Thyroid hormone non-genomically suppresses Src thereby stimulating osteocalcin expression in primary mouse calvarial osteoblasts

被引:9
作者
Asai, Shuji [1 ,2 ]
Cao, Xia [1 ]
Yamauchi, Masako [1 ]
Funahashi, Koji [1 ,2 ]
Ishiguro, Naoki [2 ]
Kambe, Fukushi [1 ]
机构
[1] Nagoya Univ, Dept Endocrinol, Environm Med Res Inst, Chikusa Ku, Nagoya, Aichi 4648601, Japan
[2] Nagoya Univ, Dept Orthoped, Sch Med, Showa Ku, Nagoya, Aichi 4668550, Japan
关键词
Thyroid hormone; Non-genomic action; Src; Osteoblasts; Osteocalcin; Phosphorylation; ACTIVATED PROTEIN-KINASE; C-SRC; SERINE PHOSPHORYLATION; NONGENOMIC ACTIONS; PLASMA-MEMBRANE; RECEPTOR; MECHANISMS; GROWTH;
D O I
10.1016/j.bbrc.2009.06.131
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
To provide further insights into non-genomic action of thyroid hormone (T3), we investigated whether Src is under control of T3 in primary calvarial osteoblasts prepared from neonatal mice. Treatment of the cells with T3 rapidly decreased Src Y416 autophosphorylation, followed by the decrease of phosphorylated extracellular signal-regulated kinases, suggesting that T3 non-genomically suppresses Src activity. Furthermore, this T3 effect was rapid and Persistent, and was associated with the increased expression of osteocalcin (OC). To confirm the contribution of Src to the effect of T3 on OC expression, a constitutively active Src (Y527F) was overexpressed in osteoblasts. In such cells, Y416 phosphorylation was markedly increased even in the presence of T3, and T3-dependent expression of OC was markedly attenuated. The present study demonstrates a novel, non-genomic action of T3 in primary Mouse osteoblasts, by which T3 suppresses Src thereby stimulating OC expression. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:92 / 96
页数:5
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