Hypoxia decreases Runx2/Cbfa1 expression in human osteoblast-like cells

被引:82
作者
Park, JH
Park, BH
Kim, HK
Park, TS
Baek, HS
机构
[1] Chonbuk Natl Univ, Sch Med, Dept Internal Med, Div Endocrinol & Metab,Dukjin Gu, Chonju 561712, Chonbuk, South Korea
[2] Res Inst Clin Med, Chonju 561712, Chonbuk, South Korea
[3] Chobuk Natl Univ, Sch Med, Dept Biochem, Chonju, South Korea
[4] Chobuk Natl Univ, Sch Med, Inst Med Sci, Chonju, South Korea
关键词
Runx2 (Cbfa1/Pebp2 alpha A/AML3); hypoxia; osteoblast;
D O I
10.1016/S0303-7207(02)00036-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To elucidate the molecular mechanism in relation to vascular supply and osteoporosis, we investigated the effect of hypoxia on Runx2 expression in MG63 cells. Also investigated was expression of type I collagen and osteocalcin, which are regulated by Runx2, alkaline phosphatase (ALPase) to see if they are affected by hypoxia. Quiescent cultures of MG63 cells were exposed to hypoxia (2% O-2) and normoxia (18% O-2) for 24, 48, 72 and 96 h. In cells exposed to hypoxia, reverse transcription-polymerase chain reaction (RT-PCR) analysis showed that mRNA expression of Runx2, type I collagen, osteocalcin, and ALPase were decreased in a time dependent manner to 96 h. Activity of ALPase was also reduced in the same manner. Western blotting showed a marked decrease in Runx2 protein at 96 h in cells under hypoxia compared to normoxia. These data indicate that Runx2 expression in osteoblasts is reduced by hypoxia, and may be a mechanism of osteoporosis by decreased vascular supply. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:197 / 203
页数:7
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