The role of Trithorax family regulating osteogenic and Chondrogenic differentiation in mesenchymal stem cells
Mesenchymal stem/stromal cells (MSCs) hold great promise and clinical efficacy in bone/cartilage regeneration. With a deeper understanding of stem cell biology over the past decade, epigenetics stands out as one of the most promising ways to control MSCs differentiation. Trithorax group (TrxG) prote...
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Published in | Cell proliferation Vol. 55; no. 5; pp. e13233 - n/a |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley & Sons, Inc
01.05.2022
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Mesenchymal stem/stromal cells (MSCs) hold great promise and clinical efficacy in bone/cartilage regeneration. With a deeper understanding of stem cell biology over the past decade, epigenetics stands out as one of the most promising ways to control MSCs differentiation. Trithorax group (TrxG) proteins, including the COMPASS family, ASH1L, CBP/p300 as histone modifying factors, and the SWI/SNF complexes as chromatin remodelers, play an important role in gene expression regulation during the process of stem cell differentiation. This review summarises the components and functions of TrxG complexes. We provide an overview of the regulation mechanisms of TrxG in MSCs osteogenic and chondrogenic differentiation, and discuss the prospects of epigenetic regulation mediated by TrxG in bone and cartilage regeneration.
TrxG family is one of the most important mechanisms for gene expression activation in epigenetics. The COMPASS family, ASH1L, and CBP/p300 are associated with histone methylation and acetylation activities. The SWI/SNF complexes have ATP‐dependent chromatin remodelling activities. By targeting differentiation‐related key genes such as RUNX2, OSX, DLX3, and SOX9, these TrxG proteins play a prominent role in the epigenetic regulation of osteogenic and chondrogenic differentiation. |
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Bibliography: | Funding information National Natural Science Foundation of China, Grant/Award Number: NSFC81825005 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Chenghao Song author contributed equally. Funding information National Natural Science Foundation of China, Grant/Award Number: NSFC81825005 |
ISSN: | 0960-7722 1365-2184 |
DOI: | 10.1111/cpr.13233 |