[Integrin expression in eutopic and ectopic endometrium]

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This study examined integrin expression in eutopic and ectopic endometrium, finding reduced alpha(2)- and alpha(v)-integrin expression in ectopic tissue compared to eutopic tissue from endometriosis patients.

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This paper investigated integrin expression in eutopic versus ectopic endometrium from endometriosis patients and controls using immunohistochemistry, motivated by the idea that integrins mediate cell–cell and cell–matrix adhesion relevant to endometriosis development. Nearly all samples showed glandular epithelial expression of α2-, α3-, α6-, and αv-integrin, with smaller proportions expressing α1-, α4-, and α5. Compared with eutopic endometrium, ectopic endometrium had reduced α2- and αv-integrin expression, while eutopic endometrium showed no differences in α2 and αv between patients and controls; the authors therefore propose that the ectopic reduction may reflect effects of the altered local environment, such as peritoneal fluid. This paper is centrally about endometriosis — it compares integrin (α2 and αv) expression in eutopic versus ectopic endometrium in endometriosis patients.

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Abstract

The significance of retrograde menstruation as a risk factor for endometriosis has been confirmed by numerous clinical observations. Integrins mediate both cell-cell and cell-matrix adhesion, and it is therefore suspected that integrins are involved in the development of endometriosis. Using immunohistochemistry, integrin expression in eutopic and ectopic endometrium is examined in endometriosis patients and control individuals. In nearly all cases, the glandular epithelial cells in the endometrium showed expression of alpha (2-), alpha (3)-, alpha (6)- and alpha (v)- integrin and a low percentage of expression of alpha (1)-, alpha (4)-, and alpha (5)-integrin. In comparison with eutopic endometrium, ectopic endometrium shows reduced expression of alpha (2)- and alpha (v)-integrin. Since no differences in alpha (2)- and alpha (v)-integrin expression were observed in eutopic endometrium between endometriosis patients and control individuals, it may be suspected that the reduced expression of these in ectopic endometrium is explained by influences in the altered environment -- e. g., in the peritoneal fluid -- on the ectopic endometrium.
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Subscribe to RSS DOI: 10.1055/s-2006-921550 © Georg Thieme Verlag Stuttgart · New York Integrinexpression im eutopen und ektopen Endometrium von Endometriosepatientinnen Integrinexpression in Eutopic and Ectopic EndometriumPublication History Publication Date: 06 June 2006 (online) Zusammenfassung Die Bedeutung der retrograden Menstruation als Risikofaktor für eine Endometriose ist durch zahlreiche klinische Beobachtungen belegt. Integrine vermitteln sowohl Zell-Zell- als auch Zell-Matrix-Adhäsion, daher wird eine Beteiligung der Integrine an der Entwicklung der Endometriose vermutet. Mit Hilfe der Immunhistochemie wird die Integrinexpression im eutopen und ektopen Endomerium von Endometriosepatientinnen und Kontrollen untersucht. Die glandulären Epithelzellen des Endometriums zeigten in nahezu allen Fällen die Expression von α2-, α3-, α6- und αv-Integrin und in einem geringen Prozentsatz die Expression von α1-, α4- und α5-Integrin. Verglichen mit dem eutopen Endometrium weist das ektope Endometrium eine verminderte Expression von α2- und αv-Integrin auf. Da im eutopen Endometrium keine Unterschiede der α2- und αv-Integrinexpression zwischen Endometriosepatientinnen und Kontrollen festzustellen waren, kann vermutet werden, dass die verminderte Expression im ektopen Endometrium durch Einflüsse der veränderten Umgebung, wie z. B. der Peritonealflüssigkeit auf das ektope Endometrium zu erklären sind. Abstract The significance of retrograde menstruation as a risk factor for endometriosis has been confirmed by numerous clinical observations. Integrins mediate both cell-cell and cell-matrix adhesion, and it is therefore suspected that integrins are involved in the development of endometriosis. Using immunohistochemistry, integrin expression in eutopic and ectopic endometrium is examined in endometriosis patients and control individuals. In nearly all cases, the glandular epithelial cells in the endometrium showed expression of α2-, α3-, α6- and αv- integrin and a low percentage of expression of α1-, α4-, and α5-integrin. In comparison with eutopic endometrium, ectopic endometrium shows reduced expression of α2- and αv-integrin. Since no differences in α2- and αv-integrin expression were observed in eutopic endometrium between endometriosis patients and control individuals, it may be suspected that the reduced expression of these in ectopic endometrium is explained by influences in the altered environment - e. g., in the peritoneal fluid - on the ectopic endometrium. Schlüsselwörter Adhäsion - Peritonealflüssigkeit - Endometriose Key words adhesion - peritoneal fluid - endometriosis Literatur - 1 Danen E HJ. Integrins: Regulators of tissue functions and cancer progression. Curr Pharm Design. 2005; 11 881-891 - 2 Lessey B A, Castelbaum A J, Buck C A, Lei Y, Yowell C W, Sun J. Further characterization of endometrial integrins during menstrual cycle and in pregnancy. Fertil Steril. 1994; 64 497-506 - 3 Sülz I, Valenzuela J P, Salvatierra A M, Ortiz M E, Croxatto H B. The expression of αv and β3 integrin subunits in the normal fallopian tube epithelium suggest the occurrence of a tubal implantation window. Hum Reprod. 1998; 12 2916-2920 - 4 Gaetje R, Kotzian S, Herrmann G, Baumann R, Starzinski-Powitz A. Non-malignant epithelial cells, potentially invasive cells in human endometriosis, lack the tumor suppressor molecule E-Cadherin. Am J Path. 1997; 150 461-467 - 5 Gaetje R, Kotzian S, Herrmann G, Baumann R, Starzinski-Powitz A. Invasiveness of endometriotic cells in vitro. Lancet. 1995; 346 1463-1464 - 6 Lessey B A, Castelbaum A J, Sawin S S, Sun J. Intergrin as markers of uterine receptivity in women with primary unexplained infertility. Fertil Steril. 1995; 63 535-542 - 7 Lessey B A. Endometrial integrins and the establishment of uterine receptivity. Hum Reprod. 1998; 13 (Suppl 3) 247-258 - 8 van der Linden P JQ, de Goeij A FPM, Dunselman G AJ, van der Linden E PM, Ramaekers F CS, Evers J LH. Expression of integrins and E-Cadherin in cells from menstrual fluid, endometrium, peritoneal fluid, peritoneum and endometriosis. Fertil Steril. 1994; 61 85-90 - 9 Bridges J E, Roche W, Englefield P, Thomas E J. Expression of integrin adhesion molecules in endometrium and endometriosis. Br J Obstet Gynaecol. 1994; 101 696-700 - 10 Beliard A, Donnez J, Nisolle M, Foidart J M. Localization of laminin, fibronectin, E-cadherin, and integrin in endometrium and endometriosis. Fertil Steril. 1997; 67 266-272 - 11 Hii L LP, Rogers P AW. Endoemtrial vascular and glandular expression of integrin αvβ3 in women with and without endometriosis. Hum Reprod. 1998; 13 1030-1035 - 12 Khorram O, Lessey B A. Alterations in expression of endometrial endothelial nitric oxide synthase and alpha(v)beta(3)integrin in women with endometriosis. Fertil Steril. 2002; 78 860-864 - 13 Illera M J, Jaun L, Stewart C L, Cullinan E, Ruman J, Lessey B A. Effect of peritoneal fluid from women with endometriosis on implantation in the mouse model. Fertil Steril. 2000; 74 41-48 PD Dr. R. Gaetje Klinik für Gynäkologie und Geburtshilfe · Johann-Wolfgang-Goethe-Universität Theodor Stern-Kai 7 60596 Frankfurt Phone: 0 69/63 01 74 38 Fax: 0 69/63 01 70 34 Email: [email protected]

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Condition tags

mesh:D004715endometriosis

MeSH descriptors

Endometriosis Endometrium Integrins Biopsy Choristoma Choristoma Choristoma Endometriosis Endometrium Endometrium Female Humans Integrins

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