Journal Article DZNE-2025-01370

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Direct interaction between TDP-43 and Tau promotes their co-condensation, while suppressing Tau fibril formation and seeding.

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2025
Nature Publishing Group UK [London]

The EMBO journal 44(24), 7395 - 7433 () [10.1038/s44318-025-00590-2]

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Abstract: Neuronal aggregates of Tau are a hallmark of Alzheimer's disease (AD), but more than half of the patients exhibit additional TDP-43 inclusions, while some have co-aggregates of the two proteins. The presence of such co-aggregates is associated with increased disease severity, although whether there is a causal relationship remains unclear. Here, we demonstrate that Tau and TDP-43 mutually promote each other's condensation through direct interaction in vitro, forming irregularly-shaped or multiphasic co-condensates with lower TDP-43 mobility, but higher Tau mobility. While Tau promotes TDP-43 aggregation in vitro, TDP-43 suppresses formation of Tau fibrils and instead causes formation of oligomeric Tau and Tau/TDP-43 species. These co-assemblies hinder Tau seeding in a biosensor assay specific for proteopathic Tau seeds. Consistent with these data, insoluble material extracted from AD patient brains with Tau/TDP-43 co-aggregates exhibits reduced Tau seeding compared to AD patient brains with Tau aggregates only. In contrast, patient-derived extracts from AD patient brains with Tau/TDP-43 co-aggregates are highly potent in seeding new TDP-43 aggregates in a TDP-43 reporter cell line. Our results suggest that direct interaction between TDP-43 and Tau may suppress Tau pathology, while promoting TDP-43 pathology in Alzheimer's disease patients.

Keyword(s): tau Proteins: metabolism (MeSH) ; tau Proteins: genetics (MeSH) ; Humans (MeSH) ; DNA-Binding Proteins: metabolism (MeSH) ; DNA-Binding Proteins: genetics (MeSH) ; Alzheimer Disease: metabolism (MeSH) ; Alzheimer Disease: pathology (MeSH) ; Alzheimer Disease: genetics (MeSH) ; Protein Aggregation, Pathological: metabolism (MeSH) ; Brain: metabolism (MeSH) ; Brain: pathology (MeSH) ; Protein Aggregates (MeSH) ; Protein Binding (MeSH) ; Alzheimer’s Disease ; Phase Separation ; Seeding ; TDP-43 ; Tau ; tau Proteins ; DNA-Binding Proteins ; TARDBP protein, human ; MAPT protein, human ; Protein Aggregates

Classification:

Contributing Institute(s):
  1. Cell Biology of Neurodegeneration (AG Edbauer)
  2. Neuronal Cell Biology (AG Misgeld)
  3. Translational Structural Biology (AG Zweckstetter)
  4. Protein Actions in Neurodegeneration (AG Wegmann)
  5. Clinical Research (Munich) (Clinical Research (Munich))
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)
  2. 351 - Brain Function (POF4-351) (POF4-351)
  3. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)

Appears in the scientific report 2025
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Medline ; Creative Commons Attribution CC BY 4.0 ; DOAJ ; OpenAccess ; Article Processing Charges ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Wiley ; DOAJ Seal ; Ebsco Academic Search ; Essential Science Indicators ; Fees ; IF >= 10 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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The record appears in these collections:
Institute Collections > M DZNE > M DZNE-Clinical Research (Munich)
Institute Collections > GÖ DZNE > GÖ DZNE-AG Zweckstetter
Document types > Articles > Journal Article
Institute Collections > M DZNE > M DZNE-AG Misgeld
Institute Collections > M DZNE > M DZNE-AG Edbauer
Institute Collections > B DZNE > B DZNE-AG Wegmann
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 Record created 2025-12-17, last modified 2025-12-17


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