Tyrosine-599 of the c-Mpl receptor is required for Shc phosphorylation and the induction of cellular differentiation
Details
Publication Year 1996-12-02,Volume 15,Issue #23,Page 6531-6540
Journal Title
EMBO JOURNAL
Publication Type
Journal Article
Abstract
Interaction of thrombopoietin (TPO) with its receptor, c-Mpl, triggers cell growth and differentiation responses controlling primitive haemopoietic cell production and megakaryocytopoiesis. To examine the important receptor domains and signal transduction pathways involved in these cellular responses, c-Mpl cytoplasmic domain truncation and tyrosine substitution mutants were generated. In the myelomonocytic leukaemia cell lines WEHI3B-D+ and M1, ectopic expression of the wild-type c-Mpl receptor induced TPO-dependent cellular differentiation characterized by increased cell migration through agar and acquisition of the morphology and molecular markers of macrophages. Consistent with the concept that proliferative and differentiation signals emanate from distinct receptor domains, the C-terminal 33 amino acids of c-Mpl were dispensable for a proliferative response in Ba/F3 cells but proved critical for WEHI3B-D+ and M1 differentiation. Finer mapping revealed that substitution of Tyr599 by phenylalanine within this c-Mpl domain was sufficient to abolish the normal differentiation response, Moreover, in contrast to the normal c-Mpl receptor, this same mplY599F mutant was also incapable of stimulating TPO-dependent She phosphorylation, the association of She with Grb2 or c-Mpl and of inducing c-fos expression, Thus activation of components of the Ras signalling cascade, initiated by interaction of She with c-Mpl Tyr599, may play a decisive role in specific differentiation signals emanating from the c-Mpl receptor.
Publisher
OXFORD UNIV PRESS
Keywords
COLONY-STIMULATING FACTOR; HUMAN MEGAKARYOCYTE GROWTH; SIGNAL-TRANSDUCTION; CYTOPLASMIC DOMAIN; IN-VITRO; LIGAND THROMBOPOIETIN; CELLS; EXPRESSION; MICE; THROMBOCYTOPENIA
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Creation Date: 1996-12-02 12:00:00
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