Literature DB >> 31983508

Maintaining Iron Homeostasis Is the Key Role of Lysosomal Acidity for Cell Proliferation.

Ross A Weber1, Frederick S Yen2, Shirony P V Nicholson3, Hanan Alwaseem4, Erol C Bayraktar2, Mohammad Alam2, Rebecca C Timson2, Konnor La2, Monther Abu-Remaileh5, Henrik Molina4, Kıvanç Birsoy6.   

Abstract

The lysosome is an acidic multi-functional organelle with roles in macromolecular digestion, nutrient sensing, and signaling. However, why cells require acidic lysosomes to proliferate and which nutrients become limiting under lysosomal dysfunction are unclear. To address this, we performed CRISPR-Cas9-based genetic screens and identified cholesterol biosynthesis and iron uptake as essential metabolic pathways when lysosomal pH is altered. While cholesterol synthesis is only necessary, iron is both necessary and sufficient for cell proliferation under lysosomal dysfunction. Remarkably, iron supplementation restores cell proliferation under both pharmacologic and genetic-mediated lysosomal dysfunction. The rescue was independent of metabolic or signaling changes classically associated with increased lysosomal pH, uncoupling lysosomal function from cell proliferation. Finally, our experiments revealed that lysosomal dysfunction dramatically alters mitochondrial metabolism and hypoxia inducible factor (HIF) signaling due to iron depletion. Altogether, these findings identify iron homeostasis as the key function of lysosomal acidity for cell proliferation. Published by Elsevier Inc.

Entities:  

Keywords:  CRISPR; Chelation; Genetic Screens; Iron Depletion; Iron Homeostasis; Iron Sulfur Clusters; Lysosomal Acidity; Lysosomal Dysfunction; Organelle Metabolism; v-ATPase

Mesh:

Substances:

Year:  2020        PMID: 31983508      PMCID: PMC7176020          DOI: 10.1016/j.molcel.2020.01.003

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  45 in total

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