Biomedical and Technology Science Section, Department of Science, Roma Tre University, Viale Marconi 446, 00146 Rome, Italy.
Centre National de la Recherche Scientifique, Institut des Neurosciences Cellulaires et Intégratives, Université de Strasbourg, 8 Allée General Rouvillois, 67000 Strasbourg, France.
Int J Mol Sci. 2020 Nov 26;21(23):8979. doi: 10.3390/ijms21238979.
Biomedical research aims to understand the molecular mechanisms causing human diseases and to develop curative therapies. So far, these goals have been achieved for a small fraction of diseases, limiting factors being the availability, validity, and use of experimental models. Niemann-Pick type C (NPC) is a prime example for a disease that lacks a curative therapy despite substantial breakthroughs. This rare, fatal, and autosomal-recessive disorder is caused by defects in NPC1 or NPC2. These ubiquitously expressed proteins help cholesterol exit from the endosomal-lysosomal system. The dysfunction of either causes an aberrant accumulation of lipids with patients presenting a large range of disease onset, neurovisceral symptoms, and life span. Here, we note general aspects of experimental models, we describe the line-up used for NPC-related research and therapy development, and we provide an outlook on future topics.
生物医学研究旨在了解导致人类疾病的分子机制,并开发治疗方法。到目前为止,这些目标仅在一小部分疾病中实现,限制因素是实验模型的可用性、有效性和使用。尼曼-匹克 C 型(NPC)是一个缺乏治疗方法的疾病的典型例子,尽管已经取得了重大突破。这种罕见的、致命的、常染色体隐性遗传病是由 NPC1 或 NPC2 的缺陷引起的。这些广泛表达的蛋白质有助于胆固醇从内体溶酶体系统中排出。这两种蛋白的功能障碍都会导致脂质的异常积累,患者的发病时间、神经内脏症状和寿命长短差异很大。在这里,我们注意到实验模型的一般方面,我们描述了用于 NPC 相关研究和治疗开发的模型,并对未来的课题进行了展望。