内皮素-1对体外人小梁网细胞吞噬功能的影响

Y. Xiang, G. Li, Lin-gang Xu, Zhiqi Chen, Rui-Lin Wang, Hong Zhang
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引用次数: 0

摘要

内皮素-1 (ET-1)是眼压的积极调节因子。在原发性开角型青光眼、正常眼内张力型青光眼和青光眼动物模型中,房水ET-1水平升高。现在有越来越多的证据表明ET-1在青光眼发病机制中的作用。然而,ET-1对小梁网细胞(TMCs)吞噬功能的影响尚不清楚。目的观察ET-1对体外培养的人tmc吞噬功能的影响。方法从健康供体获得人小梁网组织,采用外植体培养法进行体外培养和传代培养。第三代人tmc与荧光红色标记乳胶珠孵育0、4、8、12、24、48和72小时。利用荧光显微镜连续测定tmc中乳胶珠的数量,观察tmc的吞噬动力学。根据培养基中ET-1的浓度,将TMCs分为对照组(不含ET-1)、低剂量ET-1 (10~(-9)mol/L)处理组、中剂量ET-1 (10~(-8)mol/L)处理组和高剂量ET-1 (10~(-7) mol/L)处理组。此外,根据内皮素受体(ETAR)拮抗剂的添加情况,将TMCs分为对照组(未添加ETAR拮抗剂)、ET-1 (10~(-8)mol/L)处理组、ETAR拮抗剂(1×10~(-7)mol/L BQ123+10~(-8)mol/L ET-1)处理组和ETBR拮抗剂(1×10~(-7)mol/L BQ788+10~(-8) mol/L ET-1)处理组。用乳胶珠孵育各组tmc,荧光显微镜下计数tmc中乳胶珠的数量。结果培养的HTM细胞对FN、LN、NSE呈阳性反应,对FⅧRag呈阴性反应。吞噬动力学试验表明,孵育4小时后可检测到乳胶珠。乳胶珠密度随孵育时间的延长而逐渐增加,在孵育24小时达到峰值。孵育48小时后乳胶珠饱和的数量。而ET-1的加入显著降低了TMCs中乳胶珠的数量,且呈剂量依赖性(F=28.91,P<0.05)。ET-1组乳胶珠数少于对照组和ETAR受体拮抗剂组(q=13.7228,q=9.4312,P<0.05)。ET-1组与ETBR拮抗剂组的乳胶珠数差异无统计学意义(q=1.1600,P>0.05)。结论ET-1抑制人TMCs的吞噬功能,ETAR对TMCs的吞噬功能起部分作用。关键词:人小梁tmc;网状组织细胞;endothelin-1;吞噬作用;乳胶珠子
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of endothelin-1 on the phagocytic function of human trabecular meshwork cells in vitro
Background Endothelin-1 (ET-1) is an active regulator of intraocular pressure.The ET-1 level in aqueous humor is elevated in primary open-angle glaucoma,normal intraocular tension glaucoma and the animal model of glaucoma.There is now accumulating evidence for a role of ET-1 in the pathogenesis of glaucoma.However,the effect of ET-1 on the phagocytic function in trabecular meshwork cells (TMCs) is unclear.ObjectiveThis study is to observe the effect of ET-1 on the phagocytic function in cultured human TMCs.Methods Human trabecular meshwork tissue was obtained from healthy donator and cultured and subcultured in vitro by the explant culture method.The third passage of human TMCs were incubated with fluoresent red-labeled latex beads for 0,4,8,12,24,48 and 72 hours.The phagocytic kinetics of human TMCs were continuously evaluated by counting the number of latex beads in TMCs using a fluorescence microscope.Depending on the concentrations of ET-1 in culture medium,the TMCs were divided into control group (without ET-1),low-dose ET-1 (10~(-9)mol/L) treatment group,middle-dose ET-1 (10~(-8)mol/L) treatment group and high-dose ET-1 (10~(-7) mol/L) treatment group.In addition,based on the addition of endothelin receptor (ETAR) antagonist,the TMCs were divided into control group (without ETAR antagonist),ET-1 (10~(-8)mol/L) treatment group,ETAR antagonist (1×10~(-7)mol/L BQ123+10~(-8)mol/L ET-1) treatment group and ETBR antagonist(1×10~(-7) mol/L BQ788+10~(-8) mol/L ET-1)treatment group.TMCs of each group were incubated with latex beads,and the numbers of latex beads in TMCs were counted under a fluorescent microscope.Results Cultured HTM cells showed positive reactions for FN,LN,NSE and negative response for FⅧRag.The phagocytic kinetics test revealed that the latex beads were detected 4 hours after incubation.The density of latex beads was gradually increased with the delay of incubation duration and peaked at 24 hours.The number of the latex beads saturated after 48 hours of incubation.However,the number of latex beads in TMCs was significantly reduced after the addition of ET-1 in a dose-dependent manner (F=28.91,P<0.05).The number of latex beads in the ET-1 group was less than that in the control group and the ETAR receptor antagonist group (q=13.7228,q=9.4312,P<0.05).No significant difference was found in latex beads number between the ET-1 group and the ETBR antagonist group (q=1.1600,P>0.05).Conclusion ET-1 inhibits the phagocytic function of human TMCs and ETAR plays a partial role in the phagocytic function of human TMCs. Key words: trabecular human TMCs; meshwork cells; endothelin-1; phagocytosis; latex beads
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