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酶替代疗法可预防小鼠同型胱氨酸尿症中的新生儿死亡、肝损伤和骨质疏松症。

Enzyme replacement prevents neonatal death, liver damage, and osteoporosis in murine homocystinuria.

作者信息

Majtan Tomas, Hůlková Helena, Park Insun, Krijt Jakub, Kožich Viktor, Bublil Erez M, Kraus Jan P

机构信息

Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA;

Institute of Inherited Metabolic Disorders, Charles University-First Faculty of Medicine and General University Hospital, Prague, Czech Republic.

出版信息

FASEB J. 2017 Dec;31(12):5495-5506. doi: 10.1096/fj.201700565R. Epub 2017 Aug 16.

Abstract

Classical homocystinuria (HCU) is an inborn error of sulfur amino acid metabolism caused by deficient activity of cystathionine β-synthase (CBS), resulting in an accumulation of homocysteine and a concomitant decrease of cystathionine and cysteine in blood and tissues. In mice, the complete lack of CBS is neonatally lethal. In this study, newborn CBS-knockout (KO) mice were treated with recombinant polyethyleneglycolylated human truncated CBS (PEG-CBS). Full survival of the treated KO mice, along with a positive impact on metabolite levels in plasma, liver, brain, and kidneys, was observed. The PEG-CBS treatment prevented an otherwise fatal liver disease characterized by steatosis, death of hepatocytes, and ultrastructural abnormalities of endoplasmic reticulum and mitochondria. Furthermore, treatment of the KO mice for 5 mo maintained the plasma metabolite balance and completely prevented osteoporosis and changes in body composition that characterize both the KO model and human patients. These findings argue that early treatment of patients with HCU with PEG-CBS may prevent clinical symptoms of the disease possibly without the need of dietary protein restriction.-Majtan, T., Hůlková, H., Park, I., Krijt, J., Kožich, V., Bublil, E. M., Kraus, J. P. Enzyme replacement prevents neonatal death, liver damage, and osteoporosis in murine homocystinuria.

摘要

经典型同型胱氨酸尿症(HCU)是一种硫氨基酸代谢的先天性缺陷疾病,由胱硫醚β-合酶(CBS)活性不足引起,导致血液和组织中同型半胱氨酸积累,同时胱硫醚和半胱氨酸减少。在小鼠中,完全缺乏CBS在新生儿期是致死性的。在本研究中,对新生的CBS基因敲除(KO)小鼠用重组聚乙二醇化人截短型CBS(PEG-CBS)进行治疗。观察到经治疗的KO小鼠完全存活,并且对血浆、肝脏、脑和肾脏中的代谢物水平有积极影响。PEG-CBS治疗预防了一种以脂肪变性、肝细胞死亡以及内质网和线粒体超微结构异常为特征的致命性肝病。此外,对KO小鼠进行5个月的治疗维持了血浆代谢物平衡,并完全预防了KO模型和人类患者所特有的骨质疏松和身体成分变化。这些发现表明,用PEG-CBS对HCU患者进行早期治疗可能无需限制饮食蛋白质就能预防该疾病的临床症状。-马伊坦,T.,胡尔科娃,H.,朴,I.,克里伊特,J.,科齐奇,V.,布布利尔,E.M.,克劳斯,J.P.酶替代疗法可预防小鼠同型胱氨酸尿症中的新生儿死亡、肝损伤和骨质疏松。

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