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Studies with wortmannin and cytochalasins suggest a pivotal role of phosphatidylinositols in the regulation of tight junction integrity

机译:对渥曼青霉素和细胞松弛素的研究表明磷脂酰肌醇在调节紧密连接完整性中起着关键作用

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Wortmannin, a selective inhibitor of phosphatidylinositol 3-kinase (P13K), was found to give a dose and time-dependent, bimodal effect-initial increase, followed by decrease on the tight junction integrity of MDCK-1 monolayers, as assessed by electrical resistance measurement of the epithelia. Moreover, dihydrocytochalasin B inhibited the wortmannin-induced alteration, whereas cytochalasin B had a negligible influence on the wortmannin effect. Wortmannin was also found to cause changes in the cytoskeleton structure. These alterations were also seen when wortmannin was combined with cytochalasin B. However, in accordance with the electrical resistance measurements, dihydrocytochalasin B was able to abolish wortmannin-induced filamentous (F-) actin changes. These findings suggest that the P13K, phosphatidylinositols, and filamentous actin rearrangements, in combination, play an important role in the modulation of the junctional integrity.
机译:Wortmannin是磷脂酰肌醇3激酶(P13K)的选择性抑制剂,被发现具有剂量和时间依赖性,双峰效应起初增加,随后MDCK-1单层紧密连接完整性降低,通过电阻评估上皮的测量。此外,二氢细胞松弛素B抑制了渥曼青霉素诱导的改变,而细胞松弛素B对渥曼青霉素的作用可忽略不计。还发现渥曼青霉素可引起细胞骨架结构的改变。当渥曼青霉素与细胞松弛素B结合使用时,也观察到了这些变化。但是,根据电阻测量,二氢细胞松弛素B能够消除渥曼青霉素诱导的丝状(F-)肌动蛋白变化。这些发现表明,P13K,磷脂酰肌醇和丝状肌动蛋白重排组合在一起在调节连接完整性中起重要作用。

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