Regulation of trophoblast beta1-integrin expression by contact with endothelial cells

<p>Abstract</p> <p>Background</p> <p>In human and non-human primates, migratory trophoblasts penetrate the uterine epithelium, invade uterine matrix, and enter the uterine vasculature. Invasive trophoblasts show increased expression of β1 integrin. Since trophoblast mig...

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Main Authors: Thirkill Twanda L, Hendren Sonia R, Soghomonians Arlen, Mariano Natalie F, Barakat Abdul I, Douglas Gordon C
Format: Article
Language:English
Published: BMC 2004-06-01
Series:Cell Communication and Signaling
Online Access:http://www.biosignaling.com/content/2/1/4
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author Thirkill Twanda L
Hendren Sonia R
Soghomonians Arlen
Mariano Natalie F
Barakat Abdul I
Douglas Gordon C
author_facet Thirkill Twanda L
Hendren Sonia R
Soghomonians Arlen
Mariano Natalie F
Barakat Abdul I
Douglas Gordon C
author_sort Thirkill Twanda L
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>In human and non-human primates, migratory trophoblasts penetrate the uterine epithelium, invade uterine matrix, and enter the uterine vasculature. Invasive trophoblasts show increased expression of β1 integrin. Since trophoblast migration within the uterine vasculature involves trophoblast attachment to endothelial cells lining the vessel walls, this raises the possibility that cell-cell contact and/or factors released by endothelial cells could regulate trophoblast integrin expression. To test this, we used an in vitro system consisting of early gestation macaque trophoblasts co-cultured on top of uterine microvascular endothelial cells.</p> <p>Results</p> <p>When cultured alone, trophoblasts expressed low levels of β1 integrin as determined by quantitative immunofluorescence microscopy. When trophoblasts were cultured on top of endothelial cells for 24 h, the expression of trophoblast β1 integrin was significantly increased as determined by image analysis. β1 Integrin expression was not increased when trophoblasts were cultured with endothelial cell-conditioned medium, suggesting that upregulation requires direct contact between trophoblasts and endothelial cells. To identify endothelial cell surface molecules responsible for induction of trophoblast integrin expression, trophoblasts were cultured in dishes coated with recombinant platelet endothelial cell adhesion molecule-1 (PECAM-1), intercellular adhesion molecule-1 (ICAM-1), or αVβ3 integrin. Trophoblast β1 integrin expression (assessed by immunofluorescence microscopy and Western blotting) was increased when PECAM-1 or αVβ3 integrin, but not ICAM-1, was used as substrate.</p> <p>Conclusions</p> <p>Direct contact between trophoblasts and endothelial cells increases the expression of trophoblast β1 integrin.</p>
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spelling doaj.art-ed1ac978462041cb8e6c555360e55e702022-12-22T03:28:31ZengBMCCell Communication and Signaling1478-811X2004-06-0121410.1186/1478-811X-2-4Regulation of trophoblast beta1-integrin expression by contact with endothelial cellsThirkill Twanda LHendren Sonia RSoghomonians ArlenMariano Natalie FBarakat Abdul IDouglas Gordon C<p>Abstract</p> <p>Background</p> <p>In human and non-human primates, migratory trophoblasts penetrate the uterine epithelium, invade uterine matrix, and enter the uterine vasculature. Invasive trophoblasts show increased expression of β1 integrin. Since trophoblast migration within the uterine vasculature involves trophoblast attachment to endothelial cells lining the vessel walls, this raises the possibility that cell-cell contact and/or factors released by endothelial cells could regulate trophoblast integrin expression. To test this, we used an in vitro system consisting of early gestation macaque trophoblasts co-cultured on top of uterine microvascular endothelial cells.</p> <p>Results</p> <p>When cultured alone, trophoblasts expressed low levels of β1 integrin as determined by quantitative immunofluorescence microscopy. When trophoblasts were cultured on top of endothelial cells for 24 h, the expression of trophoblast β1 integrin was significantly increased as determined by image analysis. β1 Integrin expression was not increased when trophoblasts were cultured with endothelial cell-conditioned medium, suggesting that upregulation requires direct contact between trophoblasts and endothelial cells. To identify endothelial cell surface molecules responsible for induction of trophoblast integrin expression, trophoblasts were cultured in dishes coated with recombinant platelet endothelial cell adhesion molecule-1 (PECAM-1), intercellular adhesion molecule-1 (ICAM-1), or αVβ3 integrin. Trophoblast β1 integrin expression (assessed by immunofluorescence microscopy and Western blotting) was increased when PECAM-1 or αVβ3 integrin, but not ICAM-1, was used as substrate.</p> <p>Conclusions</p> <p>Direct contact between trophoblasts and endothelial cells increases the expression of trophoblast β1 integrin.</p>http://www.biosignaling.com/content/2/1/4
spellingShingle Thirkill Twanda L
Hendren Sonia R
Soghomonians Arlen
Mariano Natalie F
Barakat Abdul I
Douglas Gordon C
Regulation of trophoblast beta1-integrin expression by contact with endothelial cells
Cell Communication and Signaling
title Regulation of trophoblast beta1-integrin expression by contact with endothelial cells
title_full Regulation of trophoblast beta1-integrin expression by contact with endothelial cells
title_fullStr Regulation of trophoblast beta1-integrin expression by contact with endothelial cells
title_full_unstemmed Regulation of trophoblast beta1-integrin expression by contact with endothelial cells
title_short Regulation of trophoblast beta1-integrin expression by contact with endothelial cells
title_sort regulation of trophoblast beta1 integrin expression by contact with endothelial cells
url http://www.biosignaling.com/content/2/1/4
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AT soghomoniansarlen regulationoftrophoblastbeta1integrinexpressionbycontactwithendothelialcells
AT marianonatalief regulationoftrophoblastbeta1integrinexpressionbycontactwithendothelialcells
AT barakatabduli regulationoftrophoblastbeta1integrinexpressionbycontactwithendothelialcells
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