Calcium as a mediator between erythropoietin and protein tyrosine phosphatase 1B.

Abstract:

:Erythropoietin (Epo) is crucial for promoting the survival, proliferation, and differentiation of mammalian erythroid progenitors. The central role played by tyrosine phosphorylation of erythropoietin receptor (EpoR) in Epo-cell activation has focused attention on protein tyrosine phosphatases (PTPs) as candidates implicated in the pathogenesis of the resistance to therapy with human recombinant Epo. Prototypic member of the PTP family is PTP1B, which has been implicated in the regulation of EpoR signaling pathways. In previous reports we have shown that PTP1B is reciprocally modulated by Epo in undifferentiated UT-7 cell line. However, no information is available with respect to the modulation of this phosphatase in non-Epo depending cells or at late stages of erythroid differentiation. In order to investigate these issues we induced UT-7 cells to differentiate and studied their PTP1B expression pattern. Simultaneous observations were performed in TF-1 cells which can be cultured either with GM-CSF, IL-3 or Epo. We found that Epo induced PTP1B cleaveage in TF-1 and differentiated UT-7 cells. This pattern of PTP1B modulation may be due to an increased TRPC3/TRPC6 expression ratio which could explain the larger and sustained calcium response to Epo and calpain activation in Epo treated TF-1 and differentiated UT-7 cells.

journal_name

Arch Biochem Biophys

authors

Callero MA,Vota DM,Chamorro ME,Wenker SD,Vittori DC,Nesse AB

doi

10.1016/j.abb.2010.10.004

subject

Has Abstract

pub_date

2011-01-15 00:00:00

pages

242-9

issue

2

eissn

0003-9861

issn

1096-0384

pii

S0003-9861(10)00432-7

journal_volume

505

pub_type

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