Barabutis Nektarios
School of Basic Pharmaceutical and Toxicological Sciences, College of Pharmacy, University of Louisiana Monroe, Monroe, Louisiana, USA.
IUBMB Life. 2020 Apr;72(4):801-804. doi: 10.1002/iub.2251. Epub 2020 Feb 11.
Dysregulation of lung endothelial barrier function may lead to lethal outcomes, as demonstrated in the case of the acute respiratory distress syndrome (ARDS). p53 participates in the regulation of the lung endothelial barrier, and it has been associated both in vivo and in vitro with protective effects against the LPS-induced hyperpermeability. Family members of the never in mitosis A-related kinases (NEKs) are crucial mediators of fundamental cellular processes, including mitosis, and have been shown to posttranslationally modify p53. Since such modifications affect p53 stability and activity, it is highly probable that NEK kinases are also regulators of lung endothelial permeability. Thus, they may serve as possible therapeutic targets for treatment of pathologies associated with endothelial barrier dysfunction.
肺内皮屏障功能失调可能导致致命后果,急性呼吸窘迫综合征(ARDS)就是例证。p53参与肺内皮屏障的调节,在体内和体外均显示出对脂多糖(LPS)诱导的高通透性具有保护作用。从未在有丝分裂A相关激酶(NEKs)家族成员是包括有丝分裂在内的基本细胞过程的关键介质,并且已证明可对p53进行翻译后修饰。由于此类修饰会影响p53的稳定性和活性,因此NEK激酶很可能也是肺内皮通透性的调节因子。因此,它们可能成为治疗与内皮屏障功能障碍相关病症的潜在治疗靶点。