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Lithium enhances the neuronal differentiation of neural progenitor cells in vitro and after transplantation into the avulsed ventral horn of adult rats through the secretion of brain-derived neurotrophic factor

机译:锂通过分泌脑源性神经营养因子,在体外和移植到成年大鼠撕裂的腹侧角后增强神经祖细胞的神经元分化。

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摘要

This study was undertaken to elucidate the molecular mechanisms by which lithium regulates the development of spinal cord-derived neural progenitor cells (NPCs) in vitro and after transplanted in vivo. Our results show that lithium at the therapeutic concentration significantly increases the proliferation and neuronal differentiation of NPCs in vitro. Specific ELISAs, western blotting, and quantitative real-time RT-PCR assays demonstrate that lithium treatment significantly elevates the expression and production of brain-derived neurotrophic factor (BDNF) by NPCs in culture. Application of a BDNF neutralizing antibody in culture leads to a marked reduction in the neurogenesis of lithium-treated NPCs to the control level. However, it shows no effects on the proliferation of lithium-treated NPCs. These findings suggest that the BDNF pathway is possibly involved in the supportive role of lithium in inducing NPC neurogenesis but not proliferation. This study also provides evidence that lithium is able to elevate the neuronal generation and BDNF production of NPCs after transplantation into the adult rat ventral horn with motoneuron degeneration because of spinal root avulsion, which highlights the therapeutic potential of lithium in cell replacement strategies for spinal cord injury because of its ability to promote neuronal differentiation and BDNF production of grafted NPCs in the injured spinal cord. © 2009 International Society for Neurochemistry.
机译:进行这项研究是为了阐明锂在体外和体内移植后调控脊髓源性神经祖细胞(NPC)发育的分子机制。我们的结果表明,治疗浓度的锂在体外显着增加了NPC的增殖和神经元分化。特异性ELISA,western印迹和定量实时RT-PCR分析表明,锂处理显着提高了培养中NPC对脑源性神经营养因子(BDNF)的表达和产生。 BDNF中和抗体在培养物中的应用导致锂处理的NPC的神经发生显着降低至对照水平。但是,它对锂处理的NPC的增殖没有影响。这些发现表明,BDNF途径可能参与了锂在诱导NPC神经发生而不是增殖中的支持作用。这项研究还提供了证据,表明由于脊髓根部撕脱,锂在具有运动神经元变性的成年大鼠腹角移植到成年大鼠腹角后,能够提高NPC的神经元生成和BDNF的产生,这突出了锂在脊髓细胞替代策略中的治疗潜力。由于其能够促进受损脊髓中移植NPC的神经元分化和BDNF产生,因此具有损伤作用。 ©2009国际神经化学学会。

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