首页 | 本学科首页   官方微博 | 高级检索  
检索        

羊膜自噬的形态及其相关基因表达
引用本文:吕汕群,沈忠英.羊膜自噬的形态及其相关基因表达[J].中国医药导报,2008,5(22):11-13.
作者姓名:吕汕群  沈忠英
作者单位:1. 汕头市中心医院妇产科,广东汕头,515011
2. 汕头大学医学院病理科,广东汕头,515011
基金项目:广东省汕头市重点科技计划项目
摘    要:目的:阐明羊膜上皮细胞自噬过程的形态及其相关基因表达。方法:20片足月羊膜用透射电镜检查,用单丹磺酰戊二胺(MDC)标记自噬泡和溶酶示棕红(LTR)检查溶酶体;用RT—PCR检测beclin-1,apg-5和DAPK基因的转录。结果:在羊膜上皮可见多数双层膜包被的自噬泡,它可分为两种:一种是自噬体,其中包含细胞浆成份;另一种是自噬溶酶体。系自噬体和溶酶体融合。细胞浆成份降解。MDC和LTR染色阳性。beclin-1,apg-5和DAPK基因在多数羊膜上皮有表达。结论:在正常羊膜上皮出现自噬并有相关基因表达,羊膜上皮为适应其营养限制可诱导自噬以促进自我营养。

关 键 词:羊膜  自噬  自噬体  自噬溶酶体

Morphology of autophagy and expression of some relative genes in amnion
LU Shan-qun,SHEN Zhong-ying.Morphology of autophagy and expression of some relative genes in amnion[J].China Medical Herald,2008,5(22):11-13.
Authors:LU Shan-qun  SHEN Zhong-ying
Institution:LU Shan-qun1,SHEN Zhong-ying2
Abstract:Objective: To expose the morphology of autophagy and expression of some associated genes in the amnion. Methods: Twenty pieces of amnions in term gestation were examined by transmitted electron microscopy and by mono-dansylcadaverin (MDC) and LysoTracker Red (LTR) staining, markers for autophagic vacuole and lysosome. Autophagy-as-sociated genes, beclin-1, apg-5 and DAPK were assayed by RT-PCR. Results:Most autophagic vacuoles enclosed with double membranes were found in the amniotic epithelial cells. They were divided two kinds: autophagosomes, in which contained some cytoplasmic compartments, and autolysosomes, in which autophagosome fused with lysosomes and contained degraded cytoplasmic compartments. MDC and LTR staining was positive in the cytoplasm. beclin-1, apg-5 and DAPK genes were expressed in great proportion of amniotic epithelium. Conclusion:These results display that the phenotype of autophagy are induced in normal amniotic epithelium with some autophagy-associated genes expression, and suggest that amniotic epithelia adapt to the nutrient limitation by inducing autophagy to promote self-nourishment.
Keywords:Amnion  Autophagy  Autophagosome  Antolysosome
本文献已被 CNKI 维普 万方数据 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