Chair of Vegetative Anatomy, Faculty of Medicine, Ludwig-Maximilians-University (LMU) Munich, Pettenkoferstraße 11, 80336, Munich, Germany.
Sci Rep. 2022 Sep 2;12(1):14940. doi: 10.1038/s41598-022-18964-5.
Adducin (Add) is an actin binding protein participating in the stabilization of actin/spectrin networks, epithelial junctional turnover and cardiovascular disorders such as hypertension. Recently, we demonstrated that Add is required for adherens junctions (AJ) integrity. Here we hypothesized that Add regulates tight junctions (TJ) as well and may play a role in cAMP-mediated barrier enhancement. We evaluated the role of Add in MyEnd cells isolated from WT and Add-Knock-Out (KO) mice. Our results indicate that the lack of Add drastically alters the junctional localization and protein levels of major AJ and TJ components, including VE-Cadherin and claudin-5. We also showed that cAMP signaling induced by treatment with forskolin and rolipram (F/R) enhances the barrier integrity of WT but not Add-KO cells. The latter showed no junctional reorganization upon cAMP increase. The absence of Add also led to higher protein levels of the small GTPases Rac1 and RhoA. In vehicle-treated cells the activation level of Rac1 did not differ significantly when WT and Add-KO cells were compared. However, the lack of Add led to increased activity of RhoA. Moreover, F/R treatment triggered Rac1 activation only in WT cells. The function of Rac1 and RhoA per se was unaffected by the total ablation of Add, since direct activation with CN04 was still possible in both cell lines and led to improved endothelial barrier function. In the current study, we demonstrate that Add is required for the maintenance of endothelial barrier by regulating both AJ and TJ. Our data show that Add may act upstream of Rac1 as it is necessary for its activation via cAMP.
内收蛋白(Add)是一种肌动蛋白结合蛋白,参与肌动蛋白/ spectrin 网络的稳定、上皮连接的翻转以及高血压等心血管疾病。最近,我们证明 Add 是黏附连接(AJ)完整性所必需的。在这里,我们假设 Add 也调节紧密连接(TJ),并且可能在 cAMP 介导的屏障增强中发挥作用。我们评估了从 WT 和 Add 敲除(KO)小鼠中分离的 MyEnd 细胞中 Add 的作用。我们的结果表明,Add 的缺乏严重改变了主要 AJ 和 TJ 成分的连接定位和蛋白水平,包括 VE-钙粘蛋白和 Claudin-5。我们还表明,用 forskolin 和 rolipram(F/R)处理诱导的 cAMP 信号增强了 WT 细胞但不是 Add-KO 细胞的屏障完整性。后者在 cAMP 增加时没有连接重新组织。Add 的缺乏还导致小 GTPases Rac1 和 RhoA 的蛋白水平升高。在未处理的细胞中,当比较 WT 和 Add-KO 细胞时,Rac1 的激活水平没有显著差异。然而,Add 的缺乏导致 RhoA 的活性增加。此外,F/R 处理仅在 WT 细胞中触发 Rac1 激活。Add 的完全缺失本身并不影响 Rac1 和 RhoA 的功能,因为在两种细胞系中,用 CN04 直接激活仍然是可能的,并且导致内皮屏障功能的改善。在目前的研究中,我们证明 Add 通过调节 AJ 和 TJ 来维持内皮屏障的功能。我们的数据表明,Add 可能作为 Rac1 的上游作用,因为它是通过 cAMP 激活 Rac1 所必需的。