Krizbai I A, Deli M A
Laboratory of Molecular Neurobiology, Institute of Biophysics, Biological Research Centre of the Hungarian Academy of Sciences, P.O. Box 521, H-6701 Szeged, Hungary.
Cell Mol Biol (Noisy-le-grand). 2003 Feb;49(1):23-31.
Tight junctions (TJs) of the cerebral endothelial cells play a crucial role in the regulation of BBB permeability under physiological, as well as pathological conditions. The regulation of the junctional proteins is under a complex control. In these regulatory processes signalling molecules, some of them localized to the TJ, play an important role. Among the best characterized second messengers which regulate TJ function are the cyclic nucleotides, which, as shown in our experiments, as well, decrease paracellular permeability. Another important signalling molecule involved in TJ regulation is protein kinase C, which may affect differently the formation of TJ and the function of mature TJ. Further signalling molecules known to regulate paracellular permeability are G-proteins, both conventional and small G-proteins, MAP kinases and other protein kinases. Much of our knowledge concerning second messenger regulation of TJ arises fon the study of epithelial cells of different origin, mostly from kidney, therefore the specific regulation of the junctional complex of the BBB still remains to be elucidated.
脑内皮细胞的紧密连接(TJs)在生理和病理条件下对血脑屏障(BBB)通透性的调节中起着关键作用。连接蛋白的调节受到复杂的控制。在这些调节过程中,一些定位于紧密连接的信号分子发挥着重要作用。在调节紧密连接功能的最具特征的第二信使中,环核苷酸起着重要作用,如我们的实验所示,它也会降低细胞旁通透性。另一个参与紧密连接调节的重要信号分子是蛋白激酶C,它可能对紧密连接的形成和成熟紧密连接的功能产生不同的影响。已知调节细胞旁通透性的其他信号分子包括G蛋白(传统G蛋白和小G蛋白)、丝裂原活化蛋白激酶(MAP激酶)和其他蛋白激酶。我们关于紧密连接第二信使调节的许多知识来自对不同来源上皮细胞的研究,主要是肾脏上皮细胞,因此血脑屏障连接复合体的具体调节仍有待阐明。