Tethered epidermal growth factor provides a survival advantage to mesenchymal stem cells

被引:208
作者
Fan, Vivian H.
Au, Ada
Tamama, Kenichi
Littrell, Romie
Richardson, Llewellyn B.
Wright, John W.
Wells, Alan
Griffith, Linda G.
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[3] MIT, Dept Engn Mech, Cambridge, MA 02139 USA
[4] Harvard Univ, Sch Dent Med, Cambridge, MA 02138 USA
[5] Univ Pittsburgh, Dept Pathol, Pittsburgh, PA USA
关键词
mesenchymal stem cells; epidermal growth factor; extracellular signal-regulated protein kinase; Fas ligand; cell death; cell spreading; bone graft;
D O I
10.1634/stemcells.2006-0320
中图分类号
Q813 [细胞工程];
学科分类号
摘要
MSC can act as a pluripotent source of reparative cells during injury and therefore have great potential in regenerative medicine and tissue engineering. However, the response of MSC to many growth factors and cytokines is unknown. Many envisioned applications of MSC, such as treating large defects in bone, involve in vivo implantation of MSC attached to a scaffold, a process that creates an acute inflammatory environment that may be hostile to MSC survival. Here, we investigated cellular responses of MSC on a biomaterial surface covalently modified with epidermal growth factor (EGF). We found that surface-tethered EGF promotes both cell spreading and survival more strongly than saturating concentrations of soluble EGF. By sustaining mitogen-activated protein kinase kinase-extracellular-regulated kinase signaling, tethered EGF increases the contact of MSC with an otherwise moderately adhesive synthetic polymer and confers resistance to cell death induced by the proinflammatory cytokine, Fas ligand. We concluded that tethered EGF may offer a protective advantage to MSC in vivo during acute inflammatory reactions to tissue engineering scaffolds. The tethered EGF-modified polymers described here could be used together with structural materials to construct MSC scaffolds for the treatment of hard-tissue lesions, such as large bony defects.
引用
收藏
页码:1241 / 1251
页数:11
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