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Yap1-Usp14 轴通过调节 Beclin-1 泛素化抑制新生鼠缺氧缺血性脑病时的神经元自噬。

Yap1-Usp14 Axis Inhibits Neuronal Mitophagy During Neonatal Hypoxia-Ischemia Encephalopathy by Regulation of Beclin-1 Ubiquitination in Mouse.

机构信息

National Clinical Research Center for Child Health of the Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310052, China.

Department of Neurosurgery, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310052, China.

出版信息

Mol Neurobiol. 2023 Aug;60(8):4273-4287. doi: 10.1007/s12035-023-03344-5. Epub 2023 Apr 17.

Abstract

Neonatal hypoxic-ischemic encephalopathy (HIE) that results from perinatal cerebral hypoxia-ischemia has become one of the leading causes of acute mortality and chronic disability in infants and children. Despite that neuronal mitophagy and subsequent clearance of damaged neurons exert protective effect, the pathogenesis of HIE and effective treatment strategies for intervention of HIE remain poorly understood. Here, we report that ubiquitin-specific protease 14 (Usp14, a deubiquitinating enzyme) is closely associated with HIE progression by its negative regulation in neuronal mitophagy in mouse. The expression of Usp14 is elevated in both an oxygen-glucose deprivation (OGD) mouse neuronal cell line culture model in vitro and a HIE mouse model in vivo. Mechanistically, OGD treatment activates Hippo signaling that enhances Yap1 phosphorylation levels at Ser-127 but inhibits Yap1 protein level, which potentiates Usp14 transcription and leads to the downregulated ubiquitination at Lys-63 of Beclin-1, a key molecule in autophagy, resulting in the suppressed neuronal mitophagy, subsequent failure in the clearance of damaged neurons, and finally possible dysregulation in brain functions. Thus, our results provide with Usp14 as a novel target and treatment strategy for intervention of HIE, which may help diagnose and treat HIE in clinic.

摘要

新生儿缺氧缺血性脑病(HIE)是围产期脑缺氧缺血引起的,已成为婴儿和儿童急性死亡和慢性残疾的主要原因之一。尽管神经元细胞自噬及其随后对受损神经元的清除具有保护作用,但 HIE 的发病机制和有效的干预治疗策略仍知之甚少。在这里,我们报告泛素特异性蛋白酶 14(Usp14,一种去泛素化酶)通过其在小鼠神经元细胞自噬中的负调控,与 HIE 的进展密切相关。Usp14 的表达在体外氧葡萄糖剥夺(OGD)小鼠神经元细胞系培养模型和体内 HIE 小鼠模型中均升高。在机制上,OGD 处理激活 Hippo 信号通路,增强 Yap1 丝氨酸 127 位的磷酸化水平,但抑制 yap1 蛋白水平,从而增强 Usp14 的转录,并导致自噬关键分子 Beclin-1 的赖氨酸 63 位泛素化降低,导致神经元细胞自噬抑制,随后受损神经元清除失败,最终可能导致脑功能失调。因此,我们的研究结果为 HIE 的干预提供了 Usp14 作为一个新的靶点和治疗策略,这可能有助于临床上对 HIE 的诊断和治疗。

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