Shen Yan, Plane Jennifer M, Deng Wenbin
Department of Cell Biology, University of California, Davis, CA, USA.
J Vis Exp. 2010 May 18(39):1951. doi: 10.3791/1951.
We describe a protocol for establishing mouse models of periventricular leukomalacia (PVL). PVL is the predominant form of brain injury in premature infants and the most common antecedent of cerebral palsy. PVL is characterized by periventricular white matter damage with prominent oligodendroglial injury. Hypoxia/ischemia with or without systemic infection/inflammation are the primary causes of PVL. We use P6 mice to create models of neonatal brain injury by the induction of hypoxia/ischemia with or without systemic infection/inflammation with unilateral carotid ligation followed by exposure to hypoxia with or without injection of the endotoxin lipopolysaccharide (LPS). Immunohistochemistry of myelin basic protein (MBP) or O1 and electron microscopic examination show prominent myelin loss in cerebral white matter with additional damage to the hippocampus and thalamus. Establishment of mouse models of PVL will greatly facilitate the study of disease pathogenesis using available transgenic mouse strains, conduction of drug trials in a relatively high throughput manner to identify candidate therapeutic agents, and testing of stem cell transplantation using immunodeficiency mouse strains.
我们描述了一种建立脑室周围白质软化症(PVL)小鼠模型的方案。PVL是早产儿脑损伤的主要形式,也是脑瘫最常见的先兆。PVL的特征是脑室周围白质损伤并伴有明显的少突胶质细胞损伤。伴有或不伴有全身感染/炎症的缺氧/缺血是PVL的主要病因。我们使用出生后6天(P6)的小鼠,通过单侧颈动脉结扎诱导缺氧/缺血,伴有或不伴有全身感染/炎症(通过注射或不注射内毒素脂多糖(LPS)来暴露于缺氧环境),从而创建新生儿脑损伤模型。髓磷脂碱性蛋白(MBP)或O1的免疫组织化学以及电子显微镜检查显示,脑白质中出现明显的髓磷脂丢失,海马体和丘脑也有额外损伤。建立PVL小鼠模型将极大地促进利用现有的转基因小鼠品系研究疾病发病机制,以相对高通量的方式进行药物试验以确定候选治疗药物,以及使用免疫缺陷小鼠品系进行干细胞移植测试。