Traumatic brain injury (TBI), the leading cause of death in children and young adults [1-6], leaves many patients (1.5 million annually in the US) with substantial motor disabilities and cognitive impairments [1-4, 6]. TBI represents a significant socioeconomic burden [2, 7-9]. In 2000 civilian TBI patients incurred over $60 billion in medical costs [3, 4, 10, 11]. Furthermore, it is estimated that more than 300,000 Iraq and Afghanistan war veterans have sustained mild traumatic brain injury (mTBIs) from blast waves of wartime improvised explosive devices (20% of 1.6 million) [12, 13]. Therefore, mTBI is a serious public health problem. At present, there is no effective treatment for these TBI-associated disorders. Thus, the development of therapeutic approaches to treat these disorders following TBI would be of enormous clinical, social, and economic benefit. Recently research has identified neural stem/progenitor cells (NSCs) in the adult brain [14-17]. New neurons are continuously generated from NSCs throughout adulthood . These adult-born new neurons are a potential resource for repairing damages in the brain following TBI. In addition, these findings suggest that innate repair and/or plasticity mechanisms exit in the adult brain. However, these innate processes are often unsuccessful, and additional interventions are required to increase the innate plasticity for successfully repairing the damaged brain following TBI. Recently, it has been shown that physical exercise enhanced neurogenesis in the adult hippocampus, and moderately improved its functional performance following TBI [19-21]. This finding suggests that physical exercise-enhanced neurogenesis might be induced in patients following TBI. However, so far exercise-enhanced functional improvement have proven to be moderate, and several questions still remain: 1) Does physical exercise increase NSC proliferation or/and promote newborn neuron survival?;2) What are the molecular and cellular mechanisms that regulate exercise-enhanced neurogenesis?;3) Does exercise-enhanced neurogenesis lead to behavioral improvements in patients following TBI?;and 4) How can this effect be increased to further boost neurogenesis and to potentially greatly improve the behaviorof TBI patients? To address these questions, this proposal will investigate the molecular and cellular mechanisms that regulate exercise-enhanced neurogenesis, and use the molecules identified in this study to further increase exercise-enhanced neurogenesis in the adult hippocampus following TBI. Completion of these studies will not only provide insights into the molecular and cellular mechanisms mediating exercise- enhanced neurogenesis, but also may provide a potential approach to increase neurogenesis and facilitate functional recovery following TBI.
Traumatic brain injury (TBI) is the leading cause of death in children and young adults, and represents a significant socioeconomic burden. It leaves many patients with substantial cognitive impairments and epilepsy. Currently there is no effective treatment for these disorders. This proposal aims to investigate the molecular and cellular mechanisms underlying exercise-enhanced neurogenesis in the hippocampus following TBI, and to potentially find a novel approach to augment exercise-enhanced neurogenesis for functional recovery of patients following TBI.
|Zhao, Shu; Wang, Xiaoting; Gao, Xiang et al. (2018) Delayed and progressive damages to juvenile mice after moderate traumatic brain injury. Sci Rep 8:7339|
|Wang, Xiaoting; Romine, Jennifer Lynn; Gao, Xiang et al. (2017) Aging impairs dendrite morphogenesis of newborn neurons and is rescued by 7, 8-dihydroxyflavone. Aging Cell 16:304-311|
|Gao, Xiang; Wang, Xiaoting; Xiong, Wenhui et al. (2016) In vivo reprogramming reactive glia into iPSCs to produce new neurons in the cortex following traumatic brain injury. Sci Rep 6:22490|
|Zhao, Shu; Gao, Xiang; Dong, Weiren et al. (2016) The Role of 7,8-Dihydroxyflavone in Preventing Dendrite Degeneration in Cortex After Moderate Traumatic Brain Injury. Mol Neurobiol 53:1884-1895|
|Ding, Xue-Feng; Gao, Xiang; Ding, Xin-Chun et al. (2016) Postnatal dysregulation of Notch signal disrupts dendrite development of adult-born neurons in the hippocampus and contributes to memory impairment. Sci Rep 6:25780|
|Ibrahim, Sara; Hu, Weipeng; Wang, Xiaoting et al. (2016) Traumatic Brain Injury Causes Aberrant Migration of Adult-Born Neurons in the Hippocampus. Sci Rep 6:21793|
|Wang, Xiaoting; Gao, Xiang; Michalski, Stephanie et al. (2016) Traumatic Brain Injury Severity Affects Neurogenesis in Adult Mouse Hippocampus. J Neurotrauma 33:721-33|
|Romine, Jennifer; Gao, Xiang; Xu, Xiao-Ming et al. (2015) The proliferation of amplifying neural progenitor cells is impaired in the aging brain and restored by the mTOR pathway activation. Neurobiol Aging 36:1716-1726|
|Chen, Liang; Gao, Xiang; Zhao, Shu et al. (2015) The Small-Molecule TrkB Agonist 7, 8-Dihydroxyflavone Decreases Hippocampal Newborn Neuron Death After Traumatic Brain Injury. J Neuropathol Exp Neurol 74:557-67|
|Carlson, Shaun W; Madathil, Sindhu K; Sama, Diana M et al. (2014) Conditional overexpression of insulin-like growth factor-1 enhances hippocampal neurogenesis and restores immature neuron dendritic processes after traumatic brain injury. J Neuropathol Exp Neurol 73:734-46|
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