ERRα regulates osteoblastic and adipogenic differentiation of mouse bone marrow mesenchymal stem cells

被引:33
|
作者
Rajalin, Ann-Marie [1 ]
Pollock, Hanna [1 ]
Aarnisalo, Piia [1 ,2 ,3 ]
机构
[1] Univ Helsinki, Biomedicum Helsinki, Inst Biomed, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Dept Clin Chem, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Cent Hosp, FIN-00014 Helsinki, Finland
基金
芬兰科学院;
关键词
Estrogen-related receptor; Nuclear receptor; Osteoblast; Bone; PROLIFERATOR-ACTIVATED RECEPTOR; ORPHAN NUCLEAR RECEPTORS; FORMATION IN-VITRO; TRANSCRIPTIONAL REGULATION; SIALOPROTEIN EXPRESSION; ESTROGEN; CANCER; GENE; TISSUES;
D O I
10.1016/j.bbrc.2010.04.120
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 orphan nuclear receptor estrogen-related receptor-alpha (ERR alpha) has been reported to have both a positive and a negative regulatory role in osteoblastic and adipocytic differentiation. We have studied the role of ERR alpha in osteoblastic and adipogenic differentiation of mesenchymal stem cells. Bone marrow mesenchymal stem cells were isolated from ERR alpha deficient mice and their differentiation capacities were compared to that of the wild-type cells. ERR alpha deficient cultures displayed reduced cellular proliferation, osteoblastic differentiation, and mineralization. In the complementary experiment, overexpression of ERR alpha in MC3T3-E1 cells increased the expression of osteoblastic markers and mineralization. Alterations in the expression of bone sialoprotein (BSP) may at least partially explain the effects on mineralization as BSP expression was reduced in ERR alpha deficient MSCs and enhanced upon ERR alpha overexpression in MC3T3-E1 cells. Furthermore, a luciferase reporter construct driven by the BSP promoter was efficiently transactivated by ERR alpha. Under adipogenic conditions, ERR alpha deficient cultures displayed reduced adipocytic differentiation. Our data thus propose a positive role for ERR alpha in osteoblastic and adipocytic differentiation. The variability in the results yielded in the different studies implies that ERR alpha may play different roles in bone under different physiological conditions. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:477 / 482
页数:6
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