Connexin 43 Modulates Osteogenic Differentiation of Bone Marrow Stromal Cells Through GSK-3beta/Beta-Catenin Signaling Pathways
Author(s) -
Fei-Xiang Lin,
Guizhou Zheng,
Bo-Jui Chang,
Rongchun Chen,
Qihao Zhang,
Peng Xie,
Da Xie,
Guoyong Yu,
Qin-Xiao Hu,
Dezhong Liu,
Shixin Du,
Xuedong Li
Publication year - 2018
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000489763
Subject(s) - bone sialoprotein , chemistry , runx2 , stromal cell , gene knockdown , microbiology and biotechnology , alkaline phosphatase , osteocalcin , cellular differentiation , small hairpin rna , signal transduction , cancer research , biology , biochemistry , apoptosis , gene , enzyme
Bone marrow stromal cells (BMSCs) are multipotent precursors that give rise to osteoblasts, and contribute directly to bone formation. Connexin 43 (Cx43) is the most ubiquitous gap junction protein expressed in bone cell types, and plays crucial roles in regulating intercellular signal transmission for bone development, differentiation and pathology. However, the precise role and mechanism of Cx43 in BMSCs are less known. Here, we investigate the function of Cx43 in osteogenic differentiation of BMSCs in vitro.
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