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KMID : 0624620170500080429
BMB Reports
2017 Volume.50 No. 8 p.429 ~ p.434
Transforming growth factor ¥â1 enhances adhesion of endometrial cells to mesothelium by regulating integrin expression
Choi Hee-Jung

Park Mi-Ju
Kim Bo-Sung
Joo Bo-Sun
Lee Kyu-Sup
Choi Jung-Hye
Chung Tae-Wook
Ha Ki-Tae
Abstract
Endometriosis is the abnormal growth of endometrial cells outside the uterus, causing pelvic pain and infertility. Furthermore, adhesion of endometrial tissue fragments to pelvic mesothelium is required for the initial step of endometriosis formation outside uterus. TGF-¥â1 and adhesion molecules importantly function for adhesion of endometrial tissue fragments to mesothelium outside uterus. However, the function of TGF-¥â1 on the regulation of adhesion molecule expression for adhesion of endometrial tissue fragments to mesothelium has not been fully elucidated. Interestingly, transforming growth factor ¥â1 (TGF-¥â1) expression was higher in endome-triotic epithelial cells than in normal endometrial cells. The adhesion efficiency of endometriotic epithelial cells to meso-thelial cells was also higher than that of normal endometrial cells. Moreover, TGF-¥â1 directly induced the adhesion of endometrial cells to mesothelial cells through the regulation of integrin of ¥áV, ¥á6, ¥â1, and ¥â4 via the activation of the TGF-¥â1/TGF-¥âRI/Smad2 signaling pathway. Conversely, the adhesion of TGF-¥â1-stimulated endometrial cells to mesothelial cells was clearly reduced following treatment with neutralizing antibodies against specific TGF-¥â1-mediated integrins ¥áV, ¥â1, and ¥â4 on the endometrial cell membrane. Taken together, these results suggest that TGF-¥â1 may act to promote the initiation of endometriosis by enhancing integrin-mediated cell-cell adhesion.
KEYWORD
Endometrial cells, Endometriosis, Integrin, Mesothelial cells, TGF-¥â1
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