Adiponectin Stimulates Osteoblast Differentiation Through Induction of COX2 in Mesenchymal Progenitor Cells

被引:128
作者
Lee, Hyun Woo
Kim, Sang Yun
Kim, A. Young
Lee, Eun Jig [2 ]
Choi, Je-Yong [3 ,4 ]
Kim, Jae Bum [1 ]
机构
[1] Seoul Natl Univ, Sch Biol Sci, Inst Mol Biol & Genet, Seoul 151742, South Korea
[2] Yonsei Univ, Coll Med, Div Endocrinol, Seoul, South Korea
[3] Kyungpook Natl Univ, Sch Med, Dept Biochem & Cell Biol, Taegu, South Korea
[4] Kyungpook Natl Univ, Skeletal Dis Genome Res Ctr, Taegu, South Korea
关键词
Adiponectin; Mesenchymal progenitor cell; Osteogenesis; COX2; c-Jun; ACTIVATED PROTEIN-KINASE; BONE-MINERAL DENSITY; IN-VIVO; C-JUN; INSULIN-RESISTANCE; DIABETES-MELLITUS; VISCERAL FAT; STEM-CELLS; CYCLOOXYGENASE-2; EXPRESSION;
D O I
10.1002/stem.144
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
In bone marrow, osteoblasts and adipocytes are differentiated from mesenchymal progenitor cells and their differentiation is reciprocally regulated by largely unknown mechanisms. In this study, we investigated downstream signaling cascades of adiponectin, a member of the adipocytokine family, in the regulation of osteoblast differentiation. Adiponectin augmented expression of several osteogenic marker genes and increased osteoblast differentiation in mesenchymal progenitor cells. The expression of cyclooxygenase-2 (COX2) was potently increased by adiponectin, whereas inhibition of COX2 activity abolished the effect of adiponectin on osteogenesis. In addition, adiponectin rapidly stimulated p38 mitogen-activated protein kinase via the adiponectin receptor, AdipoR1, which resulted in c-Jun activation for COX2 expression. Adiponectin also stimulated BMP2 expression in a COX2-dependent manner. Moreover, Runx2, a key osteogenic transcription factor, contributed to the acceleration of osteogenesis in the presence of adiponectin. Collectively, the finding that adiponectin could promote osteogenesis through an intracellular signaling cascade in mesenchymal progenitor cells suggests that adiponectin would be a potential therapeutic target for bone-related diseases. STEM CELLS 2009; 27: 2254-2262
引用
收藏
页码:2254 / 2262
页数:9
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