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从人诱导多能干细胞中分离原始神经干细胞。

Derivation of primitive neural stem cells from human-induced pluripotent stem cells.

机构信息

Department of Stem Cell and Regenerative Biotechnology, KU Institute of Science and Technology, Konkuk University, Seoul, Republic of Korea.

Department of Dental Pharmacology, School of Dentistry and Institute of Oral Bioscience, BK21 Plus, Chonbuk National University, Jeonju, Republic of Korea.

出版信息

J Comp Neurol. 2019 Dec 15;527(18):3023-3033. doi: 10.1002/cne.24727. Epub 2019 Jun 20.

Abstract

Human-induced pluripotent stem cells (hiPSCs) have facilitated studies on organ development and differentiation into specific lineages in in vitro systems. Although numerous studies have focused on cellular differentiation into neural lineage using hPSCs, most studies have initially evaluated embryoid body (EB) formation, eventually yielding terminally differentiated neurons with limited proliferation potential. This study aimed to establish human primitive neural stem cells (pNSCs) from exogene-free hiPSCs without EB formation. To derive pNSCs, we optimized N2B27 neural differentiation medium through supplementation of two inhibitors, CHIR99021 (GSK-3 inhibitor) and PD0325901 (MEK inhibitor), and growth factors including basic fibroblast growth factor (bFGF) and human leukemia inhibitory factor (hLIF). Consequently, pNSCs were efficiently derived and cultured over a long term. pNSCs displayed differentiation potential into neurons, astrocytes, and oligodendrocytes. These early NSC types potentially promote the clinical application of hiPSCs to cure human neurological disorders.

摘要

人诱导多能干细胞(hiPSCs)促进了器官发育和体外特定谱系分化的研究。尽管许多研究集中在使用 hPSCs 将细胞分化为神经谱系上,但大多数研究最初评估了胚胎体(EB)的形成,最终产生了具有有限增殖潜力的终末分化神经元。本研究旨在从无 EB 形成的外源性 hiPSCs 中建立人类原始神经干细胞(pNSCs)。为了获得 pNSCs,我们通过添加两种抑制剂 CHIR99021(GSK-3 抑制剂)和 PD0325901(MEK 抑制剂)以及包括碱性成纤维细胞生长因子(bFGF)和人白血病抑制因子(hLIF)在内的生长因子来优化 N2B27 神经分化培养基。结果,pNSCs 被有效地衍生并长期培养。pNSCs 显示出分化为神经元、星形胶质细胞和少突胶质细胞的潜力。这些早期 NSC 类型可能会促进 hiPSC 在治疗人类神经疾病方面的临床应用。

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