Manchester Collaborative Centre for Inflammation Research, the University of Manchester, Manchester, UK
Department of Respiratory Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
J Exp Med. 2019 Sep 2;216(9):2184-2201. doi: 10.1084/jem.20171978. Epub 2019 Jul 9.
Epithelial cell proliferation, division, and differentiation are critical for barrier repair following inflammation, but the initial trigger for this process is unknown. Here we define that sensing of apoptotic cells by the TAM receptor tyrosine kinase Axl is a critical indicator for tracheal basal cell expansion, cell cycle reentry, and symmetrical cell division. Furthermore, once the pool of tracheal basal cells has expanded, silencing of Axl is required for their differentiation. Genetic depletion of Axl triggers asymmetrical cell division, leading to epithelial differentiation and ciliated cell regeneration. This discovery has implications for conditions associated with epithelial barrier dysfunction, basal cell hyperplasia, and continued turnover of dying cells in patients with chronic inflammatory pulmonary diseases.
上皮细胞的增殖、分裂和分化对于炎症后屏障修复至关重要,但这一过程的最初触发因素尚不清楚。在这里,我们定义了 TAM 受体酪氨酸激酶 Axl 对凋亡细胞的感应是气管基底细胞扩张、细胞周期再进入和对称分裂的关键指标。此外,一旦气管基底细胞池扩大,Axl 的沉默对于它们的分化是必需的。Axl 的基因缺失会触发不对称细胞分裂,导致上皮分化和纤毛细胞再生。这一发现对于与上皮屏障功能障碍、基底细胞增生以及慢性炎症性肺部疾病患者死亡细胞持续更替相关的疾病具有重要意义。