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亚精胺可恢复细胞转运障碍病理生理学背后的自噬缺陷。

Spermidine Recovers the Autophagy Defects Underlying the Pathophysiology of Cell Trafficking Disorders.

作者信息

Díaz-Osorio Yaiza, Gimeno-Agud Helena, Mari-Vico Rosanna, Illescas Sofía, Ramos Jose Miguel, Darling Alejandra, García-Cazorla Àngels, Oyarzábal Alfonso

机构信息

Synaptic Metabolism and Personalized Therapies Lab, Institut de Recerca Sant Joan de Déu, Department of Neurology and MetabERN; Esplugues de Llobregat, Barcelona, Spain.

Pediatric Neurometabolism + Personalized Therapies Lab, University Abat Oliba CEU, Barcelona, Spain.

出版信息

J Inherit Metab Dis. 2025 Jan;48(1):e12841. doi: 10.1002/jimd.12841.

Abstract

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.

摘要

细胞转运改变是一类日益增多的疾病,也是遗传性代谢疾病中最大的类别之一。它们具有复杂多变的临床表现。就神经学表现而言,其症状范围广泛,涵盖从神经发育障碍到神经退行性疾病。对单基因细胞转运疾病的研究为理解这一复杂的疾病群体及寻找新的治疗途径提供了一个框架。在其病理生理学中,自噬改变作为一种可靶向的疾病机制尤为突出,有望通过不同策略进行调节。在这项研究中,我们研究了由于SYNJ1和NBAS基因突变导致的两种细胞转运疾病的病理生理学。具体而言,我们评估了患者及性别/年龄匹配的对照者原代成纤维细胞培养物中的自噬通量,以及是否可以将其用于治疗目的。研究结果表明自噬是该疾病的标志之一。此外,我们在体外测试了亚精胺(一种作为自噬诱导剂的天然多胺)的作用。鉴于阳性结果,随后我们在一系列单病例临床试验中对患者进行了疗效评估,发现其在与运动能力和认知相关的一些临床方面取得了改善。将自噬改变定义为细胞转运疾病病理生理学中的一个共同特征,是朝着其治疗迈出的重要一步,因为这代表了对这些疾病进行个性化治疗的一个潜在可操作靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436d/11751594/4b961b310f9a/JIMD-48-0-g001.jpg

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