Pathways underlying selective vulnerability to Alzheimer’s disease in aminergic brainstem nuclei

Abstract Background The Neuromodulatory Subcortical System (NSS) consists of nuclei exhibiting early vulnerability to tauopathies, including Alzheimer’s Disease (AD). Within the NSS, there is a spectrum of vulnerability that becomes apparent in the earliest stages of AD, offering a chance to probe factors underlying vulnerability to AD. Method In this study, we applied bulk RNA sequencing in well‐characterized postmortem human tissue from n = 22 cases at early (Braak 0‐III) AD‐tau stages to understand why this susceptibility gradient exists by examining two nuclei with very similar neurons but differing in their vulnerability to AD the locus coeruleus (LC) and substantia nigra (SN). Result We identified 3421 differentially expressed genes between the LC and SN among Braak 0 cases. Gene set enrichment analysis directed attention towards cholesterol homeostasis, neuroinflammation, and oxidative stress as factors potentially underlying the differential vulnerability of the LC and SN to AD. Conclusion Weighing the limitations of bulk RNA sequencing against the expression patterns of the constituitive genes within each gene set, we conclude that cholesterol homeostasis likely explains the differential vulnerability of the LC and SN to AD (Figure 1).

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.095326
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
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article

Pathways underlying selective vulnerability to Alzheimer’s disease in aminergic brainstem nuclei

Lea T. Grinberg, Renata Elaine Paraízo Leite, Cathrine Petersen, Felipe Luiz Pereira et al.
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Alzheimer s & Dementia
Alzheimer's disease research and treatments
article

Pathways underlying selective vulnerability to Alzheimer’s disease in aminergic brainstem nuclei

Lea T. Grinberg, Renata Elaine Paraízo Leite, Cathrine Petersen, Felipe Luiz Pereira, Roberta Diehl Rodriguez, Carlos Augusto Pasqualucci, Salvatore Spina, Vítor Ribeiro Paes, Daniela Kaufer, Cláudia Kimie Suemoto, Ricardo Nitríni, William W. Seeley, Renata Eloah de Lucena Ferretti‐Rebustini, Alexander J. Ehrenberg, Wilson Jacob Filho, Eduardo Ferrioli, Jessica J. Buxton
article en

Abstract

Abstract Background The Neuromodulatory Subcortical System (NSS) consists of nuclei exhibiting early vulnerability to tauopathies, including Alzheimer’s Disease (AD). Within the NSS, there is a spectrum of vulnerability that becomes apparent in the earliest stages of AD, offering a chance to probe factors underlying vulnerability to AD. Method In this study, we applied bulk RNA sequencing in well‐characterized postmortem human tissue from n = 22 cases at early (Braak 0‐III) AD‐tau stages to understand why this susceptibility gradient exists by examining two nuclei with very similar neurons but differing in their vulnerability to AD the locus coeruleus (LC) and substantia nigra (SN). Result We identified 3421 differentially expressed genes between the LC and SN among Braak 0 cases. Gene set enrichment analysis directed attention towards cholesterol homeostasis, neuroinflammation, and oxidative stress as factors potentially underlying the differential vulnerability of the LC and SN to AD. Conclusion Weighing the limitations of bulk RNA sequencing against the expression patterns of the constituitive genes within each gene set, we conclude that cholesterol homeostasis likely explains the differential vulnerability of the LC and SN to AD (Figure 1).

Alzheimer s & DementiaVol. 20(S8)
Gladstone Institutes (US), Universidade de São Paulo (BR), University of California, San Francisco (US), University Memory and Aging Center (US), Innovative Genomics Institute (US), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (BR), Global Brain Health Institute (US), University of California, Berkeley (US)
Openalex Percentile: Top 65%
Alzheimer's disease research and treatments
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