Suppr超能文献

人胚胎干细胞源性运动神经元的定向分化与移植

Directed differentiation and transplantation of human embryonic stem cell-derived motoneurons.

作者信息

Lee Hyojin, Shamy George Al, Elkabetz Yechiel, Schofield Claude M, Harrsion Neil L, Panagiotakos Georgia, Socci Nicholas D, Tabar Viviane, Studer Lorenz

机构信息

Developmental Biology & Neurosurgery, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

出版信息

Stem Cells. 2007 Aug;25(8):1931-9. doi: 10.1634/stemcells.2007-0097. Epub 2007 May 3.

Abstract

Motoneurons represent a specialized class of neurons essential for the control of body movement. Motoneuron loss is the cause of a wide range of neurological disorders including amyotrophic lateral sclerosis and spinal muscular atrophy. Embryonic stem cells are a promising cell source for the study and potential treatment of motoneuron diseases. Here, we present a novel in vitro protocol of the directed differentiation of human embryonic stem cells (hESCs) into engraftable motoneurons. Neural induction of hESCs was induced on MS5 stromal feeders, resulting in the formation of neural rosettes. In response to sonic hedgehog and retinoic acid, neural rosettes were efficiently directed into spinal motoneurons with appropriate in vitro morphological, physiological, and biochemical properties. Global gene expression analysis was used as an unbiased measure to confirm motoneuron identity and type. Transplantation of motoneuron progeny into the developing chick embryo resulted in robust engraftment, maintenance of motoneuron phenotype, and long-distance axonal projections into peripheral host tissues. Transplantation into the adult rat spinal cord yielded neural grafts comprising a large number of human motoneurons with outgrowth of choline acetyltransferase positive fibers. These data provide evidence for in vivo survival of hESC-derived motoneurons, a key requirement in the development of hESC-based cell therapy in motoneuron disease. Disclosure of potential conflicts of interest is found at the end of this article.

摘要

运动神经元是一类特殊的神经元,对身体运动的控制至关重要。运动神经元的丧失是包括肌萎缩侧索硬化症和脊髓性肌萎缩症在内的多种神经疾病的病因。胚胎干细胞是研究和潜在治疗运动神经元疾病的一种有前景的细胞来源。在此,我们展示了一种将人类胚胎干细胞(hESCs)定向分化为可移植运动神经元的新型体外方案。在MS5基质饲养层上诱导hESCs进行神经诱导,从而形成神经玫瑰花结。在音猬因子和视黄酸的作用下,神经玫瑰花结被有效地定向分化为具有适当体外形态、生理和生化特性的脊髓运动神经元。全局基因表达分析被用作一种无偏倚的方法来确认运动神经元的身份和类型。将运动神经元后代移植到发育中的鸡胚中,可实现强大的植入、运动神经元表型的维持以及向周围宿主组织的长距离轴突投射。移植到成年大鼠脊髓中可产生包含大量人类运动神经元且有胆碱乙酰转移酶阳性纤维生长的神经移植物。这些数据为hESC衍生的运动神经元在体内的存活提供了证据,这是运动神经元疾病中基于hESC的细胞治疗发展的一个关键要求。潜在利益冲突的披露见本文末尾。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验