scholarly journals Branch management: mechanisms of axon branching in the developing vertebrate CNS

2013 ◽  
Vol 15 (1) ◽  
pp. 7-18 ◽  
Author(s):  
Katherine Kalil ◽  
Erik W. Dent
2018 ◽  
Vol 9 (1) ◽  
Author(s):  
Tommy L. Lewis ◽  
Seok-Kyu Kwon ◽  
Annie Lee ◽  
Reuben Shaw ◽  
Franck Polleux

Author(s):  
Satish Bodakuntla ◽  
Hana Nedozralova ◽  
Nirakar Basnet ◽  
Naoko Mizuno

Axon branching is a critical process ensuring a high degree of interconnectivity for neural network formation. As branching occurs at sites distant from the soma, it is necessary that axons have a local system to dynamically control and regulate axonal growth. This machinery depends on the orchestration of cellular functions such as cytoskeleton, subcellular transport, energy production, protein- and membrane synthesis that are adapted for branch formation. Compared to the axon shaft, branching sites show a distinct and dynamic arrangement of cytoskeleton components, endoplasmic reticulum and mitochondria. This review discusses the regulation of axon branching in the context of cytoskeleton and membrane remodeling.


Cell ◽  
2013 ◽  
Vol 153 (7) ◽  
pp. 1510-1525 ◽  
Author(s):  
Julien Courchet ◽  
Tommy L. Lewis ◽  
Sohyon Lee ◽  
Virginie Courchet ◽  
Deng-Yuan Liou ◽  
...  

Author(s):  
Katherine Kalil ◽  
Erik W. Dent ◽  
Fangjun Tang
Keyword(s):  

2014 ◽  
Vol 205 (2) ◽  
pp. 217-232 ◽  
Author(s):  
Cortney C. Winkle ◽  
Leslie M. McClain ◽  
Juli G. Valtschanoff ◽  
Charles S. Park ◽  
Christopher Maglione ◽  
...  

Developmental axon branching dramatically increases synaptic capacity and neuronal surface area. Netrin-1 promotes branching and synaptogenesis, but the mechanism by which Netrin-1 stimulates plasma membrane expansion is unknown. We demonstrate that SNARE-mediated exocytosis is a prerequisite for axon branching and identify the E3 ubiquitin ligase TRIM9 as a critical catalytic link between Netrin-1 and exocytic SNARE machinery in murine cortical neurons. TRIM9 ligase activity promotes SNARE-mediated vesicle fusion and axon branching in a Netrin-dependent manner. We identified a direct interaction between TRIM9 and the Netrin-1 receptor DCC as well as a Netrin-1–sensitive interaction between TRIM9 and the SNARE component SNAP25. The interaction with SNAP25 negatively regulates SNARE-mediated exocytosis and axon branching in the absence of Netrin-1. Deletion of TRIM9 elevated exocytosis in vitro and increased axon branching in vitro and in vivo. Our data provide a novel model for the spatial regulation of axon branching by Netrin-1, in which localized plasma membrane expansion occurs via TRIM9-dependent regulation of SNARE-mediated vesicle fusion.


Sign in / Sign up

Export Citation Format

Share Document