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Local translation of TC10 is required for membrane expansion during axon outgrowth

机译:在轴突生长过程中,需要进行TC10的局部翻译以用于膜扩张

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摘要

The surface of developing axons expands in a process mediated by the exocyst complex. The spatio-temporal regulation of the exocyst is only partially understood. Here we report that stimulated membrane enlargement in dorsal root ganglion (DRG) axons is triggered by intra-axonal synthesis of TC10, a small GTPase required for exocyst function. Induced membrane expansion and axon outgrowth are inhibited after axon-specific knockdown of TC10 mRNA. To determine the relationship of intra-axonal TC10 synthesis with the previously described stimulus-induced translation of the cytoskeletal regulator Par3, we investigate the signalling pathways controlling their local translation in response to NGF. Phosphoinositide 3-kinase (PI3K)-dependent activation of the Rheb-mTOR pathway triggers the simultaneous local synthesis of TC10 and Par3. These results reveal the importance of local translation in the control of membrane dynamics and demonstrate that localized, mTOR-dependent protein synthesis triggers the simultaneous activation of parallel pathways.RI Hengst, Ulrich/L-1413-2014OI Hengst, Ulrich/0000-0002-8061-2861
机译:发育中的轴突表面在由囊外复合物介导的过程中扩展。外囊的时空调节只是部分了解。在这里我们报告说,背根神经节(DRG)轴突的受刺激的膜增大是由TC10的轴突内合成触发的,TC10是囊外功能所需的小GTPase。 TC10 mRNA的轴突特异性敲低后,诱导的膜扩张和轴突生长受到抑制。为了确定轴突内TC10合成与先前描述的刺激诱导的细胞骨架调节剂Par3的翻译之间的关系,我们研究了控制其响应NGF的局部翻译的信号传导途径。 Rheb-mTOR途径的磷酸肌醇3激酶(PI3K)依赖性激活触发TC10和Par3的同时局部合成。这些结果揭示了局部翻译在控制膜动力学中的重要性,并证明了局部依赖于mTOR的蛋白质合成触发了并行途径的同时激活.RI Hengst,Ulrich / L-1413-2014OI Hengst,Ulrich / 0000-0002- 8061-2861

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