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生成并鉴定携带 Hermansky-Pudlak 综合征 2 型(HPS2)相关杂合复合突变 AP3B1 的人诱导多能干细胞系(iPSC 系),该突变系源自对照和患者。

Generation and characterization of a control and patient-derived human iPSC line containing the Hermansky Pudlak type 2 (HPS2) associated heterozygous compound mutation in AP3B1.

机构信息

Department of Blood Cell Research, Sanquin Research, Amsterdam University Medical Center (AUMC), University of Amsterdam, Amsterdam, The Netherlands.

Department of Molecular and Cellular Hemostasis, Sanquin Research, Amsterdam, The Netherlands.

出版信息

Stem Cell Res. 2021 Jul;54:102444. doi: 10.1016/j.scr.2021.102444. Epub 2021 Jun 23.

Abstract

Induced pluripotent stem cells (iPSCs) were generated from blood outgrowth endothelial cells (BOECs) obtained from a healthy donor and from a patient diagnosed with Hermansky Pudlak Syndrome type 2 (HPS2), caused by compound heterozygous AP3B1 mutations (c.177delA and c.1839-1842delTAGA). BOECs were reprogrammed with a hOKSM self-silencing polycistronic lentiviral vector, where the generated iPSCs showed normal karyotype, expression of pluripotency associated markers and in vitro spontaneous differentiation towards the three germ layers. The generated iPSCs can be used to study HPS2 pathophysiology and the basic functions of AP3B1 protein in different cell types.

摘要

诱导多能干细胞(iPSCs)是从一位健康供体和一位被诊断患有 Hermansky Pudlak 综合征 2 型(HPS2)的患者的血液衍生的内皮细胞(BOECs)中生成的,该患者的 HPS2 是由 AP3B1 基因突变的复合杂合子引起的(c.177delA 和 c.1839-1842delTAGA)。使用 hOKSM 自我沉默多顺反子慢病毒载体对 BOECs 进行重编程,生成的 iPSCs 显示正常核型、多能性相关标志物的表达以及体外向三个胚层的自发分化。生成的 iPSCs 可用于研究 HPS2 发病机制和 AP3B1 蛋白在不同细胞类型中的基本功能。

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