Jander Kirsten, Greulich Jan, Gonnissen Stefanie, Ale-Agha Niloofar, Goy Christine, Jakobs Philipp, Farrokh Sabrina, Marziano Corina, Sonkusare Swapnil K, Haendeler Judith, Altschmied Joachim
IUF-Leibniz Research Institute for Environmental Medicine, 40225 Düsseldorf, Germany.
Environmentally-Induced Cardiovascular Degeneration, Clinical Chemistry and Laboratory Diagnostics, Medical Faculty, University Clinics, Heinrich-Heine-University, 40225 Düsseldorf, Germany.
Antioxidants (Basel). 2021 Mar 11;10(3):428. doi: 10.3390/antiox10030428.
We previously demonstrated that the transcription factor Grainyhead-like 3 (GRHL3) has essential functions in endothelial cells by inhibiting apoptosis and promoting migration as well as activation of endothelial nitric oxide synthase (eNOS). We now show that a large portion of the protein is localized to myo-endothelial projections of murine arteries suggesting extra-nuclear functions. Therefore, we generated various deletion mutants to identify the nuclear localization signal (NLS) of GRHL3 and assessed potential extra-nuclear functions. Several large-scale deletion mutants were incapable of activating a GRHL3-dependent reporter construct, which could either be due to deficiencies in transcriptional activation or to impaired nuclear import. One of these mutants encompassed a predicted bipartite NLS whose deletion led to the retention of GRHL3 outside the nucleus. Interestingly, this mutant retained functions of the full-length protein as it could still inhibit pathways inducing endothelial cell apoptosis. As apoptosis protection by GRHL3 depends on NO-production, we examined whether GRHL3 could interact with eNOS and showed a direct interaction, which was enhanced with the extra-nuclear GRHL3 variant. The observation that endogenous GRHL3 also interacts with eNOS in intact murine arteries corroborated these findings and substantiated the notion that GRHL3 has important extra-nuclear functions in the endothelium.
我们之前证明,转录因子颗粒头样蛋白3(GRHL3)在内皮细胞中具有重要功能,它可抑制细胞凋亡、促进迁移以及激活内皮型一氧化氮合酶(eNOS)。我们现在发现,该蛋白的很大一部分定位于小鼠动脉的肌内皮突起,提示其具有核外功能。因此,我们构建了各种缺失突变体,以鉴定GRHL3的核定位信号(NLS),并评估其潜在的核外功能。几个大规模缺失突变体无法激活GRHL3依赖性报告基因构建体,这可能是由于转录激活缺陷或核输入受损所致。其中一个突变体包含一个预测的双分型NLS,其缺失导致GRHL3滞留在细胞核外。有趣的是,这个突变体保留了全长蛋白的功能,因为它仍然可以抑制诱导内皮细胞凋亡的途径。由于GRHL3对细胞凋亡的保护作用依赖于一氧化氮的产生,我们研究了GRHL3是否能与eNOS相互作用,并发现了直接相互作用,这种相互作用在核外GRHL3变体中增强。内源性GRHL3在完整的小鼠动脉中也与eNOS相互作用这一观察结果证实了这些发现,并证实了GRHL3在内皮细胞中具有重要核外功能的观点。