Master regulators of skeletal muscle lineage development and pluripotent stem cells differentiation

被引:41
作者
Esteves de Lima, Joana [1 ]
Relaix, Frederic [1 ]
机构
[1] Univ Paris Est Creteil, INSERM, EnvA, EFS,AP HP,IMRB, F-94010 Creteil, France
关键词
Myogenesis; Muscle progenitor; PAX3; PAX7; MRF; MYF5; MYOD; MYOG; hiPSC; ESC; PREMATURE MYOGENIC DIFFERENTIATION; C-MET RECEPTOR; PROGENITOR CELLS; PRECURSOR CELLS; TRANSCRIPTIONAL ACTIVITY; SATELLITE CELLS; SOMITIC ORIGIN; UP-REGULATION; TARGET GENES; LIMB;
D O I
10.1186/s13619-021-00093-5
中图分类号
Q813 [细胞工程];
学科分类号
摘要
In vertebrates, the skeletal muscles of the body and their associated stem cells originate from muscle progenitor cells, during development. The specification of the muscles of the trunk, head and limbs, relies on the activity of distinct genetic hierarchies. The major regulators of trunk and limb muscle specification are the paired-homeobox transcription factors PAX3 and PAX7. Distinct gene regulatory networks drive the formation of the different muscles of the head. Despite the redeployment of diverse upstream regulators of muscle progenitor differentiation, the commitment towards the myogenic fate requires the expression of the early myogenic regulatory factors MYF5, MRF4, MYOD and the late differentiation marker MYOG. The expression of these genes is activated by muscle progenitors throughout development, in several waves of myogenic differentiation, constituting the embryonic, fetal and postnatal phases of muscle growth. In order to achieve myogenic cell commitment while maintaining an undifferentiated pool of muscle progenitors, several signaling pathways regulate the switch between proliferation and differentiation of myoblasts. The identification of the gene regulatory networks operating during myogenesis is crucial for the development of in vitro protocols to differentiate pluripotent stem cells into myoblasts required for regenerative medicine.
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页数:13
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