Literature DB >> 24227223

Role of the unfolded protein response in organ physiology: lessons from mouse models.

Víctor Hugo Cornejo1, Philippe Pihán, René Luis Vidal, Claudio Hetz.   

Abstract

The endoplasmic reticulum (ER) is a key subcellular compartment involved in the folding and maturation of around one-third of the total proteome. Accumulation of misfolded proteins in the ER lumen engages a signal transduction pathway known as unfolded protein response (UPR) that feedback to recover ER homeostasis or to trigger apoptosis of irreversible damaged cells. The UPR is initiated by three main stress sensors including protein kinase RNA-like ER kinase (PERK), activating transcription factor 6 (ATF6), and inositol-requiring protein 1α (IRE1α), which reprogram the genome through the control of downstream transcription factors. In this article, the authors have reviewed most relevant studies uncovering the physiological function of the UPR in different organs and tissues based on the phenotypes observed after genetic manipulation of the pathway in vivo. Biomedical applications of targeting the UPR on a disease context are also discussed.
© 2013 IUBMB.

Entities:  

Keywords:  ER stress; mouse model; protein misfolding; secretory cells; unfolded protein response

Mesh:

Substances:

Year:  2013        PMID: 24227223     DOI: 10.1002/iub.1224

Source DB:  PubMed          Journal:  IUBMB Life        ISSN: 1521-6543            Impact factor:   3.885


  28 in total

Review 1.  Oxidative stress, unfolded protein response, and apoptosis in developmental toxicity.

Authors:  Allison Kupsco; Daniel Schlenk
Journal:  Int Rev Cell Mol Biol       Date:  2015-03-11       Impact factor: 6.813

Review 2.  ER stress and the unfolded protein response in neurodegeneration.

Authors:  Claudio Hetz; Smita Saxena
Journal:  Nat Rev Neurol       Date:  2017-07-21       Impact factor: 42.937

3.  Control of dopaminergic neuron survival by the unfolded protein response transcription factor XBP1.

Authors:  Pamela Valdés; Gabriela Mercado; Rene L Vidal; Claudia Molina; Geoffrey Parsons; Felipe A Court; Alexis Martinez; Danny Galleguillos; Donna Armentano; Bernard L Schneider; Claudio Hetz
Journal:  Proc Natl Acad Sci U S A       Date:  2014-04-21       Impact factor: 11.205

4.  Protein homeostasis: Modeling UPR adaptive responses.

Authors:  Danilo B Medinas; Claudio Hetz
Journal:  Nat Chem Biol       Date:  2014-11       Impact factor: 15.040

Review 5.  Unfolded Protein Response as a Therapeutic Target in Cardiovascular Disease.

Authors:  Guangyu Zhang; Xiaoding Wang; Thomas G Gillette; Yingfeng Deng; Zhao V Wang
Journal:  Curr Top Med Chem       Date:  2019       Impact factor: 3.295

6.  Recovery from temporary endoplasmic reticulum stress in plants relies on the tissue-specific and largely independent roles of bZIP28 and bZIP60, as well as an antagonizing function of BAX-Inhibitor 1 upon the pro-adaptive signaling mediated by bZIP28.

Authors:  Cristina Ruberti; YaShiuan Lai; Federica Brandizzi
Journal:  Plant J       Date:  2017-12-02       Impact factor: 6.417

7.  Targeting the unfolded protein response in heart diseases.

Authors:  Man Liu; Samuel C Dudley
Journal:  Expert Opin Ther Targets       Date:  2014-05-28       Impact factor: 6.902

Review 8.  Disturbance of endoplasmic reticulum proteostasis in neurodegenerative diseases.

Authors:  Claudio Hetz; Bertrand Mollereau
Journal:  Nat Rev Neurosci       Date:  2014-03-12       Impact factor: 34.870

Review 9.  Gene Therapy Strategies to Restore ER Proteostasis in Disease.

Authors:  Vicente Valenzuela; Kasey L Jackson; Sergio P Sardi; Claudio Hetz
Journal:  Mol Ther       Date:  2018-04-07       Impact factor: 11.454

10.  Activating transcription factor 4 underlies the pathogenesis of arsenic trioxide-mediated impairment of macrophage innate immune functions.

Authors:  Ritesh K Srivastava; Changzhao Li; Yong Wang; Zhiping Weng; Craig A Elmets; Kevin S Harrod; Jessy S Deshane; Mohammad Athar
Journal:  Toxicol Appl Pharmacol       Date:  2016-07-25       Impact factor: 4.219

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