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Blood, 15 November 2000, Vol. 96, No. 10, pp. 3406-3413
HEMATOPOIESIS
Stem cell factor induces phosphatidylinositol
3'-kinase-dependent Lyn/Tec/Dok-1 complex formation in
hematopoietic cells
Thamar B. van Dijk,
Emile van den Akker,
Martine
Parren-van Amelsvoort,
Hiroyuki Mano,
Bob Löwenberg, and
Marieke von
Lindern
From the Institute of Hematology, Erasmus University
Rotterdam, Rotterdam, The Netherlands; Department of Molecular Biology,
Jichi Medical School, Kawachi-gun, Tochigi, Japan.
Stem cell factor (SCF) has an important role in the proliferation,
differentiation, survival, and migration of hematopoietic cells. SCF
exerts its effects by binding to cKit, a receptor with intrinsic
tyrosine kinase activity. Activation of phosphatidylinositol 3'-kinase
(PI3-K) by cKit was previously shown to contribute to many SCF-induced
cellular responses. Therefore, PI3-K-dependent signaling pathways
activated by SCF were investigated. The PI3-K-dependent activation and
phosphorylation of the tyrosine kinase Tec and the adapter molecule
p62Dok-1 are reported. The study shows that Tec and Dok-1 form a stable
complex with Lyn and 2 unidentified phosphoproteins of 56 and 140 kd.
Both the Tec homology and the SH2 domain of Tec were identified as
being required for the interaction with Dok-1, whereas 2 domains in
Dok-1 appeared to mediate the association with Tec. In addition, Tec
and Lyn were shown to phosphorylate Dok-1, whereas phosphorylated Dok-1
was demonstrated to bind to the SH2 domains of several signaling
molecules activated by SCF, including Abl, CrkL, SHIP, and PLC -1,
but not those of Vav and Shc. These findings suggest that p62Dok-1 may
function as an important scaffold molecule in cKit-mediated signaling.

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