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微小RNA-181a/b通过调控视网膜轴突的特化和生长来控制视觉回路的组装。

miR-181a/b control the assembly of visual circuitry by regulating retinal axon specification and growth.

作者信息

Carrella Sabrina, D'Agostino Ylenia, Barbato Sara, Huber-Reggi Sabina P, Salierno Francesco G, Manfredi Anna, Neuhauss Stephan C F, Banfi Sandro, Conte Ivan

机构信息

Telethon Institute of Genetics and Medicine, Via Campi Flegrei 34, Pozzuoli (Naples), 80078, Italy.

Institute of Molecular Life Sciences, Division of Neurobiology, University of Zurich, Winterthurerstrasse 190, CH-8057, Zurich, Switzerland.

出版信息

Dev Neurobiol. 2015 Nov;75(11):1252-67. doi: 10.1002/dneu.22282. Epub 2015 Jun 11.

Abstract

Connectivity and function of neuronal circuitry require the correct specification and growth of axons and dendrites. Here, we identify the microRNAs miR-181a and miR-181b as key regulators of retinal axon specification and growth. Loss of miR-181a/b in medaka fish (Oryzias latipes) failed to consolidate amacrine cell processes into axons and delayed the growth of retinal ganglion cell (RGC) axons. These alterations were accompanied by defects in visual connectivity and function. We demonstrated that miR-181a/b exert these actions through negative modulation of MAPK/ERK signaling that in turn leads to RhoA reduction and proper neuritogenesis in both amacrine cells and RGCs via local cytoskeletal rearrangement. Our results identify a new pathway for axon specification and growth unraveling a crucial role of miR-181a/b in the proper establishment of visual system connectivity and function.

摘要

神经元回路的连通性和功能需要轴突和树突的正确特化与生长。在此,我们确定微小RNA miR-181a和miR-181b是视网膜轴突特化和生长的关键调节因子。在青鳉鱼(日本青鳉)中缺失miR-181a/b会导致无长突细胞的突起无法整合为轴突,并延迟视网膜神经节细胞(RGC)轴突的生长。这些改变伴随着视觉连通性和功能的缺陷。我们证明,miR-181a/b通过对MAPK/ERK信号通路的负调控发挥这些作用,进而通过局部细胞骨架重排导致无长突细胞和RGC中的RhoA减少并实现正常的神经突形成。我们的研究结果确定了轴突特化和生长的一条新途径,揭示了miR-181a/b在视觉系统连通性和功能的正确建立中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f0/5033011/410f7f8da33b/DNEU-75-1252-g001.jpg

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