首页 | 本学科首页   官方微博 | 高级检索  
检索        

增殖细胞核抗原与bc1-2在培养的人视网膜色素上皮细胞的表达
引用本文:王琳,惠延年,王雨生,惠宏襄,王剑波.增殖细胞核抗原与bc1-2在培养的人视网膜色素上皮细胞的表达[J].中华眼底病杂志,1998(1).
作者姓名:王琳  惠延年  王雨生  惠宏襄  王剑波
作者单位:第四军医大学西京医院眼科
摘    要:目的观察培养的人视网膜色素上皮细胞(retinalpigmentepithelialcels,RPE)的增殖细胞核抗原(proliferativecelnuclearantigen,PCNA)和bc1-2的表达。方法用SABC法对培养的人RPE作鼠抗人PCNA单抗及兔抗人bc1-2抗体免疫组织化学染色。结果RPE在接种后24小时和48小时,PCNA的阳性率分别为31.2%和50.6%,阳性染色位于细胞核内,斑块状。bc1-2的表达为76%~90%,阳性染色在细胞浆,细颗粒状。结论培养中一半RPE有PCNA抗原表达,提示这些细胞处于S期;bc1-2抗原在大多数RPE表达阳性。这些生物标记物可能与培养的RPE生长活性有关。

关 键 词:色素上皮.眼  细胞.培养的  增殖细胞核抗原(PCNA)  免疫组织化学  基因.抑制

Expression of PCNA and bcl 2 of cultured human retinal pigment epithelial cells
Wang Lin,Hui Yannian,Wang Yusheng,et al..Expression of PCNA and bcl 2 of cultured human retinal pigment epithelial cells[J].Chinese Journal of Ocular Fundus Diseases,1998(1).
Authors:Wang Lin  Hui Yannian  Wang Yusheng  
Institution:Wang Lin,Hui Yannian,Wang Yusheng,et al.Department of Ophthalmology,Xijing Hospital,The Fourth Military Medical University,Xian 710032,China
Abstract:Purpose To observe the expression of proliferating cell nuclear antigen(PCNA)and bcl 2 of cultured human retinal pigment epithelial cells(RPE). Methods SABC techniques were applied for immunocytochemical staining of cultured RPE with mouse anti human PCNA monoclonal antibody and rabbit anti human bcl 2 antibodies. Results 31.2% and 50.6% cultured cells were positive to anti human PCNA at 24h and 48h after seeding,respectively.The positive staining was mottled in the nucleus.Positive staining for bcl 2 was seen in 76%to 90% cells as fine granules scattered within the cytoplasm. Conclusion One half of cultured RPE expressed PCNA,indicating that the cells were in phase S of the cell cycle.Positive staining for bcl 2 appeared in much more RPE cells.These biological markers may be associated with the growth activity of cultured RPE.
Keywords:Pigment  epithelium  of  eye    Cells  Cultured    Proliferating  cell  nuclear  antigen  Immunohistochemistry    Genes  Suppressor  
本文献已被 CNKI 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号