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      Endoplasmic Reticulum Malfunction in the Nervous System

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          Abstract

          Neurodegenerative diseases often have multifactorial causes and are progressive diseases. Some are inherited while others are acquired, and both vary greatly in onset and severity. Impaired endoplasmic reticulum (ER) proteostasis, involving Ca 2+ signaling, protein synthesis, processing, trafficking, and degradation, is now recognized as a key risk factor in the pathogenesis of neurological disorders. Lipidostasis involves lipid synthesis, quality control, membrane assembly as well as sequestration of excess lipids or degradation of damaged lipids. Proteostasis and lipidostasis are maintained by interconnected pathways within the cellular reticular network, which includes the ER and Ca 2+ signaling. Importantly, lipidostasis is important in the maintenance of membranes and luminal environment that enable optimal protein processing. Accumulating evidence suggest that the loss of coordinate regulation of proteostasis and lipidostasis has a direct and negative impact on the health of the nervous system.

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          Most cited references73

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          The endoplasmic reticulum: structure, function and response to cellular signaling

          The endoplasmic reticulum (ER) is a large, dynamic structure that serves many roles in the cell including calcium storage, protein synthesis and lipid metabolism. The diverse functions of the ER are performed by distinct domains; consisting of tubules, sheets and the nuclear envelope. Several proteins that contribute to the overall architecture and dynamics of the ER have been identified, but many questions remain as to how the ER changes shape in response to cellular cues, cell type, cell cycle state and during development of the organism. Here we discuss what is known about the dynamics of the ER, what questions remain, and how coordinated responses add to the layers of regulation in this dynamic organelle.
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            Disturbance of endoplasmic reticulum proteostasis in neurodegenerative diseases.

            The unfolded protein response (UPR) is a homeostatic mechanism by which cells regulate levels of misfolded proteins in the endoplasmic reticulum (ER). Although it is well characterized in non-neuronal cells, a proliferation of papers over the past few years has revealed a key role for the UPR in normal neuronal function and as an important driver of neurodegenerative diseases. A complex scenario is emerging in which distinct UPR signalling modules have specific and even opposite effects on neurodegeneration depending on the disease context. Here, we provide an overview of the most recent findings addressing the biological relevance of ER stress in the nervous system.
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              STIM proteins: dynamic calcium signal transducers.

              Stromal interaction molecule (STIM) proteins function in cells as dynamic coordinators of cellular calcium (Ca(2+)) signals. Spanning the endoplasmic reticulum (ER) membrane, they sense tiny changes in the levels of Ca(2+) stored within the ER lumen. As ER Ca(2+) is released to generate primary Ca(2+) signals, STIM proteins undergo an intricate activation reaction and rapidly translocate into junctions formed between the ER and the plasma membrane. There, STIM proteins tether and activate the highly Ca(2+)-selective Orai channels to mediate finely controlled Ca(2+) signals and to homeostatically balance cellular Ca(2+). Details are emerging on the remarkable organization within these STIM-induced junctional microdomains and the identification of new regulators and alternative target proteins for STIM.
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                Author and article information

                Contributors
                Journal
                Front Neurosci
                Front Neurosci
                Front. Neurosci.
                Frontiers in Neuroscience
                Frontiers Media S.A.
                1662-4548
                1662-453X
                25 April 2017
                2017
                : 11
                : 220
                Affiliations
                [1] 1Department of Biochemistry, University of Alberta Edmonton, AB, Canada
                [2] 2School of Dietetics and Human Nutrition, McGill University Ste. Anne de Bellevue, QC, Canada
                Author notes

                Edited by: Cintia Roodveldt, Centro Andaluz de Biología Molecular y Medicina Regenerativa, Spain

                Reviewed by: Clara Penas, Autonomous University of Barcelona, Spain; Robert Petersen, Case Western Reserve University, USA; Gaiti Hasan, National Centre for Biological Sciences, India

                *Correspondence: Luis B. Agellon luis.agellon@ 123456mcgill.ca

                This article was submitted to Neurodegeneration, a section of the journal Frontiers in Neuroscience

                Article
                10.3389/fnins.2017.00220
                5403925
                28487627
                ce16ece9-7a12-471d-b738-5e4770738faf
                Copyright © 2017 Jung, Michalak and Agellon.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 24 January 2017
                : 31 March 2017
                Page count
                Figures: 1, Tables: 0, Equations: 0, References: 97, Pages: 7, Words: 6151
                Funding
                Funded by: Canadian Institutes of Health Research 10.13039/501100000024
                Award ID: MOP-15291
                Award ID: MOP-15415
                Award ID: MOP-53050
                Award ID: MOP-86750
                Categories
                Neuroscience
                Perspective

                Neurosciences
                calnexin,proteostasis,endoplasmic reticulum,lipidostasis,neurological disorders
                Neurosciences
                calnexin, proteostasis, endoplasmic reticulum, lipidostasis, neurological disorders

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