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早发性阿尔茨海默病患者的外周血单个核细胞重编程诱导多能干细胞(iPSCs)

Peripheral blood mononuclear cell-converted induced pluripotent stem cells (iPSCs) from an early onset Alzheimer's patient.

作者信息

Lee Han-Kyu, Morin Peter, Xia Weiming

机构信息

Department of Neurology, Rhode Island Hospital and Brown University Warren Alpert Medical School, 593 Eddy Street, Providence, RI, United States; Geriatric Research, Education and Clinical Center, Edith Nourse Rogers Memorial Veterans Hospital, Bedford, MA, United States.

Geriatric Research, Education and Clinical Center, Edith Nourse Rogers Memorial Veterans Hospital, Bedford, MA, United States.

出版信息

Stem Cell Res. 2016 Mar;16(2):213-5. doi: 10.1016/j.scr.2015.12.050. Epub 2016 Jan 15.

Abstract

Improvement in transduction efficiency makes it possible to convert blood cells into induced pluripotent stem cells (iPSC). In this study, we generated an iPSC line from peripheral blood mononuclear cells (PBMC) donated by a patient who exhibited memory deficit at age 59; outcome of positron emission tomography scan is consistent with a diagnosis of Alzheimer's disease. Integration-free CytoTune-iPS Sendai Reprogramming factors which include Sendai virus particles of the four Yamanaka factors Oct4, Sox2, Klf4, and c-Myc were introduced to PBMC to convert them to iPSCs without retention of virus. Three germ layer differentiation was induced to demonstrate the pluripotency of these iPSCs.

摘要

转导效率的提高使得将血细胞转化为诱导多能干细胞(iPSC)成为可能。在本研究中,我们从一名59岁时出现记忆缺陷的患者捐赠的外周血单个核细胞(PBMC)中生成了一条iPSC系;正电子发射断层扫描的结果与阿尔茨海默病的诊断一致。将无整合的CytoTune-iPS仙台重编程因子(其中包括四种山中因子Oct4、Sox2、Klf4和c-Myc的仙台病毒颗粒)导入PBMC,以将它们转化为不保留病毒的iPSC。诱导三胚层分化以证明这些iPSC的多能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d9/7008971/7982caf37ef8/nihms-1057986-f0001.jpg

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