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大鼠小肠吸收细胞及微绒毛膜制剂的结构特征

Structural features of absorptive cell and microvillus membrane preparations from rat small intestine.

作者信息

Bjorkman D J, Allan C H, Hagen S J, Trier J S

出版信息

Gastroenterology. 1986 Dec;91(6):1401-14. doi: 10.1016/0016-5085(86)90194-0.

DOI:10.1016/0016-5085(86)90194-0
PMID:3533700
Abstract

Absorptive cells of the small intestine are highly polarized cells with distinct microvillus membrane (MVM) and basolateral plasma membrane domains. We compared membrane structure in the following preparations of rat small intestine commonly used for in vitro study of MVM function: epithelial sheets, isolated epithelial cells, and four different MVM vesicle preparations, using electron microscopy of thin sections and freeze fracture replicas. We also quantitated mean vesicle diameter of the four MVM preparations by quasielastic light scattering and determined their actin content. Epithelial sheets maintained their plasma membrane polarity as judged by intramembrane particle (IMP) distribution for at least 30 min after isolation. In contrast, the plasma membrane of isolated cells showed redistribution of IMPs, indicating considerable loss of polarity in the few minutes required for cell recovery. The P-face IMPs in MVM prepared by Ca++ precipitation were randomly distributed but became aggregated after exposure to potassium thiocyanate, which removed approximately 50% of core actin. The P-face IMPs in Mg++ precipitated MVM were aggregated whether or not core actin was depleted with potassium thiocyanate. The shape and size of MVM vesicles differed considerably with different preparative techniques. The extremely rapid loss of plasma membrane polarity of isolated intestinal epithelial cells and the striking structural heterogeneity of MVM vesicles prepared by commonly used techniques should be considered in the interpretation of functional studies with these preparations.

摘要

小肠的吸收细胞是高度极化的细胞,具有独特的微绒毛膜(MVM)和基底外侧质膜结构域。我们使用超薄切片电子显微镜和冷冻断裂复制品,比较了以下常用于MVM功能体外研究的大鼠小肠制剂中的膜结构:上皮片、分离的上皮细胞和四种不同的MVM囊泡制剂。我们还通过准弹性光散射对四种MVM制剂的平均囊泡直径进行了定量,并测定了它们的肌动蛋白含量。分离后至少30分钟内,上皮片通过膜内颗粒(IMP)分布判断保持其质膜极性。相比之下,分离细胞的质膜显示IMP重新分布,表明在细胞恢复所需的几分钟内极性有相当大的丧失。通过Ca++沉淀制备的MVM中的P面IMP随机分布,但在暴露于硫氰酸钾后聚集,硫氰酸钾去除了约50%的核心肌动蛋白。无论核心肌动蛋白是否被硫氰酸钾耗尽,Mg++沉淀的MVM中的P面IMP都聚集。不同制备技术制备的MVM囊泡的形状和大小差异很大。在解释使用这些制剂的功能研究时,应考虑分离的肠上皮细胞质膜极性的极快速丧失以及常用技术制备的MVM囊泡的显著结构异质性。

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