Department of Paediatric Haematology, Oncology and Cell and Gene Therapy, IRCCS Bambino Gesù Children's Hospital, Piazza Sant'Onofrio 4, 00165, Rome, Italy.
IRCCS Fondazione Santa Lucia, Via del Fosso di Fiorano 64, 00143, Rome, Italy.
Nat Commun. 2019 Apr 4;10(1):1533. doi: 10.1038/s41467-019-09487-1.
Autophagy-mediated degradation of mitochondria (mitophagy) is a key process in cellular quality control. Although mitophagy impairment is involved in several patho-physiological conditions, valuable methods to induce mitophagy with low toxicity in vivo are still lacking. Herein, we describe a new optogenetic tool to stimulate mitophagy, based on light-dependent recruitment of pro-autophagy protein AMBRA1 to mitochondrial surface. Upon illumination, AMBRA1-RFP-sspB is efficiently relocated from the cytosol to mitochondria, where it reversibly mediates mito-aggresome formation and reduction of mitochondrial mass. Finally, as a proof of concept of the biomedical relevance of this method, we induced mitophagy in an in vitro model of neurotoxicity, fully preventing cell death, as well as in human T lymphocytes and in zebrafish in vivo. Given the unique features of this tool, we think it may turn out to be very useful for a wide range of both therapeutic and research applications.
自噬介导线粒体降解(mitophagy)是细胞质量控制的关键过程。虽然线粒体自噬功能障碍与多种病理生理状况有关,但在体内诱导低毒性线粒体自噬的有效方法仍然缺乏。本文描述了一种新的光遗传学工具,该工具基于光依赖性将自噬蛋白 AMBRA1 募集到线粒体表面,从而刺激线粒体自噬。光照时,AMBRA1-RFP-sspB 从细胞质有效重定位到线粒体,在那里它可逆地介导线粒体聚集体的形成和线粒体质量的减少。最后,作为该方法的生物医学相关性的概念验证,我们在神经毒性的体外模型中诱导了线粒体自噬,完全阻止了细胞死亡,并且在体内的人类 T 淋巴细胞和斑马鱼中也诱导了线粒体自噬。鉴于该工具的独特特征,我们认为它可能在广泛的治疗和研究应用中非常有用。