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New Insights into the Role of Cysteine Cathepsins in Neuroinflammation

Neuroinflammation, which is mediated by microglia and astrocytes, is associated with the progression of neurodegenerative diseases. Increasing evidence shows that activated microglia induce the expression and secretion of various lysosomal cathepsins, particularly during the early stage of neuroinfl...

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Autores principales: Pišlar, Anja, Bolčina, Lara, Kos, Janko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698589/
https://www.ncbi.nlm.nih.gov/pubmed/34944440
http://dx.doi.org/10.3390/biom11121796
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author Pišlar, Anja
Bolčina, Lara
Kos, Janko
author_facet Pišlar, Anja
Bolčina, Lara
Kos, Janko
author_sort Pišlar, Anja
collection PubMed
description Neuroinflammation, which is mediated by microglia and astrocytes, is associated with the progression of neurodegenerative diseases. Increasing evidence shows that activated microglia induce the expression and secretion of various lysosomal cathepsins, particularly during the early stage of neuroinflammation. This trigger signaling cascade that aggravate neurodegeneration. To date, most research on neuroinflammation has focused on the role of cysteine cathepsins, the largest cathepsin family. Cysteine cathepsins are primarily responsible for protein degradation in lysosomes; however, they also play a role in regulating a number of other important physiological and pathological processes. This review focuses on the functional roles of cysteine cathepsins in the central nervous system during neuroinflammation, with an emphasis on their roles in the polarization of microglia and neuroinflammation signaling, which in turn causes neuronal death and thus neurodegeneration.
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spelling pubmed-86985892021-12-24 New Insights into the Role of Cysteine Cathepsins in Neuroinflammation Pišlar, Anja Bolčina, Lara Kos, Janko Biomolecules Review Neuroinflammation, which is mediated by microglia and astrocytes, is associated with the progression of neurodegenerative diseases. Increasing evidence shows that activated microglia induce the expression and secretion of various lysosomal cathepsins, particularly during the early stage of neuroinflammation. This trigger signaling cascade that aggravate neurodegeneration. To date, most research on neuroinflammation has focused on the role of cysteine cathepsins, the largest cathepsin family. Cysteine cathepsins are primarily responsible for protein degradation in lysosomes; however, they also play a role in regulating a number of other important physiological and pathological processes. This review focuses on the functional roles of cysteine cathepsins in the central nervous system during neuroinflammation, with an emphasis on their roles in the polarization of microglia and neuroinflammation signaling, which in turn causes neuronal death and thus neurodegeneration. MDPI 2021-11-30 /pmc/articles/PMC8698589/ /pubmed/34944440 http://dx.doi.org/10.3390/biom11121796 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pišlar, Anja
Bolčina, Lara
Kos, Janko
New Insights into the Role of Cysteine Cathepsins in Neuroinflammation
title New Insights into the Role of Cysteine Cathepsins in Neuroinflammation
title_full New Insights into the Role of Cysteine Cathepsins in Neuroinflammation
title_fullStr New Insights into the Role of Cysteine Cathepsins in Neuroinflammation
title_full_unstemmed New Insights into the Role of Cysteine Cathepsins in Neuroinflammation
title_short New Insights into the Role of Cysteine Cathepsins in Neuroinflammation
title_sort new insights into the role of cysteine cathepsins in neuroinflammation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698589/
https://www.ncbi.nlm.nih.gov/pubmed/34944440
http://dx.doi.org/10.3390/biom11121796
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