Digital Library
Close Browse articles from a journal
 
<< previous    next >>
     Journal description
       All volumes of the corresponding journal
         All issues of the corresponding volume
           All articles of the corresponding issues
                                       Details for article 7 of 17 found articles
 
 
  Evolutive skin reconstructions: From the dermal collagen-glycosaminoglycan- chitosane substrate to an immunocompetent reconstructed skin
 
 
Title: Evolutive skin reconstructions: From the dermal collagen-glycosaminoglycan- chitosane substrate to an immunocompetent reconstructed skin
Author: Dezutter-Dambuyant, C.
Black, Annie
Bechetoille, Nicolas
Bouez, Charbel
Maréchal, Sylvie
Auxenfans, Céline
Cenizo, Valérie
Pascal, Pascale
Perrier, Eric
Damour, Odile
Appeared in: Bio-medical materials and engineering
Paging: Volume 16 (2006) nr. supplement-4 pages S85-S94
Year: 2006-07-13
Contents: The development of human skin models that have the same properties as genuine human skin is of particular significance. Very promising skin models are the three-dimensional artificial skin constructs, which, similar to genuine skin, consist of an epidermis of differentiated keratinocytes and a dermis. A skin equivalent based on a collagen-glycosaminoglycan-chitosan dermal substrate has been developed to meet the growing demand in tissue engineered skin equivalents. We used this model to investigate whether CD34-generated Langerhans/dendritic cell precursors could be integrated into this skin equivalent model and pursue their differentiation without addition of cytokine and growth factor. To address the issue of dendritic cell (DC) differentiation, an endothelialized skin equivalent coculture model was used to study the behaviour of haematopoietic progenitor cells (HPC) in epidermal and dermal environments. CD34+ HPC were cultured for 6 days with GM-CSF, TGFβ1 and TNFα and seeded in the endothelialized skin equivalent at different time points to favour dermal or epidermal integration. This integration (after keratinocyte seeding, only and in absence of exogenous GM-CSF, TNFα, TGFβ1) gave rise both cutaneous DC, i.e. epidermal Langerhans cells (CD1a+, HLA-DR+) and dermal DC (DC-SIGN+, HLA-DR+) while endothelial cells are sufficiently activated to acquire HLA-DR expression. For the first time, the presence of a living dermal equivalent could provide a more complex environment integrating vascular components to study the differentiation of interstitial DC in a dermis equivalent. Such sophisticated skin equivalent may clarify some intriguing aspects of the numerous regulatory mechanisms controlling skin homeostasis.
Publisher: IOS Press
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 7 of 17 found articles
 
<< previous    next >>
 
 Koninklijke Bibliotheek - National Library of the Netherlands