CNS integrins switch growth factor signalling to promote target-dependent survival

被引:201
作者
Colognato, H [1 ]
Baron, W
Avellana-Adalid, V
Relvas, JB
Baron-Van Evercooren, A
Georges-Labouesse, E
ffrench-Constant, C
机构
[1] Univ Cambridge, Dept Med Genet, Cambridge CB2 2PY, England
[2] Univ Cambridge, Dept Pathol, Cambridge CB2 2PY, England
[3] Univ Cambridge, Ctr Brain Repair, Cambridge CB2 2PY, England
[4] INSERM, CJF 97 11, Lab Pathol Myeline, F-75634 Paris 13, France
[5] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, CU De Strasbour, France
基金
英国惠康基金; 美国国家卫生研究院;
关键词
D O I
10.1038/ncb865
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Depending on the stage of development, a growth factor can mediate cell proliferation, survival or differentiation. The interaction of cell-surface integrins with extracellular matrix ligands can regulate growth factor responses and thus may influence the effect mediated by the growth factor. Here we show, by using mice lacking the alpha(6) integrin receptor for laminins, that myelin-forming oligodendrocytes activate an integrin-regulated switch in survival signalling when they contact axonal laminins. This switch alters survival signalling mediated by neuregulin from dependence on the phosphatidylinositol-3-OH kinase (PI(3)K) pathway to dependence on the mitogen-activated kinase pathway. The consequent enhanced survival provides a mechanism for target-dependent selection during development of the central nervous system. This integrin-regulated switch reverses the capacity of neuregulin to inhibit the differentiation of precursors, thereby explaining how neuregulin subsequently promotes differentiation and survival in myelinating oligodendrocytes. Our results provide a general mechanism by which growth factors can exert apparently contradictory effects at different stages of development in individual cell lineages.
引用
收藏
页码:833 / 841
页数:9
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