Cui S, Mata L, Maunsbach A B, Christensen E I
Department of Cell Biology, University of Aarhus, Denmark.
Exp Nephrol. 1998 Jul-Aug;6(4):359-67. doi: 10.1159/000020543.
To obtain insight into the basic mechanisms controlling endocytosis, we tested the effects of different perfusates containing the cytological stain light green on endocytosis and ultrastructure of the vacuolar apparatus in renal proximal tubule cells. Rat proximal tubules were microinfused in vivo for 2 min in the presence or absence of light green with the following solutions: (A) perfusates containing inorganic salts and (B) perfusates with organic components or protein. In other experiments, the tubules were first microinfused for 2 min with 0.9% NaCl in the presence or absence of light green, then 15 min later further microinfused with or without light green using either group A or B solutions in order to either aggravate or reverse possible changes. All infused tubules were fixed after 5 min with 1% glutaraldehyde and examined by electron microscopy. In tubules microinfused without light green, the endocytic vacuolar apparatus in the apical cytoplasm showed a normal ultrastructure. However, microinfusion of solutions containing light green in either inorganic salts or a low concentration of protein caused significant changes in the apical endocytic apparatus. Large endocytic vacuoles were absent, and invaginations and small endocytic vacuoles were decreased in frequency. On the other hand, the amount of dense apical tubules was significantly increased, and in some cells dense apical tubules had transformed into a cisternalike network. These changes were aggravated in tubules which received a second microinfusion of NaCl and reversed in tubules that received a second infusion of protein. Furthermore, in the tubules microinfused with light green using perfusates containing organic components or protein, the apical cytoplasm of proximal tubule cells showed an essentially normal endocytic apparatus. The present study demonstrates that microinfusion of renal proximal tubules with light green disrupted normal endocytic membrane trafficking and recycling. These changes could be prevented or reversed by microinfusion of solutions containing protein or organic components.
为深入了解控制内吞作用的基本机制,我们测试了含有细胞染色剂亮绿的不同灌注液对肾近端小管细胞内吞作用和液泡器超微结构的影响。在有或无亮绿存在的情况下,用以下溶液对大鼠近端小管进行体内微量灌注2分钟:(A) 含有无机盐的灌注液和 (B) 含有有机成分或蛋白质的灌注液。在其他实验中,小管先在有或无亮绿存在的情况下用0.9% NaCl微量灌注2分钟,然后15分钟后,使用A组或B组溶液在有或无亮绿的情况下进一步微量灌注,以加重或逆转可能的变化。所有灌注后的小管在5分钟后用1%戊二醛固定并通过电子显微镜检查。在未用亮绿微量灌注的小管中,顶端细胞质中的内吞液泡器显示出正常的超微结构。然而,用含有亮绿的无机盐溶液或低浓度蛋白质溶液进行微量灌注会导致顶端内吞器发生显著变化。大型内吞液泡缺失,内陷和小型内吞液泡的频率降低。另一方面,致密的顶端小管数量显著增加,并且在一些细胞中,致密的顶端小管已转化为类似扁平囊的网络。在接受第二次NaCl微量灌注的小管中这些变化加剧,而在接受第二次蛋白质灌注的小管中这些变化则逆转。此外,在用含有有机成分或蛋白质的灌注液进行亮绿微量灌注的小管中,近端小管细胞的顶端细胞质显示出基本正常的内吞器。本研究表明,用亮绿对肾近端小管进行微量灌注会破坏正常的内吞膜运输和再循环。通过微量灌注含有蛋白质或有机成分的溶液可以预防或逆转这些变化。