Title

BMP9 regulates endoglin-dependent chemokine responses in endothelial cells.

Document Type

Article

Publication Date

11-15-2012

Institution/Department

Maine Medical Center Research Institute

Journal Title

Blood

MeSH Headings

Activin Receptors, Type I, Activin Receptors, Type II, Animals, Antigens, CD, Aorta, Autocrine Communication, Cell Hypoxia, Cell Movement, Chemokine CXCL12, Culture Media, Conditioned, Endoglin, Endothelial Cells, Growth Differentiation Factor 2, Growth Differentiation Factors, Hindlimb, Human Umbilical Vein Endothelial Cells, Humans, Intracellular Signaling Peptides and Proteins, Ischemia, Mice, Neovascularization, Physiologic, Paracrine Communication, RNA, Messenger, RNA, Small Interfering, Real-Time Polymerase Chain Reaction, Receptors, Cell Surface, Transforming Growth Factor beta1

Abstract

BMP9 signaling has been implicated in hereditary hemorrhagic telangiectasia (HHT) and vascular remodeling, acting via the HHT target genes, endoglin and ALK1. This study sought to identify endothelial BMP9-regulated proteins that could affect the HHT phenotype. Gene ontology analysis of cDNA microarray data obtained after BMP9 treatment of primary human endothelial cells indicated regulation of chemokine, adhesion, and inflammation pathways. These responses included the up-regulation of the chemokine CXCL12/SDF1 and down-regulation of its receptor CXCR4. Quantitative mass spectrometry identified additional secreted proteins, including the chemokine CXCL10/IP10. RNA knockdown of endoglin and ALK1 impaired SDF1/CXCR4 regulation by BMP9. Because of the association of SDF1 with ischemia, we analyzed its expression under hypoxia in response to BMP9 in vitro, and during the response to hindlimb ischemia, in endoglin-deficient mice. BMP9 and hypoxia were additive inducers of SDF1 expression. Moreover, the data suggest that endoglin deficiency impaired SDF1 expression in endothelial cells in vivo. Our data implicate BMP9 in regulation of the SDF1/CXCR4 chemokine axis in endothelial cells and point to a role for BMP9 signaling via endoglin in a switch from an SDF1-responsive autocrine phenotype to an SDF1 nonresponsive paracrine state that represses endothelial cell migration and may promote vessel maturation.

ISSN

1528-0020

First Page

4263

Last Page

4273

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