Division of Neonatology, University Children's Hospital , Basel , Switzerland.
Department of Neonatology, Charité University Medical Center , Berlin , Germany.
Front Pediatr. 2015 Jan 12;2:143. doi: 10.3389/fped.2014.00143. eCollection 2014.
White matter disease in preterm infants comes along with focal destructions or with diffuse myelination disturbance. Recent experimental work with transgenic mice paves the way for a unifying molecular model for both types of brain injury, placing oxygen sensing by oligodendrocyte precursor cells (OPCs) at the center stage. Mice genetically altered to mimic high local oxygen tension in oligodendroglia lineage cells (via deletion of hypoxia-inducible factor, HIF) develop white matter disease resembling cystic periventricular leukomalacia within the first 7 days of life. Mice in which local hypoxia is mimicked in oligodendroglial cells (via genetic inhibition of HIF decay) display arrested OPC maturation and subsequent hypomyelination, reminiscent of the diffuse white matter disease observed in preterm infants and infants with congenital heart disease. These recent experimental findings on oxygen sensing and myelination are awaiting integration into a clinical framework. Gene regulation in response to hyperoxia or hypoxia, rather than oxidative stress, may be an important mechanism underlying neonatal white matter disease.
早产儿的脑白质疾病伴有局灶性破坏或弥漫性髓鞘化障碍。最近使用转基因小鼠的实验工作为这两种类型的脑损伤提供了一个统一的分子模型,将少突胶质前体细胞(OPC)的氧感应置于中心位置。通过删除缺氧诱导因子(HIF)来模拟少突胶质谱系细胞中局部高氧张力的基因改变的小鼠,在生命的头 7 天内会发展出类似于囊性脑室周围白质软化症的脑白质疾病。通过遗传抑制 HIF 降解来模拟少突胶质细胞局部缺氧的小鼠,表现出 OPC 成熟停滞和随后的少突胶质化障碍,类似于早产儿和先天性心脏病婴儿中观察到的弥漫性脑白质疾病。这些关于氧感应和髓鞘形成的最新实验发现,有待于整合到临床框架中。对高氧或低氧的基因调节,而不是氧化应激,可能是新生儿脑白质疾病的重要机制。