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子宫内膜异位症患者腹腔液中正常T淋巴细胞表达和分泌调节活化因子水平的变化及意义
引用本文:Yu J,Wang Y,Zhou WH,Wang L,Li DJ. 子宫内膜异位症患者腹腔液中正常T淋巴细胞表达和分泌调节活化因子水平的变化及意义[J]. 中华妇产科杂志, 2008, 43(5): 336-340
作者姓名:Yu J  Wang Y  Zhou WH  Wang L  Li DJ
作者单位:复旦大学附属妇产科医院生殖免疫研究室,上海,200011
基金项目:上海市重点学科建设项目 
摘    要:目的 探讨子宫内膜异位症(内异症)患者腹腔液中正常T淋巴细胞表达和分泌调节活化因子(RANTES)分泌水平的变化及其对单核巨噬细胞趋化的影响.方法 建立内异症异位病灶主要细胞--子宫内膜基质细胞(ESC)、腹膜间皮细胞(HPMC)及单核巨噬细胞系U937不同组合的直接接触(E-H-U、E-H、E-U、H-U)及间接接触共培养体系(U/E-H、H/E-U、E/H-U),然后收集共培养上清液,用酶联免疫吸附试验(ELISA)检测RANTES分泌水平的变化.利用趋化实验观察ESC、HPMC及ESC-HPMC共培养对单核巨噬细胞的趋化作用.结果 ESC、HPMC、U937单独培养时,RANTES的分泌水平分别为(5.0±0.5)、(4.0±0.3)、(254±40)ng/L;与单独培养比较,共培养明显促进RANTES的分泌,其中E-H-U培养为(2250±96) ng/L,E-U培养为(243±192) ng/L,H-U培养为(1251±73) ng/L,E-H培养为(50±40) ng/L,3种细胞直接共培养较两种细胞直接共培养时,RANTES分泌水平明显升高,差异有统计学意义(P<0.01);间接共培养时,RANTES的分泌水平分别为(1519±96) ng/L(E/H-U培养)、(912±93) ng/L(U/E-H培养)、(1201±93)ng/L(H/E-U培养).ESC、HPMC及ESC-HPMC共培养可促进单核巨噬细胞的趋化,迁移细胞数分别为(6.0±0.3)、(6.2±0.3)、(10.0±0.3)×103个.结论 内异症病灶主要细胞间存在着复杂的相互作用机制,并可促进趋化因子RANTES的分泌,从而促进腹腔内单核巨噬细胞的趋化和募集.

关 键 词:子宫内膜异位症  腹腔液  T淋巴细胞  酶联免疫吸附测定  细胞,培养的

Roles of regulated upon activation normal T cell expressed and secreted in pathogenesis of endometriosis
Yu Jing,Wang Yun,Zhou Wen-Hui,Wang Ling,Li Da-Jin. Roles of regulated upon activation normal T cell expressed and secreted in pathogenesis of endometriosis[J]. Chinese Journal of Obstetrics and Gynecology, 2008, 43(5): 336-340
Authors:Yu Jing  Wang Yun  Zhou Wen-Hui  Wang Ling  Li Da-Jin
Affiliation:Laboratory of Reproductive Immunology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.
Abstract:Objective To explore the secretion of chemokine regulated upon activation normal T cell expressed and secreted(RANTES)influenced by the complex microenvironment in the peritoneal cavity of women with endometriosis and investigate chemotaxis of RANTES on the peritoneal monocytes.Methods The contact and non-contact co-culture systems including three target cells of ectopic tissue were established.The three target cells were endometrial stromal cells(ESC),human peritoneal mesothelial cells(HPMC)and monocytes.After collection of the supernatant of co-culture systems,the levels of RANTES were detected by enzyme linked immunosorbent assay(EUSA).Migration of U937 cell,a monocyte line,was detected by chemotaxis assay.Results ESC,HPMC,and U937 cultured alone secreted slight RANTES,(5.0±0.5),(4.0±0.3),and (254±40)ng/L. Compared with the culture of the target cell alone,the levels of RANTES in each co-culture system increased significantly,with the highest level in the contact culture system of E-H-U(2250±96)ng/L. RANTES secretion of non-contact co-culture of three cells were higher than contact co-culture of two cells(P<0.01):U/E-H(912±93) vs E-H(50±40)ng/L,H/E-U(1201±93) vs E-U(243±192)ng/L,and E/H-U(1519±96) vs H-U(1251±73)ng/L. ESC,HPMC,and ESC-HPMC co-culture improved significantly migration of U937 cells [ number of cell migration respectively(6.0±0.3),(6.2±0.3),(10.0±0.3)×103,P<0.01],which could be inhibited efficiently by anti-RANTES neutralizing antibody.Condusion The target cells in the peritoneal cavity of patients with endometriosis promote the secretion of RANTES in autocrine and paracrine manners and migration of monocytes.
Keywords:RANTES
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