Morphological observation of human keratinocytes tridimensionally cocultured with xenogenic acellular dermal matrix.
- Author:
Chong-tao ZHU
1
;
Dai-zhi PENG
;
Li-hua WANG
;
Bin HE
;
Bi-xiang ZHENG
;
Xin ZHOU
;
Hai-shui LUO
;
Yong WANG
;
Jing LIU
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Cells, Cultured; Coculture Techniques; Dermis; cytology; Humans; Keratinocytes; cytology; Rats; Rats, Sprague-Dawley; Skin, Artificial; Tissue Engineering; methods
- From: Chinese Journal of Burns 2009;25(4):258-260
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo establish the tridimensional culture method for tissue-engineered skin to observe the histomorphological change in human immortal KC strain (HacaT)cocultured with xenogenic acellular dermal matrix (ADM).
METHODSThe ADM was prepared from SD rats by a modified method. HaCaTs were cultured in defined KC-serum free medium. HaCaTs in log growth phase were inoculated on ADM at the cell density of 2 x 10(5)/cm(2). They were submergedly cultured for 5 days and then changed to air-liquid phase culture for another 5 days. ADM and growth of HaCaTs on day 1 and 5 after cocultured with ADM were observed with scanning electron microscope. The histological change in ADM and HaCaTs on day 1, 5, and 10 after cocultured with ADM were examined by HE staining.
RESULTSThe gross appearance of ADM was white with smooth and soft texture, and intact collagen bundles without cellular residue. HaCaTs adhered and stretched out pseudopodia on the surface of the ADM on day 1 after combined culture, and a monolayer of cells was formed on day 5, growing into 3-6 layers of cells on day 10 with a tendency to grow into ADM.
CONCLUSIONSSD rats ADM is benefit for the adhesion of HaCaTs and the permeation of nutrient solution, from which an engineered multiple-layered human skin can be obtained within 10 days.
