CAJ | 학술논문

目的观察细胞内Ca+及MERTK基因在人视网膜色素上皮(RPE)细胞的吞噬功能中所起的作用及二者的相互关系.方法用视细胞外节膜盘(ROS)于37℃孵育培养的RPE细胞.在孵育不同终止吞噬反应.双重荧光标记法检测RPE细胞吞噬动力学;钙离子荧光探针负载法在荧光显微镜下测定RPE细胞内Ca2+的变化;半定量逆转录聚合酶链反应(RT-PCR)法检测相应时间点MERTK基因表达的变化及施加Ca2+激活剂(A23187载体)或拮抗剂(verapamile)后MERTK基因表达的变化.结果 RPE细胞与ROS孵育过程中,ROS结合于RPE细胞表面发生在15 rain时,RPE细胞吞噬ROS在24 h时达到饱和.细胞内Ca2+在孵育15 min时升高.并在24 h内保持高水平;MERTK基因表达在RPE细胞与ROS孵育5 min时增强,并在全部孵育过程中呈现出高表达状态;以A23187载体开放钙通道升高RPE细胞内Ca2+后,MERTK基因信使核糖核酸(Mrna)水平升高.并呈剂量依赖性.经A23187预处理后的孵育实验中所检测到的MERTK Mrna水平除3 h这一时间点外均高于对照组;vempamile拮抗RPE细胞内Ca2+后,MERTK基因表达明显下降并呈剂量依赖性;以verapamile预处理后继续与ROS孵育,所检测到的MERTK基因在24 h内均低于对照组.结论 MERTK基因及细胞内Ca2+发挥着维持RPE细胞吞噬过程的重要作用,MERTK作为上游调控信号启动下游的细胞内Ca2+信号来维持RPE细胞对ROS的摄入过程.
목적 관찰세포내Ca+급MERTK기인재인시망막색소상피(RPE)세포적탄서공능중소기적작용급이자적상호관계.방법용시세포외절막반(ROS)우37℃부육배양적RPE세포.재부육불동종지탄서반응.쌍중형광표기법검측RPE세포탄서동역학;개리자형광탐침부재법재형광현미경하측정RPE세포내Ca2+적변화;반정량역전록취합매련반응(RT-PCR)법검측상응시간점MERTK기인표체적변화급시가Ca2+격활제(A23187재체)혹길항제(verapamile)후MERTK기인표체적변화.결과 RPE세포여ROS부육과정중,ROS결합우RPE세포표면발생재15 rain시,RPE세포탄서ROS재24 h시체도포화.세포내Ca2+재부육15 min시승고.병재24 h내보지고수평;MERTK기인표체재RPE세포여ROS부육5 min시증강,병재전부부육과정중정현출고표체상태;이A23187재체개방개통도승고RPE세포내Ca2+후,MERTK기인신사핵당핵산(Mrna)수평승고.병정제량의뢰성.경A23187예처리후적부육실험중소검측도적MERTK Mrna수평제3 h저일시간점외균고우대조조;vempamile길항RPE세포내Ca2+후,MERTK기인표체명현하강병정제량의뢰성;이verapamile예처리후계속여ROS부육,소검측도적MERTK기인재24 h내균저우대조조.결론 MERTK기인급세포내Ca2+발휘착유지RPE세포탄서과정적중요작용,MERTK작위상유조공신호계동하유적세포내Ca2+신호래유지RPE세포대ROS적섭입과정.
Objective To investigate the role of intraeellular Ca2+ and MERTK in the phagocytosis of human retinal pigment epithelial (RPE) cells, and reveal the relationship between MERTK and intraeellular Ca2+. Methods The euhured RPE cells were incubated with rod outer segments (ROS) at 37℃, the phagoeytosis was terminated at different incubation time points. The concentration of intraeellular Ca2+ was assayed by Fluro-3/AM loading methods combined with fluorescence microscope and CCD system, and the mRNA level of MERTK gene was measured by reverse transcription polymerase chain reaction (RT-PCR). Treating the RPE cells with stimulator (A23187)or inhibitor(verapamile)of intraeellular Ca2+ to observe the changes of MERTK gene expression. Results ROS adhered to hRPE cells at the 15th minute, and the ingestion saturated at the 24th hour. The concentration of intracellular Ca2+ increased at the 15th minute, and kept the high level in 24 hours. The level of MERTK mRNA increased at the 5th minute, and kept the high level duration the whole incubation. When RPE cells were treated by A23187, the expression of MERTK increased in a dose-dependent manner. After RPE cells was pretreated by A23187, the expression level of MERTK was higher in the proceeding incubation groups than which in the control group except at the 3rd hour. When RPE cells were treated by verapamil, the expression level of MERTK decreased in a dose-dependent manner. After RPE cells were pretreated by verapamil , the expression level of MERTK was lower in all the proceeding incubation groups than which in the control group (P<0.05). Conclusion MERTK gene and Ca2+ play an important role in sustaining RPE cells phagoeytizing ROS. As an up-stream regulator, the receptor tyrosine kinase MERTK keeps RPE cells phagocytizing ROS by starting the intracellular Ca2+.