Connexin 43 Affects Osteogenic Differentiation of the Posterior Longitudinal Ligament Cells via Regulation of ERK Activity by Stabilizing Runx2 in Ossification
Author(s) -
Haisong Yang,
Lei Shi,
Guodong Shi,
Yongfei Guo,
Dechun Chen,
Deyu Chen,
Jiangang Shi
Publication year - 2016
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 - 10.1159/000438625
Subject(s) - runx2 , connexin , mapk/erk pathway , osteoblast , osteocalcin , microbiology and biotechnology , gene silencing , chemistry , biology , kinase , gap junction , in vitro , intracellular , alkaline phosphatase , biochemistry , gene , enzyme
Connexin 43 is one of the most potent gap junction proteins related to osteoblast differentiation and bone formation. We hypothesized that Connexin 43 is a significant factor in osteogenic differentiation in the posterior longitudinal ligament through the regulation of extracellular signal-regulated kinases (ERK) activity by converging on Runt-related transcription factor 2 (Runx2) activity. In this study, we mapped the activity of Connexin 43 to ERK and Runx2 by extracting longitudinal ligament cell for culture and silencing Connexin expression in addition to dexamethasone treatment in vitro.
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