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PMID: 12414810 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Stromal cell-derived factor-1alpha induces tube-like structure formation of endothelial cells through phosphoinositide 3-kinase.

The Journal of biological chemistry ·Vol. 278 ·No. 1 ·2003-01-03 ·Pages 257-62

Kanda S, Mochizuki Y, Kanetake H

Abstract

Stromal cell-derived factor-1alpha (SDF-1alpha) is a CXC chemokine, which induces tube formation of endothelial cells. Although SDF-1alpha transduces signals via CXC receptor 4 (CXCR4), resulting in activating a panel of downstream signaling molecules, such as phosphoinositide 3-kinase (PI3-kinase), little is known about the SDF-1alpha-mediated signaling pathways leading to tube formation. Here we examined the signal transduction pathway involved in SDF-1alpha-mediated tube formation by primary human umbilical endothelial cells and murine brain capillary endothelial cell line (IBE (immortalized murine brain capillary endothelial) cells). SDF-1alpha stimulated tube formation by IBE cells, which was blocked by LY294002 and pertussis toxin, suggesting that PI3-kinase and G(i) protein were involved in this process. SDF-1 also stimulated tube formation of human umbilical endothelial cells, and the response was LY294002-sensitive. SDF-1alpha activated PI3-kinase in IBE cells. In stable IBE cell lines expressing either the mutant p85 subunit of PI3-kinase (denoted Deltap85-8 cells), which lacks association with the p110 subunit, or kinase-inactive c-Fes (denoted KEFes 5-15 cells), SDF-1alpha failed to activate PI3-kinase and to stimulate tube formation. SDF-1alpha-induced tube formation was inhibited by an antibody against murine vascular endothelial cadherin. The antibody as well as LY294002 attenuated SDF-1alpha-mediated compact cell-cell contact, which proceeded to tube formation. Taken together, SDF-1alpha induces compact cell-cell contact through PI3-kinase, resulting in tube formation of endothelial cells.

MeSH Terms
Animals Antibodies/metabolism Antigens, CD Cadherins/metabolism Cell Adhesion/physiology Cell Line Chemokine CXCL12 Chemokines, CXC/pharmacology Chromones/pharmacology Endothelium, Vascular/cytology,drug effects,metabolism Enzyme Inhibitors/pharmacology Humans Immunoglobulin G/metabolism Mice Mice, Transgenic Morphogenesis Morpholines/pharmacology Phosphatidylinositol 3-Kinases/metabolism Phosphoinositide-3 Kinase Inhibitors Phosphotyrosine/metabolism Protein Serine-Threonine Kinases Proto-Oncogene Proteins/metabolism Proto-Oncogene Proteins c-akt Rats Signal Transduction/physiology
Chemicals
Antibodies Antigens, CD CXCL12 protein, human Cadherins Chemokine CXCL12 Chemokines, CXC Chromones Cxcl12 protein, mouse Enzyme Inhibitors Immunoglobulin G Morpholines Phosphoinositide-3 Kinase Inhibitors Proto-Oncogene Proteins cadherin 5 Phosphotyrosine 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one Protein Serine-Threonine Kinases Proto-Oncogene Proteins c-akt
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kanda Shigeru
Department of Molecular Microbiology and Immunology, Division of Endothelial Cell Biology, Nagasaki University Graduate School of Medical Science, 1-7-1 Sakamoto, Nagasaki 852-8501, Japan. [email protected]
Mochizuki Yasushi
Kanetake Hiroshi
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2003-01-03
Epub
2002-00-31
Pages
257-62
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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