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中文摘要
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描述(由申请人提供):中风是成人残疾的主要原因。中风是由直接阻断血流和出血引起的。脑出血是中风的第二大原因。脑出血(ICH)的恢复比例甚至低于非出血性卒中。然而,在ICH中,有一个有限的初始恢复和恢复失去的脑功能的过程。脑出血功能恢复的机制尚未研究。该应用将确定ICH后大脑中新连接形成和恢复的机制。在非出血性中风中,新的连接在中风后的第一个月形成,这一过程称为中风后轴突发芽。本申请提案的PI和其他实验室已经确定了中风后轴突发芽的分子机制,以及轴突发芽与功能恢复的关联。拟议的研究将使用新开发的技术来识别ICH后运动系统中形成的新连接模式,介导这种轴突发芽的基因系统,以及通过这些基因系统介导的轴突发芽和功能恢复之间的因果关系,从而确定可能作为这种疾病神经修复治疗靶点的分子。
英文摘要
DESCRIPTION (provided by applicant): Stroke is the leading cause of adult disability. Stroke is produced both by direct blockade of blood flow and by hemorrhage. Intracerebral hemorrhage is the second leading cause of stroke. Intracerebral hemorrhage (ICH) has even less proportionate recovery than non-hemorrhagic stroke. However, in ICH there is a limited process of initial recovery and regaining of lost brain function. The mechanisms of functional recovery in ICH have not been studied. This application will determine the mechanisms for the formation of new connections and recovery in the brain after ICH. In non-hemorrhagic stroke, new connections are formed in the first month after the stroke, a process termed post-stroke axonal sprouting. The PI on this application proposal and other labs have identified the molecular mechanisms for axonal sprouting after stroke, and the association of axonal sprouting with functional recovery. The proposed studies will use newly developed techniques to identify the new patterns of connections that form in the motor system after ICH, the gene systems that mediate this axonal sprouting, and the causal link between axonal sprouting and functional recovery mediated through these gene systems, so as to determine molecules that may serve as therapeutic targets for neural repair in this disease.
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The role of pericytes in scar formation following stroke and myocardial infarction
ASNR Annual Meeting
Mechanisms of White Matter Repair in Subcortical White Matter Ischemia
iPS-Glial Restricted Progenitors in White Matter Repair for Stroke
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