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作 者:甘胜伟[1] 孙善全[1] 冉建华[1] 陈海[2] 樊萍[3] 朱淑娟[1] 黄娟[1] 陈臻
机构地区:[1]重庆医科大学神经科学研究中心,重庆400016 [2]重庆市第三人民医院神经内科,重庆400014 [3]重庆市第五人民医院妇产科,重庆400062 [4]云南省人民医院眼科,昆明650031
出 处:《解剖学杂志》2013年第4期716-719,F0004,共5页Chinese Journal of Anatomy
基 金:国家自然科学基金(30470608,30500171);重庆市自然科学基金(cstc2011jjA10003,CSTC2010BB5098,cstc2012jjA10022)
摘 要:目的:观察急性高眼压时大鼠视网膜胶质细胞水通道蛋白-4(AQP4)内化的时空变化及其规律,并探讨其与视网膜水肿的关系.方法:建模并分组;应用免疫荧光双标鉴定视网膜AQP4阳性细胞;观察AQP4与早期内涵体抗原1(EEA1)及晚期内涵体标记物甘露糖-6-磷酸受体(MPR)的共表达规律.结果:在正常视网膜内,表达AQP4的星形胶质细胞胞体位于节细胞层,Müller细胞的胞体位于内核层.正常及假手术组未见AQP4与EEA-1、MPR的共表达;高眼压作用不同时间,AQP4与EEA1共表达细胞的分布部位及其占AQP4阳性细胞比例都有改变,在高眼压作用60 min,AQP4与EEA1共表达细胞的比例达到最高值,AQP4与MPR共表达细胞分布的部位也有变化.结论:高眼压可诱导视网膜胶质细胞AQP4的内化,即AQP4经过内吞进入早期内涵体,再转运至晚期内涵体.AQP4的内化可能对肿胀的胶质细胞起保护作用.Objective: To investigate the dynamic spatiotemporal regularity of retinal aquaporin-4 (AQP4) and the occurrence of AQP4 internalization under acute ocular hypertension (AOH), so as to study the possible role of its internalization in the glial edema of retina. Methods : The animal models of AOH were made by perfusing D-hanks buffer into the anterior chamber of rats, and double-immunofluorescence labelings were applied to identity the retinal glial cells and detect the co-expression of AQP4~EEA1 and AQP4^-MPtL Results: Double irnmunofluorescence labelings demonstrated that the cell bodies of astrocytes were located in the ganglion cell layer, while the Mialler cells in the inner nuclear layer; The distribution and proportion of AQP4~EEA1 co-expressing cells and distribution of AQP4~MPR was varied in different AOH groups: AQP4~EEA1 were co-localized in the ganglion cell layer from 5 min to 90 min of ocular hypertension, yet in the inner nuclear layer from 10 to 90 min; At the 60 min of AOH, proportion of AQP4 ~EEA1 co-expressing cells climaxed, occupying 72.97 % 9. 89 % in ganglion cell layer and 58. 94 % ~ 10. 03 ~ in the inner nuclear layer. AQP48~MPR were co-localized from 10 min to 60 min of AOH. Conelusion: AQP4 internalization can be induced by AOH. During this procedure, AQP4 is transported from the membrane to the early endosome, and then to late endosome, which has a potential protective effect on the swollen glial cells.
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