Evidence for multiple peroxisome proliferator-activated receptor γ transcripts in bone:: Fine-tuning by hormonal regulation and mRNA stability

被引:28
作者
Bruedigam, Claudia [1 ]
Koedam, Marijke [1 ]
Chiba, Hideki [2 ]
Eijken, Marco [1 ]
van Leeuwen, Johannes P. T. M. [1 ]
机构
[1] Erasmus MC, Dept Internal Med, NL-3000 CA Rotterdam, Netherlands
[2] Sapporo Med Coll, Dept Pathol, Sapporo, Hokkaido 060, Japan
关键词
peroxisome proliferator-activated receptor gamma; osteoblast; glucocorticoids; rosiglitazone; mRNA stability; alternative splicing;
D O I
10.1016/j.febslet.2008.04.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The expression, regulation and functional significance of multiple peroxisome proliferator-activated receptor gamma transcript variants in bone were studied. PPARG transcripts giving rise to PPARg-1 protein were expressed in human osteoblasts, whereas PPARG-2 transcript and protein remained virtually absent. PPARG expression underwent homologous regulation, was upregulated during differentiation and directly induced by the osteogenic hormone dexamethasone, suggesting a role for PPARg-1 in osteogenesis. Differences between the stabilities of PPARG-1, -3 and -4 were observed. We hypothesize that cell-specific expression patterns of multiple PPARG transcript variants encoding for the same protein but differing in mRNA stabilities enable a fine-tuning of PPARG action, which eventually supports a well-adjusted signal transduction between the cell and its environment. (C) 2008 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:1618 / 1624
页数:7
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