Department of Fundamental Neurosciences, University of Lausanne, Lausanne, Switzerland.
Clinic of Neonatology, Department of Women, Mother and Child, University Hospital Center and University of Lausanne, Lausanne, Switzerland.
Cell Death Dis. 2018 Aug 28;9(9):853. doi: 10.1038/s41419-018-0916-z.
Cystic periventricular leukomalacia is commonly diagnosed in premature infants, resulting from severe hypoxic-ischemic white matter injury, and also involving some grey matter damage. Very few is known concerning the cell death pathways involved in these types of premature cerebral lesions. Excitotoxicity is a predominant mechanism of hypoxic-ischemic injury in the developing brain. Concomitantly, it has been recently shown that autophagy could be enhanced in excitotoxic conditions switching this physiological intracellular degradation system to a deleterious process. We here investigated the role of autophagy in a validated rodent model of preterm excitotoxic brain damage mimicking in some aspects cystic periventricular leukomalacia. An excitotoxic lesion affecting periventricular white and grey matter was induced by injecting ibotenate, a glutamate analogue, in the subcortical white matter (subcingulum area) of five-day old rat pups. Ibotenate enhanced autophagy in rat brain dying neurons at 24 h as shown by increased presence of autophagosomes (increased LC3-II and LC3-positive dots) and enhanced autophagic degradation (SQSTM1 reduction and increased number and size of lysosomes (LAMP1- and CATHEPSIN B-positive vesicles)). Co-injection of the pharmacological autophagy inhibitor 3-methyladenine prevented not only autophagy induction but also CASPASE-3 activation and calpain-dependent cleavage of SPECTRIN 24 h after the insult, thus providing a strong reduction of the long term brain injury (16 days after ibotenate injection) including lateral ventricle dilatation, decreases in cerebral tissue volume and in subcortical white matter thickness. The autophagy-dependent neuroprotective effect of 3-methyladenine was confirmed in primary cortical neuronal cultures using not only pharmacological but also genetic autophagy inhibition of the ibotenate-induced autophagy. Strategies inhibiting autophagy could then represent a promising neuroprotective approach in the context of severe preterm brain injuries.
囊性脑室周围脑白质软化症常见于早产儿,由严重的缺氧缺血性白质损伤引起,也涉及一些灰质损伤。对于这些类型的早产儿脑损伤中涉及的细胞死亡途径知之甚少。兴奋性毒性是发育中大脑缺氧缺血损伤的主要机制。同时,最近已经表明,自噬可以在兴奋性毒性条件下增强,将这种生理细胞内降解系统转变为有害过程。我们在这里研究了自噬在一种已验证的早产兴奋性脑损伤啮齿动物模型中的作用,该模型在某些方面模拟了囊性脑室周围脑白质软化症。通过在五天大的大鼠幼仔的皮质下白质(皮层下区域)中注射谷氨酸类似物伊博霉素,诱导出一种影响脑室周围白质和灰质的兴奋性病变。伊博霉素在 24 小时内增强了大鼠脑死亡神经元中的自噬,表现为自噬体(LC3-II 和 LC3 阳性斑点增加)增加和自噬降解增强(SQSTM1 减少和溶酶体(LAMP1-和 CATHEPSIN B 阳性囊泡)数量和大小增加)。同时注射药理学自噬抑制剂 3-甲基腺嘌呤不仅可以防止自噬诱导,还可以防止 CASPASE-3 激活和钙蛋白酶依赖性切割 SPECTRIN 24 小时后,从而大大减少长期脑损伤(伊博霉素注射后 16 天),包括侧脑室扩张、脑组织结构体积减少和皮质下白质厚度减少。3-甲基腺嘌呤的自噬依赖性神经保护作用在原代皮质神经元培养物中得到了证实,不仅使用了药理学方法,还使用了基因抑制伊博霉素诱导的自噬。因此,抑制自噬的策略可能成为严重早产儿脑损伤背景下有前途的神经保护方法。