Ancestral role of TNF-R pathway in cell differentiation in the basal metazoan Hydra.
    
    
        
    
    
        
        J. Cell Sci. 134:jcs255422 (2021)
    
    
    
		
		
			
				Tumour necrosis factor receptors (TNF-Rs) and their ligands, tumour necrosis factors, are highly conserved proteins described in all metazoan phyla. They function as inducers of extrinsic apoptotic signalling and facilitate inflammation, differentiation and cell survival. TNF-Rs use distinct adaptor molecules to activate signalling cascades. Fas-associated protein with death domain (FADD) family adaptors often mediate apoptosis, and TNF-R-associated factor (TRAF) family adaptors mediate cell differentiation and inflammation. Most of these pathway components are conserved in cnidarians, and, here, we investigated the Hydra TNF-R. We report that it is related to the ectodysplasin receptor, which is involved in epithelial cell differentiation in mammals. In Hydra, it is localised in epithelial cells with incorporated nematocytes in tentacles and body column, indicating a similar function. Further experiments suggest that it interacts with the Hydra homologue of a TRAF adaptor, but not with FADD proteins. Hydra FADD proteins colocalised with Hydra caspases in death effector filaments and recruited caspases, suggesting that they are part of an apoptotic signalling pathway. Regulating epithelial cell differentiation via TRAF adaptors therefore seems to be an ancient function of TNF-Rs, whereas FADD-caspase interactions may be part of a separate apoptotic pathway.
			
			
				
			
		 
		
			
				
					
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
    
        Typ der Hochschulschrift
        
    
 
    
        Herausgeber
        
    
    
        Schlagwörter
        Hydra ; Apoptosis ; Tnf-r Superfamily ; Fadd ; Ectodysplasin; Epithelial-cells; Nurse Cells; Death; Apoptosis; Organization; Superfamily; Expression; Oogenesis; Evolution; Caspases
    
 
    
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        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2021
    
 
    
        Prepublished im Jahr 
        
    
 
    
        HGF-Berichtsjahr
        2021
    
 
    
    
        ISSN (print) / ISBN
        0021-9533
    
 
    
        e-ISSN
        1477-9137
    
 
    
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	    Band: 134,  
	    Heft: 2,  
	    Seiten: ,  
	    Artikelnummer: jcs255422 
	    Supplement: ,  
	
    
 
  
        
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            Verlag
            Company of Biologists
        
 
        
            Verlagsort
            Cambridge
        
 
	
        
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        Begutachtungsstatus
        Peer reviewed
    
 
     
    
        POF Topic(s)
        30203 - Molecular Targets and Therapies
    
 
    
        Forschungsfeld(er)
        Enabling and Novel Technologies
    
 
    
        PSP-Element(e)
        G-505700-001
    
 
    
        Förderungen
        Deutsche Forschungsgemeinschaft
    
 
    
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        Erfassungsdatum
        2021-06-29