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Title: Calmodulin physically interacts with the erythropoietin receptor and enhances Jak2-mediated signaling

Journal Article · · Biochemical and Biophysical Research Communications
 [1];  [1];  [1];  [1]
  1. Department of Hematology, Graduate School of Medicine and Dentistry, Tokyo Medical and Dental University, Tokyo 113-8519 (Japan)

Stimulation of the erythropoietin receptor (EpoR) induces a transient increase in intracellular Ca{sup 2+} level as well as activation of the Jak2 tyrosine kinase to stimulate various downstream signaling pathways. Here, we demonstrate that the universal Ca{sup 2+} receptor calmodulin (CaM) binds EpoR in a Ca{sup 2+}-dependent manner in vitro. Binding studies using various EpoR mutants in hematopoietic cells showed that CaM binds the membrane-proximal 65-amino-acid cytoplasmic region (amino acids 258-312) of EpoR that is critical for activation of Jak2-mediated EpoR signaling. Structurally unrelated CaM antagonists, W-13 and CMZ, inhibited activation of Jak2-mediated EpoR signaling pathways, whereas W-12, a W-13 analog, did not show any significant inhibitory effect. Moreover, overexpression of CaM augmented Epo-induced tyrosine phosphorylation of the EpoR. W-13, but not W-12, also inhibited Epo-induced proliferation and survival. Together, these results indicate that CaM binds to the membrane-proximal EpoR cytoplasmic region and plays an essential role in activation of Jak2-mediated EpoR signaling.

OSTI ID:
20710979
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 335, Issue 2; Other Information: DOI: 10.1016/j.bbrc.2005.07.095; PII: S0006-291X(05)01574-3; Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English

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