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轴突生长和皮质中间神经元迁移需要Rac1和Rac3 GTP酶以及双孔通道2(TPC2)。

Rac1 and Rac3 GTPases and TPC2 are required for axonal outgrowth and migration of cortical interneurons.

作者信息

Kounoupa Zouzana, Tivodar Simona, Theodorakis Kostas, Kyriakis Dimitrios, Denaxa Myrto, Karagogeos Domna

机构信息

Institute of Molecular Biology and Biotechnology (IMBB, FORTH), Heraklion 71110, Greece.

Department of Basic Science, Faculty of Medicine, University of Crete, Heraklion 71110, Greece.

出版信息

J Cell Sci. 2023 Mar 15;136(6). doi: 10.1242/jcs.260373. Epub 2023 Mar 10.

Abstract

Rho GTPases, among them Rac1 and Rac3, are major transducers of extracellular signals and are involved in multiple cellular processes. In cortical interneurons, the neurons that control the balance between excitation and inhibition of cortical circuits, Rac1 and Rac3 are essential for their development. Ablation of both leads to a severe reduction in the numbers of mature interneurons found in the murine cortex, which is partially due to abnormal cell cycle progression of interneuron precursors and defective formation of growth cones in young neurons. Here, we present new evidence that upon Rac1 and Rac3 ablation, centrosome, Golgi complex and lysosome positioning is significantly perturbed, thus affecting both interneuron migration and axon growth. Moreover, for the first time, we provide evidence of altered expression and localization of the two-pore channel 2 (TPC2) voltage-gated ion channel that mediates Ca2+ release. Pharmacological inhibition of TPC2 negatively affected axonal growth and migration of interneurons. Our data, taken together, suggest that TPC2 contributes to the severe phenotype in axon growth initiation, extension and interneuron migration in the absence of Rac1 and Rac3.

摘要

Rho GTP酶,包括Rac1和Rac3,是细胞外信号的主要转导因子,参与多种细胞过程。在控制皮质回路兴奋与抑制平衡的皮质中间神经元中,Rac1和Rac3对其发育至关重要。两者的缺失会导致小鼠皮质中成熟中间神经元数量严重减少,部分原因是中间神经元前体细胞的细胞周期进程异常以及幼龄神经元中生长锥形成缺陷。在此,我们提供新证据表明,Rac1和Rac3缺失后,中心体、高尔基体复合体和溶酶体的定位会受到显著干扰,从而影响中间神经元的迁移和轴突生长。此外,我们首次提供证据表明,介导Ca2+释放的双孔通道2(TPC2)电压门控离子通道的表达和定位发生了改变。TPC2的药理学抑制对中间神经元的轴突生长和迁移产生负面影响。综合我们的数据表明,在缺乏Rac1和Rac3的情况下,TPC2导致了轴突生长起始、延伸以及中间神经元迁移方面的严重表型。

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