Yu Ji Min, Bunnell Bruce A, Kang Soo-Kyung
Division of Regenerative Medicine, Tulane National Primate Research Center, Covington, LA, USA.
Methods Mol Biol. 2011;702:219-31. doi: 10.1007/978-1-61737-960-4_16.
While adult stem cells can be induced to transdifferentiate into multiple lineages of cells or tissues, their plasticity and utility for human therapy remains controversial. In this chapter, we describe methods for the transdifferentiation of human adipose tissue-derived stem cells (ASCs) along neural lineages using in vitro and in vivo systems. The in vitro neural differentiation of ASCs has been reported by several groups using serum-free cytokine induction, butylated hydroxyanisole (BHA) chemical induction, and neurosphere formation in combination with the cytokines, such as brain-derived neurotrophic factor (BDNF) and basic fibroblast growth factor (bFGF). For in vivo neurogenic induction, ASCs are treated with BDNF and bFGF to form neurospheres in vitro and then delivered directly to the brain. In this chapter, several detailed protocols for the effective neurogenic induction of ASCs in vitro and in vivo are described. The protocols described herein can be applied to further molecular and mechanistic studies of neurogenic induction and differentiation of ASCs. In addition, these methods can be useful for differentiating ASCs for therapeutic intervention in central nervous system disorders.
虽然成体干细胞可以被诱导转分化为多种细胞或组织谱系,但其可塑性以及在人类治疗中的效用仍存在争议。在本章中,我们描述了利用体外和体内系统使人类脂肪组织来源的干细胞(ASC)沿神经谱系进行转分化的方法。已有多个研究小组报道了利用无血清细胞因子诱导、丁基羟基茴香醚(BHA)化学诱导以及与细胞因子(如脑源性神经营养因子(BDNF)和碱性成纤维细胞生长因子(bFGF))联合形成神经球的方法,在体外对ASC进行神经分化。对于体内神经源性诱导,先在体外使用BDNF和bFGF处理ASC以形成神经球,然后直接将其移植到大脑中。在本章中,将描述几种在体外和体内有效诱导ASC神经源性的详细方案。本文所述的方案可应用于ASC神经源性诱导和分化的进一步分子及机制研究。此外,这些方法对于分化ASC以用于中枢神经系统疾病的治疗干预可能会很有用。