PUBLICATION
            Dual function of perivascular fibroblasts in vascular stabilization in zebrafish
- Authors
 - Rajan, A.M., Ma, R.C., Kocha, K.M., Zhang, D.J., Huang, P.
 - ID
 - ZDB-PUB-201027-17
 - Date
 - 2020
 - Source
 - PLoS Genetics 16: e1008800 (Journal)
 - Registered Authors
 - Huang, Peng, Kocha, Katrinka, Ma, Roger
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Pericytes/metabolism*
 - Pericytes/pathology
 - Fibroblasts/cytology
 - Fibroblasts/metabolism*
 - Fibroblasts/pathology
 - Animals
 - Zebrafish Proteins/genetics*
 - Mutant Proteins/genetics
 - Blood Vessels/growth & development
 - Blood Vessels/pathology
 - Endothelial Cells/metabolism
 - Endothelial Cells/pathology
 - Extracellular Matrix/genetics
 - Collagen/genetics*
 - Collagen/metabolism
 - Hemorrhage/genetics*
 - Hemorrhage/pathology
 - Mutation/genetics
 - Zebrafish/genetics
 - Zebrafish/growth & development
 - Myocytes, Smooth Muscle/metabolism
 - Myocytes, Smooth Muscle/pathology
 
 - PubMed
 - 33104690 Full text @ PLoS Genet.
 
            Citation
        
        
            Rajan, A.M., Ma, R.C., Kocha, K.M., Zhang, D.J., Huang, P. (2020) Dual function of perivascular fibroblasts in vascular stabilization in zebrafish. PLoS Genetics. 16:e1008800.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Blood vessels are vital to sustain life in all vertebrates. While it is known that mural cells (pericytes and smooth muscle cells) regulate vascular integrity, the contribution of other cell types to vascular stabilization has been largely unexplored. Using zebrafish, we identified sclerotome-derived perivascular fibroblasts as a novel population of blood vessel associated cells. In contrast to pericytes, perivascular fibroblasts emerge early during development, express the extracellular matrix (ECM) genes col1a2 and col5a1, and display distinct morphology and distribution. Time-lapse imaging reveals that perivascular fibroblasts serve as pericyte precursors. Genetic ablation of perivascular fibroblasts markedly reduces collagen deposition around endothelial cells, resulting in dysmorphic blood vessels with variable diameters. Strikingly, col5a1 mutants show spontaneous hemorrhage, and the penetrance of the phenotype is strongly enhanced by the additional loss of col1a2. Together, our work reveals dual roles of perivascular fibroblasts in vascular stabilization where they establish the ECM around nascent vessels and function as pericyte progenitors.
            
    
        
        
    
    
    
                
                    
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