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肠道上皮细胞旁途径生理调节的结构基础。

Structural basis for physiological regulation of paracellular pathways in intestinal epithelia.

作者信息

Madara J L, Pappenheimer J R

机构信息

Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.

出版信息

J Membr Biol. 1987;100(2):149-64. doi: 10.1007/BF02209147.

Abstract

Isolated segments of hamster small intestine were perfused with oxygenated salt-fluorocarbon emulsions with or without 10-25 mM glucose, alanine or leucine. Resistances of intercellular occluding junctions and of lateral spaces and the distributed capacitance of epithelial plasma membranes were estimated from steady-state transepithelial impedances at frequencies from 0.01-10 kHz. The segments were then fixed in situ with isorheic 2.5% glutaraldehyde while continuing to measure impedance. This method of fixation increased the resistance of lateral spaces but had little effect on the resistance of occluding junctions or on membrane capacitance. The large decreases of impedance induced by glucose or amino acids were preserved in fixed tissue and could therefore be correlated with changes in structure. The observed changes of impedance were interpreted as decreased resistance of occluding junctions and lateral spaces together with increased exposed surface of lateral membranes (capacitance). Glucose, alanine or leucine induced expansion of lateral intercellular spaces as seen by light and electron microscopy. Large dilatations within absorptive cell occluding junctions were revealed by electron microscopy. Freeze-fracture analysis revealed that these dilatations consisted of expansions of compartments bounded by strands/grooves. These solute-induced structural alterations were also associated with condensation of microfilaments in the zone of the perijunctional actomyosin ring, typical of enhanced ring tension. Similar anatomical changes were found in epithelia fixed in situ at 38 degrees C during luminal perfusion with glucose in blood-circulated intestinal segments of anesthetized animals. These structural changes support the hypothesis that Na-coupled solute transport triggers contraction of perijunctional actomyosin, thereby increasing junctional permeability and enhancing absorption of nutrients by solvent drag as described in the two accompanying papers.

摘要

用含氧盐氟碳乳液灌注仓鼠小肠的离体节段,乳液中添加或不添加10 - 25 mM的葡萄糖、丙氨酸或亮氨酸。根据0.01 - 10 kHz频率下的稳态跨上皮阻抗估算细胞间紧密连接、侧向间隙的电阻以及上皮细胞质膜的分布电容。然后在继续测量阻抗的同时,用等渗的2.5%戊二醛原位固定这些节段。这种固定方法增加了侧向间隙的电阻,但对紧密连接的电阻或膜电容影响很小。葡萄糖或氨基酸引起的阻抗大幅下降在固定组织中得以保留,因此可以与结构变化相关联。观察到的阻抗变化被解释为紧密连接和侧向间隙的电阻降低,以及侧向膜暴露表面积增加(电容增加)。光学和电子显微镜观察显示,葡萄糖、丙氨酸或亮氨酸会引起细胞间侧向间隙扩张。电子显微镜揭示了吸收细胞紧密连接内的大扩张。冷冻蚀刻分析表明,这些扩张由由股线/凹槽界定的隔室扩张组成。这些溶质诱导的结构改变还与连接周肌动球蛋白环区域微丝的凝聚有关,这是环张力增强的典型表现。在麻醉动物的血液循环肠段中,当腔内灌注葡萄糖时,在38摄氏度原位固定的上皮中也发现了类似的解剖学变化。这些结构变化支持了这样一种假说,即钠偶联溶质转运触发连接周肌动球蛋白收缩,从而增加连接通透性,并如两篇随附论文中所述通过溶剂拖曳增强营养物质的吸收。

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