Soluble factors from human endometrium promote angiogenesis and regulate the endothelial cell transcriptome

Human Reproduction · 2004 · vol. 19(10) , pp. 2356–2366 · doi:10.1093/humrep/deh411 · PMID:15242995 · W2101880027
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Human endometrial supernatants, particularly from the proliferative phase, contain soluble factors including VEGF-A that promote endothelial cell proliferation, angiogenesis, and alter the endothelial transcriptome.

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Abstract

BACKGROUND: Angiogenesis and vascular remodeling play critical roles in the cyclical growth and regression of endometrium. They also appear to play roles in the pathogenesis of endometriosis. METHODS AND RESULTS: Supernatants were collected from cultured endometrium isolated from women with and without endometriosis. These supernatants induced endothelial cell proliferation and angiogenesis in vitro. They contained vascular endothelial growth factor (VEGF)-A, and their proliferative effects on endothelial cells were partially abrogated by a blocking anti-VEGF-A antibody. Gene array analysis showed that culture supernatants from proliferative phase endometrium, and to a lesser extent secretory phase endometrium, induced significant changes in the transcriptome of endothelial cells. We could not detect any association between endometriosis and the ability of endometrial-derived soluble factors to promote angiogenesis or to regulate the endothelial transcriptome. In addition, we could not detect any association between endometriosis and the concentration of VEGF-A in supernatants from cultured endometrium or in menstrual effluent. CONCLUSIONS: We have shown that endometrium cultured in vitro produced soluble factors, including VEGF-A, that promoted angiogenesis. Proliferative phase endometrium promoted significant endothelial cell transcriptome changes that appear overall to be pro-angiogenic. These transcriptome changes provide insight into the dynamic control of vessel structure on which both eutopic endometrium and endometriotic lesions depend.

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Condition tags

endometriosis

MeSH descriptors

Endometrium Endometrium Endothelial Cells Neovascularization, Physiologic Neovascularization, Physiologic Transcription, Genetic Transcription, Genetic Case-Control Studies Cell Division Cell Division Culture Media Culture Media Culture Media Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometrium Endometrium

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