Differential Gene Expression of Integrins Alpha 2 and Beta 8 in Human Mesenchymal Stem Cells Exposed to Fluid Flow

被引:0
作者
John R. Glossop
Sarah H. Cartmell
机构
[1] University of Keele,Institute for Science and Technology in Medicine, Guy Hilton Research Centre
来源
Cellular and Molecular Bioengineering | 2009年 / 2卷
关键词
Extracellular matrix (ECM); ITGA2; ITGB8; Collagen; Shear stress; DNA microarray; Real-time RT-PCR; Mechanotransduction;
D O I
暂无
中图分类号
学科分类号
摘要
Human bone marrow-derived mesenchymal stem cells (MSCs) have potential applications for tissue engineering because they can differentiate into numerous cell lineages. Mechanical forces and mechanotransduction are important factors influencing cell responses, although such data are limited for MSCs. We investigated the gene expression response of integrin and extracellular matrix (ECM) genes in MSCs exposed to different magnitudes (1, 5, and 10 dyn/cm2) and durations (10 min, 1 h, and 24 h) of fluid flow-induced shear stress. Gene expression was examined using microarray and quantitative real-time RT-PCR analysis. In response to different magnitudes and durations of shear stress, we observed significant differential gene expression for two integrin genes: consistent up-regulation of integrin α2 subunit (ITGA2) [2- to 18-fold] and consistent down-regulation of integrin β8 subunit (ITGB8) [2- to 9-fold]. There was also evidence of ECM gene down-regulation, namely collagen type XI α1 (COL11A1), COL14A1, and COL21A1 (2- to 4-fold for each), and laminin α4 (LAMA4) [2- to 5-fold]. This indicates specific modulation of integrin gene expression in response to shear stress, supporting altered cell–ECM interactions and integrin-mediated mechanotransduction. These findings further our understanding of how mechanical stimuli regulate MSC behavior, which will be important in the development of mechanical conditioning strategies for tissue engineering.
引用
收藏
页码:544 / 553
页数:9
相关论文
共 197 条
  • [11] Calderwood DA(1994)Quantitative studies of endothelial cell adhesion. Directional remodeling of focal adhesion sites in response to flow forces J. Clin. Invest. 93 2031-2038
  • [12] Cambier S(2007)Human mesenchymal stem cells in contact with their environment: surface characteristics and the integrin system J. Cell. Mol. Med. 11 21-38
  • [13] Mu DZ(1987)Bone marrow osteogenic stem cells: in vitro cultivation and transplantation in diffusion chambers Cell Tissue Kinet. 20 263-272
  • [14] O’Connell D(2006) analysis of integrin expression during chondrogenic differentiation of mesenchymal stem cells and chondrocytes upon dedifferentiation in cell culture Int. J. Mol. Med. 17 301-307
  • [15] Boylen K(2008)Integrin expression in stem cells from bone marrow and adipose tissue during chondrogenic differentiation Int. J. Mol. Med. 21 271-279
  • [16] Travis W(2004)Cell mechanics and mechanotransduction: pathways, probes, and physiology Am. J. Physiol. Cell Physiol. 287 C1-C11
  • [17] Liu WH(1992)Integrins: versatility, modulation, and signaling in cell adhesion Cell 69 11-25
  • [18] Broaddus VC(1996)MAP kinase activation by flow in endothelial cells Circ. Res. 79 310-316
  • [19] Nishimura SL(2001)Integrin-mediated mechanotransduction requires its dynamic interaction with specific extracellular matrix (ECM) ligands Proc. Natl. Acad. Sci. USA 98 1042-1046
  • [20] Caplan AI(2008)KEGG for linking genomes to life and the environment Nucleic Acids Res. 36 D480-D484