4.3 Article

Hepatocyte growth factor enhances the generation of high-purity oligodendrocytes from human embryonic stem cells

期刊

DIFFERENTIATION
卷 78, 期 2-3, 页码 177-184

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.diff.2009.05.008

关键词

Human embryonic stem cells; Hepatocyte growth factor; G5 supplement; Oligodendrocyte

资金

  1. Yunnan Nature Science Foundation [2001C0009Z]
  2. Major State research Development Program [G200016108]
  3. Chinese Academy of Sciences [KSCX1-05]
  4. Chinese National Science Foundation [30370166]

向作者/读者索取更多资源

Generation of homogeneous oligodendrocytes as donor cells is essential for human embryonic stem cell (hESC)-based cell therapy for demylinating diseases. Herein we present a novel method for efficiently obtaining mature oligodendrocytes from hESCs with high purity (79.7 +/- 6.9%), using hepatocyte growth factor (HGF) and G5 supplement(containing insulin, transferrin, selenite, biotin, hydrocortisone, basic fibroblast growth factor and epidermal growth factor) in a four-step method. We induced hESCs into neural progenitors (NP) with HGF (5 ng/ml) and G5 (1 x) supplemented medium in an adherent differentiation system. The purified NPs were amplified in suspension as neurospheres for 1 month, and terminal oligodendrocyte differentiation was then induced by G5 supplement withdrawal and HGF treatment (20 ng/ml). The cells generated displayed typical morphologies of mature oligodendrocytes and expressed oligodendrocyte markers O4 and myelin basic protein (MBP). Our result revealed that HGF significantly enhanced the proliferation of hESC-derived NPs and promoted the differentiation as well as the maturation of oligodendrocytes from NPs. Further studies suggest that HGF/c-Met signaling pathway might play an important role in oligodendrocyte differentiation in our system. Our studies provide a means for generating the clinically relevant cell type and a platform for deciphering the molecular mechanisms that control oligodendrocyte differentiation. (C) 2009 International Society of Differentiation. Published by Elsevier Ltd. All rights reserved.

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