4.5 Article

p38-Mediated phosphorylation of Eps15 endocytic adaptor protein

Journal

FEBS LETTERS
Volume 588, Issue 1, Pages 131-137

Publisher

WILEY
DOI: 10.1016/j.febslet.2013.11.020

Keywords

Eps15; TNF-alpha; TAK1; EGF; p38

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan
  2. Institute of Natural Medicine, University of Toyama
  3. Grants-in-Aid for Scientific Research [23590071, 23590172, 24659017, 24659348, 24700971] Funding Source: KAKEN

Ask authors/readers for more resources

Epidermal growth factor receptor pathway substrate 15 (Eps15) has been suggested to be involved in the endocytosis of cell surface receptors, including epidermal growth factor receptor (EGFR). Eps15 is phosphorylated at Tyr-849 upon stimulation with EGF during endocytic processes. In the present study, we found that stimulation of HeLa cells with EGF or TNF-alpha induced transient phosphorylation of Eps15 at Ser-796. Inhibition of p38 completely blocked phosphorylation and recombinant p38 alpha directly phosphorylated the residue. These results demonstrate a novel stress kinase-mediated signaling pathway to Eps15 endocytic adapter protein. (C) 2013 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available