The steady-state expression of connexin43 is maintained by the P13K/Akt in osteoblasts

被引:30
作者
Bhattacharjee, Rajib [1 ,2 ]
Kaneda, Makoto [1 ]
Nakahama, Ken-ichi [1 ]
Morita, Ikuo [1 ,2 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138549, Japan
[2] Tokyo Med & Dent Univ, Int Res Ctr Mol Sci Tooth & Bone Dis, Global Ctr Excellence Program, Bunkyo Ku, Tokyo 1138549, Japan
基金
日本学术振兴会;
关键词
Gap junction; Gap junctional intercellular communication; Connexin43; P13K; Akt; mRNA stability; PARATHYROID-HORMONE; INTERCELLULAR COMMUNICATION; PROTEIN-KINASE; GAP-JUNCTIONS; ACTIVATION; P38; CELLS; GENE; PROLIFERATION; STIMULATION;
D O I
10.1016/j.bbrc.2009.03.044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The gap junction protein connexin43 (Cx43) plays an important role in bone development and its homeostasis. Therefore, it is important that the Cx43 expression is kept at a high-level in bone tissues under normal conditions. To investigate the mechanism to keep Cx43 expression level, the effects of protein kinase inhibitors on the basal expression of Cx43 were examined. It was found that the specific P13K inhibitor LY294002 significantly decreased the steady-state expression levels of Cx43 mRNA and protein in osteoblastic cell line, MC3T3-E1 cells. Furthermore, dominant-negative Akt expression reduced both Cx43 expression and gap junction activity. These results suggest an important role of P13k/Akt in the regulation of basal Cx43 expression. A promoter assay for Cx43 and an actinomycin D chase experiment revealed that P13K/Akt modulated Cx43 expression post-transcriptionally via mRNA stability. The present findings could provide new insights into the molecular understanding of Cx43 expression. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:440 / 444
页数:5
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