Elkjaer M L, Birn H, Agre P, Christensen E I, Nielsen S
Department of Cell Biology, University of Aarhus, Denmark.
Eur J Cell Biol. 1995 May;67(1):57-72.
Microtubules are critically involved in membrane traffic and maintenance of epithelial cell polarity. In this study we examined the effect of microtubule disruption by colchicine on 1) the subcellular organization of the apical endocytic apparatus, 2) apical endocytosis, and 3) subcellular distribution of gp330 and Aquaporin-1 water channels in renal proximal tubule cells. Rats were treated in vivo with colchicine for 5 h before fixation of the kidneys, and sections of proximal tubules were studied using electron microscopy, morphometry and immunocytochemistry. In proximal tubule cells from colchicine-treated animals, virtually no endocytic invaginations are present, indicating that colchicine blocks the formation of endocytic invaginations. Furthermore, no large endocytic vacuoles are present, also consistent with a block of endocytosis. This was confirmed by functional studies revealing a colchicine-induced arrest in apical endocytosis of peroxidase. There is a marked reduction in dense apical tubules (the exocytic vehicle for membrane recycling) but an extensive accumulation of small vesicles, suggesting a disruption in membrane recycling. This disruption may be primary or secondary to the block of endocytosis. Immunofluorescence and immunoelectron microscopy reveal extensive colchicine-induced changes in the subcellular distribution of gp330 and Aquaporin-1. The localization of gp330 is normally restricted to the apical endocytic apparatus. However, after colchicine treatment gp330 is localized to numerous vesicles distributed throughout the entire cytoplasm, as previously shown (Gutmann et al., Am. J. Physiol. 257, C397-C407 (1989). Also Aquaporin-1 water channels, which are normally almost exclusively present in the plasma membranes, are redistributed to small vesicles in addition to the plasma membrane localization after colchicine treatment. In summary, the present study suggests that cytoplasmic microtubules are critically involved in 1) formation and stabilization of endocytic invaginations, 2) formation of large endocytic vacuoles, 3) apical endocytosis, 4) maintaining the polarized distribution of vesicles in the apical part of the cell, and 5) maintaining the polarized organization of gp330 in the apical endocytic apparatus, and maintaining Aquaporin-1 water channels in the plasma membranes.
微管在膜运输和上皮细胞极性维持中起关键作用。在本研究中,我们检测了秋水仙碱破坏微管对以下方面的影响:1)顶端内吞装置的亚细胞组织;2)顶端内吞作用;3)肾近端小管细胞中gp330和水通道蛋白-1水通道的亚细胞分布。在固定肾脏前,给大鼠体内注射秋水仙碱5小时,然后使用电子显微镜、形态计量学和免疫细胞化学方法研究近端小管切片。在秋水仙碱处理动物的近端小管细胞中,几乎不存在内吞凹陷,这表明秋水仙碱阻断了内吞凹陷的形成。此外,也不存在大的内吞液泡,这也与内吞作用受阻一致。功能研究证实了这一点,该研究显示秋水仙碱诱导过氧化物酶顶端内吞作用停滞。致密的顶端小管(用于膜再循环的胞吐载体)显著减少,但小泡大量积聚,这表明膜再循环受到破坏。这种破坏可能是内吞作用受阻的原发性或继发性结果。免疫荧光和免疫电子显微镜显示,秋水仙碱诱导gp330和水通道蛋白-1的亚细胞分布发生广泛变化。gp330的定位通常局限于顶端内吞装置。然而,秋水仙碱处理后,gp330定位于分布在整个细胞质中的众多小泡中,如先前所示(古特曼等人,《美国生理学杂志》257卷,C397 - C407页(1989年))。同样,水通道蛋白-1水通道通常几乎仅存在于质膜中,秋水仙碱处理后,除了质膜定位外,还重新分布到小泡中。总之,本研究表明细胞质微管在以下方面起关键作用:1)内吞凹陷的形成和稳定;2)大内吞液泡的形成;3)顶端内吞作用;4)维持小泡在细胞顶端部分的极性分布;5)维持gp330在顶端内吞装置中的极性组织,以及维持水通道蛋白-1水通道在质膜中的分布。