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PERK signaling promotes mitochondrial elongation by remodeling membrane phosphatidic acid

https://doi.org/10.15252/embj.2023113908

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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PERK inhibition prevents tau-mediated neurodegeneration in a mouse model of frontotemporal dementia

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Mitochondria-Associated Membranes (MAMs): Overview and Its Role in Parkinson’s Disease

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The Endoplasmic Reticulum Stress Response in Neuroprogressive Diseases: Emerging Pathophysiological Role and Translational Implications

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Regulation of dynamin family proteins by post-translational modifications

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Intramitochondrial phospholipid trafficking

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Mitochondrial dynamics: Shaping and remodeling an organelle network

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The PERK Arm of the Unfolded Protein Response Regulates Mitochondrial Morphology during Acute Endoplasmic Reticulum Stress

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Stress-Regulated Translational Attenuation Adapts Mitochondrial Protein Import through Tim17A Degradation

inferredcites →https://doi.org/10.1016/j.cmet.2021.01.013openalex-snapshot

A cold-stress-inducible PERK/OGT axis controls TOM70-assisted mitochondrial protein import and cristae formation

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Mitochondria-associated ER membranes in Alzheimer disease

inferredcites →https://doi.org/10.1016/j.molcel.2016.08.013openalex-snapshot

Coincident Phosphatidic Acid Interaction Restrains Drp1 in Mitochondrial Division

inferredcites →https://doi.org/10.1016/j.molcel.2017.06.017openalex-snapshot

The Unfolded Protein Response and Cell Fate Control

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mTOR Controls Mitochondrial Dynamics and Cell Survival via MTFP1

inferredcites →https://doi.org/10.1016/j.molcel.2019.03.031openalex-snapshot

ER and Nutrient Stress Promote Assembly of Respiratory Chain Supercomplexes through the PERK-eIF2α Axis

inferredcites →https://doi.org/10.1016/j.molcel.2021.09.015openalex-snapshot

Proteome-wide mapping of short-lived proteins in human cells

inferredcites →https://doi.org/10.1016/j.tcb.2017.08.011openalex-snapshot

Phosphatidic Acid and Cardiolipin Coordinate Mitochondrial Dynamics

inferredcites →https://doi.org/10.1016/j.tcb.2018.02.009openalex-snapshot

Endoplasmic Reticulum–Mitochondrial Contactology: Structure and Signaling Functions

inferredcites →https://doi.org/10.1016/j.tem.2014.06.007openalex-snapshot

Stress-responsive regulation of mitochondria through the ER unfolded protein response

inferredcites →https://doi.org/10.1016/j.tem.2019.08.003openalex-snapshot

ER Stress Priming of Mitochondrial Respiratory suPERKomplex Assembly

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Mitochondria and T2D: Role of Autophagy, ER Stress, and Inflammasome

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Cardiolipin, Mitochondria, and Neurological Disease

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A PERKy way to make mitochondrial cristae

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Reciprocal Regulation of Mitochondrial Fission and Fusion

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PERKing up the ER stress response

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Perk Is Essential for Translational Regulation and Cell Survival during the Unfolded Protein Response

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An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative Stress

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One Step Forward for Reducing False Positive and False Negative Compound Identifications from Mass Spectrometry Metabolomics Data: New Algorithms for Constructing Extracted Ion Chromatograms and Detecting Chromatographic Peaks

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Discovery of GSK2656157: An Optimized PERK Inhibitor Selected for Preclinical Development

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Mutation of the mouse klotho gene leads to a syndrome resembling ageing.

inferredcites →https://doi.org/10.1038/78085openalex-snapshot

EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome

inferredcites →https://doi.org/10.1038/cdd.2012.74openalex-snapshot

PERK is required at the ER-mitochondrial contact sites to convey apoptosis after ROS-based ER stress

inferredcites →https://doi.org/10.1038/cddis.2015.49openalex-snapshot

Partial restoration of protein synthesis rates by the small molecule ISRIB prevents neurodegeneration without pancreatic toxicity

inferredcites →https://doi.org/10.1038/emboj.2009.89openalex-snapshot

SLP‐2 is required for stress‐induced mitochondrial hyperfusion

inferredcites →https://doi.org/10.1038/emboj.2010.169openalex-snapshot

Regulation of mitochondrial phospholipids by Ups1/PRELI‐like proteins depends on proteolysis and Mdm35

inferredcites →https://doi.org/10.1038/emboj.2012.202openalex-snapshot

Upregulated function of mitochondria‐associated ER membranes in Alzheimer disease

inferredcites →https://doi.org/10.1038/emboj.2012.279openalex-snapshot

Close encounter: mitochondria, endoplasmic reticulum and Alzheimer's disease

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Sustained translational repression by eIF2α-P mediates prion neurodegeneration

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A cross-platform toolkit for mass spectrometry and proteomics

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During autophagy mitochondria elongate, are spared from degradation and sustain cell viability

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ER-stress-induced transcriptional regulation increases protein synthesis leading to cell death

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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

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Lipid signalling drives proteolytic rewiring of mitochondria by YME1L

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Phosphatidic Acid (PA)-preferring Phospholipase A1 Regulates Mitochondrial Dynamics

inferredcites →https://doi.org/10.1074/jbc.m607279200openalex-snapshot

Mitotic Phosphorylation of Dynamin-related GTPase Drp1 Participates in Mitochondrial Fission

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Transmission of cell stress from endoplasmic reticulum to mitochondria

inferredcites →https://doi.org/10.1083/jcb.201404050openalex-snapshot

Transient assembly of F-actin on the outer mitochondrial membrane contributes to mitochondrial fission

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Metabolic regulation of mitochondrial dynamics

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Phospholipid ebb and flow makes mitochondria go

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Parkin-independent mitophagy via Drp1-mediated outer membrane severing and inner membrane ubiquitination

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The modified mitochondrial outer membrane carrier MTCH2 links mitochondrial fusion to lipogenesis

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Quantifying organellar ultrastructure in cryo-electron tomography using a surface morphometrics pipeline

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The unfolded protein response: mechanisms and therapy of neurodegeneration

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Repurposed drugs targeting eIF2α-P-mediated translational repression prevent neurodegeneration in mice

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Tauopathy-Associated PERK Alleles are Functional Hypomorphs that Increase Neuronal Vulnerability to ER Stress

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Cell death induced by endoplasmic reticulum stress

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The unfolded protein response in neurodegenerative disorders – therapeutic modulation of the PERK pathway

inferredcites →https://doi.org/10.1111/jnc.14112openalex-snapshot

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inferredcites →https://doi.org/10.1128/mcb.00063-12openalex-snapshot

PERK Utilizes Intrinsic Lipid Kinase Activity To Generate Phosphatidic Acid, Mediate Akt Activation, and Promote Adipocyte Differentiation

inferredcites →https://doi.org/10.1139/o59-099openalex-snapshot

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

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Mitochondrial Dynamics and Its Involvement in Disease

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MZmine 2: Modular framework for processing, visualizing, and analyzing mass spectrometry-based molecular profile data

inferredcites →https://doi.org/10.1186/2051-5960-1-31openalex-snapshot

The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer’s disease

inferredcites →https://doi.org/10.1242/jcs.157321openalex-snapshot

MFN1 deacetylation activates adaptive mitochondrial fusion and protects metabolically challenged mitochondria

inferredcites →https://doi.org/10.1371/journal.pone.0004170openalex-snapshot

Divergent Effects of PERK and IRE1 Signaling on Cell Viability

inferredcites →https://doi.org/10.1515/hsz-2013-0174openalex-snapshot

Stressed to death – mechanisms of ER stress-induced cell death

inferredcites →https://doi.org/10.1515/hsz-2020-0121openalex-snapshot

Lipid homeostasis in mitochondria

inferredcites →https://doi.org/10.15252/embj.2023113908openalex-snapshot

PERK signaling promotes mitochondrial elongation by remodeling membrane phosphatidic acid

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PERK-opathies: An Endoplasmic Reticulum Stress Mechanism Underlying Neurodegeneration

inferredcites →https://doi.org/10.26508/lsa.201900576openalex-snapshot

ER-resident sensor PERK is essential for mitochondrial thermogenesis in brown adipose tissue

inferredcites →https://doi.org/10.3389/fphys.2012.00263openalex-snapshot

The endoplasmic reticulum stress response in aging and age-related diseases

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Role for the Unfolded Protein Response in Heart Disease and Cardiac Arrhythmias

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Essential amino acids and glutamine regulate induction of mitochondrial elongation during autophagy

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Pharmacological brake-release of mRNA translation enhances cognitive memory

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Actin filaments target the oligomeric maturation of the dynamin GTPase Drp1 to mitochondrial fission sites

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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