TY - JOUR
T1 - Muscle Satellite Cell Heterogeneity
T2 - Does Embryonic Origin Matter?
AU - Rodriguez-Outeiriño, Lara
AU - Hernandez-Torres, Francisco
AU - Ramírez-de Acuña, F.
AU - Matías-Valiente, Lidia
AU - Sanchez-Fernandez, Cristina
AU - Franco, Diego
AU - Aranega, Amelia Eva
N1 - Publisher Copyright:
© Copyright © 2021 Rodriguez-Outeiriño, Hernandez-Torres, Ramírez-de Acuña, Matías-Valiente, Sanchez-Fernandez, Franco and Aranega.
PY - 2021/10/15
Y1 - 2021/10/15
N2 - 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.
AB - 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.
KW - adult myogenesis
KW - embryonic myogenesis
KW - muscle regeneration
KW - myogenic precursor cells
KW - satellite cell heterogeneity
UR - https://www.scopus.com/pages/publications/85118267979
U2 - 10.3389/fcell.2021.750534
DO - 10.3389/fcell.2021.750534
M3 - Review article
VL - 9
JO - Frontiers in Cell and Developmental Biology
JF - Frontiers in Cell and Developmental Biology
M1 - 750534
ER -