Skeletal Muscle Degenerative Diseases and Strategies for Therapeutic Muscle Repair

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Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells

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SATELLITE CELL OF SKELETAL MUSCLE FIBERS

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Rejuvenation of aged progenitor cells by exposure to a young systemic environment

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Dystrophin expression in the mdx mouse restored by stem cell transplantation

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Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis

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A Special Population of Regulatory T Cells Potentiates Muscle Repair

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NAD + repletion improves mitochondrial and stem cell function and enhances life span in mice

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In vivo gene editing in dystrophic mouse muscle and muscle stem cells

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Stem cell aging: mechanisms, regulators and therapeutic opportunities

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Tissue Tregs

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Exosomes from differentiating human skeletal muscle cells trigger myogenesis of stem cells and provide biochemical cues for skeletal muscle regeneration

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Muscle Expression of Mutant Androgen Receptor Accounts for Systemic and Motor Neuron Disease Phenotypes in Spinal and Bulbar Muscular Atrophy

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Physiopathology of the Permeability Transition Pore: Molecular Mechanisms in Human Pathology

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Adiponectin promotes muscle regeneration through binding to T-cadherin

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A Novel Microplate 3D Bioprinting Platform for the Engineering of Muscle and Tendon Tissues

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Barium chloride injures myofibers through calcium-induced proteolysis with fragmentation of motor nerves and microvessels

Morton, A. B., Norton, C. E., Jacobsen, N. L., Fernando, C. A., Cornelison, D., & Segal, S. S. (2019) · Skeletal Muscle · doi:10.1186/s13395-019-0213-2 · Cited by 95

Functions and Regulatory Mechanisms of lncRNAs in Skeletal Myogenesis, Muscle Disease and Meat Production

Wang, S., Jin, J., Xu, Z., & Zuo, B. (2019) · Cells · doi:10.3390/cells8091107 · Cited by 89

Magnetically Activated Electroactive Microenvironments for Skeletal Muscle Tissue Regeneration

Ribeiro, S., Ribeiro, C., Carvalho, E. O., Tubio, C. R., Castro, N., Pereira, N. M., Correia, V. M. G., Gomes, A. C., & Lanceros-Méndez, S. (2020) · ACS Applied Bio Materials · doi:10.1021/acsabm.0c00315 · Cited by 78

iPSC s: A powerful tool for skeletal muscle tissue engineering

Ortuño‐Costela, M. D. C., García‐López, M., Cerrada, V., & Gallardo, M. E. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14292 · Cited by 59

Platelet-Derived Growth Factor BB Influences Muscle Regeneration in Duchenne Muscle Dystrophy

Piñol‐Jurado, P., Gallardo, E., de Luna, N., Suárez‐Calvet, X., Riera, C. S., Fernández‐Simón, E., Gomis, C., Illa, I., & Díaz‐Manera, J. (2017) · American Journal Of Pathology · doi:10.1016/j.ajpath.2017.04.011 · Cited by 46

3D biofabrication for soft tissue and cartilage engineering

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MicroRNA-432 targeting E2F3 and P55PIK inhibits myogenesis through PI3K/AKT/mTOR signaling pathway

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An emerging role of regulatory T-cells in cardiovascular repair and regeneration

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Preparation of decellularized biphasic hierarchical myotendinous junction extracellular matrix for muscle regeneration

Zhao, C., Wang, S., Wang, G., Su, M., Song, L., Chen, J., Fan, S., & Lin, X. (2017) · Acta Biomaterialia · doi:10.1016/j.actbio.2017.12.035 · Cited by 39

The extraocular muscle stem cell niche is resistant to ageing and disease

Formicola, L., Marazzi, G., & Sassoon, D. A. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00328 · Cited by 42

The effect of hypoxia on myogenic differentiation and multipotency of the skeletal muscle-derived stem cells in mice

Elashry, M. I., Kinde, M. Z., Klymiuk, M. C., Eldaey, A., Wenisch, S., & Arnhold, S. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-02730-5 · Cited by 34

Skeletal muscle dedifferentiation during salamander limb regeneration

Wang, H., & Simon, A. (2016) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2016.06.013 · Cited by 33

Cytoskeleton and Adhesion in Myogenesis

Costa, M. L. (2014) · ISRN Developmental Biology · doi:10.1155/2014/713631 · Cited by 32

New roles for Smad signaling and phosphatidic acid in the regulation of skeletal muscle mass

Goodman, C. A., & Hornberger, T. A. (2014) · F1000Prime Reports · doi:10.12703/p6-20 · Cited by 30

Cell fusion is differentially regulated in zebrafish post-embryonic slow and fast muscle

Hromowyk, K. J., Talbot, J. C., Martin, B. L., Janssen, P. M. L., & Amacher, S. L. (2020) · Developmental Biology · doi:10.1016/j.ydbio.2020.03.005 · Cited by 29

Investigating the passive mechanical behaviour of skeletal muscle fibres: Micromechanical experiments and Bayesian hierarchical modelling

Böl, M., Kumar, R. I., Dittmann, J., Garcés-Schröder, M., & Dietzel, A. H. (2019) · Acta Biomaterialia · doi:10.1016/j.actbio.2019.05.015 · Cited by 28

Development and application of human skeletal muscle microphysiological systems

Truskey, G. A. (2018) · Lab on a Chip · doi:10.1039/c8lc00553b · Cited by 28

Hypoglycosylation of dystroglycan due to T192M mutation: A molecular insight behind the fact

Bhattacharya, S., Das, A., Ghosh, S., Dasgupta, R., & Bagchi, A. (2013) · Gene · doi:10.1016/j.gene.2013.11.071 · Cited by 24

Nanomaterial‐Mediated Reprogramming of Macrophages to Inhibit Refractory Muscle Fibrosis

Cheng, X., Sui, H., Chen, F., Li, C., Du, M., Zhang, S., Chen, J., Dou, J., Huang, Y., Xie, X., et al. (2024) · Advanced Materials · doi:10.1002/adma.202410368 · Cited by 24

Genome Editing in Neurosciences

Jaenisch, R., Gage, F. H., & Zhang, F. (2017) · Research and perspectives in neurosciences · doi:10.1007/978-3-319-60192-2 · Cited by 23

Regulatory T cells were recruited by CCL3 to promote cryo-injured muscle repair

Zhang, C., Qiao, Y., Huang, L. J., Li, F., Zhang, Z., Yü, P., Shen, Z., Lian, J., Li, F., Zhao, L., et al. (2018) · Immunology Letters · doi:10.1016/j.imlet.2018.10.004 · Cited by 21

Insights into the Notch signaling pathway in degenerative musculoskeletal disorders: Mechanisms and perspectives

Liu, G., Wei, J., Xiao, W., Xie, W., Ru, Q., Chen, L., Wu, Y., Mobasheri, A., & Li, Y. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115884 · Cited by 23

Direct measurement of the direction-dependent mechanical behaviour of skeletal muscle extracellular matrix

Kohn, S., Leichsenring, K., Kuravi, R., Ehret, A. E., & Böl, M. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.12.050 · Cited by 21

Novel Insights Into the Multifaceted Functions of RNA n6-Methyladenosine Modification in Degenerative Musculoskeletal Diseases

Li, H., Xiao, W., He, Y., Wen, Z., Cheng, S., Zhang, Y., & Li, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.766020 · Cited by 20

Effects of physical exercise on neuromuscular junction degeneration during ageing: A systematic review

Wang, Q., Cui, C., Zhang, N., Lin, W., Chai, S., Chow, S. K., Wong, R. M. Y., Hu, Y. S., Law, S. W., & Cheung, W. (2024) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2024.03.007 · Cited by 24

Myofiber-specific TEAD1 overexpression drives satellite cell hyperplasia and counters pathological effects of dystrophin deficiency

Southard, S. M., Kim, J.-R., Low, S., Tsika, R. W., & Lepper, C. (2016) · eLife · doi:10.7554/elife.15461 · Cited by 20

Targeting of miR-432 to myozenin1 to regulate myoblast proliferation and differentiation

Ren, R. M., Liu, H., Zhao, S. H., & Cao, J. H. (2016) · Genetics and Molecular Research · doi:10.4238/gmr15049313 · Cited by 19

Novel insights of EZH2-mediated epigenetic modifications in degenerative musculoskeletal diseases

Ma, Z., Chen, L., Wang, Y., Zhang, S., Zheng, J., Luo, Y., Wang, C., Zeng, H., Xue, L., Tan, Z. W., et al. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102034 · Cited by 19

LncRNAs as a new regulator of chronic musculoskeletal disorder

Huang, H., Xing, D., Zhang, Q., Li, H., Lin, J., He, Z., & Lin, J. (2021) · Cell Proliferation · doi:10.1111/cpr.13113 · Cited by 18

Two Enhancers Control Transcription of Drosophila muscleblind in the Embryonic Somatic Musculature and in the Central Nervous System

Bargiela, A., Llamusí, B., Cerro-Herreros, E., & Artero, R. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093125 · Cited by 18

Role and molecular mechanism of ghrelin in degenerative musculoskeletal disorders

Sun, J.-F., Tan, Y., Su, J.-Y., Mikhail, H., Pavel, V., Deng, Z., & Li, Y.-S. (2023) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17944 · Cited by 11

Inhibition of the Activin Receptor Type-2B Pathway Restores Regenerative Capacity in Satellite Cell-Depleted Skeletal Muscle

Formicola, L., Pannérec, A., Correra, R. M., Gayraud-Morel, B., Ollitrault, D., Besson, V., Tajbakhsh, S., Lachey, J. L., Seehra, J. S., Marazzi, G., et al. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00515 · Cited by 17

Growth and Differentiation of Circulating Stem Cells After Extensive Ex Vivo Expansion

Barbon, S., Rajendran, S., Bertalot, T., Piccione, M., Gasparella, M., Parnigotto, P. P., Liddo, R. D., & Conconi, M. T. (2021) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-021-00330-7 · Cited by 15

Wnt7a induces satellite cell expansion, myofiber hyperplasia and hypertrophy in rat craniofacial muscle

Cheng, X., Huang, H., Luo, X., Shi, B., & Li, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-28917-6 · Cited by 13

Cryoinjury Model for Tissue Injury and Repair in Bioengineered Human Striated Muscle

Mills, R. J., Voges, H. K., Porrello, E. R., & Hudson, J. E. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7283-8_15 · Cited by 10

The dual guardians of cellular stability: exploring nesprin and lamin in senescence

Zhou, Z., Qin, Q., Dong, C., Liu, Y., Cao, C., & Teng, L. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-08087-w · Cited by 10

Fatty acids impact sarcomere integrity through myristoylation and ER homeostasis

Tang, H., Cui, M., & Han, M. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109539 · Cited by 9

Metabolic adaptation orchestrates tissue context‐dependent behavior in regulatory T cells

Wang, H., Lu, C., & Ho, P. (2020) · Immunological Reviews · doi:10.1111/imr.12844 · Cited by 10

Human MuStem cells repress T-cell proliferation and cytotoxicity through both paracrine and contact-dependent pathways

Charrier, M., Lorant, J., Contreras-López, R. A., Téjédor, G., Blanquart, C., Lieubeau, B., Schleder, C., Leroux, I., Deshayes, S., Fonteneau, J., et al. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02681-3 · Cited by 9

Transplantation of Muscle Stem Cell Mitochondria Rejuvenates the Bioenergetic Function of Dystrophic MusclePreprint

Mohiuddin, M., Choi, J. J., Lee, N. H., Jeong, H., Anderson, S. E., Han, W. M., Aliya, B., Peykova, T. Z., Verma, S., Garcı́a, A. J., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.17.017822 · Cited by 8

Polymer-based stimuli-responsive biomaterials featuring self-generated electric fields for tissue repair

Li, X., Zhang, Y., Deng, Z., Zhao, X., Zhang, S., Shan, Y., Guo, B., & Han, Y. (2026) · Progress in Materials Science · doi:10.1016/j.pmatsci.2026.101660 · Cited by 8

Bioengineered human pre-vascularized microtissues reconstruct vascular niche and regenerative microenvironment to enhance functional skeletal muscle regeneration

Cheng, L., Gao, Y. P., Li, J., Liang, Q., Li, M., Yang, J., Su, X., Zhang, J., Tian, W., & Liao, L. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123645 · Cited by 8

Biomaterial-based strategies for cell-free nucleic acids scavenging and macrophage modulation in oral diseases: Mechanisms and therapeutic potential

Chen, J., Xu, C., Zhang, S., Sui, H., Fang, K., Li, S., Yang, R., Yang, C., Shao, D., Zheng, Q., et al. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123773 · Cited by 6

5-Azacytidine incorporated skeletal muscle-derived hydrogel promotes rat skeletal muscle regeneration

Ahmadi, B. M., Noori, A., Ashtiani, M. K., Rajabi, S., & Talkhabi, M. (2023) · Cells and Development · doi:10.1016/j.cdev.2023.203826 · Cited by 6

Combinations of Kinase Inhibitors Protecting Myoblasts against Hypoxia

Kang, Y., Tierney, M. T., Ong, E., Zhang, L., Piermarocchi, C., Sacco, A., & Paternostro, G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0126718 · Cited by 6

Elemental Composition of Skeletal Muscle Fibres Studied with Synchrotron Radiation X-ray Fluorescence (SR-XRF)

Kasprzyk, P., Wróbel, P., Dudała, J., Geraki, K., Szczerbowska‐Boruchowska, M., Radwańska, E., Krzyżewski, R. M., Adamek, D., & Lankosz, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147931 · Cited by 5

Transplantation-based screen identifies inducers of muscle progenitor cell engraftment across vertebrate species

Tavakoli, S., Garcia, V., Gähwiler, E. K. N., Adatto, I., Rangan, A., Messemer, K. A., Kakhki, S. A., Yang, S. P., Chan, V., Manning, M. E., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112365 · Cited by 4

Muscle Stem Cell Immunostaining

Wang, S., Zhang, B., Addicks, G. C., Zhang, H., Menzies, K. J., & Zhang, H. (2018) · Current Protocols in Mouse Biology · doi:10.1002/cpmo.47 · Cited by 4

Therapeutic Gene Editing in Muscles and Muscle Stem Cells

Tabebordbar, M., Cheng, J. K. W., & Wagers, A. J. (2017) · Research and perspectives in neurosciences · doi:10.1007/978-3-319-60192-2_10 · Cited by 3

A novel intraoral injection technique for rat levator veli palatini muscle regeneration

Cheng, X., Huang, H., Shi, B., & Li, J. (2019) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2019.01.012 · Cited by 3

Effects of the purified dry extract of fermented ginseng BST204 on muscle fiber regeneration

Jo, S. I., Park, Y. S., Chang, Y., Moon, J.-H., Lee, S. B., Lee, H., Kim, M., Kim, D. Y., Bae, S., Park, S. Y., et al. (2023) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2023.101525 · Cited by 2

XLOC_015548 Mitigates Skeletal Muscle Atrophy via the Gadd45g/MEK/ERK Pathway and Redox Regulation

Qi, T., Qin, H., Yu, F., Zhou, Z., Chen, Y., Liu, P., Zeng, H., & Weng, J. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl36233 · Cited by 3

Non-canonical muscle stem cells and other lessons from regenerative vertebrates

Jamwal, V. S., Masselink, W., Crawford, K., & Murawala, P. (2026) · npj Regenerative Medicine · doi:10.1038/s41536-026-00468-9 · Cited by 1

Enhancing Skeletal Muscle Fiber Type Transition Through Substrate Coating Alteration in Myoblast Cell Culture

Riskawati, Y. K., Lin, C., Niwa, A., & Chang, H. C. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26125637 · Cited by 2

Prospects of 3D Bioprinting as a Possible Treatment for Cancer Cachexia

Galib, M., Araf, Y., Naser, I. B., & Promon, S. K. (2021) · Journal of Clinical and Experimental Investigations · doi:10.29333/jcei/11289 · Cited by 1

Influência do tempo de irradiação da terapia por ultrassom sobre o tecido conjuntivo no processo de reparação muscular de ratos

Baldan, C. S. (2013) · doi:10.11606/t.5.2013.tde-26032013-151130

T CELL SUBSETS AND DISEASE MECHANISMS IN INFLAMMATORY MYOPATHIES

Pandya, J. M. (2014) · Figshare

Plastyczność mięśni szkieletowych: Od miogenezy po regenerację

Rędowicz, M. J., & Wojton, D. (2021) · Kosmos · doi:10.36921/kos.2020_2708

Skeletal muscle weakness and mitochondrial dysfunction in the osteogenesis imperfecta murine (oim) model

Gremminger, V. L. (2021) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/85774

Sub-cellular elemental imaging of human muscle tissues affected by neuromuscular diseases

Śliż-Szpytma, P., Lankosz, M., Dudała, J., Adamek, D., Radwańska, E., Kwinta, B. M., Jakšić, M., Mihalić, I. B., & Provatas, G. (2021) · Nukleonika · doi:10.2478/nuka-2021-0024

Transplantation-based screen uncovers inducers of muscle progenitor cell engraftment across vertebrate speciesPreprint

Tavakoli, S., Adatto, I., Kakhki, S. A., Chan, V., Fotowat, H., Gähwiler, E. K. N., Manning, M. E., Messemer, K. A., Rangan, A., Yang, S. P., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.13.523942

Defining Threshold values of Paraspinal Sarcopenia in Patients with Degenerative Lumbar DiseasesPreprint

Kiram, A., Wang, M., Li, J., Xu, Y., Hu, J., Liu, Q., Hu, Z., Qiu, Y., Zhu, Z., & Liu, Z. (2025) · Research Square · doi:10.21203/rs.3.rs-7085436/v1

Study of the biomolecular composition of skeletal muscle fibres affected by different types of pathology using by FTIR microspectroscopy

Kasprzyk, P., Dudała, J., Lankosz, M., Adamek, D., Kwinta, B. M., Radwańska, E., Lekkas, J., Cinque, G., & Szczerbowska‐Boruchowska, M. (2025) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2025.126727

Additional file 1 of The effect of hypoxia on myogenic differentiation and multipotency of the skeletal muscle-derived stem cells in mice

Elashry, M. I., Kinde, M., Klymiuk, M. C., Eldaey, A., Wenisch, S., & Arnhold, S. (2022) · Figshare · doi:10.6084/m9.figshare.19128863

Role of Nutraceuticals in the Treatment of Degenerative Muscle Diseases

Sahu, R., Thapa, A., Ashraf, G. J., Das, P., Maiti, P. P., Paul, P., Dua, T. K., & Nandi, G. (2026) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9798898813369126010009

Skeletal muscle growth and maintenance depend on BMP signaling

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Deficiency of G9a boosts muscle regeneration through IL13/Musclin-mediated crosstalk between macrophage and myofiber

Jin, Y., Zhou, K., Hao, S., Hu, Y., Wang, H., Liu, Z., Zhou, Y., Xie, Y., Liu, X., Chen, H., et al. (2026) · Cell Death and Disease · doi:10.1038/s41419-026-08944-2

Beyond immune suppression: regenerative programs in regulatory T cells

You, Y., Hu, X., Xue, Y., & Liu, Z. (2026) · Cell Insight · doi:10.1016/j.cellin.2026.100355

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

Stem Cells in Skeletal Muscle

Polesskaya, A., & Rudnicki, M. A. (2004) · Humana Press eBooks · doi:10.1007/978-1-59259-732-1_3

Regenerative Therapy

Morgan, J. E., Brimah, K., & Collins, C. A. (2006) · CRC Press eBooks · doi:10.3109/9780849374456-16

Downstream Pathways of Dystrophin Deficiency in Duchenne Muscular Dystrophy: Implications for Muscle Degeneration and Regeneration

Epis, R., Rovetta, G., Ferrari, G., Bonfanti, C., Careccia, G., & Messina, G. (2026) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.70333 · Cited by 1

Attenuating Muscle Wasting: Cell and Gene Therapy Approaches

Musarò, A., & Rosenthal, N. (2003) · Current Genomics · doi:10.2174/1389202033490222 · Cited by 5