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Lysosomes: multifunctional compartments ruled by a complex regulatory network

More than 50 years have passed since Nobel laureate Cristian de Duve described for the first time the presence of tiny subcellular compartments filled with hydrolytic enzymes: the lysosome. For a long time, lysosomes were deemed simple waste bags exerting a plethora of hydrolytic activities involved...

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Autores principales: Martinez‐Fabregas, Jonathan, Tamargo‐Azpilicueta, Joaquin, Diaz‐Moreno, Irene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8972048/
https://www.ncbi.nlm.nih.gov/pubmed/35218162
http://dx.doi.org/10.1002/2211-5463.13387
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author Martinez‐Fabregas, Jonathan
Tamargo‐Azpilicueta, Joaquin
Diaz‐Moreno, Irene
author_facet Martinez‐Fabregas, Jonathan
Tamargo‐Azpilicueta, Joaquin
Diaz‐Moreno, Irene
author_sort Martinez‐Fabregas, Jonathan
collection PubMed
description More than 50 years have passed since Nobel laureate Cristian de Duve described for the first time the presence of tiny subcellular compartments filled with hydrolytic enzymes: the lysosome. For a long time, lysosomes were deemed simple waste bags exerting a plethora of hydrolytic activities involved in the recycling of biopolymers, and lysosomal genes were considered to just be simple housekeeping genes, transcribed in a constitutive fashion. However, lysosomes are emerging as multifunctional signalling hubs involved in multiple aspects of cell biology, both under homeostatic and pathological conditions. Lysosomes are involved in the regulation of cell metabolism through the mTOR/TFEB axis. They are also key players in the regulation and onset of the immune response. Furthermore, it is becoming clear that lysosomal hydrolases can regulate several biological processes outside of the lysosome. They are also implicated in a complex communication network among subcellular compartments that involves intimate organelle‐to‐organelle contacts. Furthermore, lysosomal dysfunction is nowadays accepted as the causative event behind several human pathologies: low frequency inherited diseases, cancer, or neurodegenerative, metabolic, inflammatory, and autoimmune diseases. Recent advances in our knowledge of the complex biology of lysosomes have established them as promising therapeutic targets for the treatment of different pathologies. Although recent discoveries have started to highlight that lysosomes are controlled by a complex web of regulatory networks, which in some cases seem to be cell‐ and stimuli‐dependent, to harness the full potential of lysosomes as therapeutic targets, we need a deeper understanding of the little‐known signalling pathways regulating this subcellular compartment and its functions.
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spelling pubmed-89720482022-04-05 Lysosomes: multifunctional compartments ruled by a complex regulatory network Martinez‐Fabregas, Jonathan Tamargo‐Azpilicueta, Joaquin Diaz‐Moreno, Irene FEBS Open Bio Reviews More than 50 years have passed since Nobel laureate Cristian de Duve described for the first time the presence of tiny subcellular compartments filled with hydrolytic enzymes: the lysosome. For a long time, lysosomes were deemed simple waste bags exerting a plethora of hydrolytic activities involved in the recycling of biopolymers, and lysosomal genes were considered to just be simple housekeeping genes, transcribed in a constitutive fashion. However, lysosomes are emerging as multifunctional signalling hubs involved in multiple aspects of cell biology, both under homeostatic and pathological conditions. Lysosomes are involved in the regulation of cell metabolism through the mTOR/TFEB axis. They are also key players in the regulation and onset of the immune response. Furthermore, it is becoming clear that lysosomal hydrolases can regulate several biological processes outside of the lysosome. They are also implicated in a complex communication network among subcellular compartments that involves intimate organelle‐to‐organelle contacts. Furthermore, lysosomal dysfunction is nowadays accepted as the causative event behind several human pathologies: low frequency inherited diseases, cancer, or neurodegenerative, metabolic, inflammatory, and autoimmune diseases. Recent advances in our knowledge of the complex biology of lysosomes have established them as promising therapeutic targets for the treatment of different pathologies. Although recent discoveries have started to highlight that lysosomes are controlled by a complex web of regulatory networks, which in some cases seem to be cell‐ and stimuli‐dependent, to harness the full potential of lysosomes as therapeutic targets, we need a deeper understanding of the little‐known signalling pathways regulating this subcellular compartment and its functions. John Wiley and Sons Inc. 2022-03-08 /pmc/articles/PMC8972048/ /pubmed/35218162 http://dx.doi.org/10.1002/2211-5463.13387 Text en © 2022 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Martinez‐Fabregas, Jonathan
Tamargo‐Azpilicueta, Joaquin
Diaz‐Moreno, Irene
Lysosomes: multifunctional compartments ruled by a complex regulatory network
title Lysosomes: multifunctional compartments ruled by a complex regulatory network
title_full Lysosomes: multifunctional compartments ruled by a complex regulatory network
title_fullStr Lysosomes: multifunctional compartments ruled by a complex regulatory network
title_full_unstemmed Lysosomes: multifunctional compartments ruled by a complex regulatory network
title_short Lysosomes: multifunctional compartments ruled by a complex regulatory network
title_sort lysosomes: multifunctional compartments ruled by a complex regulatory network
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8972048/
https://www.ncbi.nlm.nih.gov/pubmed/35218162
http://dx.doi.org/10.1002/2211-5463.13387
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