Aix-Marseille Université, Institut de Biologie du Développement de Marseille de Luminy, Unité Mixte de Recherche 7288, 13288 Marseille, France.
J Neurosci. 2013 Feb 13;33(7):3240-50. doi: 10.1523/JNEUROSCI.2579-12.2013.
Ciliary neurotrophic factor (CNTF) has been shown to be expressed after brain lesions and in particular after demyelination. Here, we addressed the role of this cytokine in the regulation of neural progenitor migration in the adult rodent brain. Using an acute model of demyelination, we show that CNTF is strongly re-expressed after lesion and is involved in the postlesional mobilization of endogenous progenitors that participate in the myelin regenerative process. We show that CNTF controls the migration of subventricular zone (SVZ)-derived neural progenitors toward the demyelinated corpus callosum. Furthermore, an ectopic source of CNTF in adult healthy brains changes SVZ-derived neural progenitors' migratory behavior that migrate toward the source by activation of the Janus kinase/signal transducer and activator of transcription 3 (JAK/STAT3) pathway. Using various in vitro assays (Boyden chambers, explants, and video time-lapse imaging), we demonstrate that CNTF controls the directed migration of SVZ-derived progenitors and oligodendrocyte precursors. Altogether, these results demonstrate that in addition to its neuroprotective activity and its role in progenitor survival and maturation, CNTF acts as a chemoattractant and participates in the recruitment of endogenous progenitors during myelin repair.
睫状神经营养因子 (CNTF) 在脑损伤后特别是脱髓鞘后被证明有表达。在这里,我们研究了这种细胞因子在调节成年啮齿动物大脑中神经祖细胞迁移中的作用。我们使用脱髓鞘的急性模型,表明 CNTF 在损伤后强烈重新表达,并参与参与髓鞘再生过程的内源性祖细胞的损伤后动员。我们表明 CNTF 控制脑室下区 (SVZ) 衍生的神经祖细胞向脱髓鞘胼胝体的迁移。此外,成年健康大脑中的 CNTF 异位源改变 SVZ 衍生的神经祖细胞的迁移行为,通过激活 Janus 激酶/信号转导和转录激活因子 3 (JAK/STAT3) 途径向源迁移。通过使用各种体外测定法(Boyden 室、外植体和视频延时成像),我们证明 CNTF 控制 SVZ 衍生祖细胞和少突胶质前体细胞的定向迁移。总之,这些结果表明,除了其神经保护活性及其在祖细胞存活和成熟中的作用外,CNTF 还作为趋化因子起作用,并在髓鞘修复过程中参与内源性祖细胞的募集。