Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada.
PLoS One. 2011;6(6):e21744. doi: 10.1371/journal.pone.0021744. Epub 2011 Jun 30.
Neural stem/progenitor cells (NSPCs) have great potential as a cell replacement therapy for spinal cord injury. However, poor control over transplant cell differentiation and survival remain major obstacles. In this study, we asked whether dibutyryl cyclic-AMP (dbcAMP), which was shown to induce up to 85% in vitro differentiation of NSPCs into neurons would enhance survival of transplanted NSPCs through prolonged exposure either in vitro or in vivo through the controlled release of dbcAMP encapsulated within poly(lactic-co-glycolic acid) (PLGA) microspheres and embedded within chitosan guidance channels. NSPCs, seeded in fibrin scaffolds within the channels, differentiated in vitro to betaIII-tubulin positive neurons by immunostaining and mRNA expression, in response to dbcAMP released from PLGA microspheres. After transplantation in spinal cord injured rats, the survival and differentiation of NSPCs was evaluated. Untreated NSPCs, NSPCs transplanted with dbcAMP-releasing microspheres, and NSPCs pre-differentiated with dbcAMP for 4 days in vitro were transplanted after rat spinal cord transection and assessed 2 and 6 weeks later. Interestingly, NSPC survival was highest in the dbcAMP pre-treated group, having approximately 80% survival at both time points, which is remarkable given that stem cell transplantation often results in less than 1% survival at similar times. Importantly, dbcAMP pre-treatment also resulted in the greatest number of in vivo NSPCs differentiated into neurons (37±4%), followed by dbcAMP-microsphere treated NSPCs (27±14%) and untreated NSPCs (15±7%). The reverse trend was observed for NSPC-derived oligodendrocytes and astrocytes, with these populations being highest in untreated NSPCs. This combination strategy of stem cell-loaded chitosan channels implanted in a fully transected spinal cord resulted in extensive axonal regeneration into the injury site, with improved functional recovery after 6 weeks in animals implanted with pre-differentiated stem cells in chitosan channels.
神经干细胞/祖细胞 (NSPCs) 具有作为脊髓损伤细胞替代治疗的巨大潜力。然而,对移植细胞分化和存活的控制仍然是主要障碍。在这项研究中,我们询问了二丁酰环 AMP(dbcAMP) 是否可以通过体外或体内延长暴露来增强移植 NSPCs 的存活,方法是将 dbcAMP 包封在聚 (乳酸-共-乙醇酸) (PLGA) 微球中并嵌入壳聚糖导向通道内进行受控释放。将 NSPC 接种在通道内的纤维蛋白支架中,通过免疫染色和 mRNA 表达,对 PLGA 微球释放的 dbcAMP 作出反应,在体外分化为β III-微管蛋白阳性神经元。在脊髓损伤大鼠中移植后,评估 NSPC 的存活和分化。未经处理的 NSPCs、用释放 dbcAMP 的微球移植的 NSPCs 以及在体外用 dbcAMP 预分化 4 天的 NSPCs 在大鼠脊髓横断后进行移植,并在 2 和 6 周后进行评估。有趣的是,dbcAMP 预处理组的 NSPC 存活率最高,在两个时间点均有约 80%的存活率,考虑到干细胞移植通常在类似时间导致不到 1%的存活率,这是非常显著的。重要的是,dbcAMP 预处理还导致了最多数量的体内 NSPC 分化为神经元 (37±4%),其次是 dbcAMP-微球处理的 NSPCs(27±14%)和未经处理的 NSPCs(15±7%)。相反,NSPC 衍生的少突胶质细胞和星形胶质细胞的趋势相反,未经处理的 NSPCs 中这两种细胞的数量最多。在完全横断的脊髓中植入负载干细胞的壳聚糖通道的这种组合策略导致广泛的轴突再生进入损伤部位,在植入壳聚糖通道中预先分化的干细胞的动物中,在 6 周后功能恢复得到改善。