Peng Hongmei, Chen Gui'an
Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing 100083, China.
Sci China C Life Sci. 2005 Jun;48(3):295-9. doi: 10.1360/062004-83.
Human embryonic stem (hES) cells provide a promising supply of specific cell types for transplantation therapy. We presented here the method to induce differentiation of purified neural precursors from hES cells. hES cells (Line PKU-1 and Line PKU-2) were cultured in suspension in bacteriological Petri dishes, which differentiated into cystic embryoid bodies (EBs). The EBs were then cultured in N2 medium containing bFGF in poly-L-lysine-coated tissue culture dishes for two weeks. The central, small cells with 2-3 short processes of the spreading outgrowth were isolated mechanically and replated. The resulting neurospheres were cultured in suspension for 10 days, then dissociated into single cell suspension with a Pasteur pipette and plated. Cells grew vigorously in an attached way and were passed every 4-5 days. Almost all the cells were proved nestin positive by immunostaining. Following withdrawal of bFGF, they differentiated into neurons expressing beta-tubulin isotype(III), GABA, serotonin and synaptophysin. Through induction of PDGF-AA, they differentiated into astrocytes expressing GFAP and oligodendrocytes expressing O4. The results showed that hES cells can differentiate into typical neural precursors expressing the specific marker nestin and capable of generating all three cell types of the central nervous system (CNS) in vitro.
人胚胎干细胞(hES细胞)为移植治疗提供了有前景的特定细胞类型来源。我们在此展示了从hES细胞诱导分化出纯化神经前体细胞的方法。hES细胞(PKU - 1系和PKU - 2系)在细菌培养皿中悬浮培养,分化形成囊性胚状体(EBs)。然后将EBs在含有碱性成纤维细胞生长因子(bFGF)的N2培养基中,于聚-L-赖氨酸包被的组织培养皿中培养两周。机械分离出具有2 - 3个短突起且向外伸展的中央小细胞并重新接种。将得到的神经球悬浮培养10天,然后用巴氏吸管解离成单细胞悬液并接种。细胞贴壁生长旺盛,每4 - 5天传代一次。免疫染色证明几乎所有细胞巢蛋白呈阳性。去除bFGF后,它们分化为表达β-微管蛋白同型物(III)、γ-氨基丁酸(GABA)、5-羟色胺和突触素的神经元。通过血小板源性生长因子-AA(PDGF-AA)诱导,它们分化为表达胶质纤维酸性蛋白(GFAP)的星形胶质细胞和表达O4的少突胶质细胞。结果表明,hES细胞能够分化为表达特定标志物巢蛋白的典型神经前体细胞,并在体外能够生成中枢神经系统(CNS)的所有三种细胞类型。