首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >Effects of cytochalasin D on occluding junctions of intestinal absorptive cells: further evidence that the cytoskeleton may influence paracellular permeability and junctional charge selectivity
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Effects of cytochalasin D on occluding junctions of intestinal absorptive cells: further evidence that the cytoskeleton may influence paracellular permeability and junctional charge selectivity

机译:细胞松弛素D对肠道吸收细胞闭塞连接的影响:进一步的证据表明细胞骨架可能影响细胞旁通透性和连接电荷选择性

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摘要

Intestinal absorptive cells may modulate both the structure and function of occluding junctions by a cytoskeleton dependent mechanism (Madara, J. L., 1983, J. Cell Biol., 97:125-136). To further examine the putative relationship between absorptive cell occluding junctions and the cytoskeleton, we assessed the effects of cytochalasin D (CD) on occluding junction function and structure in guinea pig ileum using ultrastructural and Ussing chamber techniques. Maximal decrements in transepithelial resistance and junctional charge selectivity were obtained with 10 micrograms/ml CD and the dose-response curves for these two functional parameters were highly similar. Analysis of simultaneous flux studies of sodium and the nonabsorbable extracellular tracer mannitol suggested that CD opened a transjunctional shunt and that this shunt could fully account for the increase in sodium permeability and thus the decrease in resistance. Structural studies including electron microscopy of detergent-extracted cytoskeletal preparations revealed that 10 micrograms/ml CD produced condensation of filamentous elements of the peri-junctional contractile ring and that this was associated with brush border contraction as assessed by scanning electron microscopy. Quantitative freeze-fracture studies revealed marked aberrations in absorptive cell occluding junction structure including diminished strand number, reduced strand-strand cross-linking, and failure of strands to impede the movement of intramembrane particles across them. In aggregate these studies show that CD-induced perturbation of the absorptive cell cytoskeleton results in production of a transepithelial shunt which is fully explained by a defect in the transjunctional pathway. Furthermore, substantial structural abnormalities in occluding junction structure accompany this response. Lastly, the abnormalities in occluding junction structure and function coincide with structural changes in and contraction of the peri-junctional actin-myosin ring. These data suggest that a functionally relevant association may exist between the cytoskeleton and the occluding junction of absorptive cells. We speculate that such an association may serve as a mechanism by which absorptive cells regulate paracellular transport.
机译:肠吸收性细胞可通过细胞骨架依赖性机制调节闭塞连接的结构和功能(Madara,J.L.,1983,J.Cell Biol。,97:125-136)。为了进一步检查吸收性细胞闭塞连接与细胞骨架之间的假定关系,我们使用超微结构和Ussing室技术评估了细胞松弛素D(CD)对豚鼠回肠闭塞连接功能和结构的影响。使用10微克/毫升CD获得的跨上皮电阻和结合电荷选择性的最大降低,这两个功能参数的剂量反应曲线高度相似。对钠和不可吸收的细胞外示踪甘露醇同时进行通量研究的分析表明,CD打开了一个跨结分流器,该分流器可以充分说明钠渗透性的增加,从而降低了电阻的降低。结构研究包括去污剂提取的细胞骨架制剂的电子显微镜检查表明,10微克/毫升CD会产生结周收缩环丝状元件的凝结,这与通过扫描电子显微镜观察到的刷缘收缩有关。定量的冷冻断裂研究显示,吸收性细胞闭塞的连接结构存在明显的畸变,包括减少的链数,减少的链-股交联,以及股线无法阻止跨膜运动。总的来说,这些研究表明,CD引起的吸收性细胞骨架的扰动导致跨上皮分流的产生,这完全可以通过跨结途径的缺陷来解释。此外,闭塞连接结构中的实质性结构异常伴随该响应。最后,闭塞连接结构和功能的异常与结周肌动蛋白-肌球蛋白环的结构变化和收缩相吻合。这些数据表明功能相关的关联可能存在于吸收性细胞的细胞骨架与闭塞连接之间。我们推测这种关联可以作为吸收性细胞调节旁细胞运输的机制。

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