Exploring molecular signatures of vulnerable vs resilient RORB excitatory neurons of the entorhinal cortex in Alzheimer's disease

Our findings suggest that transcriptomic signatures of vulnerable and resilient RORB excitatory neurons in the EC, in early Braak stages, may reveal key pathways leading to tau accumulation and neuronal loss. Notably, vulnerable RORB neurons upregulated cytoskeletal organization pathways and downregulated proteostasis pathways. Ongoing analyses on this RORB subpopulation and trajectory analyses on additional excitatory neuronal subpopulations in the EC will refine our understanding of the pathways that potentially lead to selective vulnerability in AD.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70855_107472
Primary Topic
Barrier Structure and Function Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Exploring molecular signatures of vulnerable vs resilient RORB excitatory neurons of the entorhinal cortex in Alzheimer's disease

Lea T. Grinberg, Renata Elaine Paraízo Leite, Cláudia Kimie Suemoto, Alexander Soloviev et al.
Alzheimer s & Dementia
Barrier Structure and Function Studies
article

Exploring molecular signatures of vulnerable vs resilient RORB excitatory neurons of the entorhinal cortex in Alzheimer's disease

Lea T. Grinberg, Renata Elaine Paraízo Leite, Cláudia Kimie Suemoto, Alexander Soloviev, Martin Kampmann, Felipe Luiz Pereira, Kun Leng
article en

Abstract

Our findings suggest that transcriptomic signatures of vulnerable and resilient RORB excitatory neurons in the EC, in early Braak stages, may reveal key pathways leading to tau accumulation and neuronal loss. Notably, vulnerable RORB neurons upregulated cytoskeletal organization pathways and downregulated proteostasis pathways. Ongoing analyses on this RORB subpopulation and trajectory analyses on additional excitatory neuronal subpopulations in the EC will refine our understanding of the pathways that potentially lead to selective vulnerability in AD.

Alzheimer s & DementiaVol. 21(S1)
Universidade de São Paulo (BR), University of California, San Francisco (US), Microsoft (Brazil) (BR), University Memory and Aging Center (US)
Openalex Percentile: Top 38%
Barrier Structure and Function Studies
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