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Usage Information

Integrin adhesion molecules in the human endometrium. Correlation with the normal and abnormal menstrual cycle.
B A Lessey, L Damjanovich, C Coutifaris, A Castelbaum, S M Albelda, C A Buck
B A Lessey, L Damjanovich, C Coutifaris, A Castelbaum, S M Albelda, C A Buck
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Research Article

Integrin adhesion molecules in the human endometrium. Correlation with the normal and abnormal menstrual cycle.

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Abstract

Integrins are a class of cell adhesion molecules that participate in cell-cell and cell-substratum interactions and are present on essentially all human cells. The distribution of nine different alpha and beta integrin subunits in human endometrial tissue at different stages of the menstrual cycle was determined using immunoperoxidase staining. Glandular epithelial cells expressed primarily alpha 2, alpha 3, and alpha 6 (collagen/laminin receptors), while stromal cells expressed predominantly alpha 5 (fibronectin receptor). The presence of alpha 1 on glandular epithelial cells was cycle specific, found only during the secretory phase. Expression of both subunits of the vitronectin receptor, alpha v beta 3, also underwent cycle specific changes on endometrial epithelial cells. Immunostaining for alpha v increased throughout the menstrual cycle, while the beta 3 subunit appeared abruptly on cycle day 20 on luminal as well as glandular epithelial cells. Discordant luteal phase biopsies (greater than or equal to 3 d "out of phase") from infertility patients exhibited delayed epithelial beta 3 immunostaining. These results demonstrate similarities, as well as specific differences, between endometrium and other epithelial tissues. Certain integrin moieties appear to be regulated within the cycling endometrium and disruption of integrin expression may be associated with decreased uterine receptivity and infertility.

Authors

B A Lessey, L Damjanovich, C Coutifaris, A Castelbaum, S M Albelda, C A Buck

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Usage data is cumulative from August 2025 through August 2026.

Usage JCI PMC
Text version 711 121
PDF 201 51
Scanned page 641 0
Citation downloads 206 0
Totals 1,759 172
Total Views 1,931
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ISSN: 0021-9738 (print), 1558-8238 (online)

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