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Extracellular Monomeric Tau Is Internalized by Astrocytes

https://doi.org/10.3389/fnins.2019.00442

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What this work says

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

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Neuropathological stageing of Alzheimer-related changes

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The role of tau phosphorylation in transfected COS-1 cells

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Mechanisms of secretion and spreading of pathological tau protein

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Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy

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Pathogenesis of the Tauopathies

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Investigation of tau-2 positive microglia-like cells in the subcortical nuclei of human neurodegenerative disorders

inferredcites →https://doi.org/10.1016/j.brainresbull.2016.08.018openalex-snapshot

Tau and tauopathies

inferredcites →https://doi.org/10.1016/j.celrep.2015.04.043openalex-snapshot

Synaptic Contacts Enhance Cell-to-Cell Tau Pathology Propagation

inferredcites →https://doi.org/10.1016/j.celrep.2018.04.056openalex-snapshot

Unconventional Secretion Mediates the Trans-cellular Spreading of Tau

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Characteristics and consequences of muscarinic receptor activation by tau protein

inferredcites →https://doi.org/10.1016/j.expneurol.2018.08.007openalex-snapshot

Dephosphorylated rather than hyperphosphorylated Tau triggers a pro-inflammatory profile in microglia through the p38 MAPK pathway

inferredcites →https://doi.org/10.1016/j.febslet.2006.07.078openalex-snapshot

Extracellular tau is toxic to neuronal cells

inferredcites →https://doi.org/10.1016/j.febslet.2011.11.022openalex-snapshot

Proteostasis of tau. Tau overexpression results in its secretion via membrane vesicles

inferredcites →https://doi.org/10.1016/j.neulet.2016.09.026openalex-snapshot

Secretion of full-length tau or tau fragments in a cell culture model

inferredcites →https://doi.org/10.1016/j.neuron.2014.06.004openalex-snapshot

Tau Propagation, Different Tau Phenotypes, and Prion-like Properties of Tau

inferredcites →https://doi.org/10.1016/j.tins.2008.11.007openalex-snapshot

Tau pathophysiology in neurodegeneration: a tangled issue

inferredcites →https://doi.org/10.1021/cn500143nopenalex-snapshot

Advances in Therapeutics for Neurodegenerative Tauopathies: Moving toward the Specific Targeting of the Most Toxic Tau Species

inferredcites →https://doi.org/10.1038/embor.2013.15openalex-snapshot

Physiological release of endogenous tau is stimulated by neuronal activity

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Tau-mediated neurodegeneration in Alzheimer's disease and related disorders

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Soluble Tau has devastating effects on the structural plasticity of hippocampal granule neurons

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Internalization mechanisms of brain-derived tau oligomers from patients with Alzheimer’s disease, progressive supranuclear palsy and dementia with Lewy bodies

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Cellular internalization of alpha-synuclein aggregates by cell surface heparan sulfate depends on aggregate conformation and cell type

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Tau Internalization is Regulated by 6-O Sulfation on Heparan Sulfate Proteoglycans (HSPGs)

inferredcites →https://doi.org/10.1038/srep11161openalex-snapshot

Microglial internalization and degradation of pathological tau is enhanced by an anti-tau monoclonal antibody

inferredcites →https://doi.org/10.1073/pnas.1301440110openalex-snapshot

Heparan sulfate proteoglycans mediate internalization and propagation of specific proteopathic seeds

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A protein factor essential for microtubule assembly.

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The sulfation code for propagation of neurodegeneration

inferredcites →https://doi.org/10.1074/jbc.r114.549295openalex-snapshot

Prion-like Properties of Tau Protein: The Importance of Extracellular Tau as a Therapeutic Target

inferredcites →https://doi.org/10.1074/jbc.ra117.000378openalex-snapshot

Specific glycosaminoglycan chain length and sulfation patterns are required for cell uptake of tau versus α-synuclein and β-amyloid aggregates

inferredcites →https://doi.org/10.1083/jcb.103.6.2739openalex-snapshot

Tau protein function in living cells.

inferredcites →https://doi.org/10.1084/jem.20172158openalex-snapshot

TFEB enhances astroglial uptake of extracellular tau species and reduces tau spreading

inferredcites →https://doi.org/10.1093/brain/awv081openalex-snapshot

Reactive microglia drive tau pathology and contribute to the spreading of pathological tau in the brain

inferredcites →https://doi.org/10.1097/nen.0b013e318220a658openalex-snapshot

Soluble tau Species, Not Neurofibrillary Aggregates, Disrupt Neural System Integration in a tau Transgenic Model

inferredcites →https://doi.org/10.1111/bpa.12593openalex-snapshot

Aging‐related tau astrogliopathy (ARTAG): not only tau phosphorylation in astrocytes

inferredcites →https://doi.org/10.1111/j.1750-3639.1999.tb00550.xopenalex-snapshot

Comparative Biochemistry of Tau in Progressive Supranuclear Palsy, Corticobasal Degeneration, FTDP‐17 and Pick's Disease

inferredcites →https://doi.org/10.1126/science.6120571openalex-snapshot

Alzheimer's Disease: Insolubility of Partially Purified Paired Helical Filaments in Sodium Dodecyl Sulfate and Urea

inferredcites →https://doi.org/10.1186/s13024-016-0143-yopenalex-snapshot

The release and trans-synaptic transmission of Tau via exosomes

inferredcites →https://doi.org/10.1186/s13024-017-0192-xopenalex-snapshot

Glial contributions to neurodegeneration in tauopathies

inferredcites →https://doi.org/10.1186/s13024-017-0200-1openalex-snapshot

Absence of CX3CR1 impairs the internalization of Tau by microglia

inferredcites →https://doi.org/10.3233/jad-140755openalex-snapshot

Is Tau a Prion-Like Protein?

inferredcites →https://doi.org/10.3233/jad-150704openalex-snapshot

Direct Evidence of Internalization of Tau by Microglia In Vitro and In Vivo

inferredcites →https://doi.org/10.3389/fnagi.2016.00262openalex-snapshot

Tau Structures

inferredcites →https://doi.org/10.3389/fnagi.2020.00096openalex-snapshot

Astroglia and Tau: New Perspectives

inferredcites →https://doi.org/10.3389/fncel.2014.00113openalex-snapshot

The role of extracellular Tau in the spreading of neurofibrillary pathology

inferredcites →https://doi.org/10.3389/fncel.2018.00172openalex-snapshot

The Role of Microglia in the Spread of Tau: Relevance for Tauopathies

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Are Tau Aggregates Toxic or Protective in Tauopathies?

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Neurons Expressing Pathological Tau Protein Trigger Dramatic Changes in Microglial Morphology and Dynamics

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New Features about Tau Function and Dysfunction

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Methylene Blue Blocks and Reverses the Inhibitory Effect of Tau on PMCA Function

What points at this work

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

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Heparan Sulfate Proteoglycans (HSPGs) Serve as the Mediator Between Monomeric Tau and Its Subsequent Intracellular ERK1/2 Pathway Activation

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p38 Inhibition Decreases Tau Toxicity in Microglia and Improves Their Phagocytic Function

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LC3-associated endocytosis facilitates extracellular Tau aggregate internalization and degradation in microglia

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G-protein coupled purinergic P2Y12 receptor interacts and internalizes TauRD-mediated by membrane-associated actin cytoskeleton remodeling in microglia

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Ext1-targeted gene therapy ameliorates tauopathy by inhibiting heparan sulfate-dependent tau propagation

inferred← citeshttps://doi.org/10.1021/acsomega.1c01678openalex-snapshot

Amyloid and Tau Induce Cell Death Independently of TSPO Polymerization and Density Changes

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Internalization mechanisms of brain-derived tau oligomers from patients with Alzheimer’s disease, progressive supranuclear palsy and dementia with Lewy bodies

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Filamentous recombinant human Tau activates primary astrocytes via an integrin receptor complex

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Cellular and pathological functions of tau

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p38 activation occurs mainly in microglia in the P301S Tauopathy mouse model

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Astroglial contribution to tau-dependent neurodegeneration

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Tau fibrils induce nanoscale membrane damage and nucleate cytosolic tau at lysosomes

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Properties of Alzheimer’s disease brain-derived tau aggregates define tau processing by human astrocytes

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Microglia undergoes chemokine receptor, CX3CR1-mediated internalization of extracellular Tau

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Neurons expressing pathological Tau protein trigger dramatic changes in microglial morphology and dynamics

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Distinct regulation of Tau Monomer and aggregate uptake and intracellular accumulation in human neurons

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Astrocytic Propagation of Tau in the Context of Alzheimer's Disease

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Astrocytes in Tauopathies

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Neurons Expressing Pathological Tau Protein Trigger Dramatic Changes in Microglial Morphology and Dynamics

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Heparan Sulfate Proteoglycans in Tauopathy

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Critical Molecular and Cellular Contributors to Tau Pathology

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Tau Transfer via Extracellular Vesicles Disturbs the Astrocytic Mitochondrial System

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Methylene Blue Blocks and Reverses the Inhibitory Effect of Tau on PMCA Function

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Endosomal-Lysosomal Processing of Neurodegeneration-Associated Proteins in Astrocytes

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Sorcin Activates the Brain PMCA and Blocks the Inhibitory Effects of Molecular Markers of Alzheimer’s Disease on the Pump Activity

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Astroglial and Microglial Purinergic P2X7 Receptor as a Major Contributor to Neuroinflammation during the Course of Multiple Sclerosis

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Neurodegeneration and Astrogliosis in the Human CA1 Hippocampal Subfield Are Related to hsp90ab1 and bag3 in Alzheimer’s Disease

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Transgenic Mouse Models of Alzheimer’s Disease: An Integrative Analysis

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Pathological and Functional Brain Amyloids: A New Concept Explaining the Differences

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The Function of Tau in Astrocytes: Advantage or Damage

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Role of non-neuronal cells in neurorepair: a focus on proteinopathy and neurodegeneration

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Additional file 1 of Determinants of astrocytic pathology in stem cell models of primary tauopathies

inferred← citeshttps://doi.org/10.6084/m9.figshare.26623753openalex-snapshot

Additional file 2 of Determinants of astrocytic pathology in stem cell models of primary tauopathies

inferred← citeshttps://doi.org/10.64898/2026.01.07.698214openalex-snapshot

A Joint Tau Propagation and Neuroinflammation Model Reinforces Inflammatory Modulation of Network-Driven Spread in Alzheimer’s Disease

inferred← citeshttps://doi.org/10.70675/04658671zaca3z4fefza24dz2f5a011bebfeopenalex-snapshot

Study of the Neuron-Astrocyte Relationship in a Rodent Model of Tauopathy

inferred← citeshttps://doi.org/10.70675/a6b6a2f4zff42z4987z9ca0z62aca30c291copenalex-snapshot

Astrocytes dysfunction in tauopathies

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