Faculty Bibliography

Objectives: Given that epidemiologic studies have shown that diabetes mellitus increases the risk of Alzheimer's disease (AD), our objective was to examine the mechanistic links between the two diseases in a non-human primate. Methods: Tissue from multiple brain regions of a vervet monkey model of streptozotocin-induced type 1 diabetes (n=10 control; n=7 diabetic) was examined by Western blot analysis, sandwich ELISA, and qPCR for biochemical changes in tau protein and Abeta peptide, as well as changes in key enzymes that contribute to their processing and posttranslational modification. Results: Regional brain analyses showed a global increase in tau phosphorylation in areas vulnerable to AD pathology as well as in spared structures such as the cerebellum. An examination of tau phosphatases and kinases showed a brain-wide increase in active ERK1/2. A diabetes-induced increase in Abeta levels, however, was specific to brain regions affected during the early stages of AD pathogenesis, with the greatest increase observed in the hippocampus. Examination of the amyloid precursor protein, its metabolites, and proteins involved in the clearance and degradation of brain Abeta indicated that a hippocampal-specific decrease in the Abeta-degrading enzyme neprilysin is a major contributor to this localized Abeta increase. Conclusions: Our study suggests protein changes in the brain that link diabetes to AD risk: decreased neprilysin expression leads to an increase in Abeta in the temporal lobe structures that are at the earliest risk in AD while increased ERK1/2 activity appears to contribute to a brain-wide increase in tau phosphorylation

Neurotrophins play a crucial role in mediating neuronal survival and synaptic plasticity. A lack of trophic factor support in the peripheral nervous system (PNS) is associated with a transcription-dependent programmed cell death process in developing sympathetic neurons. While most of the attention has been upon events culminating in cell death in the PNS, the earliest events that occur after trophic factor withdrawal in the central nervous system (CNS) have not been investigated. In the CNS, brain-derived neurotrophic factor (BDNF) is widely expressed and is released in an activity-dependent manner to shape the structure and function of neuronal populations. Reduced neurotrophic factor support has been proposed as a mechanism to account for changes in synaptic plasticity during neurodevelopment to aging and neurodegenerative disorders. To this end, we performed transcriptional profiling in cultured rat hippocampal neurons. We used a TrkB ligand scavenger (TrkB-FC ) to sequester endogenous neurotrophic factor activity from hippocampal neurons in culture. Using a high-density microarray platform, we identified a significant decrease in genes that are associated with vesicular trafficking and synaptic function, as well as selective increases in MAP kinase phosphatases. A comparison of these changes with recent studies of Alzheimer's disease and cognitive impairment in post mortem brain tissue revealed striking similarities in gene expression changes for genes involved in synaptic function. These changes are relevant to a wide number of conditions in which levels of BDNF are compromised. (c) 2014 Wiley Periodicals, Inc. Develop Neurobiol, 2014.

Down syndrome (DS) is the most prevalent cause of intellectual disability (ID). Individuals with DS show a variety of cognitive deficits, most notably in hippocampal learning and memory, and display pathological hallmarks of Alzheimer's disease (AD), with neurodegeneration of cholinergic basal forebrain (CBF) neurons. Elucidation of the molecular and cellular underpinnings of neuropathology has been assessed via gene expression analysis in a relevant animal model, termed the Ts65Dn mouse. The Ts65Dn mouse is a segmental trisomy model of DS which mimics DS/AD pathology, notably age-related cognitive dysfunction and degeneration of basal forebrain cholinergic neurons (BFCNs). To determine expression level changes, molecular fingerprinting of Cornu Ammonis 1 (CA1) pyramidal neurons was performed in adult (4-9 month old) Ts65Dn mice, at the initiation of BFCN degeneration. To quantitate transcriptomic changes during this early time period, laser capture microdissection (LCM), terminal continuation (TC) RNA amplification, custom-designed microarray analysis, and subsequent validation of individual transcripts by qPCR and protein analysis via immunoblotting was performed. Results indicate significant alterations within CA1 pyramidal neurons of Ts65Dn mice compared to normal disomic (2N) littermates, notably in the downregulation of neurotrophins and their cognate neurotrophin receptors among other classes of transcripts relevant to neurodegeneration. These results of this single population gene expression analysis at the time of septohippocampal deficits in a trisomic mouse model shed light on a vulnerable circuit that may cause the AD-like pathology invariably seen in DS that could help to identify mechanisms of degeneration, and provide novel gene targets for therapeutic interventions. J. Comp. Neurol., 2014. (c) 2014 Wiley Periodicals, Inc.

A major feature of Alzheimer's disease (AD) is the loss of noradrenergic locus coeruleus (LC) projection neurons that mediate attention, memory, and arousal. However, the extent to which the LC projection system degenerates during the initial stages of AD remains unclear. To address this question, we performed tyrosine hydroxylase (TH) immunohistochemistry and unbiased stereology of LC neurons in tissue harvested postmortem from subjects who died with a clinical diagnosis of no cognitive impairment (NCI), amnestic mild cognitive impairment (aMCI, a prodromal AD stage), or mild AD (n = 5-6/group). Stereologic estimates of total LC neuron number revealed a 30-35% decrease in aMCI versus NCI (p < 0.01) and a 45% loss of cells in mild AD compared to NCI (p < 0.01). Furthermore, LC fiber density was selectively reduced in the hippocampus compared to the neocortex of aMCI subjects, suggesting that coeruleohippocampal pathway degeneration marks the transition from normal cognition to prodromal disease. To examine the molecular pathogenic processes underlying LC neurodegeneration in aMCI, we combined laser capture microdissection with custom microarray technology to quantify gene expression patterns in individual TH-immunopositive neurons accessed from LC tissue samples. These studies revealed significant reductions in select functional classes of mRNAs regulating mitochondrial metabolism (e.g., cytochrome c1, cytochrome oxidase subunit 5a, p < 0.01), redox homeostasis (e.g., superoxide dismutase 2, glutathione peroxidase 1, p < 0.01), and cytoskeletal plasticity (e.g., microtubule-associated binding protein 1a, utrophin, p < 0.01) in both aMCI and AD subjects compared to NCI. Taken together, these observations show that LC projection system degeneration is a prominent feature during the transition from NCI to aMCI. In this regard, we are currently examining the extent of LC neuropathology in tissue from "preclinical AD" subjects who died with a clinical diagnosis of NCI but who displayed high postmortem Braak pathology. Targeting the noradrenergic LC system may present a novel disease-modifying strategy for cognitive protection in the elderly

Calorie restriction (CR) enhances longevity and mitigates aging phenotypes in numerous species. Physiological responses to CR are cell-type specific and variable throughout the lifespan. However, the mosaic of molecular changes responsible for CR benefits remains unclear, particularly in brain regions susceptible to deterioration during aging. We examined the influence of long-term CR on the CA1 hippocampal region, a key learning and memory brain area that is vulnerable to age-related pathologies, such as Alzheimer's disease (AD). Through mRNA sequencing and NanoString nCounter analysis, we demonstrate that one year of CR feeding suppresses age-dependent signatures of 882 genes functionally associated with synaptic transmission-related pathways, including calcium signaling, long-term potentiation (LTP), and Creb signaling in wild-type mice. By comparing the influence of CR on hippocampal CA1 region transcriptional profiles at younger-adult (5 months, 2.5 months of feeding) and older-adult (15 months, 12.5 months of feeding) timepoints, we identify conserved upregulation of proteome quality control and calcium buffering genes, including heat shock 70 kDa protein 1b (Hspa1b) and heat shock 70 kDa protein 5 (Hspa5), protein disulfide isomerase family A member 4 (Pdia4) and protein disulfide isomerase family A member 6 (Pdia6), and calreticulin (Calr). Expression levels of putative neuroprotective factors, klotho (Kl) and transthyretin (Ttr), are also elevated by CR in adulthood, although the global CR-specific expression profiles at younger and older timepoints are highly divergent. At a previously unachieved resolution, our results demonstrate conserved activation of neuroprotective gene signatures and broad CR-suppression of age-dependent hippocampal CA1 region expression changes, indicating that CR functionally maintains a more youthful transcriptional state within the hippocampal CA1 sector.

Maternal choline supplementation (MCS) induces lifelong cognitive benefits in the Ts65Dn mouse, a trisomic mouse model of Down syndrome and Alzheimer's disease. To gain insight into the mechanisms underlying these beneficial effects, we conducted a study to test the hypothesis that MCS alters choline metabolism in adult Ts65Dn offspring. Deuterium-labeled methyl-d9-choline was administered to adult Ts65Dn and disomic (2N) female littermates born to choline-unsupplemented or choline-supplemented Ts65Dn dams. Enrichment of d9-choline metabolites (derived from intact choline) and d3 + d6-choline metabolites [produced when choline-derived methyl groups are used by phosphatidylethanolamine N-methyltransferase (PEMT)] was measured in harvested tissues. Adult offspring (both Ts65Dn and 2N) of choline-supplemented (vs. choline-unsupplemented) dams exhibited 60% greater (P