Literature DB >> 17896870

How transmembrane proteins sense endoplasmic reticulum stress.

Kenji Kohno1.   

Abstract

The unfolded protein response (UPR) is an adaptive stress response in which cells recover from the accumulation of unfolded or misfolded proteins in the endoplasmic reticulum (ER) by increasing its protein-folding capacity. The IRE1 pathway in the UPR is evolutionarily conserved from yeast to human, and two other pathways involving PERK and ATF6 have also evolved in higher eukaryotes. These three intracellular signaling pathways originate in the ER lumen, where unfolded or misfolded proteins are recognized by the three transmembrane ER stress sensors IRE1, PERK, and ATF6. This review focuses on current progress with efforts to elucidate how stress sensors recognize the accumulation of unfolded proteins.

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Year:  2007        PMID: 17896870     DOI: 10.1089/ars.2007.1819

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  32 in total

Review 1.  The UPR and cell fate at a glance.

Authors:  Philip I Merksamer; Feroz R Papa
Journal:  J Cell Sci       Date:  2010-04-01       Impact factor: 5.285

2.  Total and mitochondrial nitrosative stress, decreased brain-derived neurotrophic factor (BDNF) levels and glutamate uptake, and evidence of endoplasmic reticulum stress in the hippocampus of vitamin A-treated rats.

Authors:  Marcos Roberto de Oliveira; Ricardo Fagundes da Rocha; Laura Stertz; Gabriel Rodrigo Fries; Diogo Losch de Oliveira; Flávio Kapczinski; José Cláudio Fonseca Moreira
Journal:  Neurochem Res       Date:  2010-12-28       Impact factor: 3.996

Review 3.  The role of the unfolded protein response in the heart.

Authors:  Christopher C Glembotski
Journal:  J Mol Cell Cardiol       Date:  2007-12-03       Impact factor: 5.000

4.  Mutual cross talk between the regulators Hac1 of the unfolded protein response and Gcn4 of the general amino acid control of Saccharomyces cerevisiae.

Authors:  Britta Herzog; Blagovesta Popova; Antonia Jakobshagen; Hedieh Shahpasandzadeh; Gerhard H Braus
Journal:  Eukaryot Cell       Date:  2013-06-21

5.  CREB3L1 is a metastasis suppressor that represses expression of genes regulating metastasis, invasion, and angiogenesis.

Authors:  Paul Mellor; Leah Deibert; Brian Calvert; Keith Bonham; Svein A Carlsen; Deborah H Anderson
Journal:  Mol Cell Biol       Date:  2013-10-14       Impact factor: 4.272

6.  4-Phenylbutyric acid protects against vasculitic peripheral neuropathy induced by ischaemia-reperfusion through attenuating endoplasmic reticulum stress.

Authors:  Cay-Huyen Chen; Ping-Chen Shih; Han-Yu Lin; Po-Kai Wang; Po-Ting Pan; Ching-Wei Chuang; Ming-Chang Kao
Journal:  Inflammopharmacology       Date:  2019-05-22       Impact factor: 4.473

7.  Heat shock transcriptional factor mediates mitochondrial unfolded protein response.

Authors:  Naoki Koike; Yuuki Hatano; Takashi Ushimaru
Journal:  Curr Genet       Date:  2018-02-08       Impact factor: 3.886

Review 8.  ER stress and unfolded protein response in amyotrophic lateral sclerosis.

Authors:  Kohsuke Kanekura; Hiroaki Suzuki; Sadakazu Aiso; Masaaki Matsuoka
Journal:  Mol Neurobiol       Date:  2009-01-30       Impact factor: 5.590

9.  N-acetylcysteine protects against cadmium-induced germ cell apoptosis by inhibiting endoplasmic reticulum stress in testes.

Authors:  Yan-Li Ji; Hua Wang; Cheng Zhang; Ying Zhang; Mei Zhao; Yuan-Hua Chen; De-Xiang Xu
Journal:  Asian J Androl       Date:  2013-01-28       Impact factor: 3.285

10.  Cryptosporidium parvum induces an endoplasmic stress response in the intestinal adenocarcinoma HCT-8 cell line.

Authors:  Mary Morada; Lakhsmi Pendyala; Gang Wu; Salim Merali; Nigel Yarlett
Journal:  J Biol Chem       Date:  2013-08-28       Impact factor: 5.157

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