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线粒体自噬可减少衰老过程中细胞溶质中线粒体DNA依赖性的cGAS/STING炎症激活。

Mitophagy curtails cytosolic mtDNA-dependent activation of cGAS/STING inflammation during aging.

作者信息

Jiménez-Loygorri Juan Ignacio, Villarejo-Zori Beatriz, Viedma-Poyatos Álvaro, Zapata-Muñoz Juan, Benítez-Fernández Rocío, Frutos-Lisón María Dolores, Tomás-Barberán Francisco A, Espín Juan Carlos, Area-Gómez Estela, Gomez-Duran Aurora, Boya Patricia

机构信息

Department of Cellular and Molecular Biology, Centro de Investigaciones Biológicas Margarita Salas, CSIC, Madrid, Spain.

Department of Neuroscience and Movement Science, Section of Medicine, University of Fribourg, Fribourg, Switzerland.

出版信息

Nat Commun. 2024 Jan 27;15(1):830. doi: 10.1038/s41467-024-45044-1.

Abstract

Macroautophagy decreases with age, and this change is considered a hallmark of the aging process. It remains unknown whether mitophagy, the essential selective autophagic degradation of mitochondria, also decreases with age. In our analysis of mitophagy in multiple organs in the mito-QC reporter mouse, mitophagy is either increased or unchanged in old versus young mice. Transcriptomic analysis shows marked upregulation of the type I interferon response in the retina of old mice, which correlates with increased levels of cytosolic mtDNA and activation of the cGAS/STING pathway. Crucially, these same alterations are replicated in primary human fibroblasts from elderly donors. In old mice, pharmacological induction of mitophagy with urolithin A attenuates cGAS/STING activation and ameliorates deterioration of neurological function. These findings point to mitophagy induction as a strategy to decrease age-associated inflammation and increase healthspan.

摘要

巨自噬随年龄增长而减少,这种变化被认为是衰老过程的一个标志。线粒体自噬作为线粒体必需的选择性自噬降解过程,是否也随年龄增长而减少仍不清楚。在我们对线粒体质量控制(mito-QC)报告基因小鼠多个器官的线粒体自噬分析中,老年小鼠与年轻小鼠相比,线粒体自噬要么增加,要么不变。转录组分析显示,老年小鼠视网膜中I型干扰素反应显著上调,这与细胞质中线粒体DNA水平的增加以及cGAS/STING通路的激活相关。至关重要的是,这些相同的改变在老年供体的原代人成纤维细胞中也能重现。在老年小鼠中,用尿石素A进行线粒体自噬的药理学诱导可减弱cGAS/STING激活,并改善神经功能的衰退。这些发现表明,诱导线粒体自噬是一种减少与年龄相关的炎症并延长健康寿命的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d04c/10821893/c101907fa08c/41467_2024_45044_Fig1_HTML.jpg

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