| Literature DB >> 34783657 |
Titas Sengupta1, Noelle L Koonce1, Nabor Vázquez-Martínez1, Mark W Moyle1, Leighton H Duncan1, Sarah E Emerson1, Xiaofei Han2, Lin Shao1, Yicong Wu2, Anthony Santella3, Li Fan3, Zhirong Bao3, William A Mohler4, Hari Shroff2,5, Daniel A Colón-Ramos1,5,6,7.
Abstract
During development, neurites and synapses segregate into specific neighborhoods or layers within nerve bundles. The developmental programs guiding placement of neurites in specific layers, and hence their incorporation into specific circuits, are not well understood. We implement novel imaging methods and quantitative models to document the embryonic development of the C. elegans brain neuropil, and discover that differential adhesion mechanisms control precise placement of single neurites onto specific layers. Differential adhesion is orchestrated via developmentally regulated expression of the IgCAM SYG-1, and its partner ligand SYG-2. Changes in SYG-1 expression across neuropil layers result in changes in adhesive forces, which sort SYG-2-expressing neurons. Sorting to layers occurs, not via outgrowth from the neurite tip, but via an alternate mechanism of retrograde zippering, involving interactions between neurite shafts. Our study indicates that biophysical principles from differential adhesion govern neurite placement and synaptic specificity in vivo in developing neuropil bundles.Entities:
Keywords: C. elegans; IgCAM; developmental biology; differential adhesion; neurite placement; neuroscience
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Year: 2021 PMID: 34783657 PMCID: PMC8843091 DOI: 10.7554/eLife.71171
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140