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REP1 缺失导致脉络膜白化病的脂质代谢和氧化应激的全身功能障碍。

REP1 deficiency causes systemic dysfunction of lipid metabolism and oxidative stress in choroideremia.

机构信息

Department of Development, Ageing and Disease, UCL Institute of Ophthalmology, London, United Kingdom.

Department of Genetics, Moorfields Eye Hospital NHS Foundation Trust, London, United Kingdom.

出版信息

JCI Insight. 2021 May 10;6(9):146934. doi: 10.1172/jci.insight.146934.

Abstract

Choroideremia (CHM) is an X-linked recessive chorioretinal dystrophy caused by mutations in CHM, encoding for Rab escort protein 1 (REP1). Loss of functional REP1 leads to the accumulation of unprenylated Rab proteins and defective intracellular protein trafficking, the putative cause for photoreceptor, retinal pigment epithelium (RPE), and choroidal degeneration. CHM is ubiquitously expressed, but adequate prenylation is considered to be achieved, outside the retina, through the isoform REP2. Recently, the possibility of systemic features in CHM has been debated; therefore, in this study, whole metabolomic analysis of plasma samples from 25 CHM patients versus age- and sex-matched controls was performed. Results showed plasma alterations in oxidative stress-related metabolites, coupled with alterations in tryptophan metabolism, leading to significantly raised serotonin levels. Lipid metabolism was disrupted with decreased branched fatty acids and acylcarnitines, suggestive of dysfunctional lipid oxidation, as well as imbalances of several sphingolipids and glycerophospholipids. Targeted lipidomics of the chmru848 zebrafish provided further evidence for dysfunction, with the use of fenofibrate over simvastatin circumventing the prenylation pathway to improve the lipid profile and increase survival. This study provides strong evidence for systemic manifestations of CHM and proposes potentially novel pathomechanisms and targets for therapeutic consideration.

摘要

脉络膜视网膜变性(CHM)是一种 X 连锁隐性视网膜营养不良,由 CHM 基因突变引起,该基因编码 Rab 衔接蛋白 1(REP1)。功能性 REP1 的丧失导致未酰化 Rab 蛋白的积累和细胞内蛋白转运的缺陷,这是光感受器、视网膜色素上皮(RPE)和脉络膜变性的潜在原因。CHM 广泛表达,但在视网膜外,通过 REP2 同工型,认为可以实现适当的预酰化。最近,CHM 是否存在全身特征一直存在争议;因此,在这项研究中,对 25 名 CHM 患者与年龄和性别匹配的对照者的血浆样本进行了全代谢组学分析。结果表明,氧化应激相关代谢物的血浆发生改变,同时色氨酸代谢发生改变,导致血清素水平显著升高。脂代谢受到破坏,支链脂肪酸和酰基肉碱减少,表明脂质氧化功能障碍,以及几种鞘脂和甘油磷脂的失衡。chmru848 斑马鱼的靶向脂质组学提供了进一步的功能障碍证据,使用非诺贝特而不是辛伐他汀绕过预酰化途径,改善脂质谱并提高存活率。这项研究为 CHM 的全身表现提供了强有力的证据,并提出了潜在的新的病理机制和治疗考虑的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/236c/8262314/8809f3c0e452/jciinsight-6-146934-g113.jpg

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