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从尼曼-匹克病C型患者来源的成纤维细胞中生成患者特异性人类神经干细胞。

Generation of patient specific human neural stem cells from Niemann-Pick disease type C patient-derived fibroblasts.

作者信息

Sung Eun-Ah, Yu Kyung-Rok, Shin Ji-Hee, Seo Yoojin, Kim Hyung-Sik, Koog Myung Guen, Kang Insung, Kim Jae-Jun, Lee Byung-Chul, Shin Tae-Hoon, Lee Jin Young, Lee Seunghee, Kang Tae-Wook, Choi Soon Won, Kang Kyung-Sun

机构信息

Adult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul 08826, Republic of Korea.

Research Institute for Veterinary Science, College of Veterinary Medicine, Seoul National University, Seoul 08826, Republic of Korea.

出版信息

Oncotarget. 2017 Aug 7;8(49):85428-85441. doi: 10.18632/oncotarget.19976. eCollection 2017 Oct 17.

Abstract

Niemann-Pick disease type C (NPC) is a neurodegenerative and lysosomal lipid storage disorder, characterized by the abnormal accumulation of unesterified cholesterol and glycolipids, which is caused by mutations in the genes. Here, we report the generation of human induced neural stem cells from NPC patient-derived fibroblasts (NPC-iNSCs) using only two reprogramming factors and without going through the pluripotent state. NPC-iNSCs were stably expandable and differentiated into neurons, astrocytes, and oligodendrocytes. However, NPC-iNSCs displayed defects in self-renewal and neuronal differentiation accompanied by cholesterol accumulation, suggesting that NPC-iNSCs retain the main features of NPC. This study revealed that the cholesterol accumulation and the impairments in self-renewal and neuronal differentiation in NPC-iNSCs were significantly improved by valproic acid. Additionally, we demonstrated that the inhibition of cholesterol transportation by U18666A in WT-iNSCs mimicked the impaired self-renewal and neuronal differentiation of NPC-iNSCs, indicating that the regulation of cholesterol homeostasis is a crucial determinant for the neurodegenerative features of NPC. Taken together, these findings suggest that NPC-iNSCs can serve as an unlimited source of neural cells for pathological study or drug screening in a patient specific manner. Furthermore, this direct conversion technology might be extensively applicable for other human neurodegenerative diseases.

摘要

尼曼-匹克C型病(NPC)是一种神经退行性和溶酶体脂质贮积病,其特征是未酯化胆固醇和糖脂异常蓄积,由基因突变所致。在此,我们报告仅使用两种重编程因子从NPC患者来源的成纤维细胞生成人诱导神经干细胞(NPC-iNSCs),且不经过多能状态。NPC-iNSCs可稳定扩增并分化为神经元、星形胶质细胞和少突胶质细胞。然而,NPC-iNSCs在自我更新和神经元分化方面存在缺陷,并伴有胆固醇蓄积,提示NPC-iNSCs保留了NPC的主要特征。本研究表明,丙戊酸可显著改善NPC-iNSCs中的胆固醇蓄积以及自我更新和神经元分化障碍。此外,我们证明U18666A对野生型诱导神经干细胞(WT-iNSCs)胆固醇转运的抑制模拟了NPC-iNSCs自我更新和神经元分化受损的情况,表明胆固醇稳态调节是NPC神经退行性特征的关键决定因素。综上所述,这些发现提示NPC-iNSCs可以作为一种无限的神经细胞来源,以患者特异性方式用于病理研究或药物筛选。此外,这种直接转化技术可能广泛适用于其他人类神经退行性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb0c/5689620/c6d0d4a46696/oncotarget-08-85428-g001.jpg

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