Faculty of Medical Sciences, Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, UK.
Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, KS, USA.
Autophagy. 2024 Dec;20(12):2599-2601. doi: 10.1080/15548627.2024.2408712. Epub 2024 Oct 6.
Mitochondria are crucial organelles in maintaining cellular homeostasis. They are involved in processes such as energy production, metabolism of lipids and glucose, and cell death regulation. Mitochondrial dysfunction can lead to various health issues such as aging, cancer, neurodegenerative diseases, and chronic liver diseases. While mitophagy is the main process for getting rid of excess or damaged mitochondria, there are additional mechanisms for preserving mitochondrial quality. One such alternative mechanism we have discovered is a hybrid organelle called mitochondrial-lysosome-related-organelle (MLRO), which functions independently of the typical autophagy process. More recently, another type of vesicle called vesicle derived from the inner mitochondrial membrane (VDIM) has been identified to break down the inner mitochondrial membrane without involving the standard autophagy pathway. In this article, we will delve into the similarities and differences between MLRO and VDIM, including their structure, regulation, and relevance to human diseases.
线粒体是维持细胞内稳态的关键细胞器。它们参与能量产生、脂质和葡萄糖代谢以及细胞死亡调节等过程。线粒体功能障碍可导致各种健康问题,如衰老、癌症、神经退行性疾病和慢性肝病。虽然自噬是清除多余或受损线粒体的主要过程,但还有其他维持线粒体质量的机制。我们发现的一种这样的替代机制是一种称为线粒体-溶酶体相关细胞器(MLRO)的混合细胞器,它独立于典型的自噬过程发挥作用。最近,另一种称为源自线粒体内膜的囊泡(VDIM)的囊泡也被鉴定出来,它可以在不涉及标准自噬途径的情况下分解线粒体内膜。在本文中,我们将深入探讨 MLRO 和 VDIM 之间的相似之处和不同之处,包括它们的结构、调节以及与人类疾病的关系。