Selective vulnerability of layer 5a corticostriatal neurons in Huntington's disease.

ATAC-seq CAG repeat expansion Huntington’s disease RNA-seq RNAscope human post-mortem cortex neuronal vulnerability serial fluorescence-activated nuclei sorting snRNA-seq

Journal

Neuron
ISSN: 1097-4199
Titre abrégé: Neuron
Pays: United States
ID NLM: 8809320

Informations de publication

Date de publication:
11 Jan 2024
Historique:
received: 15 06 2023
revised: 18 08 2023
accepted: 13 12 2023
medline: 19 1 2024
pubmed: 19 1 2024
entrez: 18 1 2024
Statut: aheadofprint

Résumé

The properties of the cell types that are selectively vulnerable in Huntington's disease (HD) cortex, the nature of somatic CAG expansions of mHTT in these cells, and their importance in CNS circuitry have not been delineated. Here, we employed serial fluorescence-activated nuclear sorting (sFANS), deep molecular profiling, and single-nucleus RNA sequencing (snRNA-seq) of motor-cortex samples from thirteen predominantly early stage, clinically diagnosed HD donors and selected samples from cingulate, visual, insular, and prefrontal cortices to demonstrate loss of layer 5a pyramidal neurons in HD. Extensive mHTT CAG expansions occur in vulnerable layer 5a pyramidal cells, and in Betz cells, layers 6a and 6b neurons that are resilient in HD. Retrograde tracing experiments in macaque brains identify layer 5a neurons as corticostriatal pyramidal cells. We propose that enhanced somatic mHTT CAG expansion and altered synaptic function act together to cause corticostriatal disconnection and selective neuronal vulnerability in HD cerebral cortex.

Identifiants

pubmed: 38237588
pii: S0896-6273(23)00968-6
doi: 10.1016/j.neuron.2023.12.009
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Christina Pressl (C)

Laboratory of Molecular Biology, The Rockefeller University, New York, NY, USA.

Kert Mätlik (K)

Laboratory of Molecular Biology, The Rockefeller University, New York, NY, USA.

Laura Kus (L)

Laboratory of Molecular Biology, The Rockefeller University, New York, NY, USA.

Paul Darnell (P)

Laboratory of Molecular Biology, The Rockefeller University, New York, NY, USA.

Ji-Dung Luo (JD)

Bioinformatics Resource Center, The Rockefeller University, New York, NY, USA.

Matthew R Paul (MR)

Bioinformatics Resource Center, The Rockefeller University, New York, NY, USA.

Alison R Weiss (AR)

Division of Neuroscience, Oregon National Primate Research Center, Beaverton, OR, USA.

William Liguore (W)

Division of Neuroscience, Oregon National Primate Research Center, Beaverton, OR, USA.

Thomas S Carroll (TS)

Bioinformatics Resource Center, The Rockefeller University, New York, NY, USA.

David A Davis (DA)

Department of Neurology, University of Miami Miller School of Medicine, Miami, FL, USA.

Jodi McBride (J)

Division of Neuroscience, Oregon National Primate Research Center, Beaverton, OR, USA.

Nathaniel Heintz (N)

Laboratory of Molecular Biology, The Rockefeller University, New York, NY, USA. Electronic address: heintz@rockefeller.edu.

Classifications MeSH