No description available.

Cognitive aging is a biological process characterized by physical changes in the brain and subsequent alterations in cognitive function. While neurodegenerative diseases result in extensive neuronal death and anatomical abnormalities, normal aging has subtle changes resulting in a range of cognitive abilities. Early studies of cognitive aging focused on changes in the neuronal population, but evidence has demonstrated that forebrain neurons are largely preserved with age. Furthermore, the proliferation of new neurons in the adult brain has generated great speculation regarding the role and contribution of new neurons to cognitive function. Conversely, both imaging and ultrastructural analyses have shown that age-related alterations in white matter and myelin are good predictors of cognitive impairment, suggesting that alterations in connectivity between brain regions may result in cognitive decline. In this dissertation, a rhesus monkey model of normal aging was used to assess the contribution of adult-neurogenesis and oligodendrogenesis to cognitive function. First, cell proliferation and adult neurogenesis were assessed in the subgranular zone of the hippocampal dentate gyrus. Aged animals demonstrated a decline in proliferating cells and neurogenesis but only limited correlations with behavioral impairment. Immature neurons were also identified in temporal lobe cortices, but results indicate these immature cortical neurons are most likely not adult-generated. Moreover, despite an age-related decline in numbers, they persist throughout the lifespan and many differentiate into Calretinin neurons. Further investigation of white matter alterations used immunohistochemistry and diffusion spectrum imaging to correlate oligodendrocyte numbers with white matter connectivity. In the corpus callosum and cingulum bundle, there were no correlations with age, but cognitive impairment was associated with increased oligodendrocyte number and decreased white matter connectivity. These correlations were only present in the anterior aspect of the cingulum bundle, not the posterior cingulum suggesting differential oligodendrocyte responses along the anterior-posterior axis of the brain. Together, these data demonstrate an age-related decline in adult neurogenesis may be only a small contributor to cognitive impairment. Additionally, a reserve pool of immature neurons continues to differentiate in the temporal cortex potentially contributing to local plasticity. Furthermore, cognitive impairment rather than aging has a stronger correlation with oligodendrocytes alterations and connectivity.

Demyelinating disorders affect many people around the globe and are characterized by loss of myelin sheaths and oligodendrocyte death, ultimately compromising neuronal signal transmission across the Central Nervous System (CNS). Adult Neural Stem Cells (NSC) are multipotent stem cells with the ability to differentiate into the three types of CNS cells: oligodendrocytes, neurons and astrocytes. Hydrogen peroxide (H2O2) is an inflammatory mediator, often present in demyelinating events, commonly associated with oxidative stress and cell death. However, H2O2 also plays a major role as an intracellular signaling molecule. It has been seen that NSC exposed to H2O2 revealed an increase in proliferation and oligodendrogenesis. In this project, we tried to understand how oligodendrogenesis is modulated at a transcriptional level by H2O2. We have identified the genes Hes1, Foxo1, Nrf2 and Prdx6 as being downregulated in the presence of H2O2 when compared to the non-exposed controls. In order to understand if the differential gene expression is involved in the H2O2-induced oligodendrogenesis, we silenced the genes through siRNA transfection (mimicking the downregulation observed after H2O2 exposure) and analyzed the effects on the transcriptome of NSCs and the impact on cell proliferation and differentiation. Our findings indicate that Foxo1 silencing induced the greatest increase in cell proliferation and that Nrf2 silencing revealed the greatest impact on oligodendrogenesis. While not very significant, Foxo1 silencing seems to induce oligodendrogenesis, and Prdx6 silencing seems to inhibit it. The results obtained give important hints on the role that these genes play in NSCs differentiation and fate determination when exposed to oxidative stress and might allow a better understanding of this complex system.

No description available.