ApoE and TDP-43 neuropathology in two siblings with familial FTLD-motor neuron disease.

两名患有家族性FTLD-运动神经元疾病的兄弟姐妹的ApoE和TDP-43神经病理学

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作者:Vossel Keith A, Bien-Ly Nga, Bernardo Aubrey, Rascovsky Katya, Karydas Anna, Rabinovici Gil D, Sidhu Manu, Huang Eric J, Miller Bruce L, Huang Yadong, Seeley William W
Frontotemporal lobar degeneration with motor neuron disease (FTLD-MND) is characterized by neuronal cytoplasmic inclusions containing TDP-43. Apolipoprotein E4 (apoE4), derived from the apoE ϵ4 allele, enhances brain atrophy in FTLD through unknown mechanisms. Here, we studied two siblings with C9ORF72-linked familial FTLD-MND, an apoE ϵ4 homozygote and an apoE ϵ3 homozygote. The apoE ϵ4 homozygote had more cognitive-behavioral symptoms, fronto-insulo-temporal atrophy, and apoE fragments and aggregates in the anterior cingulate cortex. ApoE formed complexes with TDP-43 that were more abundant in the apoE ϵ4 homozygote. Although differences seen in a sibling pair could arise due to chance, these findings raise the possibility that apoE4 exacerbates brain pathology in FTLD through formation of neurotoxic apoE fragments and interactions with TDP-43.

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