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<p>Lysosomes are integral organelles that communicate cellular status to an entire tissue through mechanisms that are poorly defined. Here we developed an unbiased platform, integrating human plasma metabolomes and single-lysosome metabolomics, and show the byproducts of proteolysis are an unexpected class of signalling molecules. We show that dimethylarginine is a lysosomal-derived metabolite and a predictor of patient morbidity. Genetic depletion of a lysosomal exporter, cystinosin, accumulated dimethylarginine in lysosomes. Leveraging a lysosomal storage disease with cystinosin mutations, we show that the rapid plasticity of dimethylarginine compartmentalization ensures cell and tissue homeostasis. Strikingly, lysosomal entrapment of dimethylarginine in patients and disease models corresponds with lipid accumulation, lipid droplets and lipotoxicity. Exogenously restoring asymmetric dimethylarginine buffers oxidative stress, decreasing lipid peroxidation and cell death. These data show that dimethylarginine engages an interorganellar process—with peroxisomes, lysosomes and lipid droplets—that confers a crucial adaptive response mechanism.</p>

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Lysosome-derived methylated arginine is a signalling metabolite controlling the lipidome

  • 期刊论文

  • 发表日期：

    2026年6月19日

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  • Steven T. Nguyen,
  • Richard L. Watson,
  • Fangyuan Gao,
  • Melissa Campos,
  • Sunhee Jung,
  • Laurence J. Seabrook,
  • Maxwell C. Kim,
  • Eric A. Hanse,
  • Ying Yang,
  • Mei Kong,
  • Jonathan E. Zuckerman,
  • Renata C. Pereira,
  • Isidro B. Salusky,
  • Sergio D. Catz,
  • Cholsoon Jang,
  • Dorota Skowronska-Krawczyk,
  • Lauren V. Albrecht

摘要

Lysosomes are integral organelles that communicate cellular status to an entire tissue through mechanisms that are poorly defined. Here we developed an unbiased platform, integrating human plasma metabolomes and single-lysosome metabolomics, and show the byproducts of proteolysis are an unexpected class of signalling molecules. We show that dimethylarginine is a lysosomal-derived metabolite and a predictor of patient morbidity. Genetic depletion of a lysosomal exporter, cystinosin, accumulated dimethylarginine in lysosomes. Leveraging a lysosomal storage disease with cystinosin mutations, we show that the rapid plasticity of dimethylarginine compartmentalization ensures cell and tissue homeostasis. Strikingly, lysosomal entrapment of dimethylarginine in patients and disease models corresponds with lipid accumulation, lipid droplets and lipotoxicity. Exogenously restoring asymmetric dimethylarginine buffers oxidative stress, decreasing lipid peroxidation and cell death. These data show that dimethylarginine engages an interorganellar process—with peroxisomes, lysosomes and lipid droplets—that confers a crucial adaptive response mechanism.