Literature DB >> 32917789

The GTPase Arl8B Plays a Principle Role in the Positioning of Interstitial Axon Branches by Spatially Controlling Autophagosome and Lysosome Location.

Gee Adnan1, Aine Rubikaite1, Moqadisa Khan1, Michael Reber2, Philip Suetterlin1,3, Robert Hindges1,4, Uwe Drescher5,4.   

Abstract

Interstitial axon branching is an essential step during the establishment of neuronal connectivity. However, the exact mechanisms on how the number and position of branches are determined are still not fully understood. Here, we investigated the role of Arl8B, an adaptor molecule between lysosomes and kinesins. In chick retinal ganglion cells (RGCs), downregulation of Arl8B reduces axon branch density and shifts their location more proximally, while Arl8B overexpression leads to increased density and more distal positions of branches. These alterations correlate with changes in the location and density of lysosomes and autophagosomes along the axon shaft. Diminishing autophagy directly by knock-down of atg7, a key autophagy gene, reduces branch density, while induction of autophagy by rapamycin increases axon branching, indicating that autophagy plays a prominent role in axon branch formation. In vivo, local inactivation of autophagy in the retina using a mouse conditional knock-out approach disturbs retino-collicular map formation which is dependent on the formation of interstitial axon branches. These data suggest that Arl8B plays a principal role in the positioning of axon branches by spatially controlling autophagy, thus directly controlling formation of neural connectivity in the brain.SIGNIFICANCE STATEMENT The formation of interstitial axonal branches plays a prominent role in numerous places of the developing brain during neural circuit establishment. We show here that the GTPase Arl8B controls density and location of interstitial axon branches, and at the same time controls also density and location of the autophagy machinery. Upregulation or downregulation of autophagy in vitro promotes or inhibits axon branching. Local disruption of autophagy in vivo disturbs retino-collicular mapping. Our data suggest that Arl8B controls axon branching by controlling locally autophagy. This work is one of the first reports showing a role of autophagy during early neural circuit development and suggests that autophagy in general plays a much more prominent role during brain development than previously anticipated.
Copyright © 2020 the authors.

Entities:  

Keywords:  autophagy; axon branching; lysosomes; neural circuit development; retinotectal projection; vesicle trafficking

Mesh:

Substances:

Year:  2020        PMID: 32917789      PMCID: PMC7574663          DOI: 10.1523/JNEUROSCI.1759-19.2020

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  82 in total

1.  BORC/kinesin-1 ensemble drives polarized transport of lysosomes into the axon.

Authors:  Ginny G Farías; Carlos M Guardia; Raffaella De Pace; Dylan J Britt; Juan S Bonifacino
Journal:  Proc Natl Acad Sci U S A       Date:  2017-03-20       Impact factor: 11.205

2.  An Arf-like small G protein, ARL-8, promotes the axonal transport of presynaptic cargoes by suppressing vesicle aggregation.

Authors:  Matthew P Klassen; Ye E Wu; Celine I Maeder; Isei Nakae; Juan G Cueva; Emily K Lehrman; Minoru Tada; Keiko Gengyo-Ando; George J Wang; Miriam Goodman; Shohei Mitani; Kenji Kontani; Toshiaki Katada; Kang Shen
Journal:  Neuron       Date:  2010-06-10       Impact factor: 17.173

3.  Terminal axon branching is regulated by the LKB1-NUAK1 kinase pathway via presynaptic mitochondrial capture.

Authors:  Julien Courchet; Tommy L Lewis; Sohyon Lee; Virginie Courchet; Deng-Yuan Liou; Shinichi Aizawa; Franck Polleux
Journal:  Cell       Date:  2013-06-20       Impact factor: 41.582

4.  The autophagy-inducing kinases, ULK1 and ULK2, regulate axon guidance in the developing mouse forebrain via a noncanonical pathway.

Authors:  Bo Wang; Rekha Iyengar; Xiujie Li-Harms; Joung Hyuck Joo; Christopher Wright; Alfonso Lavado; Linda Horner; Mao Yang; Jun-Lin Guan; Sharon Frase; Douglas R Green; Xinwei Cao; Mondira Kundu
Journal:  Autophagy       Date:  2017-12-24       Impact factor: 16.016

Review 5.  Moving and positioning the endolysosomal system.

Authors:  Juan S Bonifacino; Jacques Neefjes
Journal:  Curr Opin Cell Biol       Date:  2017-02-21       Impact factor: 8.382

Review 6.  Metabolic control of autophagy.

Authors:  Lorenzo Galluzzi; Federico Pietrocola; Beth Levine; Guido Kroemer
Journal:  Cell       Date:  2014-12-04       Impact factor: 41.582

7.  Essential role for autophagy protein Atg7 in the maintenance of axonal homeostasis and the prevention of axonal degeneration.

Authors:  Masaaki Komatsu; Qing Jun Wang; Gay R Holstein; Victor L Friedrich; Jun-ichi Iwata; Eiki Kominami; Brian T Chait; Keiji Tanaka; Zhenyu Yue
Journal:  Proc Natl Acad Sci U S A       Date:  2007-08-28       Impact factor: 11.205

8.  RNA Docking and Local Translation Regulate Site-Specific Axon Remodeling In Vivo.

Authors:  Hovy Ho-Wai Wong; Julie Qiaojin Lin; Florian Ströhl; Cláudio Gouveia Roque; Jean-Michel Cioni; Roberta Cagnetta; Benita Turner-Bridger; Romain F Laine; William A Harris; Clemens F Kaminski; Christine E Holt
Journal:  Neuron       Date:  2017-08-03       Impact factor: 17.173

9.  Autophagy linked FYVE (Alfy/WDFY3) is required for establishing neuronal connectivity in the mammalian brain.

Authors:  Joanna M Dragich; Takaaki Kuwajima; Megumi Hirose-Ikeda; Michael S Yoon; Evelien Eenjes; Joan R Bosco; Leora M Fox; Alf H Lystad; Tinmarla F Oo; Olga Yarygina; Tomohiro Mita; Satoshi Waguri; Yoshinobu Ichimura; Masaaki Komatsu; Anne Simonsen; Robert E Burke; Carol A Mason; Ai Yamamoto
Journal:  Elife       Date:  2016-09-20       Impact factor: 8.140

10.  Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons.

Authors:  Jean-Michel Cioni; Julie Qiaojin Lin; Anne V Holtermann; Max Koppers; Maximilian A H Jakobs; Afnan Azizi; Benita Turner-Bridger; Toshiaki Shigeoka; Kristian Franze; William A Harris; Christine E Holt
Journal:  Cell       Date:  2019-01-03       Impact factor: 41.582

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  2 in total

1.  RUFY3 and RUFY4 are ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin.

Authors:  Tal Keren-Kaplan; Amra Sarić; Saikat Ghosh; Chad D Williamson; Rui Jia; Yan Li; Juan S Bonifacino
Journal:  Nat Commun       Date:  2022-03-21       Impact factor: 14.919

Review 2.  Ubiquitination-Dependent Regulation of Small GTPases in Membrane Trafficking: From Cell Biology to Human Diseases.

Authors:  Zehui Lei; Jing Wang; Lingqiang Zhang; Cui Hua Liu
Journal:  Front Cell Dev Biol       Date:  2021-07-01
  2 in total

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