Developmental regulation of a neuron cell-type-specific antigen recognized by a monoclonal antibody 10G4 in C. elegans

1992 ◽  
Vol 17 ◽  
pp. 171
Author(s):  
Shohei Mitani
2019 ◽  
Vol 111 (4) ◽  
pp. 95-107 ◽  
Author(s):  
Jyothi S. Akella ◽  
Malan Silva ◽  
Natalia S. Morsci ◽  
Ken C. Nguyen ◽  
William J. Rice ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (10) ◽  
pp. e0164601 ◽  
Author(s):  
Holly Stevens ◽  
Ashley B. Williams ◽  
W. Matthew Michael

2003 ◽  
Vol 39 (13) ◽  
pp. 783-789 ◽  
Author(s):  
Richard H Weisbart ◽  
Fusheng Yang ◽  
Grace Chan ◽  
Rika Wakelin ◽  
Kevin Ferreri ◽  
...  

2019 ◽  
Vol 7 (3) ◽  
pp. 17 ◽  
Author(s):  
Devyn Oliver ◽  
Emily Norman ◽  
Heather Bates ◽  
Rachel Avard ◽  
Monika Rettler ◽  
...  

Formation of the nervous system requires a complex series of events including proper extension and guidance of neuronal axons and dendrites. Here we investigate the requirement for integrins, a class of transmembrane cell adhesion receptors, in regulating these processes across classes of C. elegans motor neurons. We show α integrin/ina-1 is expressed by both GABAergic and cholinergic motor neurons. Despite this, our analysis of hypomorphic ina-1(gm144) mutants indicates preferential involvement of α integrin/ina-1 in GABAergic commissural development, without obvious involvement in cholinergic commissural development. The defects in GABAergic commissures of ina-1(gm144) mutants included both premature termination and guidance errors and were reversed by expression of wild type ina-1 under control of the native ina-1 promoter. Our results also show that α integrin/ina-1 is important for proper outgrowth and guidance of commissures from both embryonic and post-embryonic born GABAergic motor neurons, indicating an ongoing requirement for integrin through two phases of GABAergic neuron development. Our findings provide insights into neuron-specific roles for integrin that would not be predicted based solely upon expression analysis.


2005 ◽  
Vol 102 (3) ◽  
pp. 737-747 ◽  
Author(s):  
Claudia Strehblow ◽  
Maj Schuster ◽  
Thomas Moritz ◽  
Hans-Christoph Kirch ◽  
Bertram Opalka ◽  
...  

2020 ◽  
Author(s):  
Wendy Fung ◽  
Leigh Wexler ◽  
Maxwell G. Heiman

ABSTRACTGlia shape the development and function of the C. elegans nervous system, especially its sense organs and central neuropil (nerve ring). Cell-type-specific promoters allow investigators to label or manipulate individual glial cell types, and therefore provide a key tool for deciphering glial function. In this technical resource, we compare the specificity, brightness, and consistency of cell-type-specific promoters for C. elegans glia. We identify a set of promoters for the study of seven glial cell types (F16F9.3, amphid and phasmid sheath glia; F11C7.2, amphid sheath glia only; grl-2, amphid and phasmid socket glia; hlh-17, cephalic (CEP) sheath glia; and grl-18, inner labial (IL) socket glia) as well as a pan-glial promoter (mir-228). We compare these promoters to promoters that are expressed more variably in combinations of glial cell types (delm-1 and itx-1). We note that the expression of some promoters depends on external conditions or the internal state of the organism, such as developmental stage, suggesting glial plasticity. Finally, we demonstrate an approach for prospectively identifying cell-type-specific glial promoters using existing single-cell sequencing data, and we use this approach to identify two novel promoters specific to IL socket glia (col-53 and col-177).


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