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成纤维细胞中包被小泡形成的三维可视化。

Three-dimensional visualization of coated vesicle formation in fibroblasts.

作者信息

Heuser J

出版信息

J Cell Biol. 1980 Mar;84(3):560-83. doi: 10.1083/jcb.84.3.560.

Abstract

Fibroblasts apparently ingest low density lipoproteins (LDL) by a selective mechanism of receptor-mediated endocytosis involving the formation of coated vesicles from the plasma membrane. However, it is not known exactly how coated vesicles collect LDL receptors and pinch off from the plasma membrane. In this report, the quick-freeze, deep-etch, rotary-replication method has been applied to fibroblasts; it displays with unusual clarity the coats that appear under the plasma membrane at the start of receptor-mediated endocytosis. These coats appear to be polygonal networks of 7-nm strands or struts arranged into 30-nm polygons, most of which are hexagons but some of which are 5- and 7-sided rings. The proportion of pentagons in each network increases as the coated area of the plasma membrane puckers up from its planar configuration (where the network is mostly hexagons) to its most sharply curved condition as a pinched-off coated vesicle. Coats around the smallest vesicles (which are icosahedrons of hexagons and pentagons) appear only slightly different from "empty coats" purified from homogenized brain, which are less symmetrical baskets containing more pentagons than hexagons. A search for structural intermediates in this coat transformation allows a test of T. Kanaseki and K. Kadota's (1969. J. Cell Biol. 42:202--220.) original idea that an internal rearrangement in this basketwork from hexagons to pentagons could "power" coated vesicle formation. The most noteworthy variations in the typical hexagonal honeycomb are focal juxtapositions of 5- and 7-sided polygons at points of partial contraction and curvature in the basketwork. These appear to precede complete contraction into individual pentagons completely surrounded by hexagons, which is the pattern that characterizes the final spherical baskets around coated vesicles.

摘要

成纤维细胞显然通过受体介导的内吞作用的选择性机制摄取低密度脂蛋白(LDL),该机制涉及从质膜形成被膜小泡。然而,目前尚不清楚被膜小泡究竟是如何收集LDL受体并从质膜上脱离的。在本报告中,快速冷冻、深度蚀刻、旋转复制方法已应用于成纤维细胞;它异常清晰地显示了在受体介导的内吞作用开始时出现在质膜下的衣被。这些衣被似乎是由7纳米的链或支柱组成的多边形网络,排列成30纳米的多边形,其中大多数是六边形,但有些是五边形和七边形环。随着质膜的被膜区域从其平面构型(此时网络大多为六边形)皱缩到其作为脱离的被膜小泡时最急剧弯曲的状态,每个网络中五边形的比例会增加。最小的小泡(由六边形和五边形组成的二十面体)周围的衣被与从匀浆脑中纯化的“空衣被”仅略有不同,“空衣被”是对称性较低的篮状结构,其中五边形比六边形多。对这种衣被转变过程中结构中间体的寻找,使得对T. Kanaseki和K. Kadota(1969年。《细胞生物学杂志》42:202 - 220)最初的想法进行了检验,即这种篮状结构从六边形到五边形的内部重排可以“驱动”被膜小泡的形成。典型六边形蜂巢结构中最值得注意的变化是在篮状结构的部分收缩和弯曲点处五边形和七边形的局部并列。这些似乎先于完全收缩成被六边形完全包围的单个五边形,而这是围绕被膜小泡的最终球形篮状结构的特征模式。

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