Barabino Silvia, Lombardi Silvia, Zilocchi Mara
Department of Biotechnology and Biosciences, University of Milano-Bicocca, 20126, Milan, Italy.
Cell Death Discov. 2023 Nov 16;9(1):417. doi: 10.1038/s41420-023-01710-9.
Mitochondria have been the focus of extensive research for decades since their dysfunction is linked to more than 150 distinct human disorders. Despite considerable efforts, researchers have only been able to skim the surface of the mitochondrial social complexity and the impact of inter-organelle and inter-organ communication alterations on human health. While some progress has been made in deciphering connections among mitochondria and other cytoplasmic organelles through direct (i.e., contact sites) or indirect (i.e., inter-organelle trafficking) crosstalk, most of these efforts have been restricted to a limited number of proteins involved in specific physiological pathways or disease states. This research bottleneck is further narrowed by our incomplete understanding of the cellular alteration timeline in a specific pathology, which prevents the distinction between a primary organelle dysfunction and the defects occurring due to the disruption of the organelle's interconnectivity. In this perspective, we will (i) summarize the current knowledge on the mitochondrial crosstalk within cell(s) or tissue(s) in health and disease, with a particular focus on neurodegenerative disorders, (ii) discuss how different large-scale and targeted approaches could be used to characterize the different levels of mitochondrial social complexity, and (iii) consider how investigating the different expression patterns of mitochondrial proteins in different cell types/tissues could represent an important step forward in depicting the distinctive architecture of inter-organelle communication.
几十年来,线粒体一直是广泛研究的焦点,因为它们的功能障碍与150多种不同的人类疾病有关。尽管付出了巨大努力,但研究人员仅触及了线粒体社交复杂性的表面,以及细胞器间和器官间通讯改变对人类健康的影响。虽然通过直接(即接触位点)或间接(即细胞器间运输)串扰来破译线粒体与其他细胞质细胞器之间的联系已取得了一些进展,但这些努力大多局限于参与特定生理途径或疾病状态的有限数量的蛋白质。由于我们对特定病理学中细胞改变时间线的理解不完整,这一研究瓶颈进一步缩小,这使得区分原发性细胞器功能障碍和由于细胞器互连性破坏而出现的缺陷变得困难。从这个角度来看,我们将(i)总结目前关于健康和疾病状态下细胞内或组织内线粒体串扰的知识,特别关注神经退行性疾病;(ii)讨论如何使用不同的大规模和靶向方法来表征线粒体社交复杂性的不同水平;(iii)考虑研究线粒体蛋白在不同细胞类型/组织中的不同表达模式如何代表描绘细胞器间通讯独特结构方面向前迈出的重要一步。