The sphingomyelin/ceramide pathway is involved in ERK1/2 phosphorylation, cell proliferation, and uPAR overexpression induced by tissue‐type plasminogen activator-Reference-Cited by-同舟云学术

The sphingomyelin/ceramide pathway is involved in ERK1/2 phosphorylation, cell proliferation, and uPAR overexpression induced by tissue‐type plasminogen activator

Published:2004-07 Issue:12 Volume:18 Page:1398-1400
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Maupas‐Schwalm Françoise¹,Augé Nathalie¹,Robinet Catherine¹,Cambus Jean‐Pierre²,Parsons Sarah J.³,Salvayre Robert¹,Nègre‐Salvayre Anne¹

Affiliation:

1. Inserm U‐466CHU Rangueil31043 Cedex 4, IFR31ToulouseFrance

2. Laboratoire d'HematologieCHU RangueilToulouseFrance

3. Microbiology Dept. and Cancer CenterUniversity of Virginia, CharlottesvilleVirginiaUSA

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.03-1123fje

Reference53 articles.

1. uPAR: a versatile signalling orchestrator

2. Plasminogen activator inhibitor 1. Structure of the native serpin, comparison to its other conformers and implications for serpin inactivation

3. Plasminogen activator inhibitor 1: Physiological and pathophysiological roles;Binder B. R.;News Physiol. Sci.,2002

4. Direct Binding of Occupied Urokinase Receptor (uPAR) to LDL Receptor-related Protein Is Required for Endocytosis of uPAR and Regulation of Cell Surface Urokinase Activity

5. Receptor-mediated internalization and degradation of urokinase is caused by its specific inhibitor PAI-1.

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