Witz Craig A, Allsup Karen T, Montoya-Rodriguez Iris A, Vaughan Shelby L, Centonze Victoria E, Schenken Robert S
Department of Obstetrics and Gynecology, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900, USA.
Hum Fertil (Camb). 2003 Feb;6(1):34-40. doi: 10.1080/1464770312331368973.
Proliferative, secretory and menstrual endometrial cells of both the stroma and epithelium adhere to intact peritoneal mesothelium and mesothelial monolayers. Endometrial attachment to the mesothelium appears to occur rapidly (within 1 h) and transmesothelial invasion occurs between 1 and 18-24 h. These results demonstrate that the mesothelium is not a 'no-stick' surface and indicates that molecules present at the surface of the mesothelium are involved in the pathogenesis of the early endometriotic lesion. The inhibition of endometrial cell adherence to peritoneal mesothelium by hyaluronidase indicates that CD44-hyaluronan binding is at least one of the mechanisms involved in the pathogenesis of endometriosis. We believe that investigation of mesothelial cell adhesion molecules is central to understanding the pathogenesis of endometriosis.
基质和上皮的增殖期、分泌期及月经期子宫内膜细胞均能黏附于完整的腹膜间皮和间皮单层。子宫内膜与间皮的黏附似乎迅速发生(1小时内),而跨间皮侵袭发生在1至18 - 24小时之间。这些结果表明,间皮并非“不黏附”表面,提示间皮表面存在的分子参与了早期子宫内膜异位症病变的发病机制。透明质酸酶抑制子宫内膜细胞与腹膜间皮的黏附,表明CD44 - 透明质酸结合至少是子宫内膜异位症发病机制中的一种机制。我们认为,对间皮细胞黏附分子的研究是理解子宫内膜异位症发病机制的核心。