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泛酸激酶相关神经变性中的精准医学

Precision medicine in pantothenate kinase-associated neurodegeneration.

作者信息

Alvarez-Cordoba Mónica, Villanueva-Paz Marina, Villalón-García Irene, Povea-Cabello Suleva, Suárez-Rivero Juan M, Talaverón-Rey Marta, Abril-Jaramillo Javier, Vintimilla-Tosi Ana Belén, Sánchez-Alcázar José A

机构信息

Centro Andaluz de Biología del Desarrollo (CABD-CSIC-Universidad Pablo de Olavide), and Centro de Investigación Biomédica en Red: Enfermedades Raras, Instituto de Salud Carlos III, Sevilla, Spain.

Centro de Neurología Avanzada, Sevilla, Spain.

出版信息

Neural Regen Res. 2019 Jul;14(7):1177-1185. doi: 10.4103/1673-5374.251203.

DOI:10.4103/1673-5374.251203
PMID:30804242
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6425824/
Abstract

Neurodegeneration with brain iron accumulation is a broad term that describes a heterogeneous group of progressive and invalidating neurologic disorders in which iron deposits in certain brain areas, mainly the basal ganglia. The predominant clinical symptoms include spasticity, progressive dystonia, Parkinson's disease-like symptoms, neuropsychiatric alterations, and retinal degeneration. Among the neurodegeneration with brain iron accumulation disorders, the most frequent subtype is pantothenate kinase-associated neurodegeneration (PKAN) caused by defects in the gene encoding the enzyme pantothenate kinase 2 (PANK2) which catalyzed the first reaction of the coenzyme A biosynthesis pathway. Currently there is no effective treatment to prevent the inexorable course of these disorders. The aim of this review is to open up a discussion on the utility of using cellular models derived from patients as a valuable tool for the development of precision medicine in PKAN. Recently, we have described that dermal fibroblasts obtained from PKAN patients can manifest the main pathological changes of the disease such as intracellular iron accumulation accompanied by large amounts of lipofuscin granules, mitochondrial dysfunction and a pronounced increase of markers of oxidative stress. In addition, PKAN fibroblasts showed a morphological senescence-like phenotype. Interestingly, pantothenate supplementation, the substrate of the PANK2 enzyme, corrected all pathophysiological alterations in responder PKAN fibroblasts with low/residual PANK2 enzyme expression. However, pantothenate treatment had no favourable effect on PKAN fibroblasts harbouring mutations associated with the expression of a truncated/incomplete protein. The correction of pathological alterations by pantothenate in individual mutations was also verified in induced neurons obtained by direct reprograming of PKAN fibroblasts. Our observations indicate that pantothenate supplementation can increase/stabilize the expression levels of PANK2 in specific mutations. Fibroblasts and induced neurons derived from patients can provide a useful tool for recognizing PKAN patients who can respond to pantothenate treatment. The presence of low but significant PANK2 expression which can be increased in particular mutations gives valuable information which can support the treatment with high dose of pantothenate. The evaluation of personalized treatments in vitro of fibroblasts and neuronal cells derived from PKAN patients with a wide range of pharmacological options currently available, and monitoring its effect on the pathophysiological changes, can help for a better therapeutic strategy. In addition, these cell models will be also useful for testing the efficacy of new therapeutic options developed in the future.

摘要

脑铁沉积神经退行性疾病是一个广义术语,用于描述一组异质性的进行性且使人衰弱的神经系统疾病,其中铁在某些脑区沉积,主要是基底神经节。主要临床症状包括痉挛、进行性肌张力障碍、帕金森病样症状、神经精神改变和视网膜变性。在脑铁沉积神经退行性疾病中,最常见的亚型是泛酸激酶相关神经退行性疾病(PKAN),它由编码泛酸激酶2(PANK2)的基因突变引起,该酶催化辅酶A生物合成途径的第一步反应。目前尚无有效的治疗方法来阻止这些疾病的不可阻挡的病程。本综述的目的是开启一场关于使用源自患者的细胞模型作为PKAN精准医学发展的有价值工具的实用性的讨论。最近,我们描述了从PKAN患者获得的皮肤成纤维细胞可以表现出该疾病的主要病理变化,如细胞内铁积累伴有大量脂褐素颗粒、线粒体功能障碍以及氧化应激标志物的显著增加。此外,PKAN成纤维细胞表现出一种形态学上类似衰老的表型。有趣的是,补充泛酸(PANK2酶的底物)可纠正具有低/残余PANK2酶表达的有反应的PKAN成纤维细胞中的所有病理生理改变。然而,泛酸治疗对携带与截短/不完整蛋白表达相关突变的PKAN成纤维细胞没有有利影响。通过直接重编程PKAN成纤维细胞获得的诱导神经元中也验证了泛酸对个别突变的病理改变的纠正作用。我们的观察结果表明,补充泛酸可以增加/稳定特定突变中PANK2的表达水平。源自患者的成纤维细胞和诱导神经元可以为识别能够对泛酸治疗产生反应的PKAN患者提供有用的工具。存在低但显著的PANK2表达,其在特定突变中可以增加,这提供了有价值的信息,可支持高剂量泛酸治疗。利用目前可用的广泛的药理学选择对源自PKAN患者的成纤维细胞和神经元细胞进行体外个性化治疗评估,并监测其对病理生理变化的影响,有助于制定更好的治疗策略。此外,这些细胞模型对于测试未来开发的新治疗选择的疗效也将是有用的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cd8/6425824/46aa7d147707/NRR-14-1177-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cd8/6425824/46aa7d147707/NRR-14-1177-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cd8/6425824/46aa7d147707/NRR-14-1177-g001.jpg

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本文引用的文献

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Application of Precision Medicine in Neurodegenerative Diseases.精准医学在神经退行性疾病中的应用。
Front Neurol. 2018 Aug 23;9:701. doi: 10.3389/fneur.2018.00701. eCollection 2018.
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Pantothenate Rescues Iron Accumulation in Pantothenate Kinase-Associated Neurodegeneration Depending on the Type of Mutation.泛酸激酶相关神经变性中,根据突变类型,泛酸盐可挽救铁蓄积。
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