Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Hum Mol Genet. 2023 Jun 5;32(12):1988-2004. doi: 10.1093/hmg/ddad031.
SURF1 deficiency (OMIM # 220110) causes Leigh syndrome (LS, OMIM # 256000), a mitochondrial disorder typified by stress-induced metabolic strokes, neurodevelopmental regression and progressive multisystem dysfunction. Here, we describe two novel surf1-/- zebrafish knockout models generated by CRISPR/Cas9 technology. While gross larval morphology, fertility, and survival into adulthood appeared unaffected, surf1-/- mutants manifested adult-onset ocular anomalies and decreased swimming activity, as well as classical biochemical hallmarks of human SURF1 disease, including reduced complex IV expression and enzymatic activity and increased tissue lactate. surf1-/- larvae also demonstrated oxidative stress and stressor hypersensitivity to the complex IV inhibitor, azide, which exacerbated their complex IV deficiency, reduced supercomplex formation, and induced acute neurodegeneration typical of LS including brain death, impaired neuromuscular responses, reduced swimming activity, and absent heartrate. Remarkably, prophylactic treatment of surf1-/- larvae with either cysteamine bitartrate or N-acetylcysteine, but not other antioxidants, significantly improved animal resiliency to stressor-induced brain death, swimming and neuromuscular dysfunction, and loss of heartbeat. Mechanistic analyses demonstrated cysteamine bitartrate pretreatment did not improve complex IV deficiency, ATP deficiency, or increased tissue lactate but did reduce oxidative stress and restore glutathione balance in surf1-/- animals. Overall, two novel surf1-/- zebrafish models recapitulate the gross neurodegenerative and biochemical hallmarks of LS, including azide stressor hypersensitivity that was associated with glutathione deficiency and ameliorated by cysteamine bitartrate or N-acetylcysteine therapy.
SURF1 缺乏症(OMIM#220110)导致 Leigh 综合征(LS,OMIM#256000),这是一种线粒体疾病,其特征为应激诱导的代谢性中风、神经发育倒退和进行性多系统功能障碍。在这里,我们描述了两种由 CRISPR/Cas9 技术产生的新型 surf1-/-斑马鱼敲除模型。虽然大体幼虫形态、生育力和成年期的存活率似乎没有受到影响,但 surf1-/-突变体表现出成年期眼部异常和游泳活动减少,以及人类 SURF1 疾病的典型生化特征,包括复合物 IV 表达和酶活性降低以及组织内乳酸增加。surf1-/-幼虫还表现出氧化应激和对复合物 IV 抑制剂叠氮化物的应激敏感性增加,这加剧了它们的复合物 IV 缺乏,减少了超复合物形成,并诱导了典型的 LS 急性神经退行性变,包括脑死亡、神经肌肉反应受损、游泳活动减少和心率缺失。值得注意的是,预防性地用半胱胺二氢盐或 N-乙酰半胱氨酸治疗 surf1-/-幼虫,但不是其他抗氧化剂,可显著改善动物对应激诱导的脑死亡、游泳和神经肌肉功能障碍以及心率缺失的应激耐受力。机制分析表明,半胱胺二氢盐预处理并没有改善复合物 IV 缺乏、ATP 缺乏或组织内乳酸增加,但确实减轻了氧化应激并恢复了 surf1-/-动物的谷胱甘肽平衡。总体而言,两种新型 surf1-/-斑马鱼模型重现了 LS 的大体神经退行性和生化特征,包括对叠氮化物应激的敏感性增加,这与谷胱甘肽缺乏有关,并通过半胱胺二氢盐或 N-乙酰半胱氨酸治疗得到改善。