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Exp Cell Res ; 313(15): 3308-18, 2007 Sep 10.
Article in English | MEDLINE | ID: mdl-17643421

ABSTRACT

Sphingosine kinase 1 catalyzes the formation of sphingosine-1-phosphate, a lipid mediator involved in the regulation of angiogenesis. Sphingosine kinase 1 is constitutively released from cells, even though it lacks a classical signal peptide sequence. Because copper-dependent non-classical stress-induced release of FGF1 also regulates angiogenesis, we questioned whether sphingosine kinase 1 is involved in the FGF1 release pathway. We report that (i) the coexpression of sphingosine kinase 1 with FGF1 inhibited the release of sphingosine kinase 1 at 37 degrees C; (ii) sphingosine kinase 1 was released at 42 degrees C in complex with FGF1; (iii) sphingosine kinase 1 null cells failed to release FGF1 at stress; (iv) sphingosine kinase 1 is a high affinity copper-binding protein which formed a complex with FGF1 in a cell-free system, and (v) sphingosine kinase 1 over expression rescued the release of FGF1 from inhibition by the copper chelator, tetrathiomolybdate. We propose that sphingosine kinase 1 is a component of the copper-dependent FGF1 release pathway.


Subject(s)
Copper/metabolism , Fibroblast Growth Factor 1/metabolism , Phosphotransferases (Alcohol Group Acceptor)/metabolism , Animals , Cells, Cultured , Chelating Agents/pharmacology , Cloning, Molecular , Fibroblasts/metabolism , Mice , Mice, Knockout , Molybdenum/pharmacology , NIH 3T3 Cells , Phosphotransferases (Alcohol Group Acceptor)/genetics , Protein Transport , Temperature
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