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Gata2 Is a Rheostat for Mesenchymal Stem Cell Fate in Male Mice
Author(s) -
Xiaoxiao Li,
HoangDinh Huynh,
Hao Zuo,
Marjo Salminen,
Yihong Wan
Publication year - 2016
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/en.2015-1827
Subject(s) - adipogenesis , mesenchymal stem cell , gata2 , biology , microbiology and biotechnology , transcription factor , cellular differentiation , adipocyte , haematopoiesis , stem cell , cell fate determination , zinc finger transcription factor , endocrinology , medicine , genetics , adipose tissue , zinc finger , gene
Gata2 is a zinc finger transcription factor that is important in hematopoiesis and neuronal development. However, the roles of Gata2 in the mesenchymal lineages are poorly understood. In vitro studies suggest that Gata2 modulates adipocyte differentiation and mesenchymal stem cell (MSC) proliferation. To systematically determine the in vivo functions of Gata2 in the MSC lineage commitment and development, we have generated three mouse models in which Gata2 is specifically deleted in MSCs, adipocytes, or osteoblasts. During the MSC expansion stage, Gata2 promotes proliferation and attenuates differentiation; thereby Gata2 loss in MSCs results in enhanced differentiation of both adipocytes and osteoblasts. During the differentiation stage, Gata2 also plays MSC-independent roles to impede lineage commitment; hence, Gata2 loss in adipocyte or osteoblast lineages also augments adipogenesis and osteoblastogenesis, respectively. These findings reveal Gata2 as a crucial rheostat of MSC fate to control osteoblast and adipocyte lineage development.

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