Phosphatidylinositol-3' kinase is not required for mitogenesis or internalization of the Flt3/Flk2 receptor tyrosine kinase

被引:29
作者
Beslu, N
LaRose, J
Casteran, N
Birnbaum, D
Lecoq, E
Dubreuil, P
Rottapel, R
机构
[1] INSERM, U119, MOL HEMATOL LAB, F-13009 MARSEILLE, FRANCE
[2] INSERM, U119, MOL ONCOL LAB, F-13009 MARSEILLE, FRANCE
[3] UNIV TORONTO, WELLESLEY HOSP, RES INST, TORONTO, ON M4Y 1J3, CANADA
[4] UNIV TORONTO, DEPT MED, TORONTO, ON M56 1A1, CANADA
[5] UNIV TORONTO, DEPT IMMUNOL, TORONTO, ON M56 1A1, CANADA
关键词
D O I
10.1074/jbc.271.33.20075
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
Flt3/Flk2 is a receptor tyrosine kinase that is expressed on early hematopoietic progenitor cells. Flt3/Flk2 belongs to a family of receptors, including Kit and colony-stimulating factor-1R, which support growth and differentiation within the hematopoietic system, The Flt3/Flk2 ligand, in combination with other growth factors, tors, stimulates the proliferation of hematopoietic progenitors of both lymphoid and myeloid lineages in vitro. We report that phosphatidylinositol 3'-kinase (PI3K) binds to a unique site in the carboxy tail of murine Flt3/Flk2. In distinction to Kit and colony-stimulating factor-1R, mutant receptors unable to couple to PI3K and expressed in rodent fibroblasts or in the interleukin 3-dependent cell line Ba/F3 provide a mitogenic signal comparable to wild-type receptors, Flt3/Flk2 receptors that do not bind to PI3K also normally down-regulate, a function ascribed to PI3K in the context of other receptor systems, These data point to the existence of other unidentified pathways that, alone or in combination with PI3K, transduce these cellular responses following the activation of Flt3/Flk2.
引用
收藏
页码:20075 / 20081
页数:7
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