Aging Institute, University of Pittsburgh School of Medicine/University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Department of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
EMBO Rep. 2023 Nov 6;24(11):e57265. doi: 10.15252/embr.202357265. Epub 2023 Oct 9.
Dysfunction of lysosomes, the primary hydrolytic organelles in animal cells, is frequently associated with aging and age-related diseases. At the cellular level, lysosomal dysfunction is strongly linked to cellular senescence or the induction of cell death pathways. However, the precise mechanisms by which lysosomal dysfunction participates in these various cellular or organismal phenotypes have remained elusive. The ability of lysosomes to degrade diverse macromolecules including damaged proteins and organelles puts lysosomes at the center of multiple cellular stress responses. Lysosomal activity is tightly regulated by many coordinated cellular processes including pathways that function inside and outside of the organelle. Here, we collectively classify these coordinated pathways as the lysosomal processing and adaptation system (LYPAS). We review evidence that the LYPAS is upregulated by diverse cellular stresses, its adaptability regulates senescence and cell death decisions, and it can form the basis for therapeutic manipulation for a wide range of age-related diseases and potentially for aging itself.
溶酶体是动物细胞中主要的水解细胞器,其功能障碍常与衰老和衰老相关疾病有关。在细胞水平上,溶酶体功能障碍与细胞衰老或诱导细胞死亡途径密切相关。然而,溶酶体功能障碍参与这些不同的细胞或机体表型的确切机制仍不清楚。溶酶体降解各种大分子的能力,包括受损的蛋白质和细胞器,使溶酶体处于多种细胞应激反应的中心。溶酶体的活性受到许多协调一致的细胞过程的严格调控,包括在细胞器内外起作用的途径。在这里,我们将这些协调的途径统称为溶酶体加工和适应系统(LYPAS)。我们综述了证据表明,LYPAS 被多种细胞应激上调,其适应性调节衰老和细胞死亡决策,并且可以为广泛的与年龄相关的疾病和潜在的衰老本身提供治疗干预的基础。