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Review
. 2021 Jul;288(14):4168-4182.
doi: 10.1111/febs.15602. Epub 2020 Nov 12.

The lysosomal membrane-export of metabolites and beyond

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Free article
Review

The lysosomal membrane-export of metabolites and beyond

Sönke Rudnik et al. FEBS J. 2021 Jul.
Free article

Abstract

Lysosomes are degradative organelles in eukaryotic cells mediating the hydrolytic catabolism of various macromolecules to small basic building blocks. These low-molecular-weight metabolites are transported across the lysosomal membrane and reused in the cytoplasm and other organelles for biosynthetic pathways. Even though in the past 20 years our understanding of the lysosomal membrane regarding various transporters, other integral and peripheral membrane proteins, the lipid composition, but also its turnover has dramatically improved, there are still many unresolved questions concerning key aspects of the function of the lysosomal membrane. These include a possible function of lysosomes as a cellular storage compartment, yet unidentified transporters mediating the export such as various amino acids, mechanisms mediating the transport of lysosomal membrane proteins from the Golgi apparatus to lysosomes, and the turnover of lysosomal membrane proteins. Here, we review the current knowledge about the lysosomal membrane and identify some of the open questions that need to be solved in the future for a comprehensive and complete understanding of how lysosomes communicate with other organelles, cellular processes, and pathways.

Keywords: accessory subunits; lysosomal membrane; lysosomal storage diseases; transporter.

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References

    1. Appelmans F, Wattiaux R & De Duve C (1955) Tissue fractionation studies. 5. The association of acid phosphatase with a special class of cytoplasmic granules in rat liver. Biochem J. 59, 438-445.
    1. Bijvoet AG, van de Kamp EH, Kroos MA, Ding JH, Yang BZ, Visser P, Bakker CE, Verbeet MP, Oostra BA, Reuser AJ et al. (1998) Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe disease. Hum Mol Genet. 7, 53-62.
    1. Forster S & Lloyd JB (1988) Solute translocation across the mammalian lysosome membrane. Biochim Biophys Acta. 947, 465-491.
    1. Van Acker ZP, Bretou M & Annaert W (2019) Endo-lysosomal dysregulations and late-onset Alzheimer's disease: impact of genetic risk factors. Mol Neurodegener 14, 20.
    1. Di Malta C, Siciliano D, Calcagni A, Monfregola J, Punzi S, Pastore N, Eastes AN, Davis O, De Cegli R, Zampelli A et al. (2017) Transcriptional activation of RagD GTPase controls mTORC1 and promotes cancer growth. Science 356, 1188-1192.

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