Hyperosmotic stress induces Axl activation and cleavage in cerebral endothelial cells.

Abstract:

:Because of the relative impermeability of the blood-brain barrier (BBB), many drugs are unable to reach the CNS in therapeutically relevant concentration. One method to deliver drugs to the CNS is the osmotic opening of the BBB using mannitol. Hyperosmotic mannitol induces a strong phosphorylation on tyrosine residues in a broad spectrum of proteins in cerebral endothelial cells, the principal components of the BBB. Previously, we have shown that among targets of tyrosine phosphorylation are beta-catenin, extracellular signal-regulated kinase 1/2 and the non-receptor tyrosine kinase Src. The aim of this study was to identify new signalling pathways activated by hypertonicity in cerebral endothelial cells. Using an antibody array and immunoprecipitation we identified the receptor tyrosine kinase Axl to become tyrosine phosphorylated in response to hyperosmotic mannitol. Besides activation, Axl was also cleaved in response to osmotic stress. Degradation of Axl proved to be metalloproteinase- and proteasome-dependent and resulted in 50-55 kDa C-terminal products which remained phosphorylated even after degradation. Specific knockdown of Axl increased the rate of apoptosis in hyperosmotic mannitol-treated cells; therefore, we assume that activation of Axl may be a protective mechanism against hypertonicity-induced apoptosis. Our results identify Axl as an important element of osmotic stress-induced signalling.

journal_name

J Neurochem

authors

Wilhelm I,Nagyoszi P,Farkas AE,Couraud PO,Romero IA,Weksler B,Fazakas C,Dung NT,Bottka S,Bauer H,Bauer HC,Krizbai IA

doi

10.1111/j.1471-4159.2008.05590.x

subject

Has Abstract

pub_date

2008-10-01 00:00:00

pages

116-26

issue

1

eissn

0022-3042

issn

1471-4159

pii

JNC5590

journal_volume

107

pub_type

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