Bauer Sylvian, Patterson Paul H
Biology Division, California Institute of Technology, Pasadena, California 91125, USA.
J Neurosci. 2006 Nov 15;26(46):12089-99. doi: 10.1523/JNEUROSCI.3047-06.2006.
Although neural stem cells (NSCs) persist in various areas of the adult brain, their contribution to brain repair after injury is very limited. Treatment with exogenous growth factors can mitigate this limitation, suggesting that the brain environment is normally deficient in permissive cues and that it may be possible to stimulate the latent regenerative potential of endogenous progenitors with appropriate signals. We analyzed the effects of overexpressing the cytokine leukemia inhibitory factor (LIF) on adult neurogenesis in the normal brain. We found that LIF reduces neurogenesis in the olfactory bulb and subventricular zone by acting directly on NSCs. LIF appears to promote NSC self-renewal, preventing the emergence of more differentiated cell types. This ultimately leads to an expansion of the NSC pool. Our results have implications for the development of therapeutic strategies for brain repair and suggest that LIF may be useful, in combination with other factors, in promoting regeneration in the adult brain.
尽管神经干细胞(NSCs)存在于成人大脑的各个区域,但它们在损伤后对脑修复的贡献非常有限。外源性生长因子治疗可以减轻这种限制,这表明大脑环境通常缺乏允许性信号,并且有可能通过适当的信号刺激内源性祖细胞的潜在再生潜力。我们分析了细胞因子白血病抑制因子(LIF)过表达对正常大脑中成年神经发生的影响。我们发现,LIF通过直接作用于神经干细胞来减少嗅球和脑室下区的神经发生。LIF似乎促进神经干细胞的自我更新,阻止更多分化细胞类型的出现。这最终导致神经干细胞池的扩大。我们的研究结果对脑修复治疗策略的开发具有启示意义,并表明LIF与其他因素联合使用,可能有助于促进成人大脑的再生。