The current knowledge and recent advances on how this sensory organelle controls muscle stem cell quiescence, enables mechano-sensation, and regulates activation following tissue injury and during asymmetric self-renewal are synthesized.
Abstract
Adult muscle stem cells are responsible for skeletal muscle regeneration, a process where quiescent muscle stem cells activate, enter the cell cycle, and proliferate to give rise to either lineage-committed myoblasts for new muscle fiber formation, or self-renewing cells to replenish the stem cell reservoir. The regenerative capacity of muscle stem cells relies on their precise reception of environmental cues and appropriate intracellular responses. Quiescent muscle stem cells display a primary cilium, a microtubule-based organelle that protrudes from the cell surface and acts as a hub for chemical and mechanical signal transduction. Recent work has significantly increased our understanding of this organelle, demonstrating that the primary cilium actively regulates signaling pathways that are essential for maintenance of muscle stem cell quiescence, proliferation, and fate decision. In this review, we synthesize the current knowledge and recent advances on how this sensory organelle controls muscle stem cell quiescence, enables mechano-sensation, and regulates activation following tissue injury and during asymmetric self-renewal.
The current evidence regarding the role of primary cilium in skeletal, cardiac, and smooth muscle and its potential relevance in muscle disease are examined, providing an integrated overview of cilium-dependent signaling across muscle tissues.
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Muscle stem cells (MuSCs) represent a subset of satellite cells (SCs) and constitute the stem cell compartment of the skeletal muscle tissue. MuSCs and SCs are quiescent under homeostatic conditions but activate upon injury to drive regeneration and repopulation of the stem cell pool. Heterogeneity has become a central...
O. Ashekyan, Marie J. Catenacci, Corentin Guilhot et al.· Frontiers in Cell and Develo...· 0 citations
Skeletal muscle maintenance and regeneration are highly regulated by cell fate decisions made by muscle stem cells and their progeny, myoblasts. Although the transcription factor p53 is well known for its role in cellular stress responses, cell cycle regulation, and tumor prevention, emerging evidence suggests that p53...
Ingrid R. Aragon, Neha Patole, Ajay Vachanaram et al.· Frontiers in Cell and Develo...· 0 citations
Interactions between myogenesis, angiogenesis, and reinnervation provide synergistic support as muscle structure and function are restored as muscle structure and function are restored.
Steven S. Segal· American Journal of Physiolo...· 0 citations
Molecular, cellular, and niche-level evidence across these settings are integrated to explain why FGF signaling produces divergent outcomes and to clarify how cellular context and timing should inform therapeutic modulation.
Multinucleated skeletal muscle cells are stably withdrawn from the cell cycle in most vertebrates. Muscle dedifferentiation, however, naturally occurs during limb regeneration in newts and can be experimentally induced in mammalian myotubes. Here we addressed the dynamics of centrosomes, which are key organelles for ce...