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压电陶瓷(PZT)通过 RhoA、Rac1 和 Cdc42 途径调节大鼠皮质神经元的轴突导向生长。

Piezoelectric ceramic (PZT) modulates axonal guidance growth of rat cortical neurons via RhoA, Rac1, and Cdc42 pathways.

机构信息

Underwater Acoustic Transducer and Testing Laboratory, Institute of Acoustics, Chinese Academy of Sciences, Beijing, 100190, China,

出版信息

J Mol Neurosci. 2014 Mar;52(3):323-30. doi: 10.1007/s12031-013-0149-7. Epub 2013 Nov 8.

Abstract

Electrical stimulation is critical for axonal connection, which can stimulate axonal migration and deformation to promote axonal growth in the nervous system. Netrin-1, an axonal guidance cue, can also promote axonal guidance growth, but the molecular mechanism of axonal guidance growth under indirect electric stimulation is still unknown. We investigated the molecular mechanism of axonal guidance growth under piezoelectric ceramic lead zirconate titanate (PZT) stimulation in the primary cultured cortical neurons. PZT induced marked axonal elongation. Moreover, PZT activated the excitatory postsynaptic currents (EPSCs) by increasing the frequency and amplitude of EPSCs of the cortical neurons in patch clamp assay. PZT downregulated the expression of Netrin-1 and its receptor Deleted in Colorectal Cancer (DCC). Rho GTPase signaling is involved in interactions of Netrin-1 and DCC. PZT activated RhoA. Dramatic decrease of Cdc42 and Rac1 was also observed after PZT treatment. RhoA inhibitor Clostridium botulinum C3 exoenzyme (C3-Exo) prevented the PZT-induced downregulation of Netrin-1 and DCC. We suggest that PZT can promote axonal guidance growth by downregulation of Netrin-1 and DCC to mediate axonal repulsive responses via the Rho GTPase signaling pathway. Obviously, piezoelectric materials may provide a new approach for axonal recovery and be beneficial for clinical therapy in the future.

摘要

电刺激对于轴突连接至关重要,它可以刺激轴突迁移和变形,从而促进神经系统中的轴突生长。神经导向因子 netrin-1 也可以促进轴突导向生长,但间接电刺激下轴突导向生长的分子机制尚不清楚。我们研究了压电陶瓷锆钛酸铅(PZT)刺激下原代培养皮质神经元中轴突导向生长的分子机制。PZT 诱导明显的轴突伸长。此外,在膜片钳检测中,PZT 通过增加皮质神经元 EPSC 的频率和幅度来激活兴奋性突触后电流(EPSC)。PZT 下调了 netrin-1 及其受体结直肠癌缺失基因(DCC)的表达。Rho GTPase 信号通路参与了 netrin-1 和 DCC 的相互作用。PZT 激活了 RhoA。在 PZT 处理后,还观察到 Cdc42 和 Rac1 的明显减少。RhoA 抑制剂肉毒梭菌 C3 外毒素(C3-Exo)可阻止 PZT 诱导的 netrin-1 和 DCC 下调。我们认为,PZT 通过下调 netrin-1 和 DCC 来促进轴突导向生长,从而通过 Rho GTPase 信号通路介导轴突排斥反应。显然,压电材料可能为轴突恢复提供一种新方法,对未来的临床治疗有益。

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