Parsons Xuejun H, Teng Yang D, Parsons James F, Snyder Evan Y, Smotrich David B, Moore Dennis A
San Diego Regenerative Medicine Institute, USA.
J Vis Exp. 2011 Oct 28(56):e3273. doi: 10.3791/3273.
There is a large unfulfilled need for a clinically-suitable human neuronal cell source for repair or regeneration of the damaged central nervous system (CNS) structure and circuitry in today's healthcare industry. Cell-based therapies hold great promise to restore the lost nerve tissue and function for CNS disorders. However, cell therapies based on CNS-derived neural stem cells have encountered supply restriction and difficulty to use in the clinical setting due to their limited expansion ability in culture and failing plasticity after extensive passaging(1-3). Despite some beneficial outcomes, the CNS-derived human neural stem cells (hNSCs) appear to exert their therapeutic effects primarily by their non-neuronal progenies through producing trophic and neuroprotective molecules to rescue the endogenous cells(1-3). Alternatively, pluripotent human embryonic stem cells (hESCs) proffer cures for a wide range of neurological disorders by supplying the diversity of human neuronal cell types in the developing CNS for regeneration(1,4-7). However, how to channel the wide differentiation potential of pluripotent hESCs efficiently and predictably to a desired phenotype has been a major challenge for both developmental study and clinical translation. Conventional approaches rely on multi-lineage inclination of pluripotent cells through spontaneous germ layer differentiation, resulting in inefficient and uncontrollable lineage-commitment that is often followed by phenotypic heterogeneity and instability, hence, a high risk of tumorigenicity(7-10). In addition, undefined foreign/animal biological supplements and/or feeders that have typically been used for the isolation, expansion, and differentiation of hESCs may make direct use of such cell-specialized grafts in patients problematic(11-13). To overcome these obstacles, we have resolved the elements of a defined culture system necessary and sufficient for sustaining the epiblast pluripotence of hESCs, serving as a platform for de novo derivation of clinically-suitable hESCs and effectively directing such hESCs uniformly towards clinically-relevant lineages by small molecules(14) (please see a schematic in Fig. 1). Retinoic acid (RA) does not induce neuronal differentiation of undifferentiated hESCs maintained on feeders(1, 14). And unlike mouse ESCs, treating hESC-differentiated embryoid bodies (EBs) only slightly increases the low yield of neurons(1, 14, 15). However, after screening a variety of small molecules and growth factors, we found that such defined conditions rendered retinoic acid (RA) sufficient to induce the specification of neuroectoderm direct from pluripotent hESCs that further progressed to neuroblasts that generated human neuronal progenitors and neurons in the developing CNS with high efficiency (Fig. 2). We defined conditions for induction of neuroblasts direct from pluripotent hESCs without an intervening multi-lineage embryoid body stage, enabling well-controlled efficient derivation of a large supply of human neuronal cells across the spectrum of developmental stages for cell-based therapeutics.
在当今医疗行业中,对于用于修复或再生受损中枢神经系统(CNS)结构和神经回路的临床适用人类神经元细胞来源,存在着巨大的未满足需求。基于细胞的疗法有望恢复中枢神经系统疾病中丧失的神经组织和功能。然而,基于中枢神经系统来源的神经干细胞的细胞疗法,由于其在培养中的有限扩增能力以及在大量传代后失去可塑性,在临床应用中面临供应限制和使用困难(1 - 3)。尽管有一些有益的结果,但中枢神经系统来源的人类神经干细胞(hNSCs)似乎主要通过其非神经元后代产生营养和神经保护分子来拯救内源性细胞,从而发挥其治疗作用(1 - 3)。另外,多能性人类胚胎干细胞(hESCs)通过为发育中的中枢神经系统提供多种人类神经元细胞类型用于再生,为多种神经系统疾病提供了治疗方法(1,4 - 7)。然而,如何将多能性hESCs的广泛分化潜能有效且可预测地引导至所需表型,一直是发育研究和临床转化面临的主要挑战。传统方法依赖于多能细胞通过自发胚层分化进行多谱系分化,导致效率低下且无法控制的谱系定向,随后往往伴随着表型异质性和不稳定性,因此具有高致瘤风险(7 - 10)。此外,通常用于hESCs分离、扩增和分化的未定义的外源/动物生物补充剂和/或饲养层,可能使此类细胞特异性移植物在患者中的直接使用存在问题(11 - 13)。为了克服这些障碍,我们确定了维持hESCs上胚层多能性所需且足够的确定培养系统要素,作为从头衍生临床适用hESCs的平台,并通过小分子有效地将此类hESCs均匀地引导至临床相关谱系(14)(见图1示意图)。视黄酸(RA)不会诱导饲养层上未分化的hESCs发生神经元分化(1, 14)。与小鼠胚胎干细胞不同,处理hESC分化的胚状体(EBs)只会略微提高神经元的低产量(1, 14, 15)。然而,在筛选了多种小分子和生长因子后,我们发现这种确定的条件使视黄酸(RA)足以诱导直接从多能性hESCs形成神经外胚层,进而进一步发育为神经母细胞,这些神经母细胞在发育中的中枢神经系统中高效地产生人类神经元祖细胞和神经元(图2)。我们确定了直接从多能性hESCs诱导神经母细胞的条件,无需中间的多谱系胚状体阶段,从而能够在发育阶段范围内良好控制地高效衍生大量人类神经元细胞用于基于细胞的治疗。