Center for Translational Cancer Research (TranslaTUM), Technical University of Munich, Munich, Germany.
Department of Internal Medicine II, Klinikum Rechts der Isar, Technical University of Munich, Munich, Germany.
Front Immunol. 2018 Apr 10;9:766. doi: 10.3389/fimmu.2018.00766. eCollection 2018.
Autophagy is a pathway that allows cells to target organelles, protein complexes, or invading microorganisms for lysosomal degradation. The specificity of autophagic processes is becoming increasingly recognized and is conferred by selective autophagy receptors such as Optineurin (OPTN). As an autophagy receptor, OPTN controls the clearance of infection and mediates mitochondrial turnover. Recent studies demonstrated that OPTN is critically required for pathogen clearance and an appropriate cytokine response in macrophages. Moreover, OPTN emerges as a critical regulator of inflammation emanating from epithelial cells in the intestine. OPTN directly interacts with and promotes the removal of inositol-requiring enzyme 1α, a central inflammatory signaling hub of the stressed endoplasmic reticulum (ER). Perturbations of ER and autophagy functions have been linked to inflammatory bowel disease (IBD) and specifically Crohn's disease. Collectively, these studies may explain how perturbations at the ER can be resolved by selective autophagy to restrain inflammatory processes in the intestine and turn the spotlight on OPTN as a key autophagy receptor. This review covers a timely perspective on the regulation and function of OPTN in health and IBD.
自噬是一种途径,使细胞能够针对溶酶体降解细胞器、蛋白质复合物或入侵的微生物。自噬过程的特异性越来越被认识到,这是由选择性自噬受体如 Optineurin(OPTN)赋予的。作为一种自噬受体,OPTN 控制着感染的清除和线粒体的周转。最近的研究表明,OPTN 对巨噬细胞中病原体的清除和适当的细胞因子反应至关重要。此外,OPTN 作为肠道上皮细胞中炎症的关键调节因子出现。OPTN 直接相互作用,并促进肌醇需求酶 1α 的去除,肌醇需求酶 1α 是应激内质网(ER)的中央炎症信号枢纽。ER 和自噬功能的紊乱与炎症性肠病(IBD),特别是克罗恩病有关。总的来说,这些研究可能解释了 ER 的紊乱如何通过选择性自噬来解决,以限制肠道中的炎症过程,并将 OPTN 作为关键的自噬受体成为焦点。这篇综述涵盖了 OPTN 在健康和 IBD 中的调节和功能的及时观点。