期刊文献+

热休克蛋白-70在人类糖尿病性白内障晶状体上皮细胞中的表达及意义 被引量:9

Expression and significance of heat shock protin-70 in human diabetic cataract lens epithelial cells
下载PDF
导出
摘要 目的 :探讨热休克蛋白 70在人类糖性白内障晶状体上皮细胞中的表达及意义。方法 :采用链霉菌抗生物素蛋白碱性磷酸酶 (streptavidin alkalinephosphatase ,S P)免疫组化技术检测热休克蛋白 70 (heatshockprotin 70 ,HSP 70 )在人类糖性白内障 (2 5例 )和正常晶状体 (7例 )上皮细胞中的表达情况。结果 :热休克蛋白 70在人类糖性白内障晶状体上皮中全部为阳性表达 ,而在正常晶状体上皮细胞中全部为阴性表达 ,二者差异有显著性 (χ2 =2 6 .4 2 ,P <0 .0 1)。结论 :热休克蛋白 70在人类糖尿病性白内障发生、发展中起重要作用。 Objective:To investigate the expression and significance of HSP 70(heat shock protin 70) in human diabetic cataract lens epithelial cells(LECs).Methods:The expression of HSP 70 was assayed using immunohistochemistry(streptavidin alkaline phosphatase,S P) in human diabetic cataract LECs(25 cases) and human normal LECs(7 cases).Results:There was significant expression of HSP 70(χ 2=26.42,P<0.01) in human diabetic LECs(25 cases) but there was no expression of HSP 70 in human normal LECs(7 cases).Conclusion:HSP 70 may play a critical role during the development and formation of human diabetic cataract.[
出处 《眼视光学杂志》 CAS 2003年第2期72-74,共3页 Chinese Journal of Optometry & Ophthalmology
基金 福建省自然科学基金资助项目 ( 2 0 0 1Z0 3 3 )
关键词 糖尿病性白内障 晶状体 上皮细胞 热休克蛋白—70 免疫组织化学 链霉菌抗生物素蛋白碱性磷酸酶 heat shock protin/physiopathology immunohistochemistry human diabetic cataracts/physiopathology
  • 相关文献

参考文献11

二级参考文献47

  • 1[1]Vinores SA,Herman MM,et al.A morphological & immunohistochemical study of human RPE cells,retinal glia,& fibroblasts grown on gelfoam matrix in an organ culture system[J].Graefes Arch Clin Exp Ophthalmol,1993,231:279-288.
  • 2[2]Xu Guoxing.Effects of LPA on DNA synthesis and proliferation in cultured human RPE cells[J].Invest Ophthalmol Vis Sci,1997,38(4):671.
  • 3[3]Glaser BM,Cardin A,Biscoe B.Proliferative vitreoretinopathy the mechanism of developement of vetreoretinal traction[J].Ophthalmology,1987,94:327-332.
  • 4Ellis M. Studies on lens vimentin[J]. Exp Eye Res, 1984,38:195.
  • 5Sandilands A. Vimentin and CP49/filensin form distinct lens fibre cell differentiation[ J]. J Cell Sci, 1995,108:1397.
  • 6Nishida S. Age-related cataract in the hereditary cataract rat(ICR/1 ):development and classification[ J]. Ophthalmic Res, 1992,24(1): 253-259.
  • 7UgaS,TsuchiyaK,IshikawaS. Histopathologicalstudy of emorymouse cataract[J]. Graefes Arch Clin Exp Ophthalmol, 1988,226(1):15-21.
  • 8Hosakawa M , Ashida Y , Tsuooyama T , et al . Cataract in senescence accelerated mouse (SAM)2: development of a new strain of mouse with late-appearing catuact[J]. Exp Eye Res,1988,47(2) :629 - 640.
  • 9Bloemendal H. Transgenic mice carrying chimeric or mutated type Ⅲintermediate filament(IF) genes[J]. Cell Mol Life Sci, 1997,53:1.
  • 10Li C J;Li C.查看详情,1998(03).

共引文献40

同被引文献83

引证文献9

二级引证文献22

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部