Activation of Sirt1 Decreases Adipocyte Formation during Osteoblast Differentiation of Mesenchymal Stem Cells

被引:84
作者
Backesjo, Carl-Magnus [1 ]
Li, Yan [1 ]
Lindgren, Urban [1 ]
Haldosen, Lars-Arne [2 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Dept Clin Sci Intervent & Technol, Huddinge, Sweden
[2] Karolinska Inst, Novum, Dept Med Nutr, Huddinge, Sweden
关键词
Sirt1; PPAR gamma; Mesenchymal stem cells; Osteoblast; Adipocyte; PPAR-GAMMA; BONE; MARROW; OSTEOPOROSIS;
D O I
10.1159/000151744
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Mesenchymal stem cells ( MSC) can differentiate into osteoblasts, adipocytes, chondrocytes and myoblasts. It has been suggested that a reciprocal relationship exists between the differentiation of MSC into osteoblasts and adipocytes. Peroxisome proliferator-activated receptor gamma 2 (PPAR gamma 2) is a key element for the differentiation into adipocytes. Activation of the nuclear protein deacetylase Sirt1 has recently been shown to decrease adipocyte development from preadipocytes via inhibition of PPAR gamma 2. In vitro, MSC differentiate to osteoblasts when exposed to bone-inducing medium. However, adipocytes are also developed. In the present study we have targeted Sirt1 to control adipocyte development during differentiation of MSC into osteoblasts. The finding that resveratrol and isonicotinamide markedly inhibited adipocyte and promoted osteoblast differentiation demonstrates an interesting alternative to PPAR gamma antagonists. These results are important for the evolving field of cell-based tissue engineering, but may also be relevant in the search for new treatments of osteoporosis. Copyright (C) 2008 S. Karger AG, Basel
引用
收藏
页码:93 / 97
页数:5
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