RRC ID 86440
著者 Loo TM, Zhou X, Tanaka Y, Sugawara S, Yamauchi S, Kawasaki H, Matsuoka Y, Sugiura Y, Sakuma S, Yamanishi Y, Yotsumoto S, Dodo K, Shirasaki Y, Kamatani T, Takahashi A.
タイトル Senescence-associated lysosomal dysfunction impairs cystine deprivation-induced lipid peroxidation and ferroptosis.
ジャーナル Nat Commun
Abstract Senescent cells, characterized by irreversible cell cycle arrest and inflammatory factor secretion, promote various age-related pathologies. Senescent cells exhibit resistance to ferroptosis, a form of iron-dependent cell death; however, the underlying mechanisms remain unclear. Here, we discovered that lysosomal acidity was crucial for lipid peroxidation and ferroptosis induction by cystine deprivation. In senescent cells, lysosomal alkalinization causes the aberrant retention of ferrous iron in lysosomes, resulting in resistance to ferroptosis. Treatment with the V-ATPase activator EN6 restored lysosomal acidity and ferroptosis sensitivity in senescent cells. A similar ferroptosis resistance mechanism involving lysosomal alkalinization was observed in pancreatic cancer cell lines. EN6 treatment prevented pancreatic cancer development in xenograft and Kras mutant mouse models. Our findings reveal a link between lysosomal dysfunction and the regulation of ferroptosis, suggesting a therapeutic strategy for the treatment of age-related diseases.
巻・号 16(1)
ページ 6617
公開日 2025-7-29
DOI 10.1038/s41467-025-61894-9
PII 10.1038/s41467-025-61894-9
PMID 40731111
PMC PMC12307602
MeSH Animals Cell Line, Tumor Cellular Senescence* / physiology Cystine* / deficiency Cystine* / metabolism Ferroptosis* / drug effects Ferroptosis* / physiology Humans Iron / metabolism Lipid Peroxidation* / drug effects Lysosomes* / drug effects Lysosomes* / metabolism Mice Pancreatic Neoplasms / metabolism Pancreatic Neoplasms / pathology
IF 12.121
リソース情報
実験動物マウス RBRC10170