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The GTPase Arl8B Plays a Principle Role in the Positioning of Interstitial Axon Branches by Spatially Controlling Autophagosome and Lysosome Location.
- Source :
-
The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] 2020 Oct 14; Vol. 40 (42), pp. 8103-8118. Date of Electronic Publication: 2020 Sep 11. - Publication Year :
- 2020
-
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.<br /> (Copyright © 2020 the authors.)
- Subjects :
- ADP-Ribosylation Factors metabolism
Animals
Autophagosomes enzymology
Autophagosomes ultrastructure
Autophagy genetics
Axons enzymology
Axons ultrastructure
Chick Embryo
Down-Regulation
Gene Knockdown Techniques
Lysosomes enzymology
Lysosomes ultrastructure
Mice, Knockout
Primary Cell Culture
Retinal Ganglion Cells metabolism
Retinal Ganglion Cells ultrastructure
ADP-Ribosylation Factors physiology
Autophagosomes physiology
Axons physiology
Lysosomes physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1529-2401
- Volume :
- 40
- Issue :
- 42
- Database :
- MEDLINE
- Journal :
- The Journal of neuroscience : the official journal of the Society for Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 32917789
- Full Text :
- https://doi.org/10.1523/JNEUROSCI.1759-19.2020