中华临床医师杂志(电子版)
中華臨床醫師雜誌(電子版)
중화림상의사잡지(전자판)
CHINESE JOURNAL OF CLINICIANS(ELECTRONIC VERSION)
2013年
4期
1436-1440
,共5页
周雯慧%任亮%刘越%张元珍
週雯慧%任亮%劉越%張元珍
주문혜%임량%류월%장원진
母-胎界面%滋养细胞%蜕膜基质细胞%CXCR7%CXCR4
母-胎界麵%滋養細胞%蛻膜基質細胞%CXCR7%CXCR4
모-태계면%자양세포%세막기질세포%CXCR7%CXCR4
Materno-fetal interface%Trophoblasts%Decidual stromal cells%CXCR7%CXCR4
目的研究趋化因子受体CXCR7在人早孕期母-胎界面的表达特征。方法收集人早孕期绒毛与蜕膜组织,免疫组织化学技术分析趋化因子受体CXCR7及CXCR4在母-胎界面的表达情况;分别分离培养人早孕期滋养细胞及蜕膜基质细胞,免疫细胞化学技术分析CXCR7和CXCR4在两种细胞的表达。结果人早孕期绒毛与蜕膜组织及体外分离培养的人早孕期滋养细胞、蜕膜基质细胞均可观察到特异性CXCR7和CXCR4阳性染色,但两种细胞CXCR7染色强度(平均光密度值)均略低于CXCR4,差异有统计学意义(P<0.05)。结论人早孕期滋养细胞及蜕膜基质细胞共表达趋化因子受体CXCR7和CXCR4,提示CXCR7可能在母-胎免疫微环境形成中也起重要作用。
目的研究趨化因子受體CXCR7在人早孕期母-胎界麵的錶達特徵。方法收集人早孕期絨毛與蛻膜組織,免疫組織化學技術分析趨化因子受體CXCR7及CXCR4在母-胎界麵的錶達情況;分彆分離培養人早孕期滋養細胞及蛻膜基質細胞,免疫細胞化學技術分析CXCR7和CXCR4在兩種細胞的錶達。結果人早孕期絨毛與蛻膜組織及體外分離培養的人早孕期滋養細胞、蛻膜基質細胞均可觀察到特異性CXCR7和CXCR4暘性染色,但兩種細胞CXCR7染色彊度(平均光密度值)均略低于CXCR4,差異有統計學意義(P<0.05)。結論人早孕期滋養細胞及蛻膜基質細胞共錶達趨化因子受體CXCR7和CXCR4,提示CXCR7可能在母-胎免疫微環境形成中也起重要作用。
목적연구추화인자수체CXCR7재인조잉기모-태계면적표체특정。방법수집인조잉기융모여세막조직,면역조직화학기술분석추화인자수체CXCR7급CXCR4재모-태계면적표체정황;분별분리배양인조잉기자양세포급세막기질세포,면역세포화학기술분석CXCR7화CXCR4재량충세포적표체。결과인조잉기융모여세막조직급체외분리배양적인조잉기자양세포、세막기질세포균가관찰도특이성CXCR7화CXCR4양성염색,단량충세포CXCR7염색강도(평균광밀도치)균략저우CXCR4,차이유통계학의의(P<0.05)。결론인조잉기자양세포급세막기질세포공표체추화인자수체CXCR7화CXCR4,제시CXCR7가능재모-태면역미배경형성중야기중요작용。
Objective To explore the expression of chemokine receptor CXCR 7 at the materno-fetal interface during human first-trimester pregnancy .Methods Human first-trimester pregnancy villous and decidual tissues were collected , and primary trophoblast cells ( TC ) and dedidual stromal cells ( DSC ) were isolated and cultured.The protein expression of CXCR7 and CXCR4 were examined by immunohistochemistry ( IHC ) and immunocytochemistry(ICC),respectively.Results IHC and ICC disclosed specific staining for both CXCR 7 and CXCR4 protein in TC and DSC ,respectively .However ,the mean density of CXCR 7 in TC and DSC was significantly lower than that of CXCR4(P<0.05).Conclusions CXCR7 and CXCR4 are co-expressed in human first-trimester pregnancy TC and DSC ,which contributes to the establishment of materno-fetal immune microenvironment .