F.M. Kirby Neurobiology Center, Children's Hospital Boston, Boston, MA, USA.
Glia. 2013 Jul;61(7):1029-40. doi: 10.1002/glia.22491. Epub 2013 Apr 2.
Upon peripheral nerve injury, specific molecular events, including increases in the expression of selected neurotrophic factors, are initiated to prepare the tissue for regeneration. However, the mechanisms underlying these events and the nature of the cells involved are poorly understood. We used the injury-induced upregulation of glial cell-derived neurotrophic factor (GDNF) expression as a tool to gain insights into these processes. We found that both myelinating and nonmyelinating Schwann cells are responsible for the dramatic increase in GDNF expression after injury. We also demonstrate that the GDNF upregulation is mediated by a signaling cascade involving activation of Schwann cell purinergic receptors, followed by protein kinase C signaling which activates protein kinase D (PKD), which leads to increased GDNF transcription. Given the potent effects of GDNF on survival and repair of injured peripheral neurons, we propose that targeting these pathways may yield therapeutic tools to treat peripheral nerve injury and neuropathies.
在外周神经损伤后,会启动特定的分子事件,包括选定神经营养因子的表达增加,为组织再生做准备。然而,这些事件背后的机制以及涉及的细胞类型尚不清楚。我们利用损伤诱导的神经胶质细胞衍生的神经营养因子(GDNF)表达上调作为一种工具来深入了解这些过程。我们发现,髓鞘形成和非髓鞘形成 Schwann 细胞都负责损伤后 GDNF 表达的急剧增加。我们还证明,GDNF 的上调是由涉及 Schwann 细胞嘌呤能受体激活的信号级联介导的,随后是蛋白激酶 C 信号激活蛋白激酶 D(PKD),从而导致 GDNF 转录增加。鉴于 GDNF 对损伤外周神经元的存活和修复有很强的作用,我们提出靶向这些途径可能为治疗外周神经损伤和神经病变提供治疗工具。