HORMONAL-REGULATION OF CONNEXIN-43 EXPRESSION AND GAP JUNCTIONAL COMMUNICATION IN HUMAN OSTEOBLASTIC CELLS

被引:36
作者
CHIBA, H [1 ]
SAWADA, N [1 ]
OYAMADA, M [1 ]
KOJIMA, T [1 ]
IBA, K [1 ]
ISHII, S [1 ]
MORI, M [1 ]
机构
[1] SAPPORO MED UNIV, SCH MED, DEPT ORTHOPED SURG, SAPPORO 060, JAPAN
关键词
HUMAN OSTEOBLASTS; GAP JUNCTIONS; CONNEXINS; RETINOIC ACID; TRANSFORMING GROWTH FACTOR-BETA;
D O I
10.1247/csf.19.173
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have recently shown that connexin 43 (Cx43), a major gap junction protein in osteoblasts, is expressed with an increase in cell density (CHIBA, H. et al. (1993). Cell Struc. Funct., 18: 419-426). In the present study, we examined what kinds of hormones and cytokines regulate the gap junction protein in osteoblastic cells, using a human osteoblastic cell line (SV-HFO) after reaching a confluent density to avoid influence of cell proliferation. Either retinoic acid (RA) or transforming growth factor-beta(1) (TGF-beta(1)) induced the Cx43 expression of SV-HFO cells, as revealed by Northern blot analysis and immunocytochemistry. These modulators also increased gap junctional intercellular communication, in terms of the extent of dye transfer. On the other hand, 1 alpha, 25-dihydroxyvitamin D-3 did not influence the Cx43 expression and gap junctional intercellular communication of the cells. These results suggest that RA and TGF-beta(1) might maintain bone tissue as an organized tissue in vivo by increasing intercellular communication of osteoblastic cells.
引用
收藏
页码:173 / 177
页数:5
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