Endoplasmic reticulum stress signalling – from basic mechanisms to clinical applications

Author:

Almanza Aitor1,Carlesso Antonio2,Chintha Chetan1,Creedican Stuart3,Doultsinos Dimitrios45,Leuzzi Brian1,Luís Andreia6,McCarthy Nicole7,Montibeller Luigi8,More Sanket9,Papaioannou Alexandra45,Püschel Franziska10,Sassano Maria Livia9,Skoko Josip11,Agostinis Patrizia9,de Belleroche Jackie8,Eriksson Leif A.2,Fulda Simone7,Gorman Adrienne M.1ORCID,Healy Sandra1,Kozlov Andrey6,Muñoz‐Pinedo Cristina10ORCID,Rehm Markus11,Chevet Eric45ORCID,Samali Afshin1

Affiliation:

1. Apoptosis Research Centre National University of Ireland Galway Ireland

2. Department of Chemistry and Molecular Biology University of Gothenburg Göteborg Sweden

3. Randox Teoranta Dungloe County Donegal Ireland

4. INSERM U1242 University of Rennes France

5. Centre de Lutte Contre le Cancer Eugène Marquis Rennes France

6. Ludwig Boltzmann Institute for Experimental and Clinical Traumatology AUVA Research Centre Vienna Austria

7. Institute for Experimental Cancer Research in Paediatrics Goethe‐University Frankfurt Germany

8. Neurogenetics Group Division of Brain Sciences Faculty of Medicine Imperial College London UK

9. Department Cellular and Molecular Medicine Laboratory of Cell Death and Therapy KU Leuven Belgium

10. Cell Death Regulation Group Oncobell Program Bellvitge Biomedical Research Institute (IDIBELL) Barcelona Spain

11. Institute of Cell Biology and Immunology University of Stuttgart Germany

Abstract

The endoplasmic reticulum (ER) is a membranous intracellular organelle and the first compartment of the secretory pathway. As such, the ER contributes to the production and folding of approximately one‐third of cellular proteins, and is thus inextricably linked to the maintenance of cellular homeostasis and the fine balance between health and disease. Specific ER stress signalling pathways, collectively known as the unfolded protein response (UPR), are required for maintaining ER homeostasis. The UPR is triggered when ER protein folding capacity is overwhelmed by cellular demand and the UPR initially aims to restore ER homeostasis and normal cellular functions. However, if this fails, then the UPR triggers cell death. In this review, we provide a UPR signalling‐centric view of ER functions, from the ER's discovery to the latest advancements in the understanding of ER and UPR biology. Our review provides a synthesis of intracellular ER signalling revolving around proteostasis and the UPR, its impact on other organelles and cellular behaviour, its multifaceted and dynamic response to stress and its role in physiology, before finally exploring the potential exploitation of this knowledge to tackle unresolved biological questions and address unmet biomedical needs. Thus, we provide an integrated and global view of existing literature on ER signalling pathways and their use for therapeutic purposes.

Funder

Erzincan Üniversitesi

Federación Española de Enfermedades Raras

Ministerio de Economía y Competitividad

Publisher

Wiley

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