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单基因神经退行性疾病的复杂性:尼曼-匹克 C 病治疗驱动研究的 20 多年。

The complexity of a monogenic neurodegenerative disease: More than two decades of therapeutic driven research into Niemann-Pick type C disease.

机构信息

School of Biological Sciences, Victoria University of Wellington, Wellington 6012, New Zealand.

School of Biological Sciences, Victoria University of Wellington, Wellington 6012, New Zealand.

出版信息

Biochim Biophys Acta Mol Cell Biol Lipids. 2019 Aug;1864(8):1109-1123. doi: 10.1016/j.bbalip.2019.04.002. Epub 2019 Apr 17.

DOI:10.1016/j.bbalip.2019.04.002
PMID:31002946
Abstract

Niemann-Pick type C (NP-C) disease is a rare and fatal neurodegenerative disease typified by aberrations in intracellular lipid transport. Cholesterol and other lipids accumulate in the late endosome/lysosome of all diseased cells thereby causing neuronal and visceral atrophy. A cure for NP-C remains elusive despite the extensive molecular advances emanating from the identification of the primary genetic defect in 1997. Penetration of the blood-brain barrier and efficacy in the viscera are prerequisites for effective therapy, however the rarity of NP-C disease is the major impediment to progress. Disease diagnosis is challenging and establishment of appropriate test populations for clinical trials difficult. Fortunately, disease models that span the diversity of microbial and metazoan life have been utilized to advance the quest for a therapy. The complexity of lipid storage in this disorder and in the model systems, has led to multiple theories on the primary disease mechanism and consequently numerous and varied proposed interventions. Here, we conduct an evaluation of these studies.

摘要

尼曼-皮克 C 型(NP-C)疾病是一种罕见且致命的神经退行性疾病,其特征是细胞内脂质运输异常。胆固醇和其他脂质在内体/溶酶体的晚期在所有患病细胞中积累,从而导致神经元和内脏萎缩。尽管自 1997 年确定主要遗传缺陷以来,分子学取得了广泛的进展,但 NP-C 疾病的治疗方法仍然难以捉摸。穿透血脑屏障和在内脏中的疗效是有效治疗的前提条件,然而 NP-C 疾病的罕见性是阻碍进展的主要因素。疾病诊断具有挑战性,临床试验的合适测试人群的建立也具有难度。幸运的是,跨越微生物和后生动物生命多样性的疾病模型已被用于推进治疗方法的研究。该疾病中脂质储存的复杂性以及模型系统中的复杂性,导致了对主要疾病机制的多种理论,进而提出了许多不同的干预措施。在这里,我们对这些研究进行了评估。

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