Menstrual endometrial cells from women with endometriosis demonstrate increased adherence to peritoneal cells and increased expression of CD44 splice variants.
Menstrual endometrial cells from women with endometriosis demonstrate increased adherence to peritoneal cells and increased expression of CD44 splice variants.
复制标题
DOI:
10.1016/j.fertnstert.2008.12.012
复制
发表时间:
2010-04
影响因子:
6.7
通讯作者:
Schenken RS
中科院分区:
文献类型:
--
作者:
Griffith JS;Liu YG;Tekmal RR;Binkley PA;Holden AE;Schenken RS
We previously demonstrated that adherence of endometrial epithelial (EECs) and stromal cells (ESCs) to peritoneal mesothelial cells (PMCs) is partly regulated by ESC/EEC CD44 interactions with PMC associated hyaluronan. CD44, a transmembrane glycoprotein and major ligand for hyaluronan, has numerous splice variants which may impact hyaluronan binding. Here, we assessed whether ESCs and EECs from women with endometriosis demonstrate increased adherence to PMCs and examined CD44 splice variants’ potential role in this process. In vitro study. Academic medical Center Fertility patients with and without endometriosis Menstrual endometrium was collected from women with and without endometriosis confirmed surgically. The adherence of ESC/EECs to PMCs was measured. ESC/EEC CD44 splice variants were assessed using dot blot analysis. ESCs and EECs from women with endometriosis demonstrated increased adherence to PMCs. The predominant CD44 splice variants expressed by ESCs and EECs from women with and without endometriosis were v3, v6, v7, v8, v9, and v10. ESCs and EECs from women with endometriosis were more likely to express v6, v7, v8 or v9. Increased eutopic endometrial-PMC adherence and CD44 splice variant expression may contribute to the histogenesis of endometriotic lesions. Elucidation of factors controlling this expression may lead to novel endometriosis therapies.
登录
查看更多内容
影响因子:
6
作者:
Lessan, K;Aguiar, DJ;Skubitz, APN
通讯作者:
Skubitz, APN
DOI:
10.1083/jcb.131.6.1623
发表时间:
1995-12
期刊:
The Journal of cell biology
影响因子:
--
作者:
Bennett KL;Modrell B;Greenfield B;Bartolazzi A;Stamenkovic I;Peach R;Jackson DG;Spring F;Aruffo A
通讯作者:
Aruffo A
影响因子:
3.3
作者:
YAEGASHI, N;FUJITA, N;NAKAMURA, M
通讯作者:
NAKAMURA, M
DOI:
10.1016/s0889-8545(05)70302-8
发表时间:
1997-06-01
影响因子:
3.2
作者:
Eskenazi, B;Warner, ML
通讯作者:
Warner, ML
DOI:
10.1084/jem.182.2.431
发表时间:
1995-08-01
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Lesley J;English N;Perschl A;Gregoroff J;Hyman R
通讯作者:
Hyman R