Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Mol Metab. 2022 Jun;60:101481. doi: 10.1016/j.molmet.2022.101481. Epub 2022 Mar 25.
Spatial compartmentalization of metabolic pathways within membrane-separated organelles is key to the ability of eukaryotic cells to precisely regulate their biochemical functions. Membrane-bound organelles such as mitochondria, endoplasmic reticulum (ER) and lysosomes enable the concentration of metabolic precursors within optimized chemical environments, greatly accelerating the efficiency of both anabolic and catabolic reactions, enabling division of labor and optimal utilization of resources. However, metabolic compartmentalization also poses a challenge to cells because it creates spatial discontinuities that must be bridged for reaction cascades to be connected and completed. To do so, cells employ different methods to coordinate metabolic fluxes occurring in different organelles, such as membrane-localized transporters to facilitate regulated metabolite exchange between mitochondria and lysosomes, non-vesicular transport pathways via physical contact sites connecting the ER with both mitochondria and lysosomes, as well as localized regulatory signaling processes that coordinately regulate the activity of all these organelles.
This review covers how cells use membrane transporters, membrane contact sites, and localized signaling pathways to mediate inter-organelle communication and coordinate metabolism. We also describe how disruption of inter-organelle communication is an emerging driver in a multitude of diseases, from cancer to neurodegeneration.
Effective communication among organelles is essential to cellular health and function. Identifying the major molecular players involved in mediating metabolic coordination between organelles will further our understanding of cellular metabolism in health and lead us to design better therapeutics against dysregulated metabolism in disease.
代谢途径在膜分离细胞器内的空间分隔是真核细胞精确调节其生化功能的关键。诸如线粒体、内质网(ER)和溶酶体等膜结合细胞器能够使代谢前体在优化的化学环境中浓缩,极大地加速了合成和分解反应的效率,实现分工和资源的最佳利用。然而,代谢分隔也给细胞带来了挑战,因为它造成了空间不连续性,必须通过桥接来连接和完成反应级联。为此,细胞采用不同的方法来协调发生在不同细胞器中的代谢通量,例如膜定位的转运蛋白,以促进线粒体和溶酶体之间受调控的代谢物交换;通过内质网与线粒体和溶酶体相连的物理接触点的非囊泡运输途径;以及协调调节所有这些细胞器活性的局部调节信号过程。
本文综述了细胞如何利用膜转运蛋白、膜接触位点和局部信号通路来介导细胞器间的通讯和协调代谢。我们还描述了细胞器间通讯的破坏如何成为从癌症到神经退行性疾病等多种疾病的新兴驱动因素。
细胞器之间的有效通讯对于细胞的健康和功能至关重要。确定参与细胞器间代谢协调的主要分子参与者将进一步加深我们对细胞代谢在健康中的理解,并促使我们针对疾病中失调的代谢设计更好的治疗方法。