Muscle Satellite Cell Heterogeneity: Does Embryonic Origin Matter?
- PMID: 34722534
- PMCID: PMC8554119
- DOI: 10.3389/fcell.2021.750534
Muscle Satellite Cell Heterogeneity: Does Embryonic Origin Matter?
Abstract
Muscle regeneration is an important homeostatic process of adult skeletal muscle that recapitulates many aspects of embryonic myogenesis. Satellite cells (SCs) are the main muscle stem cells responsible for skeletal muscle regeneration. SCs reside between the myofiber basal lamina and the sarcolemma of the muscle fiber in a quiescent state. However, in response to physiological stimuli or muscle trauma, activated SCs transiently re-enter the cell cycle to proliferate and subsequently exit the cell cycle to differentiate or self-renew. Recent evidence has stated that SCs display functional heterogeneity linked to regenerative capability with an undifferentiated subgroup that is more prone to self-renewal, as well as committed progenitor cells ready for myogenic differentiation. Several lineage tracing studies suggest that such SC heterogeneity could be associated with different embryonic origins. Although it has been established that SCs are derived from the central dermomyotome, how a small subpopulation of the SCs progeny maintain their stem cell identity while most progress through the myogenic program to construct myofibers is not well understood. In this review, we synthesize the works supporting the different developmental origins of SCs as the genesis of their functional heterogeneity.
Keywords: adult myogenesis; embryonic myogenesis; muscle regeneration; myogenic precursor cells; satellite cell heterogeneity.
Copyright © 2021 Rodriguez-Outeiriño, Hernandez-Torres, Ramírez-de Acuña, Matías-Valiente, Sanchez-Fernandez, Franco and Aranega.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Figures
References
Publication types
LinkOut - more resources
Full Text Sources
