Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis
Abstract: Diverse cellular processes depend on the lysosomal protease system but how cells regulate lysosomal proteolytic capacity is only partly understood. We show here that cells can respond to protease/substrate imbalance in this compartment by de novo expression of multiple lysosomal hydrolases. This response, exemplified here either by loss of asparagine endopeptidase (AEP) or other lysosomal cysteine proteases, or by increased endocytic substrate load, is not dependent on the transcription factor EB (TFEB) but rather is triggered by STAT3 activation downstream of lysosomal oxidative stress. Similar lysosomal adaptations are seen in mice and cells expressing a constitutively active form of STAT3. Our results reveal how cells can increase lysosomal protease capacity under ‘fed’ rather than ‘starved’ conditions that activate the TFEB system. In addition, STAT3 activation due to lysosomal stress likely explains the hyperproliferative kidney disease and splenomegaly observed in AEP-deficient mice
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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Nature communications. - 9, 1 (2018) , 5343, ISSN: 2041-1723
- Event
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Veröffentlichung
- (where)
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Freiburg
- (who)
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Universität
- (when)
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2019
- Creator
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Martínez-Fábregas, Jonathan
Prescott, Alan
Kasteren, Sander van
Pedrioli, Deena Leslie
McLean, Irwin
Moles, Anna
Reinheckel, Thomas
Poli, Valeria
Watts, Colin
- Contributor
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Zentrum für Biochemie und Molekulare Zellforschung
- DOI
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10.1038/s41467-018-07741-6
- URN
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urn:nbn:de:bsz:25-freidok-1479253
- Rights
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Kein Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:02 AM CEST
Data provider
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Martínez-Fábregas, Jonathan
- Prescott, Alan
- Kasteren, Sander van
- Pedrioli, Deena Leslie
- McLean, Irwin
- Moles, Anna
- Reinheckel, Thomas
- Poli, Valeria
- Watts, Colin
- Zentrum für Biochemie und Molekulare Zellforschung
- Universität
Time of origin
- 2019
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Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis
Lysosomal SLC46A3 modulates hepatic cytosolic copper homeostasis
The lysosomal protein cathepsin L is a progranulin protease
Helicobacter pylori and gastric cancer: a lysosomal protease perspective
Regulation of lysosomal ion homeostasis by channels and transporters
Lysosomal function in macromolecular homeostasis and bioenergetics in Parkinson's disease
Lysosomal dysfunction and overload of nucleosides in thymidine phosphorylase deficiency of MNGIE
Methods for investigating STAT3 regulation of lysosomal function in mammary epithelial cells
Lysosomal storage disease: aspartylglycosaminuria
Lysosomal processing of progranulin
Lysosomal enzyme trafficking factor LYSET in lysosomal catabolism, nutrient generation, and pathology
STAT3 associates with vacuolar H+-ATPase and regulates cytosolic and lysosomal pH
Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis
Lysosomal SLC46A3 modulates hepatic cytosolic copper homeostasis
The lysosomal protein cathepsin L is a progranulin protease
Helicobacter pylori and gastric cancer: a lysosomal protease perspective
Regulation of lysosomal ion homeostasis by channels and transporters
Lysosomal function in macromolecular homeostasis and bioenergetics in Parkinson's disease
Lysosomal dysfunction and overload of nucleosides in thymidine phosphorylase deficiency of MNGIE
Methods for investigating STAT3 regulation of lysosomal function in mammary epithelial cells
Lysosomal storage disease: aspartylglycosaminuria
Lysosomal processing of progranulin
Lysosomal enzyme trafficking factor LYSET in lysosomal catabolism, nutrient generation, and pathology