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Mol. Hum. Reprod. Advance Access originally published online on November 6, 2007
Molecular Human Reproduction 2007 13(12):875-886; doi:10.1093/molehr/gam073
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© The Author 2007. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Identification of novel antigens in blood vessels in rectovaginal endometriosis

A. Van Langendonckt1, C. Punyadeera2,4, R. Kamps2, G. Dunselman2, L. Klein-Hitpass5, L.J. Schurgers3, J. Squifflet1, J. Donnez1,6 and P. Groothuis2

1Department of Gynecology, Université Catholique de Louvain, 1200 Brussels, Belgium 2Department of Obstetrics and Gynecology, Research Institute for Growth and Development, The Netherlands 3Cardiovascular Research Institute and VitaK BV, Maastricht University and University Hospital, 6202 AZ Maastricht, The Netherlands 4Department of Molecular Diagnostics, Philips Research Europe, High Tech Campus 11, 5656AE Eindhoven, The Netherlands 5Institute of Cell Biology, University Medical Center, D-45122 Essen, Germany

6 Correspondence address. E-mail: donnez{at}gyne.ucl.ac.be

To identify specific markers of rectovaginal endometriotic nodule vasculature, highly enriched preparations of vascular endothelial cells and pericytes were obtained from endometriotic nodules and control endometrial and myometrial tissue by laser capture microdissection (LCM), and gene expression profiles were screened by microarray analysis. Of the 18 400 transcripts on the arrays, 734 were significantly overexpressed in vessels from fibromuscular tissue and 923 in vessels from stromal tissue of endometriotic nodules, compared with vessels dissected from control tissues. The most frequently expressed transcripts included known endothelial cell-associated genes, as well as transcripts with little or no previous association with vascular cells. The higher expression in blood vessels was further corroborated by immunohistochemical staining of six potential markers, five of which showed strong expression in pericytes. The most promising marker was matrix Gla protein, which was found to be present in both glandular epithelial cells and vascular endothelial cells of endometriotic lesions, although it was barely expressed at all in normal endometrium. LCM, combined with microarray analysis, constitutes a powerful tool for mapping the transcriptome of vascular cells. After immunohistochemical validation, markers of vascular endothelial and perivascular cells from endometriotic nodules could be identified, which may provide targets to improve early diagnosis or to selectively deliver therapeutic agents.

Key words: angiogenesis/rectovaginal endometriosis/laser capture microdissection/microarray/vascular targeting

Submitted on June 12, 2007; accepted on September 21, 2007.


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A. Van Langendonckt, J. Donnez, S. Defrere, G. A.J. Dunselman, and P. G. Groothuis
Antiangiogenic and vascular-disrupting agents in endometriosis: pitfalls and promises
Mol. Hum. Reprod., May 1, 2008; 14(5): 259 - 268.
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