CTE-Type Tau Filaments in Alzheimer’s Disease with Co-morbid LATE-NC

Authors:
  • JRJaimin K. Rana
    Jaimin K. Rana
  • EPEmile S. Pinarbasi
    Emile S. Pinarbasi
  • MFMartin G. Fernandez
    Martin G. Fernandez
  • VNVikas Navratna
    Vikas Navratna
  • KCKyle S. Conway
    Kyle S. Conway
  • ALAndrew P. Lieberman
    Andrew P. Lieberman
  • SMShyamal Mosalaganti
    Shyamal Mosalaganti
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Abstract
Alzheimer’s disease (AD), the most common neurodegenerative disease, is defined by β-amyloid plaques and tau neurofibrillary tangles. Tau filaments in AD adopt the “Alzheimer’s fold”, which is distinct from other tauopathies and highly conserved across sporadic and familial AD. However, to date, structural studies have focused on pure AD, despite the high prevalence of comorbid pathologies. In particular, up to half of AD patients harbor limbic-predominant age-related TDP-43 encephalopathy neuropathologic change (LATE-NC). This co-pathology— consisting of mislocalized and aggregated TDP-43, mainly restricted to the medial temporal lobe—is associated with accelerated clinical decline and more severe tau pathology. Whether there is a structural basis for this clinical synergy remains unknown. Here, using cryo-electron microscopy, we determine the structure of tau filaments from three AD patients with LATE-NC. We show that in addition to the expected Alzheimer’s fold tau filaments, all cases exhibit a distinct fibril morphology identical to chronic traumatic encephalopathy (CTE) fold tau. Additional sampling revealed CTE neuropathology in one patient, suggestive features without definitive CTE in the second, and no evidence of CTE in the third. These findings raise questions about the relationship between LATE-NC and CTE, the effect of TDP-43 on tau conformation, and the etiology of LATE-NC.

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