PUBLICATION
            CSF-contacting neurons regulate locomotion by relaying mechanical stimuli to spinal circuits
- Authors
 - Böhm, U. L., Prendergast, A., Djenoune, L., Nunes Figueiredo, S., Gomez, J., Stokes, C., Kaiser, S., Suster, M., Kawakami, K., Charpentier, M., Concordet, J. P., Rio, J. P., Del Bene, F., Wyart, C.
 - ID
 - ZDB-PUB-160805-7
 - Date
 - 2016
 - Source
 - Nature communications 7: 10866 (Journal)
 - Registered Authors
 - Del Bene, Filippo, Djenoune, Lydia, Kawakami, Koichi, Prendergast, Andrew, Stokes, Caleb, Suster, Maximiliano, Wyart, Claire
 - Keywords
 - Biological sciences, Cell biology, Neuroscience
 - MeSH Terms
 - 
    
        
        
            
                
- Neurons/cytology*
 - Neurons/metabolism
 - Male
 - Mechanoreceptors/cytology
 - Mechanoreceptors/metabolism
 - Cell Movement
 - Animals
 - Biomechanical Phenomena
 - Spinal Cord/chemistry
 - Spinal Cord/cytology*
 - Spinal Cord/metabolism
 - Zebrafish Proteins/genetics
 - Zebrafish Proteins/metabolism
 - Zebrafish/genetics
 - Zebrafish/metabolism
 - Transient Receptor Potential Channels/genetics
 - Transient Receptor Potential Channels/metabolism
 - Female
 - Cerebrospinal Fluid/cytology*
 - Cerebrospinal Fluid/metabolism
 
 - PubMed
 - 26946992 Full text @ Nat. Commun.
 
            Citation
        
        
            Böhm, U. L., Prendergast, A., Djenoune, L., Nunes Figueiredo, S., Gomez, J., Stokes, C., Kaiser, S., Suster, M., Kawakami, K., Charpentier, M., Concordet, J. P., Rio, J. P., Del Bene, F., Wyart, C. (2016) CSF-contacting neurons regulate locomotion by relaying mechanical stimuli to spinal circuits. Nature communications. 7:10866.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Throughout vertebrates, cerebrospinal fluid-contacting neurons (CSF-cNs) are ciliated cells surrounding the central canal in the ventral spinal cord. Their contribution to modulate locomotion remains undetermined. Recently, we have shown CSF-cNs modulate locomotion by directly projecting onto the locomotor central pattern generators (CPGs), but the sensory modality these cells convey to spinal circuits and their relevance to innate locomotion remain elusive. Here, we demonstrate in vivo that CSF-cNs form an intraspinal mechanosensory organ that detects spinal bending. By performing calcium imaging in moving animals, we show that CSF-cNs respond to both passive and active bending of the spinal cord. In mutants for the channel Pkd2l1, CSF-cNs lose their response to bending and animals show a selective reduction of tail beat frequency, confirming the central role of this feedback loop for optimizing locomotion. Altogether, our study reveals that CSF-cNs constitute a mechanosensory organ operating during locomotion to modulate spinal CPGs.
            
    
        
        
    
    
    
                
                    
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