首页> 外文期刊>Journal of cellular physiology. >miR-22-3p enhances the intrinsic regenerative abilities of primary sensory neurons via the CBL/p-EGFR/p-STAT3/ GAP43/p-GAP43 axis
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miR-22-3p enhances the intrinsic regenerative abilities of primary sensory neurons via the CBL/p-EGFR/p-STAT3/ GAP43/p-GAP43 axis

机译:miR-22-3p提高内在再生初级感觉神经元通过能力

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摘要

Spinal cord injury (SCI) is a devastating disease. Strategies that enhance the intrinsic regenerative ability are very important for the recovery of SCI to radically prevent the occurrence of sensory disorders. Epidermal growth factor (EGF) showed a limited effect on the growth of primary sensory neuron neurites due to the degradation of phosphorylated-epidermal growth factor receptor (p-EGFR) in a manner dependent on Casitas B-lineage lymphoma (CBL) (an E3 ubiquitin-protein ligase). MiR-22-3p predicted from four databases could target CBL to inhibit the expression of CBL, increase p-EGFR levels and neurites length via STAT3/GAP43 pathway rather than Erk1/2 axis. EGF, EGFR, and miR-22-3p were downregulated sharply after injury. In vivo miR-22-3p Agomir application could regulate CBL/p-EGFR/p-STAT3/GAP43/p-GAP43 axis, and restore spinal cord sensory conductive function. This study clarified the mechanism of the limited promotion effect of EGF on adult primary sensory neuron neurite and targeting miR-22-3p could be a novel strategy to treat sensory dysfunction after SCI.
机译:脊髓损伤(SCI)是一种毁灭性的疾病。策略增强内在再生能力是非常重要的科学从根本上防止复苏感觉障碍的发生。因子(EGF)显示有限的影响增长的初级感觉神经元由于神经突phosphorylated-epidermal退化生长因子受体(p-EGFR)的方式依赖于小屋B-lineage淋巴瘤(CBL)(一个E3 ubiquitin-protein连接酶)。从四个数据库可以目标CBL抑制CBL的表达,增加p-EGFR水平和探明长度通过STAT3 / GAP43通路比Erk1/2轴。受伤后大幅下调。miR-22-3p Agomir应用程序可以调节恢复脊髓感觉传导功能。本研究阐明有限的机制促进EGF对成人的影响主要的感觉神经元轴突和定位miR-22-3p可能新策略来治疗后感觉功能障碍科学。

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