thomas-Ahner, J., Wang, J., Bloomston, M., Muscarella, P., Nau, P., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci68523 · Cited by 357 · see citing works

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 353 · see citing works

Adipogenesis at a glance

Lowe, C. E., O’Rahilly, S., & Rochford, J. J. (2011) · Journal of Cell Science · doi:10.1242/jcs.079699 · Cited by 342 · see citing works

PTEN Loss in the Myf5 Lineage Redistributes Body Fat and Reveals Subsets of White Adipocytes that Arise from Myf5 Precursors

Sánchez-Gurmaches, J., Hung, C., Sparks, C. A., Tang, Y., Li, H., & Guertin, D. A. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.08.003 · Cited by 342 · see citing works

Skeletal muscle regeneration is modulated by inflammation

Yang, W.-J., & Hu, P. (2018) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2018.01.002 · Cited by 303 · see citing works

Tissue Stem Cells: Architects of Their Niches

Fuchs, E., & Blau, H. M. (2020) · Cell Stem Cell · doi:10.1016/j.stem.2020.09.011 · Cited by 332 · see citing works

Multipotent progenitors resident in the skeletal muscle interstitium exhibit robust BMP-dependent osteogenic activity and mediate heterotopic ossification

Wosczyna, M. N., Biswas, A. A., Cogswell, C. A., & Goldhamer, D. J. (2012) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1562 · Cited by 325 · see citing works

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 · see citing works

Denervation-activated STAT3–IL-6 signalling in fibro-adipogenic progenitors promotes myofibres atrophy and fibrosis

Madaro, L., Passafaro, M., Sala, D., Etxaniz, U., Lugarini, F., Proietti, D., Alfonsi, M. V., Nicoletti, C., Gatto, S., De Bardi, M., et al. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0151-y · Cited by 310 · see citing works

Molecular circuitry of stem cell fate in skeletal muscle regeneration, ageing and disease

Almada, A. E., & Wagers, A. J. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.7 · Cited by 314 · see citing works

Defining dermal adipose tissue

Driskell, R. R., Jahoda, C. A. B., Chuong, C., Watt, F. M., & Horsley, V. (2014) · Experimental Dermatology · doi:10.1111/exd.12450 · Cited by 316 · see citing works

Connective tissue fibroblasts and Tcf4 regulate myogenesis

Mathew, S. J., Hansen, J. M., Merrell, A. J., Murphy, M. M., Lawson, J. A., Hutcheson, D. A., Hansen, M. S. T., Angus-Hill, M. L., & Kardon, G. (2010) · Development · doi:10.1242/dev.057463 · Cited by 309 · see citing works

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 313 · see citing works

Cellular Mechanisms of Tissue Fibrosis. 4. Structural and functional consequences of skeletal muscle fibrosis

Lieber, R. L., & Ward, S. R. (2013) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00173.2013 · Cited by 303 · see citing works

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 307 · see citing works

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 · see citing works

MicroRNA-133 Controls Brown Adipose Determination in Skeletal Muscle Satellite Cells by Targeting Prdm16

Yin, H., Pasut, A., Soleimani, V. D., Bentzinger, C. F., Antoun, G., Thorn, S., Seale, P., Fernando, P., van IJcken, W., Grosveld, F., et al. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.01.004 · Cited by 293 · see citing works

Macrophage Plasticity and the Role of Inflammation in Skeletal Muscle Repair

Kharraz, Y., Guerra, J., Mann, C. J., Serrano, A. L., & Muñoz‐Cánoves, P. (2013) · Mediators of Inflammation · doi:10.1155/2013/491497 · Cited by 302 · see citing works

Intradermal adipocytes mediate fibroblast recruitment during skin wound healing

Schmidt, B. A., & Horsley, V. (2013) · Development · doi:10.1242/dev.087593 · Cited by 318 · see citing works

Regulation and dysregulation of fibrosis in skeletal muscle

Serrano, A. L., & Muñoz‐Cánoves, P. (2010) · Experimental Cell Research · doi:10.1016/j.yexcr.2010.05.035 · Cited by 291 · see citing works

A PDGFRα-Mediated Switch toward CD9high Adipocyte Progenitors Controls Obesity-Induced Adipose Tissue Fibrosis

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 280 · see citing works

Temporal Dynamics and Heterogeneity of Cell Populations during Skeletal Muscle Regeneration

Oprescu, S. N., Yue, F., Qiu, J., Brito, L. F., & Kuang, S. (2020) · iScience · doi:10.1016/j.isci.2020.100993 · Cited by 288 · see citing works

Stem Cell Differentiation is Regulated by Extracellular Matrix Mechanics

Smith, L., Cho, S., & Discher, D. E. (2017) · Physiology · doi:10.1152/physiol.00026.2017 · Cited by 280 · see citing works

Identification of an Adipogenic Niche for Adipose Tissue Remodeling and Restoration

Lee, Y., Petkova, A. P., & Granneman, J. G. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.08.003 · Cited by 274 · see citing works

Bioengineered constructs combined with exercise enhance stem cell-mediated treatment of volumetric muscle loss

Quarta, M., Cromie, M. J., Chacon, R., Blonigan, J., Garcia, V., Akimenko, I., Hamer, M., Paine, P., Stok, M., Shrager, J. B., et al. (2017) · Nature Communications · doi:10.1038/ncomms15613 · Cited by 280 · see citing works

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 274 · see citing works

Cardiac Fibroblast Diversity

Tallquist, M. D. (2020) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021119-034527 · Cited by 276 · see citing works

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 · see citing works

Inflammation induced loss of skeletal muscle

Londhe, P., & Guttridge, D. C. (2015) · Bone · doi:10.1016/j.bone.2015.03.015 · Cited by 276 · see citing works

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 · see citing works

Adipocyte lineages: Tracing back the origins of fat

Sánchez-Gurmaches, J., & Guertin, D. A. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.05.027 · Cited by 260 · see citing works

Tissue Engineering and Regenerative Medicine: Recent Innovations and the Transition to Translation

Fisher, M. B., & Mauck, R. L. (2012) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2012.0723 · Cited by 262 · see citing works

MEAT SCIENCE AND MUSCLE BIOLOGY SYMPOSIUM: Manipulating mesenchymal progenitor cell differentiation to optimize performance and carcass value of beef cattle1,2

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 · see citing works

A Tppp3+Pdgfra+ tendon stem cell population contributes to regeneration and reveals a shared role for PDGF signalling in regeneration and fibrosis

Harvey, T., Flamenco, S., & Fan, C. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0417-z · Cited by 262 · see citing works

Fibroadipogenic progenitors mediate the ability of HDAC inhibitors to promote regeneration in dystrophic muscles of young, but not old Mdx mice

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 · see citing works

Atrial fibrillation is associated with the fibrotic remodelling of adipose tissue in the subepicardium of human and sheep atria

Haemers, P., Hamdi, H., Guedj, K., Suffee, N., Farahmand, P., Popović, N., Claus, P., Leprince, P. N., Nicoletti, A., Jalife, J., et al. (2015) · European Heart Journal · doi:10.1093/eurheartj/ehv625 · Cited by 260 · see citing works

Myogenic regulatory factors: The orchestrators of myogenesis after 30 years of discovery

Asfour, H. A., Allouh, M. Z., & Said, R. S. (2018) · Experimental Biology and Medicine · doi:10.1177/1535370217749494 · Cited by 257 · see citing works

Defining the Cardiac Fibroblast

Ivey, M. J., & Tallquist, M. D. (2016) · Circulation Journal · doi:10.1253/circj.cj-16-1003 · Cited by 258 · see citing works

Foxc1 is a critical regulator of haematopoietic stem/progenitor cell niche formation

Omatsu, Y., Seike, M., Sugiyama, T., Kume, T., & Nagasawa, T. (2014) · Nature · doi:10.1038/nature13071 · Cited by 254 · see citing works

Mechanisms Regulating Muscle Regeneration: Insights into the Interrelated and Time-Dependent Phases of Tissue Healing

Forcina, L., Cosentino, M., & Musarò, A. (2020) · Cells · doi:10.3390/cells9051297 · Cited by 252 · see citing works

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 251 · see citing works

NAD ⁺ repletion improves muscle function in muscular dystrophy and counters global PARylation

Ryu, D., Zhang, H., Ropelle, E. R., Sorrentino, V., Mázala, D. A. G., Mouchiroud, L., Marshall, P. L., Campbell, M. D., Ali, A. S., Knowels, G. M., et al. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf5504 · Cited by 256 · see citing works

The effects of obesity on skeletal muscle regeneration

Akhmedov, D., & Berdeaux, R. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00371 · Cited by 241 · see citing works

Fat1 deletion enhances Fibro-Adipogenic Differentiation and Adipogenic expansion following injury in skeletal musclePreprint

Ferracci, P.-A., & Helmbacher, F. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.21.719880

Fibro-adipogenic progenitors in healthy and dystrophic human skeletal muscles : characterization and interactions with myogenic progenitors and macrophages

Moratal, C. (2016) · theses.fr (ABES)

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 193 · see citing works

Fibro-Adipogenic Progenitors: Versatile keepers of skeletal muscle homeostasis, beyond the response to myotrauma

Wei, X., Nicoletti, C., & Puri, P. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.07.013 · Cited by 21 · see citing works

Adipose tissue is a source of regenerative cells that augment the repair of skeletal muscle after injury

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 · see citing works