培养肾细胞的扫描电镜:极化上皮的表面特征。

Scanning electron microscopy Pub Date : 1986-01-01
J A McAteer, G S Dougherty, K D Gardner, A P Evan
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引用次数: 0

摘要

我们使用扫描电子显微镜(SEM)检查肾上皮细胞系MDCK和LLC-PKl的表面形态,以确定替代培养底物条件对细胞极性的影响。我们观察到,无论在何种物理培养条件下,细胞都能建立并保持极性,这表现在细胞的顶端和基部表面特征上。然而,培养条件确实影响细胞在体外的极性取向。MDCK细胞在胶原凝胶中生长,单个细胞表现出克隆生长,形成充满液体的上皮囊肿。mdck -囊肿细胞呈两极分化,顶面朝向管腔,底面朝向周围的胶原凝胶。这种结构使得通过扫描电镜,通过去除支持性胶原晶格,可以直接看到基底表面。mdck包囊顶端表面排列有短微绒毛。每个细胞都有一个单独的纤毛。相比之下,基部表面几乎没有附属物,尽管细胞边界以交错的短突为标志。单层培养的lc - pkl细胞顶端表面有单生纤毛和长微绒毛。参与圆顶形成的细胞的基底表面被观察到只有稀疏的短钝突。当lc - pkl细胞在固定悬浮培养中或在非培养级塑料上单层培养时,它们形成囊,细胞尖端面向周围培养基。这些细胞表现出不同的顶端形态。大的、高度扩张的囊肿的细胞通常是衰减的,有一个相对光滑的根尖表面。骨折的lc - pkl囊肿的细胞基表面通常也是光滑的,没有明显的附属物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Scanning electron microscopy of kidney cells in culture: surface features of polarized epithelia.

We have used scanning electron microscopy (SEM) to examine the surface morphology of the renal epithelial cell lines MDCK and LLC-PKl to determine the influence of alternative culture substrate conditions on cell polarity. We observed that regardless of physical culture conditions, cells established and maintained polarity, expressed by the characteristics of apical and basal surfaces. Culture conditions did, however, influence the orientation of cell polarity in vitro. MDCK cells were grown within collagen gel, in which individual cells exhibited clonal growth to form fluid-filled epithelial cysts. The cells of MDCK-cysts were polarized with apical surface facing the lumen and basal surface against the surrounding collagen gel. This configuration made it possible to gain direct visual access, by SEM, to the basal surface by removing the supportive collagen lattice. The apical surface of MDCK-cysts was lined by short microvilli. Each cell possessed a solitary cilium. In comparison, the basal surface had few appendages, although cell boundaries were marked by interdigitating short processes. LLC-PKl cells in monolayer culture bore solitary cilia and long microvilli at their apical surface. The basal surface of cells involved in dome formation was observed to possess only a sparse population of short, blunt processes. When LLC-PKl cells were raised in stationary suspension culture or in monolayer atop non-culture grade plastic, they formed cysts with the cell apex facing the surrounding medium. These cells showed variable apical morphology. The cells of large, highly expanded cysts were often attenuated and had a relatively smooth apical surface. The basal surface of cells of fractured LLC-PKl cysts commonly was also smooth, without prominent appendages.

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