Endocytic vesicle rupture is a conserved mechanism of cellular invasion by amyloid proteins

scientific article published on 19 May 2017

Endocytic vesicle rupture is a conserved mechanism of cellular invasion by amyloid proteins is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1085444184
P356DOI10.1007/S00401-017-1722-X
P698PubMed publication ID28527044

P50authorJeffrey H KordowerQ67168846
Ronald MelkiQ30123639
P2093author name stringEdward M Campbell
Luc Bousset
Yaping Chu
Michael J Chaney
Stratos Skarpathiotis
William P Flavin
Zachary C Green
P2860cites workTracking the dynamic interplay between bacterial and host factors during pathogen-induced vacuole rupture in real timeQ48827027
Lysosomal membrane permeabilization in Parkinson diseaseQ57245740
Galectin 8 targets damaged vesicles for autophagy to defend cells against bacterial invasionQ24301905
Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathiesQ24307627
α-Synuclein propagates from mouse brain to grafted dopaminergic neurons and seeds aggregation in cultured human cellsQ24633663
Transmission and spreading of tauopathy in transgenic mouse brainQ24651334
Inclusion formation and neuronal cell death through neuron-to-neuron transmission of alpha-synucleinQ24655848
Cytoplasmic penetration and persistent infection of mammalian cells by polyglutamine aggregatesQ24657543
Self-propagation of pathogenic protein aggregates in neurodegenerative diseasesQ26996441
Autophagy in the regulation of pathogen replication and adaptive immunityQ27023949
Alpha-Synuclein Induces Lysosomal Rupture and Cathepsin Dependent Reactive Oxygen Species Following EndocytosisQ27323098
Mutation in the alpha-synuclein gene identified in families with Parkinson's diseaseQ27860459
Exogenous induction of cerebral beta-amyloidogenesis is governed by agent and hostQ28264821
Lewy body-like pathology in long-term embryonic nigral transplants in Parkinson's diseaseQ28275257
The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementiaQ29547174
AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's diseaseQ29547175
Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagationQ29615640
Pathological α-Synuclein Transmission Initiates Parkinson-like Neurodegeneration in Nontransgenic MiceQ29620597
VCP/p97 cooperates with YOD1, UBXD1 and PLAA to drive clearance of ruptured lysosomes by autophagyQ30274624
Spatiotemporal dynamics of adenovirus membrane rupture and endosomal escapeQ30525259
Autophagy sequesters damaged lysosomes to control lysosomal biogenesis and kidney injuryQ30544606
Lysosomes and α-synuclein form a dangerous duet leading to neuronal cell death.Q34043163
G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndromeQ34335126
Seeding of normal Tau by pathological Tau conformers drives pathogenesis of Alzheimer-like tanglesQ34869120
Transfer of human α-synuclein from the olfactory bulb to interconnected brain regions in miceQ34909750
Molecular interaction between the chaperone Hsc70 and the N-terminal flank of huntingtin exon 1 modulates aggregationQ35048841
Addition of exogenous α-synuclein preformed fibrils to primary neuronal cultures to seed recruitment of endogenous α-synuclein to Lewy body and Lewy neurite-like aggregates.Q35215169
Exogenous α-synuclein fibrils induce Lewy body pathology leading to synaptic dysfunction and neuron deathQ35484581
Peripherally applied Abeta-containing inoculates induce cerebral beta-amyloidosisQ35601755
Lewy-body formation is an aggresome-related process: a hypothesisQ35840040
Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in miceQ35946149
Fibrillar α-Synuclein and Huntingtin Exon 1 Assemblies Are Toxic to the CellsQ36045483
Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration.Q36066469
Purified and synthetic Alzheimer’s amyloid beta (Aβ) prionsQ36079533
Sensitive detection of lysosomal membrane permeabilization by lysosomal galectin puncta assay.Q36111729
α-synuclein assemblies sequester neuronal α3-Na+/K+-ATPase and impair Na+ gradientQ36148374
α-Synuclein-induced lysosomal dysfunction occurs through disruptions in protein trafficking in human midbrain synucleinopathy modelsQ36607556
Synthetic Tau Fibrils Mediate Transmission of Neurofibrillary Tangles in a Transgenic Mouse Model of Alzheimer's-Like TauopathyQ36617500
Prion-like spreading of pathological α-synuclein in brainQ36732844
Effects of Serine 129 Phosphorylation on α-Synuclein Aggregation, Membrane Association, and InternalizationQ36744478
Structural and functional properties of prefibrillar α-synuclein oligomersQ36796130
Lewy Body-like α-Synuclein Aggregates Resist Degradation and Impair MacroautophagyQ36873680
Autophagic failure promotes the exocytosis and intercellular transfer of α-synuclein.Q36907208
Autophagy failure in Alzheimer's disease and the role of defective lysosomal acidificationQ36960882
The role of autophagy-lysosome pathway in neurodegeneration associated with Parkinson's diseaseQ37054679
Activation of β-Glucocerebrosidase Reduces Pathological α-Synuclein and Restores Lysosomal Function in Parkinson's Patient Midbrain Neurons.Q37110592
Widespread transneuronal propagation of α-synucleinopathy triggered in olfactory bulb mimics prodromal Parkinson's diseaseQ37197984
Structural and functional characterization of two alpha-synuclein strainsQ37305236
Nanomechanical properties of distinct fibrillar polymorphs of the protein α-synucleinQ37453948
Lysosomal impairment in Parkinson's diseaseQ37461364
A deadly spread: cellular mechanisms of α-synuclein transferQ37874930
Lysosome-dependent pathways as a unifying theme in Parkinson's disease.Q38038561
Cell-to-cell transmission of pathogenic proteins in neurodegenerative diseasesQ38185934
What lysosomes actually tell us about Parkinson's disease?Q38762469
Cellular response of human neuroblastoma cells to α-synuclein fibrils, the main constituent of Lewy bodiesQ38827784
Binding, internalization and fate of Huntingtin Exon1 fibrillar assemblies in mitotic and nonmitotic neuroblastoma cellsQ38860098
Lysosomal dysfunction increases exosome-mediated alpha-synuclein release and transmission.Q39595928
Galectin-3, a marker for vacuole lysis by invasive pathogens.Q39768742
Assembly-dependent endocytosis and clearance of extracellular alpha-synuclein.Q40010392
Wild-type alpha-synuclein interacts with pro-apoptotic proteins PKCdelta and BAD to protect dopaminergic neuronal cells against MPP+-induced apoptotic cell deathQ40405034
α-Synuclein strains cause distinct synucleinopathies after local and systemic administrationQ41681113
TRIMs and Galectins Globally Cooperate and TRIM16 and Galectin-3 Co-direct Autophagy in Endomembrane Damage HomeostasisQ41863769
Distinct tau prion strains propagate in cells and mice and define different tauopathiesQ41904960
Alzheimer brain-derived tau oligomers propagate pathology from endogenous tauQ41979763
Tunneling nanotubes spread fibrillar α-synuclein by intercellular trafficking of lysosomesQ42388077
Cell-to-Cell Transmission of α-Synuclein AggregatesQ42426303
Role of galectin-3 in prion infections of the CNS.Q44545489
PA700, the regulatory complex of the 26S proteasome, interferes with alpha-synuclein assemblyQ46648354
Alterations in lysosomal and proteasomal markers in Parkinson's disease: relationship to alpha-synuclein inclusionsQ48581414
P921main subjectcellular invasionQ130614649
P577publication date2017-05-19
P1433published inActa NeuropathologicaQ343168
P1476titleEndocytic vesicle rupture is a conserved mechanism of cellular invasion by amyloid proteins

Reverse relations

cites work (P2860)
Q572982682D polarization imaging as a low-cost fluorescence method to detect α-synuclein aggregation ex vivo in models of Parkinson's disease
Q58596800Alpha-synuclein fibrils recruit TBK1 and OPTN to lysosomal damage sites and induce autophagy in microglial cells
Q92049502C-terminal α-synuclein truncations are linked to cysteine cathepsin activity in Parkinson's disease
Q102220321CMT-3 targets different α-synuclein aggregates mitigating their toxic and inflammogenic effects
Q61797575Clustering of Tau fibrils impairs the synaptic composition of α3-Na/K-ATPase and AMPA receptors
Q47619917Critical appraisal of pathology transmission in the α-synuclein fibril model of Lewy body disorders.
Q89720828Differential Membrane Binding and Seeding of Distinct α-Synuclein Fibrillar Polymorphs
Q41378022Following the fate of endocytosed fibrils
Q98177882Galectin-3 Secreted by Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells Reduces Aberrant Tau Phosphorylation in an Alzheimer Disease Model
Q92377188Galectin-3 is required for the microglia-mediated brain inflammation in a model of Huntington's disease
Q47251029Galectin-8-mediated selective autophagy protects against seeded tau aggregation
Q38631574Impaired endo-lysosomal membrane integrity accelerates the seeding progression of α-synuclein aggregates
Q55339738Import and Export of Misfolded α-Synuclein.
Q91474636Increased Dynamics of α-Synuclein Fibrils by β-Synuclein Leads to Reduced Seeding and Cytotoxicity
Q48103278Intracellular tracing of amyloid vaccines through direct fluorescent labelling
Q91862920K63-Linked Ubiquitin Is Required for Restriction of HIV-1 Reverse Transcription and Capsid Destabilization by Rhesus TRIM5α
Q64966531LRRK2 modifies α-syn pathology and spread in mouse models and human neurons.
Q92104903Lipids as Trans-Acting Effectors for α-Synuclein in the Pathogenesis of Parkinson's Disease
Q54988763Microglial Lectins in Health and Neurological Diseases.
Q95940310Phagocytic glia are obligatory intermediates in transmission of mutant huntingtin aggregates across neuronal synapses
Q64867396Prion-like propagation of pathology in Parkinson disease
Q64238991Propagation of α-Synuclein Strains within Human Reconstructed Neuronal Network
Q90591155Protein transmission in neurodegenerative disease
Q92063917Proteostasis Failure in Neurodegenerative Diseases: Focus on Oxidative Stress
Q92235387Reducing INS-IGF1 signaling protects against non-cell autonomous vesicle rupture caused by SNCA spreading
Q64115757Repeat domain-associated O-glycans govern PMEL fibrillar sheet architecture
Q94686336Restoration of lysosomal function after damage is accompanied by recycling of lysosomal membrane proteins
Q41378010Selective imaging of internalized proteopathic α-synuclein seeds in primary neurons reveals mechanistic insight into transmission of synucleinopathies.
Q64968356The Role of Antibodies and Their Receptors in Protection Against Ordered Protein Assembly in Neurodegeneration.
Q53841253The concept of alpha-synuclein as a prion-like protein: ten years after
Q90408376The expression level of alpha-synuclein in different neuronal populations is the primary determinant of its prion-like seeding
Q57838382Transcellular Spreading of Tau in Tauopathies
Q47844521Transcriptional Effects of ApoE4: Relevance to Alzheimer's Disease
Q59137099Unraveling the enigma: elucidating the relationship between the physicochemical properties of aluminium-based adjuvants and their immunological mechanisms of action

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