a INSERM U1152, DHU FIRE, Labex Inflamex , Université Paris Diderot, Sorbonne Paris Cité , Paris , France.
b INSERM U1085, IRSET Institut de Recherche sur la Santé, l'Environnement et le Travail , Université de Rennes-1 , Rennes , France.
Cell Cycle. 2017;16(21):2108-2118. doi: 10.1080/15384101.2017.1371882. Epub 2017 Sep 21.
It has become more and more evident that the BCL-2 family proteins mediate a wide range of non-apoptotic functions. The pro-apoptotic BAX protein has been reported in interphasic nuclei. Whether the nuclear form of BAX could be involved in non-apoptotic function is still unknown. Our study showed for the first time that BAX was associated with chromatin in vitro. Next, we used gain and loss of function approaches to decipher the potential role of nuclear BAX in non-apoptotic cells. In vitro, nuclear BAX promoted cell proliferation in lung epithelial cells and primary human lung fibroblasts by modulating CDKN1A expression. Interestingly, BAX occupancy of CDKN1A promoter was specifically enriched close to the transcription-starting site. Nuclear BAX also modulated the basal myofibroblastic differentiation and migration of primary human lung fibroblasts. Finally, BAX nuclear localization was associated in vivo with the remodelling of lung parenchyma during development, tumorigenesis as well as fibrosis compared to control adult human lungs. Hence, our study established for the first time, a strong link between the nuclear localization of the pro-apoptotic BAX protein and key basic cellular functions in the non-apoptotic setting.
越来越明显的是,BCL-2 家族蛋白介导了广泛的非凋亡功能。促凋亡的 BAX 蛋白已在间期中核中被报道。核 BAX 是否能参与非凋亡功能尚不清楚。我们的研究首次表明 BAX 可以在体外与染色质结合。接下来,我们使用功能获得和功能丧失的方法来解析核 BAX 在非凋亡细胞中的潜在作用。在体外,核 BAX 通过调节 CDKN1A 的表达,促进肺上皮细胞和原代人肺成纤维细胞的增殖。有趣的是,BAX 占据 CDKN1A 启动子的位置特别靠近转录起始位点。核 BAX 还调节原代人肺成纤维细胞的基础肌成纤维分化和迁移。最后,与对照成人肺相比,BAX 的核定位在体内与发育、肿瘤发生和纤维化过程中肺实质的重塑有关。因此,我们的研究首次建立了促凋亡 BAX 蛋白的核定位与非凋亡环境中关键基本细胞功能之间的紧密联系。