65,68,69 Given their differential nature of see more expression and because of the local regulation of mRNA translation, the role of miRNAs in numerous biological phenomena, including neuronal development, cell proliferation, cell cycle, neurogenesis, synaptic development, axon guidance, and neuronal plasticity, have been studied.70-73 miRNAs: potential regulators of neurogenesis and neural plasticity Inhibitors,research,lifescience,medical miRNAs in neurogenesis Adult neurogenesis, the process of generating
new neurons from neural stem cells, plays a critical role in synaptic plasticity, learning and memory, and mood regulation.74,75 In the mammalian brain, neurogenesis occurs throughout adulthood in the hippocampus (subgranular zone [SGZ] of the dentate gyrus) and olfactory bulb (subventricular zone [SVZ]). Neurogenesis in the SVZ is important for olfactory learning,76 whereas hippocampal neurogenesis is involved in memory and spatial learning.77 Numerous studies suggest that stress and MDD are associated with decreased hippocampal neurogenesis.78-80 Additionally, disturbed adult neurogenesis, possibly resulting Inhibitors,research,lifescience,medical in a malfunctioning of hippocampus, may contribute to cognitive deficits.81 Conversely, hippocampal neurogenesis buffers stress responses and depressive behavior.82
Enriched environment, exercise, electroconvulsive therapy, deep brain stimulation, and antidepressants Inhibitors,research,lifescience,medical increase hippocampal neurogenesis.83 The regulatory factors that control adult neurogenesis are currently under investigation; however, recent studies demonstrate Inhibitors,research,lifescience,medical that miRNAs play a role in both embryonic as well as adult neurogenesis.84 For example, Choi et al56 demonstrated
that olfactory tissues express more than 100 distinct miRNAs, the most abundant being the miR-124a and let-7 variants and the family of miR-200. To determine whether miRNAs are required during olfactory neuronal development, these investigators analyzed embryonic tissues in which Dicer function was specifically ablated in olfactory progenitor cells. They showed that the loss of miRNA function from olfactory progenitor cells produced Inhibitors,research,lifescience,medical no alterations in patterning. In contrast, they noted that terminal differentiation of the olfactory progenitor pool into mature olfactory neurons does not occur and that to the olfactory precursor cell population is not maintained. Dicer depletion also impacts proliferation and cell death, migration, and differentiation during corticogenesis as assessed by McLoughlin et al85 in the developing brain. Using markers for proliferation and in vivo labeling, they showed reduced numbers of proliferating cells, altered cell cycle kinetics from embryonic day 15.5 (E15.5), distributed progenitor cells throughout the cortex (rather than restricted to the SVZ and ventricular zones), and increased cortical cell death as early as E15.5. DGCR8 heterozygous mice also show reduced cell proliferation and neurogenesis in adult hippocampus.