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Molecular Perspective on Skeletal Muscle Regeneration

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Biology".

Deadline for manuscript submissions: 28 February 2026 | Viewed by 143

Special Issue Editor


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Guest Editor
Department of Orthopedic Surgery, University of California, San Francisco, CA 94121, USA
Interests: skeletal muscle regeneration; skeletal muscle stem; progenitor cells; Duchenne muscular dystrophy; intercellular mitochondria transfer

Special Issue Information

Dear Colleagues,

Skeletal muscle possesses a remarkable regenerative capacity that depends on the coordinated activity of stem cells and their niche. Satellite cells remain the primary drivers of regeneration, activating and proliferating in response to injury before differentiating into new myofibers. Their function is tightly regulated by molecular signals within the niche, including Notch, Wnt, FGF, and other pathways that govern quiescence, activation, and self-renewal.  

Emerging evidence highlights the critical contributions of other niche-resident cell types, including fibro/adipogenic progenitors (FAPs), immune cells, and vascular components. These cells engage in dynamic, reciprocal communication with satellite cells through diverse molecular signals—such as TGF-β, interleukins (ILs), PDGFRα, and WISP1—as well as through intercellular organelle exchange. Together, these interactions orchestrate tissue repair and remodeling during muscle regeneration.  

Aging and chronic disease disrupt these finely tuned signaling networks, shifting the muscle niche toward a pro-fibrotic and adipogenic state. This maladaptive environment diminishes satellite cell function, impairs regenerative signaling, and drives pathological outcomes such as fibrosis and fatty infiltration, ultimately leading to compromised muscle repair and functional decline. 

This Special Issue brings together cutting-edge research on stem cell biology, cell–cell communication, and niche regulation, with an emphasis on novel molecular approaches, such as scRNA sequencing, spatial transcriptomes, and small-molecule approaches, as well as translational strategies to restore muscle function in aging, injury, and disease contexts.

Prof. Dr. Xuhui Liu
Guest Editor

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Keywords

  • skeletal muscle regeneration
  • satellite cells
  • stem cell niche
  • fibro/adipogenic progenitors
  • aging
  • muscle stem cells
  • cell–cell interactions
  • fibrosis and fatty infiltration
  • translational therapeutics

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Published Papers (1 paper)

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Research

19 pages, 4855 KB  
Article
An Integrated Multi-Omics Study of Mammalian Skeletal, Cardiac, and Smooth Muscles
by Shengguo Tang, Kaiming Wang, Dongfang Li, Yanna Ma, Liangyuan Peng, Shuchao Liao, Haiming Ma and Hongjiang Wei
Int. J. Mol. Sci. 2026, 27(1), 242; https://doi.org/10.3390/ijms27010242 - 25 Dec 2025
Abstract
Muscle tissue, as a major tissue type, is classified by its structure and function into smooth, cardiac, and skeletal muscle. However, comprehensive studies on the evolutionary conservation of molecular differences among these three muscle tissues have been limited. In this study, we employed [...] Read more.
Muscle tissue, as a major tissue type, is classified by its structure and function into smooth, cardiac, and skeletal muscle. However, comprehensive studies on the evolutionary conservation of molecular differences among these three muscle tissues have been limited. In this study, we employed pigs and mice as models to perform multi-omics profiling (transcriptome, proteome, and metabolome) of these three muscle tissues in order to define their molecular landscapes. Furthermore, we characterized skeletal muscle metabolic heterogeneity. We identified 207 genes enriched in striated muscle, including poorly characterized genes such as LRRC2 and PPP1R14C. Distinct sets of genes and metabolites, conserved between the two species, were specifically enriched in each tissue: skeletal muscle (121 genes and 6 metabolites), cardiac muscle (57 genes and no specific metabolites), and smooth muscle (349 genes and 11 metabolites). Notably, the currently unannotated gene LRRC20 was most enriched in skeletal muscle, followed by cardiac muscle, and showed negligible expression in smooth muscle, suggesting its potential as a functional research target. Within skeletal muscle, 14 fast-twitch and 6 slow-twitch fiber-enriched metabolites were identified. In particular, 10-Deacetylbaccatin III was enriched in skeletal muscle and, more specifically, highly enriched in fast-twitch fibers, marking it as a promising and novel research target. These results provide a resource for research in both medicine and agricultural science. Full article
(This article belongs to the Special Issue Molecular Perspective on Skeletal Muscle Regeneration)
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