[受体介导的内吞作用对临时蛙肾中黄色荧光蛋白重吸收的影响]。

E V Seliverstova, N P Prutskova
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引用次数: 0

摘要

研究了黄荧光蛋白(YFP)在临时蛙肾近端小管(PT)中的吸收及内吞受体巨噬蛋白苷和立方蛋白的表达。采用共聚焦显微镜和免疫组织化学方法。注射后2 h,分析YFP的吸收动力学。结果显示,注射后90 ~ 120min,含yfp的内吞囊泡在PT细胞内的积累与吸收过程的完成呈对数时间依赖性。与引入YFP后15-30分钟大量表达meggalin和cubilin不同,2小时后在PT细胞中未检测到免疫标记的内吞受体。再注射YFP导致出现含有与YFP共定位的meggalin或cubilin的根尖内吞小泡。同时,YFP摄取的减少与含有受体的囊泡数量的减少有关,表明megalin和cubilin表达的失败。再注射YFP后PT细胞吸收能力的下降与之前绿色荧光蛋白(GFP)和不同序列注射YFP竞争吸收的情况相似。这些数据进一步证明了所提出的限制蛙肾小管蛋白吸收的机制,并表明巨噬细胞苷和立方蛋白参与了YFP的吸收和囊泡运输。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Reabsorption of yellow fluorescent protein in the Rana temporaria kidney by receptor-mediated endocytosis].

The absorption of yellow fluorescent protein (YFP) and the expression of the endocytic receptors, megalin and cubilin, were investigated in the renal proximal tubules (PT) in frogs Rana temporaria after parenteral YFP injections. The methods of confocal microscopy and immunohistochemistry were used. The dynamics of YFP absorption was analyzed 2 h after injection. The logarithmic time dependence of the accumulation of YFP-containing endocytic vesicles in PT cells and the completion of absorption process 90-120 min after injection were shown. Unlike substantial megalin and cubilin expression 15-30 min after YFP introduction, immunolabeled endocytic receptors were not detected in PT cells after 2 h. The re-injection of YFP led to the appearance of apical endocytic vesicles containing megalin or cubilin colocalized with YFP. At the same time, the decrease of YFP uptake associated with reduction in the number of receptor-containing vesicles was demonstrated, suggesting a failure of megalin and cubilin expression. The decrease of absorption capacity of PT cells after YFP re-injection was similar to that found previously under conditions of the competitive absorption of green fluorescent protein (GFP) and YFP injected in different sequences. The data are the further demonstration of the proposed mechanism limiting the tubular protein absorption in the frog kidney and suggest the involvement of megalin and cubilin in uptake and vesicular transport of YFP.

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