Control of immune cell function by the unfolded protein response.

Détails

ID Serval
serval:BIB_84EB04B67D6F
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Control of immune cell function by the unfolded protein response.
Périodique
Nature reviews. Immunology
Auteur⸱e⸱s
Di Conza G., Ho P.C., Cubillos-Ruiz J.R., Huang S.C.
ISSN
1474-1741 (Electronic)
ISSN-L
1474-1733
Statut éditorial
Publié
Date de publication
09/2023
Peer-reviewed
Oui
Volume
23
Numéro
9
Pages
546-562
Langue
anglais
Notes
Publication types: Journal Article ; Review ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
Publication Status: ppublish
Résumé
Initiating and maintaining optimal immune responses requires high levels of protein synthesis, folding, modification and trafficking in leukocytes, which are processes orchestrated by the endoplasmic reticulum. Importantly, diverse extracellular and intracellular conditions can compromise the protein-handling capacity of this organelle, inducing a state of 'endoplasmic reticulum stress' that activates the unfolded protein response (UPR). Emerging evidence shows that physiological or pathological activation of the UPR can have effects on immune cell survival, metabolism, function and fate. In this Review, we discuss the canonical role of the adaptive UPR in immune cells and how dysregulation of this pathway in leukocytes contributes to diverse pathologies such as cancer, autoimmunity and metabolic disorders. Furthermore, we provide an overview as to how pharmacological approaches that modulate the UPR could be harnessed to control or activate immune cell function in disease.
Mots-clé
Humans, Unfolded Protein Response, Endoplasmic Reticulum Stress, Neoplasms/pathology, Immunity, Endoplasmic Reticulum/metabolism
Pubmed
Web of science
Création de la notice
03/03/2023 15:21
Dernière modification de la notice
24/10/2023 7:09
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