Harnessing nanotopography and integrin-matrix interactions to influence stem cell fate
Harnessing nanotopography and integrin-matrix interactions to influence stem cell fate
  Stem cells respond to nanoscale surface features, with changes in cell growth and differentiation mediated by alterations in cell adhesion. The interaction of nanotopographical features with integrin receptors in the cells' focal adhesions alters how the cells adhere to materials surfaces, and defines cell fate through changes in both cell biochemistry and cell morphology. In this Review, we discuss how cell adhesions interact with nanotopography, and we provide insight as to how materials scientists can exploit these interactions to direct stem cell fate and to understand how the behaviour of stem cells in their niche can be controlled. We expect knowledge gained from the study of cell-nanotopography interactions to accelerate the development of next-generation stem cell culture materials and implant interfaces, and to fuel discovery of stem cell therapeutics to support regenerative therapies.
  
  
  558-569
  
    
      Dalby, Matthew J.
      
        25dcae6a-8289-4169-abb7-c45fff0bafdc
      
     
  
    
      Gadegaard, Nikolaj
      
        bf72c3d1-e6a7-48b4-a968-c496b655bd98
      
     
  
    
      Oreffo, Richard O.C.
      
        ff9fff72-6855-4d0f-bfb2-311d0e8f3778
      
     
  
  
   
  
  
    
    
  
    
      21 May 2014
    
    
  
  
    
      Dalby, Matthew J.
      
        25dcae6a-8289-4169-abb7-c45fff0bafdc
      
     
  
    
      Gadegaard, Nikolaj
      
        bf72c3d1-e6a7-48b4-a968-c496b655bd98
      
     
  
    
      Oreffo, Richard O.C.
      
        ff9fff72-6855-4d0f-bfb2-311d0e8f3778
      
     
  
       
    
 
  
    
      
  
  
  
  
  
  
    Dalby, Matthew J., Gadegaard, Nikolaj and Oreffo, Richard O.C.
  
  
  
  
   
    (2014)
  
  
    
    Harnessing nanotopography and integrin-matrix interactions to influence stem cell fate.
  
  
  
  
    Nature Materials, 13 (6), .
  
   (doi:10.1038/nmat3980). 
  
  
  
    (PMID:24845995)
   
  
  
  
  
  
   
  
    
    
      
        
          Abstract
          Stem cells respond to nanoscale surface features, with changes in cell growth and differentiation mediated by alterations in cell adhesion. The interaction of nanotopographical features with integrin receptors in the cells' focal adhesions alters how the cells adhere to materials surfaces, and defines cell fate through changes in both cell biochemistry and cell morphology. In this Review, we discuss how cell adhesions interact with nanotopography, and we provide insight as to how materials scientists can exploit these interactions to direct stem cell fate and to understand how the behaviour of stem cells in their niche can be controlled. We expect knowledge gained from the study of cell-nanotopography interactions to accelerate the development of next-generation stem cell culture materials and implant interfaces, and to fuel discovery of stem cell therapeutics to support regenerative therapies.
         
      
      
        
          
            
  
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 Harnessing nanotopography and integrin-matrix interactions to influence stem cell fate  Nature Materials  Nature Publishing Group.mht
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      e-pub ahead of print date: 21 May 2014
 
    
      Published date: 21 May 2014
 
    
  
  
    
  
    
  
    
  
    
  
    
  
    
  
    
     
        Organisations:
        Human Development & Health
      
    
  
    
  
  
  
    
  
  
        Identifiers
        Local EPrints ID: 365185
        URI: http://eprints.soton.ac.uk/id/eprint/365185
        
          
        
        
        
          ISSN: 1476-1122
        
        
          PURE UUID: d1905c83-b84c-4ffd-8947-abbdf927cef1
        
  
    
        
          
        
    
        
          
        
    
        
          
            
              
            
          
        
    
  
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  Date deposited: 27 May 2014 11:48
  Last modified: 22 Aug 2025 01:45
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      Contributors
      
          
          Author:
          
            
            
              Matthew J. Dalby
            
          
        
      
          
          Author:
          
            
            
              Nikolaj Gadegaard
            
          
        
      
        
      
      
      
    
  
   
  
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