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Role of Proteasomes in Inflammation

The ubiquitin–proteasome system (UPS) is involved in multiple cellular functions including the regulation of protein homeostasis, major histocompatibility (MHC) class I antigen processing, cell cycle proliferation and signaling. In humans, proteasome loss-of-function mutations result in autoinflamma...

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Detalles Bibliográficos
Autores principales: Goetzke, Carl Christoph, Ebstein, Frédéric, Kallinich, Tilmann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072576/
https://www.ncbi.nlm.nih.gov/pubmed/33923887
http://dx.doi.org/10.3390/jcm10081783
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author Goetzke, Carl Christoph
Ebstein, Frédéric
Kallinich, Tilmann
author_facet Goetzke, Carl Christoph
Ebstein, Frédéric
Kallinich, Tilmann
author_sort Goetzke, Carl Christoph
collection PubMed
description The ubiquitin–proteasome system (UPS) is involved in multiple cellular functions including the regulation of protein homeostasis, major histocompatibility (MHC) class I antigen processing, cell cycle proliferation and signaling. In humans, proteasome loss-of-function mutations result in autoinflammation dominated by a prominent type I interferon (IFN) gene signature. These genomic alterations typically cause the development of proteasome-associated autoinflammatory syndromes (PRAAS) by impairing proteasome activity and perturbing protein homeostasis. However, an abnormal increased proteasomal activity can also be found in other human inflammatory diseases. In this review, we cast a light on the different clinical aspects of proteasomal activity in human disease and summarize the currently studied therapeutic approaches.
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spelling pubmed-80725762021-04-27 Role of Proteasomes in Inflammation Goetzke, Carl Christoph Ebstein, Frédéric Kallinich, Tilmann J Clin Med Review The ubiquitin–proteasome system (UPS) is involved in multiple cellular functions including the regulation of protein homeostasis, major histocompatibility (MHC) class I antigen processing, cell cycle proliferation and signaling. In humans, proteasome loss-of-function mutations result in autoinflammation dominated by a prominent type I interferon (IFN) gene signature. These genomic alterations typically cause the development of proteasome-associated autoinflammatory syndromes (PRAAS) by impairing proteasome activity and perturbing protein homeostasis. However, an abnormal increased proteasomal activity can also be found in other human inflammatory diseases. In this review, we cast a light on the different clinical aspects of proteasomal activity in human disease and summarize the currently studied therapeutic approaches. MDPI 2021-04-20 /pmc/articles/PMC8072576/ /pubmed/33923887 http://dx.doi.org/10.3390/jcm10081783 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
Goetzke, Carl Christoph
Ebstein, Frédéric
Kallinich, Tilmann
Role of Proteasomes in Inflammation
title Role of Proteasomes in Inflammation
title_full Role of Proteasomes in Inflammation
title_fullStr Role of Proteasomes in Inflammation
title_full_unstemmed Role of Proteasomes in Inflammation
title_short Role of Proteasomes in Inflammation
title_sort role of proteasomes in inflammation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072576/
https://www.ncbi.nlm.nih.gov/pubmed/33923887
http://dx.doi.org/10.3390/jcm10081783
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