Basal Forebrain Cholinergic Neurons: Linking Down Syndrome and Alzheimer's Disease

• Published in: Frontiers in aging neuroscience Vol. 13; p. 703876
• Main Authors: Martinez, Jose L, Zammit, Matthew D, West, Nicole R, Christian, Bradley T, Bhattacharyya, Anita
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 12-07-2021; Frontiers Media S.A
• Subjects: Age; Aging; Alzheimer's disease; Amygdala; Basal forebrain; basal forebrain cholinergic neurons; Cerebral cortex; Cognition & reasoning; Cognitive ability; Dementia; Down syndrome; Down's syndrome; Forebrain; Information processing; Innervation; Life span; Memory; Neurodegeneration; Neurodegenerative diseases; Neuroimaging; Neurons; Neuroscience; Parkinson's disease; Pathology; pluripotent stem cell; Schizophrenia; Trisomy; neurodegeneration; down syndrome; Alzheimer’s disease; basal forebrain cholinergic neurons; pluripotent stem cell
• ISSN: 1663-4365; 1663-4365
• DOI: 10.3389/fnagi.2021.703876

Down syndrome (DS, trisomy 21) is characterized by intellectual impairment at birth and Alzheimer's disease (AD) pathology in middle age. As individuals with DS age, their cognitive functions decline as they develop AD pathology. The susceptibility to degeneration of a subset of neurons, known as basal forebrain cholinergic neurons (BFCNs), in DS and AD is a critical link between cognitive impairment and neurodegeneration in both disorders. BFCNs are the primary source of cholinergic innervation to the cerebral cortex and hippocampus, as well as the amygdala. They play a critical role in the processing of information related to cognitive function and are directly engaged in regulating circuits of attention and memory throughout the lifespan. Given the importance of BFCNs in attention and memory, it is not surprising that these neurons contribute to dysfunctional neuronal circuitry in DS and are vulnerable in adults with DS and AD, where their degeneration leads to memory loss and disturbance in language. BFCNs are thus a relevant cell target for therapeutics for both DS and AD but, despite some success, efforts in this area have waned. There are gaps in our knowledge of BFCN vulnerability that preclude our ability to effectively design interventions. Here, we review the role of BFCN function and degeneration in AD and DS and identify under-studied aspects of BFCN biology. The current gaps in BFCN relevant imaging studies, therapeutics, and human models limit our insight into the mechanistic vulnerability of BFCNs in individuals with DS and AD.