Use of an in vitro model of tissue-engineered human skin to study keratinocyte attachment and migration in the process of reepithelialization
- PMID: 16630110
- DOI: 10.1111/j.1743-6109.2006.00111.x
Use of an in vitro model of tissue-engineered human skin to study keratinocyte attachment and migration in the process of reepithelialization
Abstract
To produce a stable epidermis, keratinocytes need to be firmly attached to the basement membrane. However, following wounding, keratinocytes are required to develop a migratory phenotype in order to reepithelialize the wound. To investigate some of the issues underlying reepithelialization, we have developed a three-dimensional in vitro model of tissue-engineered skin, comprising sterilized human dermis seeded with human keratinocytes and dermal fibroblasts. Using this model, we have shown that the inclusion of fibroblasts within the model increases the stability of keratinocyte attachment. We have also demonstrated that keratinocyte migration occurs most effectively in the absence of a basement membrane and following the inclusion of fibroblasts in the model. In addition, subjecting the keratinocyte layer to mechanical trauma induces a migratory phenotype. We conclude that this three-dimensional in vitro wound model can be used to increase our understanding of the factors that enhance keratinocyte migration and hence wound healing in vivo.
Similar articles
-
Enhancement of keratinocyte performance in the production of tissue-engineered skin using a low-calcium medium.Wound Repair Regen. 2007 Sep-Oct;15(5):718-26. doi: 10.1111/j.1524-475X.2007.00275.x. Wound Repair Regen. 2007. PMID: 17971018
-
Characterization of wound reepithelialization using a new human tissue-engineered corneal wound healing model.Invest Ophthalmol Vis Sci. 2008 Apr;49(4):1376-85. doi: 10.1167/iovs.07-0904. Invest Ophthalmol Vis Sci. 2008. PMID: 18385053
-
Re-epithelialization. Human keratinocyte locomotion.Dermatol Clin. 1993 Oct;11(4):641-6. Dermatol Clin. 1993. PMID: 8222348 Review.
-
Streptolysin O enhances keratinocyte migration and proliferation and promotes skin organ culture wound healing in vitro.Wound Repair Regen. 2007 Jan-Feb;15(1):71-9. doi: 10.1111/j.1524-475X.2006.00187.x. Wound Repair Regen. 2007. PMID: 17244322
-
Skin tissue engineering.J Biomater Sci Polym Ed. 2008;19(8):955-68. doi: 10.1163/156856208784909417. J Biomater Sci Polym Ed. 2008. PMID: 18644224 Review.
Cited by
-
Overcoming scarring in the urethra: Challenges for tissue engineering.Asian J Urol. 2018 Apr;5(2):69-77. doi: 10.1016/j.ajur.2018.02.002. Epub 2018 Feb 12. Asian J Urol. 2018. PMID: 29736368 Free PMC article. Review.
-
Intravital insights in skin wound healing using the mouse dorsal skin fold chamber.J Anat. 2007 Dec;211(6):810-8. doi: 10.1111/j.1469-7580.2007.00822.x. Epub 2007 Nov 13. J Anat. 2007. PMID: 18005122 Free PMC article.
-
Impaired keratinocyte function on matrix metalloproteinase-1 (MMP-1) damaged collagen.Arch Dermatol Res. 2009 Aug;301(7):497-506. doi: 10.1007/s00403-009-0948-4. Epub 2009 Apr 8. Arch Dermatol Res. 2009. PMID: 19352688 Free PMC article.
-
Generation of a three-dimensional full thickness skin equivalent and automated wounding.J Vis Exp. 2015 Feb 26;(96):52576. doi: 10.3791/52576. J Vis Exp. 2015. PMID: 25741763 Free PMC article.
-
A review of tissue-engineered skin bioconstructs available for skin reconstruction.J R Soc Interface. 2010 Feb 6;7(43):229-58. doi: 10.1098/rsif.2009.0403. Epub 2009 Oct 28. J R Soc Interface. 2010. PMID: 19864266 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources