84
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      The integrated stress response

      review-article

      Read this article at

      ScienceOpenPublisherPMC
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          In response to diverse stress stimuli, eukaryotic cells activate a common adaptive pathway, termed the integrated stress response ( ISR), to restore cellular homeostasis. The core event in this pathway is the phosphorylation of eukaryotic translation initiation factor 2 alpha ( eIF2α) by one of four members of the eIF2α kinase family, which leads to a decrease in global protein synthesis and the induction of selected genes, including the transcription factor ATF4, that together promote cellular recovery. The gene expression program activated by the ISR optimizes the cellular response to stress and is dependent on the cellular context, as well as on the nature and intensity of the stress stimuli. Although the ISR is primarily a pro‐survival, homeostatic program, exposure to severe stress can drive signaling toward cell death. Here, we review current understanding of the ISR signaling and how it regulates cell fate under diverse types of stress.

          Related collections

          Most cited references212

          • Record: found
          • Abstract: found
          • Article: not found

          Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response.

          PERK and IRE1 are type-I transmembrane protein kinases that reside in the endoplasmic reticulum (ER) and transmit stress signals in response to perturbation of protein folding. Here we show that the lumenal domains of these two proteins are functionally interchangeable in mediating an ER stress response and that, in unstressed cells, both lumenal domains form a stable complex with the ER chaperone BiP. Perturbation of protein folding promotes reversible dissociation of BiP from the lumenal domains of PERK and IRE1. Loss of BiP correlates with the formation of high-molecular-mass complexes of activated PERK or IRE1, and overexpression of BiP attenuates their activation. These findings are consistent with a model in which BiP represses signalling through PERK and IRE1 and protein misfolding relieves this repression by effecting the release of BiP from the PERK and IRE1 lumenal domains.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Protein misfolding in the endoplasmic reticulum as a conduit to human disease.

            In eukaryotic cells, the endoplasmic reticulum is essential for the folding and trafficking of proteins that enter the secretory pathway. Environmental insults or increased protein synthesis often lead to protein misfolding in the organelle, the accumulation of misfolded or unfolded proteins - known as endoplasmic reticulum stress - and the activation of the adaptive unfolded protein response to restore homeostasis. If protein misfolding is not resolved, cells die. Endoplasmic reticulum stress and activation of the unfolded protein response help to determine cell fate and function. Furthermore, endoplasmic reticulum stress contributes to the aetiology of many human diseases.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              The biology of proteostasis in aging and disease.

              Loss of protein homeostasis (proteostasis) is a common feature of aging and disease that is characterized by the appearance of nonnative protein aggregates in various tissues. Protein aggregation is routinely suppressed by the proteostasis network (PN), a collection of macromolecular machines that operate in diverse ways to maintain proteome integrity across subcellular compartments and between tissues to ensure a healthy life span. Here, we review the composition, function, and organizational properties of the PN in the context of individual cells and entire organisms and discuss the mechanisms by which disruption of the PN, and related stress response pathways, contributes to the initiation and progression of disease. We explore emerging evidence that disease susceptibility arises from early changes in the composition and activity of the PN and propose that a more complete understanding of the temporal and spatial properties of the PN will enhance our ability to develop effective treatments for protein conformational diseases.
                Bookmark

                Author and article information

                Contributors
                adrienne.gorman@nuigalway.ie
                Journal
                EMBO Rep
                EMBO Rep
                10.1002/(ISSN)1469-3178
                EMBR
                embor
                EMBO Reports
                John Wiley and Sons Inc. (Hoboken )
                1469-221X
                1469-3178
                14 September 2016
                October 2016
                : 17
                : 10 ( doiID: 10.1002/embr.v17.10 )
                : 1374-1395
                Affiliations
                [ 1 ] Apoptosis Research Centre National University of Ireland Galway Galway Ireland
                [ 2 ] School of Natural Sciences National University of Ireland Galway Galway Ireland
                Author notes
                [*] [* ]Corresponding author. Tel: +353 91 492417; E‐mail: adrienne.gorman@ 123456nuigalway.ie
                [†]

                These authors contributed equally to this work

                Author information
                http://orcid.org/0000-0002-8610-8375
                http://orcid.org/0000-0002-6068-0058
                Article
                PMC5048378 PMC5048378 5048378 EMBR201642195
                10.15252/embr.201642195
                5048378
                27629041
                faec55c2-d85e-490c-b126-c40fb91cc84b
                © 2016 The Authors
                History
                : 12 February 2016
                : 03 August 2016
                : 23 August 2016
                Page count
                Figures: 4, Tables: 2, Pages: 22, Words: 21611
                Funding
                Funded by: Health Research Board
                Award ID: HRA/2009/59
                Award ID: HRA‐POR‐2014‐643
                Funded by: Belgian Science Policy Office Interuniversity Attraction Poles program
                Award ID: IAP 7/32
                Funded by: Breast Cancer Campaign
                Award ID: 2010NovPR13
                Funded by: Science Foundation Ireland (SFI)
                Award ID: 13/RC/2073
                Funded by: Irish Research Council
                Award ID: GOIPG/2014/508
                Award ID: GOIPD/2014/53
                Funded by: Thomas Crawford Hayes Fund
                Categories
                Review
                Review
                Custom metadata
                2.0
                embr201642195
                October 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.4 mode:remove_FC converted:04.10.2016

                activating transcription factor 4,Signal Transduction,Autophagy & Cell Death,integrated stress response,eukaryotic translation initiation factor 2 alpha, eIF2α kinase

                Comments

                Comment on this article