亚精胺恢复细胞运输障碍病理生理学基础上的自噬缺陷。

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Yaiza Díaz-Osorio, Helena Gimeno-Agud, Rosanna Mari-Vico, Sofía Illescas, Jose Miguel Ramos, Alejandra Darling, Àngels García-Cazorla, Alfonso Oyarzábal
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引用次数: 0

摘要

细胞运输改变是一种日益增长的疾病,也是遗传性代谢疾病的最大类别之一。其临床表现复杂多变。关于神经系统的表现,他们可以表现出广泛的症状,从神经发育到神经退行性疾病。单基因细胞运输疾病的研究为理解这一复杂的疾病群体和寻找新的治疗途径提供了一个场景。在它们的病理生理学中,自噬的改变作为一种可靶向的疾病机制而突出,可以通过不同的策略进行调节。在这项工作中,我们研究了SYNJ1和NBAS基因突变引起的两种细胞运输障碍的病理生理学。具体来说,我们已经评估了患者和性别/年龄匹配对照的原代成纤维细胞培养中的自噬通量,以及是否可以用于治疗目的。结果使自噬成为该疾病的标志之一。此外,我们在体外测试了亚精胺的作用,亚精胺是一种天然多胺,可作为自噬诱导剂。由于阳性结果,随后对患者也进行了疗效评估,在一系列n-of-1的临床试验中,在运动和认知方面的一些临床方面取得了改善。将自噬改变定义为细胞运输障碍病理生理学中的一个共同特征是朝着治疗这些疾病迈出的一大步,因为它代表了这些疾病个性化治疗的潜在可行目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spermidine Recovers the Autophagy Defects Underlying the Pathophysiology of Cell Trafficking Disorders.

Cell trafficking alterations are a growing group of disorders and one of the largest categories of Inherited Metabolic Diseases. They have complex and variable clinical presentation. Regarding neurological manifestations they can present a wide repertoire of symptoms ranging from neurodevelopmental to neurodegnerative disorders. The study of monogenic cell trafficking diseases draws an scenario to understanding this complex group of disorders and to find new therapeutic avenues. Within their pathophysiology, alterations in autophagy outstand as a targetable mechanism of disease, ammended to be modulated through different strategies. In this work we have studied the pathophysiology of two cell trafficking disorders due to mutations in SYNJ1 and NBAS genes. Specifically, we have assesed the autophagic flux in primary fibroblast cultures of the patients and gender/age-matched controls and whether it could be address with a therapeutic purpose. The results have shaped autophagy as one of the hallmarks of the disease. Moreover, we tested in vitro the effect of spermidine, a natural polyamine that acts as an autopagy inductor. Due to the positive results, its efficacy was evaluated later on the patients as well, in a series of n-of-1 clinical trials, achieving improvement in some clinical aspects related to motricity and cognition. Defining autophagy alterations as a common feature in the pathophysiology of cell trafficking disorders is a great step towards their treatment, as it represents a potential actionable target for the personalized treatement of these disorders.

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来源期刊
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease 医学-内分泌学与代谢
CiteScore
9.50
自引率
7.10%
发文量
117
审稿时长
4-8 weeks
期刊介绍: The Journal of Inherited Metabolic Disease (JIMD) is the official journal of the Society for the Study of Inborn Errors of Metabolism (SSIEM). By enhancing communication between workers in the field throughout the world, the JIMD aims to improve the management and understanding of inherited metabolic disorders. It publishes results of original research and new or important observations pertaining to any aspect of inherited metabolic disease in humans and higher animals. This includes clinical (medical, dental and veterinary), biochemical, genetic (including cytogenetic, molecular and population genetic), experimental (including cell biological), methodological, theoretical, epidemiological, ethical and counselling aspects. The JIMD also reviews important new developments or controversial issues relating to metabolic disorders and publishes reviews and short reports arising from the Society''s annual symposia. A distinction is made between peer-reviewed scientific material that is selected because of its significance for other professionals in the field and non-peer- reviewed material that aims to be important, controversial, interesting or entertaining (“Extras”).
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