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KIAA1199:调控 MEK/ERK 诱导雪旺细胞去分化的新分子。

KIAA1199: A novel regulator of MEK/ERK-induced Schwann cell dedifferentiation.

机构信息

GIGA-Neurosciences, University of Liège, Belgium.

GIGA-Molecular Biology of Diseases, University of Liège, Belgium.

出版信息

Glia. 2017 Oct;65(10):1682-1696. doi: 10.1002/glia.23188. Epub 2017 Jul 12.

DOI:10.1002/glia.23188
PMID:28699206
Abstract

The molecular mechanisms that regulate Schwann cell (SC) plasticity and the role of the Nrg1/ErbB-induced MEK1/ERK1/2 signalling pathway in SC dedifferentiation or in myelination remain unclear. It is currently believed that different levels of MEK1/ERK1/2 activation define the state of SC differentiation. Thus, the identification of new regulators of MEK1/ERK1/2 signalling could help to decipher the context-specific aspects driving the effects of this pathway on SC plasticity. In this perspective, we have investigated the potential role of KIAA1199, a protein that promotes ErbB and MEK1/ERK1/2 signalling in cancer cells, in SC plasticity. We depleted KIAA1199 in the SC-derived MSC80 cell line with RNA-interference-based strategy and also generated Tamoxifen-inducible and conditional mouse models in which KIAA1199 is inactivated through homologous recombination, using the Cre-lox technology. We show that the invalidation of KIAA1199 in SC decreases the expression of cJun and other negative regulators of myelination and elevates Krox20, driving them towards a pro-myelinating phenotype. We further show that in dedifferentiation conditions, SC invalidated for KIAA1199 exhibit lower myelin clearance as well as increased myelination capacity. Finally, the Nrg1-induced activation of the MEK/ERK/1/2 pathway is severely reduced when KIAA1199 is absent, indicating that KIAA1199 promotes Nrg1-dependent MEK1 and ERK1/2 activation in SCs. In conclusion, this work identifies KIAA1199 as a novel regulator of MEK/ERK-induced SC dedifferentiation and contributes to a better understanding of the molecular control of SC dedifferentiation.

摘要

调控许旺细胞(Schwann cell,SC)可塑性的分子机制,以及 Nrg1/ErbB 诱导的 MEK1/ERK1/2 信号通路在 SC 去分化或髓鞘形成中的作用尚不清楚。目前认为,MEK1/ERK1/2 激活的不同水平决定了 SC 分化的状态。因此,鉴定新的 MEK1/ERK1/2 信号转导调节剂可能有助于解析驱动该通路对 SC 可塑性影响的特定作用。在这方面,我们研究了 KIAA1199(一种在癌细胞中促进 ErbB 和 MEK1/ERK1/2 信号转导的蛋白)在 SC 可塑性中的潜在作用。我们利用 RNA 干扰策略在 SC 源性 MSC80 细胞系中敲低 KIAA1199,并且还利用 Cre-lox 技术生成了 Tamoxifen 诱导和条件性小鼠模型,通过同源重组使 KIAA1199 失活。结果显示,SC 中 KIAA1199 的失活降低了 cJun 和其他髓鞘形成负调节剂的表达,并升高了 Krox20,使它们向促髓鞘形成表型转变。我们进一步显示,在去分化条件下,缺失 KIAA1199 的 SC 表现出较低的髓鞘清除率和增强的髓鞘形成能力。最后,当 KIAA1199 缺失时,Nrg1 诱导的 MEK/ERK/1/2 通路的激活严重降低,表明 KIAA1199 促进了 Nrg1 依赖的 MEK1 和 ERK1/2 在 SC 中的激活。总之,这项工作鉴定了 KIAA1199 作为 MEK/ERK 诱导的 SC 去分化的新型调节因子,并有助于更好地理解 SC 去分化的分子调控。

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