Growth Cone Tctp Is Dynamically Regulated by Guidance Cues

被引:12
|
作者
Roque, Claudio Gouveia [1 ,2 ]
Holtz, Christine E. [1 ]
机构
[1] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge, England
[2] Univ Coimbra, Doctoral Programme Expt Biol & Biomed, Ctr Neurosci & Cell Biol, Coimbra, Portugal
来源
FRONTIERS IN MOLECULAR NEUROSCIENCE | 2018年 / 11卷
基金
英国惠康基金; 欧洲研究理事会;
关键词
Tctp; mTORC; Netrin-1; Ephrin-A1; axon guidance; retinal ganglion cell; growth cone; protein translation; CONTROLLED TUMOR PROTEIN; EHRLICH ASCITES TUMOR; MESSENGER-RNA; LOCAL TRANSLATION; DEGRADATION; MECHANISMS; EXPRESSION; PROMOTES; GENE; IDENTIFICATION;
D O I
10.3389/fnmol.2018.00399
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Translationally controlled tumor protein (Tctp) contributes to retinal circuitry formation by promoting axon growth and guidance, but it remains unknown to what extent axonal Tctp specifically influences axon development programs. Various genome-wide profiling studies have ranked tctp transcripts among the most enriched in the axonal compartment of distinct neuronal populations, including embryonic retinal ganglion cells (RGCs), suggesting its expression can be regulated locally and that this may be important during development. Here, we report that growth cone Tctp levels change rapidly in response to Netrin-1 and Ephrin-A1, two guidance cues encountered by navigating RGC growth cones. This regulation is opposite in effect, as we observed protein synthesisand mTORC1-dependent increases in growth cone Tctp levels after acute treatment with Netrin-1, but a decline upon exposure to Ephrin-A1, an inhibitor of mTORC1. Live imaging with translation reporters further showed that Netrin-1-induced synthesis of Tctp in growth cones is driven by a short 3' untranslated region (3'UTR) tctp mRNA isoform. However, acute inhibition of de novo Tctp synthesis in axons did not perturb the advance of retinal projections through the optic tract in vivo, indicating that locally produced Tctp is not necessary for normal axon growth and guidance.
引用
收藏
页数:14
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