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Immunocytochemical Studies of Adhesion Molecules on Mouse UNK Cells and Their Extracellular Matrix Ligands During Mouse Pregnancy

整合素 纤维连接蛋白 层粘连蛋白 生物 蜕膜 子宫 内科学 细胞外基质 内分泌学 子宫内膜 胎盘 受体 细胞生物学 怀孕 胎儿 生物化学 医学 遗传学
作者
Bruno Zavan,Andréa Mollica Amarante Paffaro,Paulo Pinto Joazeiro,Áureo T. Yamada,Valdemar A. Paffaro
出处
期刊:Anatomical Record-advances in Integrative Anatomy and Evolutionary Biology [Wiley]
卷期号:293 (6): 1081-1088 被引量:10
标识
DOI:10.1002/ar.21117
摘要

Abstract Uterine natural killer (uNK) cells are the dominant lymphocytes of pregnant mammals' uterus. Studies have identified four differentiation stage of mouse uNK cells based on Dolichos biflorus lectin cytochemistry, and their distribution showed preferential domain in the uterus through out the pregnancy. This work was done to investigate the expression of α5, α6, and β7 integrins on uNK cells and their ligands distribution. Section of mouse uterus from sixth to seventeenth gestational days were submitted to immunocytochemistry and positive reactions for α5, α6, and β7 integrins were found on uNK from eighth to tenth gestational days but not after twelfth gestational days. Fibronectin reactions were seemed from sixth to tenth gestational days around uNK from the myometrium and endometrium close to the myometrium. No reaction for fibronectin was seen in the decidualized and nondecidualized endometrium near the placenta. Laminin reaction was seen just in the antimesometrial side. β7 integrin seems to be the active receptor to bind with VCAM‐1 or MAdCAM‐1 of endothelial cells, promoting the uNK cross through the vessels. The absence of laminin in an uNK domain suggests these cells are not dependent of laminin and α6 integrin for their establishment. However, fibronectin seems to support uNK migration, proliferation, differentiation, and survival in the uterus by binding with α5 integrin. The loss of α5 integrin ligation by the down regulation of fibronectin could inhibits these events and further studies are need to investigate whether unligated α5 can actively and initiate apoptosis, maybe in a caspase 8‐dependent way that has been called integrin‐mediated death. Anat Rec, 2010. © 2010 Wiley‐Liss, Inc.
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