Insulin-like growth factor 1 enhances the migratory capacity of mesenchymal stem cells

被引:193
作者
Li, Yangxin
Yu, XiYong [1 ]
Lin, ShuGuang
Li, XiaoHong
Zhang, Saidan
Song, Yao-Hua
机构
[1] Guangdong Prov Peoples Hosp, Guangdong Prov Cardiovasc Inst, Res Ctr Med Sci, Guangzhou 510080, Guangdong, Peoples R China
[2] Texas Heart Inst, Lab Heart Failure & Stem Cell, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Mol Pathol, Houston, TX 77030 USA
[4] Cent S Univ, Cardiol Sect, Xiangya Hosp, Changsha 410008, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
IGF-1; stem cell; CXCR4; migration; SDF-1;
D O I
10.1016/j.bbrc.2007.03.049
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
Mesenchymal stem cells (MSCs) are attractive candidates for cell based therapies. However, the mechanisms responsible for stem cell migration and homing after transplantation remain unknown. It has been shown that insulin-like growth factor-1 (IGF-1) induces proliferation and migration of some cell types, but its effects on stem cells have not been investigated. We isolated and cultured MSC from rat bone marrow, and found that IGF-1 increased the expression levels of the chemokine receptor CXCR4 (receptor for stromal cell-derived factor-1, SDF-1). Moreover, IGF-1 markedly increased the migratory response of MSC to SDF-1. The IGF-1-induced increase in MSC migration in response to SDF-1 was attenuated by PI3 kinase inhibitor (LY294002 and wortmannin) but not by mitogen-activated protein/ERK kinase inhibitor PD98059. Our data indicate that IGF-1 increases MSC migratory responses via CXCR4 chemokine receptor signaling which is P13/Akt dependent. These findings provide a new paradigm for biological effects of IGF-1 on MSC and have implications for the development of novel stem cell therapeutic strategies. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:780 / 784
页数:5
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