Mitochondrial Chaperones in the Brain: Safeguarding Brain Health and Metabolism?

scientific article published on 26 April 2018

Mitochondrial Chaperones in the Brain: Safeguarding Brain Health and Metabolism? is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.3389/FENDO.2018.00196
P932PMC publication ID5932182
P698PubMed publication ID29755410

P50authorAndré KleinriddersQ55164881
José Pedro CastroQ92616183
Tilman GruneQ42577412
P2093author name stringKristina Wardelmann
P2860cites workRole of Protein Aggregation in Mitochondrial Dysfunction and Neurodegeneration in Alzheimer's and Parkinson's DiseasesQ22241397
Characterization of the human HSC20, an unusual DnaJ type III protein, involved in iron–sulfur cluster biogenesisQ24293446
Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assemblyQ24299292
Mitochondria-associated endoplasmic reticulum membrane (MAM) integrity is required for insulin signaling and is implicated in hepatic insulin resistanceQ24299552
The role of oxidative stress in Parkinson's diseaseQ24307946
Disease-causing mutations in parkin impair mitochondrial ubiquitination, aggregation, and HDAC6-dependent mitophagyQ24311582
Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunitQ24337773
Molecular chaperone TRAP1 regulates a metabolic switch between mitochondrial respiration and aerobic glycolysisQ24337960
Molecular chaperones Hsp90 and Hsp70 deliver preproteins to the mitochondrial import receptor Tom70Q24338681
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60Q24563811
A hitchhiker's guide to the human Hsp70 familyQ24597572
Autophagy, mitochondria and oxidative stress: cross-talk and redox signallingQ24608960
Tid1, a cochaperone of the heat shock 70 protein and the mammalian counterpart of the Drosophila tumor suppressor l(2)tid, is critical for early embryonic development and cell survivalQ24629776
SirT3 is a nuclear NAD+-dependent histone deacetylase that translocates to the mitochondria upon cellular stressQ24670578
Metabolic regulation of mitochondrial dynamicsQ26768130
Insulin receptor signaling in normal and insulin-resistant statesQ26823171
Structural and functional analysis of the ligand specificity of the HtrA2/Omi PDZ domainQ27646892
Mitochondrial heat-shock protein hsp60 is essential for assembly of proteins imported into yeast mitochondriaQ27933539
Mitochondrial ClpX Activates a Key Enzyme for Heme Biosynthesis and Erythropoiesis.Q27933616
The molecular chaperone Hsp78 confers compartment-specific thermotolerance to mitochondriaQ27937401
Role of the chaperonin cofactor Hsp10 in protein folding and sorting in yeast mitochondriaQ27938263
Mdj1p, a novel chaperone of the DnaJ family, is involved in mitochondrial biogenesis and protein foldingQ27939869
Protein disaggregation mediated by heat-shock protein Hsp104.Q27940314
Dysregulation of autophagy and mitochondrial function in Parkinson's diseaseQ28071890
Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant miceQ28208193
Brain insulin-like growth factor and neurotrophin resistance in Parkinson's disease and dementia with Lewy bodies: potential role of manganese neurotoxicityQ28394667
Protein misfolding and aggregation in Alzheimer's disease and type 2 diabetes mellitusQ28397425
Neuroprotective role of the Reaper-related serine protease HtrA2/Omi revealed by targeted deletion in miceQ28507648
Measures of striatal insulin resistance in a 6-hydroxydopamine model of Parkinson's diseaseQ37151436
Oxidative stress and insulin resistance: the coronary artery risk development in young adults study.Q37235949
Leptin regulation of Hsp60 impacts hypothalamic insulin signalingQ37259229
Effects of a Mutation in the HSPE1 Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental Disorder.Q37318048
Mitofusin 2 in POMC neurons connects ER stress with leptin resistance and energy imbalance.Q37339111
Mitochondrial dysfunction in SOD1G93A-bearing astrocytes promotes motor neuron degeneration: prevention by mitochondrial-targeted antioxidantsQ37352307
Diabetes mellitus and the risk of Alzheimer's disease: a nationwide population-based studyQ37529582
Mitochondrial dynamics in mammalian health and diseaseQ37543838
Role of mitochondrial dysfunction in the pathogenesis of Huntington's diseaseQ37557789
Mitochondria in Huntington's diseaseQ37580111
Happily (n)ever after: Aging in the context of oxidative stress, proteostasis loss and cellular senescenceQ37581663
Somatic mitochondrial DNA mutations in mammalian agingQ37720726
Mitochondrial proteolytic stress induced by loss of mortalin function is rescued by Parkin and PINK1.Q37726096
Mitochondrial dysfunction, proteotoxicity, and aging: causes or effects, and the possible impact of NAD+-controlled protein glycation.Q37762513
The mitochondrial UPR - protecting organelle protein homeostasisQ37806885
Mitochondrial protein quality control during biogenesis and agingQ37847411
Mitochondrial stress: a bridge between mitochondrial dysfunction and metabolic diseases?Q37880356
Quality control of mitochondrial proteostasisQ37882863
TRAP-1, the mitochondrial Hsp90.Q37924023
Brain energy metabolism: focus on astrocyte-neuron metabolic cooperationQ37966074
Cellular Links between Neuronal Activity and Energy HomeostasisQ37999314
Shared dysregulated pathways lead to Parkinson's disease and diabetesQ38078667
The brain modulates insulin sensitivity in multiple tissuesQ38204663
Mitochondrial dysfunction and mitophagy in Parkinson's: from familial to sporadic diseaseQ38372209
Lipid Biosynthesis Coordinates a Mitochondrial-to-Cytosolic Stress Response.Q38747462
A Mutation in the Flavin Adenine Dinucleotide-Dependent Oxidoreductase FOXRED1 Results in Cell-Type-Specific Assembly Defects in Oxidative Phosphorylation Complexes I and II.Q38769102
A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndromeQ38816704
Modulation of Molecular Chaperones in Huntington's Disease and Other Polyglutamine Disorders.Q38818474
Insulin Receptor Signaling in POMC, but Not AgRP, Neurons Controls Adipose Tissue Insulin ActionQ38849153
Dynamin-Related Protein 1-Dependent Mitochondrial Fission Changes in the Dorsal Vagal Complex Regulate Insulin ActionQ38920715
Mitochondrial Dysfunction and Biogenesis in Neurodegenerative diseases: Pathogenesis and Treatment.Q39016389
Cellular Regulation of Amyloid Formation in Aging and DiseaseQ39162492
Cytochrome c oxidase deficiency accelerates mitochondrial apoptosis by activating ceramide synthase 6.Q39251334
Mitochondrial dysfunction in glial cells: Implications for neuronal homeostasis and survivalQ39401287
Water maze learning and hippocampal synaptic plasticity in streptozotocin-diabetic rats: effects of insulin treatmentQ39472298
Chronic intracerebroventricular infusion of insulin reduces food intake and body weight of baboonsQ39695680
Hsp78 chaperone functions in restoration of mitochondrial network following heat stress.Q50736251
Protein Misfolding Diseases.Q51036364
CLPP deficiency protects against metabolic syndrome but hinders adaptive thermogenesis.Q51758932
Chaperoning extended life.Q52559924
Type 2 diabetes and the risk of Parkinson's disease.Q53016612
Protein folding in mitochondria requires complex formation with hsp60 and ATP hydrolysisQ57073746
Mutational screening of the mortalin gene (HSPA9) in Parkinson's diseaseQ64763346
Selective induction of mitochondrial chaperones in response to loss of the mitochondrial genomeQ71513482
Familial longevity is marked by enhanced insulin sensitivityQ39818313
Decreased expression of the mitochondrial matrix proteases Lon and ClpP in cells from a patient with hereditary spastic paraplegia (SPG13).Q39996799
Mitochondrial heat shock protein (Hsp) 70 and Hsp10 cooperate in the formation of Hsp60 complexesQ40166169
Differential effects of mitochondrial heat shock protein 60 and related molecular chaperones to prevent intracellular beta-amyloid-induced inhibition of complex IV and limit apoptosisQ40248003
Somatic mitochondrial DNA mutations in cortex and substantia nigra in aging and Parkinson's diseaseQ40607421
The relationship between diabetes mellitus and Parkinson's diseaseQ40701172
Novel signal transduction pathway utilized by extracellular HSP70: role of toll-like receptor (TLR) 2 and TLR4.Q40751982
ClpX stimulates the mitochondrial unfolded protein response (UPRmt) in mammalian cellsQ40768669
Endocytosed HSP60s use toll-like receptor 2 (TLR2) and TLR4 to activate the toll/interleukin-1 receptor signaling pathway in innate immune cellsQ40799740
Intrathecal heat shock protein 60 mediates neurodegeneration and demyelination in the CNS through a TLR4- and MyD88-dependent pathwayQ41050313
Dysregulation of parkin in the substantia nigra of db/db and high-fat diet miceQ41206122
Increased oxidative stress and mitochondrial dysfunction in zucker diabetic rat liver and brain.Q41232824
An update on the oxygen stress-mitochondrial mutation theory of aging: genetic and evolutionary implicationsQ41702999
A computational model of motor neuron degenerationQ41826395
Drosophila Trap1 protects against mitochondrial dysfunction in a PINK1/parkin model of Parkinson's disease.Q41892915
Mitochondrial contribution to lipofuscin formation.Q42042230
Brain mitochondrial dysfunction in aging, neurodegeneration and Parkinson's diseaseQ42176073
Inflammatory response of microglial BV-2 cells includes a glycolytic shift and is modulated by mitochondrial glucose-regulated protein 75/mortalinQ43223701
Hypothalamic insulin signaling is required for inhibition of glucose productionQ44212603
Increased risk of type 2 diabetes in Alzheimer diseaseQ44745172
Mitochondrial dysfunction triggered by loss of HtrA2 results in the activation of a brain-specific transcriptional stress responseQ46131495
Higher levels of heat shock proteins in longer-lived mammals and birdsQ46193463
SGLT2-inhibitor and DPP-4 inhibitor improve brain function via attenuating mitochondrial dysfunction, insulin resistance, inflammation, and apoptosis in HFD-induced obese ratsQ46321209
Time course of high-fat diet-induced reductions in adipose tissue mitochondrial proteins: potential mechanisms and the relationship to glucose intoleranceQ46379414
Compartment-specific perturbation of protein handling activates genes encoding mitochondrial chaperonesQ47069260
Activation of the mitochondrial unfolded protein response promotes longevity and dopamine neuron survival in Parkinson's disease modelsQ47160614
Crosstalk between Lysosomes and Mitochondria in Parkinson's DiseaseQ47169769
Role of brain insulin receptor in control of body weight and reproductionQ47229086
Obesity-induced CerS6-dependent C16:0 ceramide production promotes weight gain and glucose intoleranceQ47431942
Mitostasis in Neurons: Maintaining Mitochondria in an Extended Cellular ArchitectureQ47449361
Analysis of HSPA8 and HSPA9 mRNA expression and promoter methylation in the brain and blood of Alzheimer's disease patientsQ47771671
Alfalfa-derived HSP70 administered intranasally improves insulin sensitivity in miceQ47932196
The association between insulin resistance and depression in the Korean general populationQ48037132
Computed tomography and positron emission transaxial tomography evaluations of normal aging and Alzheimer's disease.Q48747176
Hippocampal insulin resistance links maternal obesity with impaired neuronal plasticity in adult offspringQ50088049
Loss of mitochondrial protease ClpP protects mice from diet-induced obesity and insulin resistance.Q50115832
Exercise training and experimental diabetes modulate heat shock protein response in brainQ28583889
Mammalian copper chaperone Cox17p has an essential role in activation of cytochrome C oxidase and embryonic developmentQ28587981
Knockdown of human COX17 affects assembly and supramolecular organization of cytochrome c oxidaseQ28910461
A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicineQ29547303
Mitochondrial formation of reactive oxygen speciesQ29547906
HSP90 at the hub of protein homeostasis: emerging mechanistic insightsQ29616824
Molecular chaperones and protein quality controlQ29617795
Mitochondrial dysfunction and type 2 diabetesQ29617913
Regulation of the heat shock transcriptional response: cross talk between a family of heat shock factors, molecular chaperones, and negative regulatorsQ29618401
High frequency of mitochondrial complex I mutations in Parkinson's disease and agingQ30434711
Parkinson's disease brain mitochondrial complex I has oxidatively damaged subunits and is functionally impaired and misassembled.Q30440422
Neuronal circuitry regulates the response of Caenorhabditis elegans to misfolded proteinsQ30503728
Insulin resistance in brain alters dopamine turnover and causes behavioral disorders.Q30631520
Extended longevity of Caenorhabditis elegans by knocking in extra copies of hsp70F, a homolog of mot-2 (mortalin)/mthsp70/Grp75.Q31048734
The chop gene contains an element for the positive regulation of the mitochondrial unfolded protein responseQ33298588
Hsp90 inhibition decreases mitochondrial protein turnoverQ33303676
Heat shock protein 60: an endogenous inducer of dopaminergic cell death in Parkinson diseaseQ33602136
The accumulation of misfolded proteins in the mitochondrial matrix is sensed by PINK1 to induce PARK2/Parkin-mediated mitophagy of polarized mitochondriaQ33638683
European contribution to the study of ROS: A summary of the findings and prospects for the future from the COST action BM1203 (EU-ROS).Q33761211
Hypothalamic and pituitary c-Jun N-terminal kinase 1 signaling coordinately regulates glucose metabolismQ33778499
Insulin action in brain regulates systemic metabolism and brain functionQ33789365
The impact of dietary energy intake on cognitive agingQ33868403
Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency.Q33921000
Different responses of astrocytes and neurons to nitric oxide: the role of glycolytically generated ATP in astrocyte protection.Q33953141
Deletion of the mitochondrial chaperone TRAP-1 uncovers global reprogramming of metabolic networksQ34022075
Mitochondrial dynamics controlled by mitofusins regulate Agrp neuronal activity and diet-induced obesityQ34080716
A mitochondrial specific stress response in mammalian cellsQ34090940
ERAL1 is associated with mitochondrial ribosome and elimination of ERAL1 leads to mitochondrial dysfunction and growth retardationQ34122622
An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex.Q34123789
The mitochondrial chaperone protein TRAP1 mitigates α-Synuclein toxicityQ34154475
Mitochondrial involvement in brain function and dysfunction: relevance to aging, neurodegenerative disorders and longevityQ34344644
Molecular chaperone functions in protein folding and proteostasisQ34349321
Loss of mitochondrial fission depletes axonal mitochondria in midbrain dopamine neuronsQ34383447
Essential role of TID1 in maintaining mitochondrial membrane potential homogeneity and mitochondrial DNA integrityQ34402031
Absence of BiP co-chaperone DNAJC3 causes diabetes mellitus and multisystemic neurodegenerationQ34451639
CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorderQ34458607
CLPB variants associated with autosomal-recessive mitochondrial disorder with cataract, neutropenia, epilepsy, and methylglutaconic aciduriaQ34458614
The biology of proteostasis in aging and diseaseQ34467650
TRAP1 controls mitochondrial fusion/fission balance through Drp1 and Mff expressionQ34532535
Hsp90 functions in the targeting and outer membrane translocation steps of Tom70-mediated mitochondrial importQ34565583
Metabolism regulates the spontaneous firing of substantia nigra pars reticulata neurons via KATP and nonselective cation channelsQ34614572
Ageing and diabetes: implications for brain functionQ34635793
Oxidative stress and the etiology of insulin resistance and type 2 diabetesQ34768229
Diabetes and the risk of developing Parkinson's disease in Denmark.Q35043736
Reduced levels of Hspa9 attenuate Stat5 activation in mouse B cellsQ35220373
Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria.Q35544534
Stimulatory effect of insulin on glucose uptake by muscle involves the central nervous system in insulin-sensitive miceQ35561118
The small Tim proteins and the twin Cx3C motifQ35632006
Cerebral metabolic and cognitive decline in persons at genetic risk for Alzheimer's diseaseQ35758632
Type 2 diabetes as a protein misfolding disease.Q35822682
Metabolic alterations induced by sucrose intake and Alzheimer's disease promote similar brain mitochondrial abnormalitiesQ35902875
The groES and groEL heat shock gene products of Escherichia coli are essential for bacterial growth at all temperaturesQ36174913
Regulation of the cellular heat shock response in Caenorhabditis elegans by thermosensory neuronsQ36194343
Loss of prohibitin membrane scaffolds impairs mitochondrial architecture and leads to tau hyperphosphorylation and neurodegenerationQ36384373
SIRT3 functions in the nucleus in the control of stress-related gene expressionQ36435193
Quality control of mitochondria: protection against neurodegeneration and ageingQ36446844
Glial cell inhibition of neurons by release of ATPQ36569710
Oxidative stress, insulin signaling, and diabetes.Q36570342
Central insulin action regulates peripheral glucose and fat metabolism in miceQ36597490
The mTOR pathway in the control of protein synthesisQ36600753
Hippocampal hypometabolism predicts cognitive decline from normal agingQ36725261
Mitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophyQ36744667
Role for neuronal insulin resistance in neurodegenerative diseasesQ36853917
Mitonuclear protein imbalance as a conserved longevity mechanismQ36873369
Maintenance and propagation of a deleterious mitochondrial genome by the mitochondrial unfolded protein responseQ36917773
TRAP1 rescues PINK1 loss-of-function phenotypesQ36950677
Mitochondrial Stress Induces Chromatin Reorganization to Promote Longevity and UPR(mt).Q36956834
Brain mitochondrial dysfunction in agingQ37141862
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P921main subjectmolecular chaperonesQ422496
P304page(s)196
P577publication date2018-04-26
P1433published inFrontiers in EndocrinologyQ27723680
P1476titleMitochondrial Chaperones in the Brain: Safeguarding Brain Health and Metabolism?
P478volume9

Reverse relations

cites work (P2860)
Q90632658Hsp90 and Its Co-Chaperones in Neurodegenerative Diseases
Q64246566Insulin action in the brain regulates mitochondrial stress responses and reduces diet-induced weight gain
Q100533628Modeling alcohol-induced neurotoxicity using human induced pluripotent stem cell-derived three-dimensional cerebral organoids

Search more.