Improvement of epidermal barrier properties in cultured skin substitutes after grafting onto athymic mice

被引:11
作者
Barai, Namrata D.
Supp, Andrew P.
Kasting, Gerald B.
Visscher, Marty O.
Boyce, Steven T.
机构
[1] Univ Cincinnati, Med Ctr, Coll Pharm, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Dept Surg, Cincinnati, OH 45267 USA
[3] Shriners Hosp Children, Dept Res, Cincinnati, OH USA
[4] Childrens Hosp, Med Ctr, Skin Sci Inst, Cincinnati, OH 45229 USA
关键词
barrier permeability; cultured skin substitutes; niacinamide flux; transepidermal water loss;
D O I
10.1159/000096168
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Barrier function in cultured skin substitutes (CSS) prepared from human cell sources was measured by noninvasive (surface hydration, transepidermal water loss) and invasive methods (water permeation, niacinamide flux) before and after grafting onto athymic mice. In vitro measurements were made on days 7 and 14. Although three of the four measures of barrier function improved markedly from day 7 to 14, the values obtained were still far from those obtained with native human skin controls. Additional CSS were grafted onto athymic mice on day 14, and skin was harvested 2 and 6 weeks after grafting. Grafting brought about a substantial decrease in all measurements by 2 weeks and almost complete normalization of barrier function after 6 weeks. The most sensitive measure of this recovery was niacinamide permeability, which decreased from (280 +/- 40) x 10(-4) cm/h in vitro to (17 +/- 30) x 10(-4) cm/h(2) weeks after grafting and (5 +/- 2) x 10(-4) cm/h 6 weeks after grafting, versus control values of (2 +/- 2) x 10(-4) cm/h in human cadaver skin and (0.6 +/- 0.4) x 10(-4) cm/h in human epidermal membrane prepared from freshly excised breast skin. These results demonstrate the reformation of epidermal barrier function after transplantation and provide insights for the development of a functional epidermal barrier in CSS in vitro. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:21 / 28
页数:8
相关论文
共 42 条
[31]   BARRIER FUNCTION OF HUMAN SKIN AND HUMAN RECONSTRUCTED EPIDERMIS [J].
REGNIER, M ;
CARON, D ;
REICHERT, U ;
SCHAEFER, H .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1993, 82 (04) :404-407
[32]   TERMINAL EPIDERMAL DIFFERENTIATION OF HUMAN KERATINOCYTES GROWN IN CHEMICALLY DEFINED MEDIUM ON INERT FILTER SUBSTRATES AT THE AIR-LIQUID INTERFACE [J].
ROSDY, M ;
CLAUSS, LC .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 95 (04) :409-414
[33]   PERMEABILITIES OF ALKYL P-AMINOBENZOATES THROUGH LIVING SKIN EQUIVALENT AND CADAVER SKIN [J].
ROY, SD ;
FUJIKI, J ;
FLEITMAN, JS .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1993, 82 (12) :1266-1268
[34]   Comparison of human skin or epidermis models with human and animal skin in in-vitro percutaneous absorption [J].
Schmook, FP ;
Meingassner, JG ;
Billich, A .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 215 (1-2) :51-56
[35]   CHARACTERIZATION, BARRIER FUNCTION, AND DRUG-METABOLISM OF AN INVITRO SKIN MODEL [J].
SLIVKA, SR ;
LANDEEN, LK ;
ZEIGLER, F ;
ZIMBER, MP ;
BARTEL, RL .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1993, 100 (01) :40-46
[36]   Incubation of cultured skin substitutes in reduced humidity promotes cornification in vitro and stable engraftment in athymic mice [J].
Supp, AP ;
Wickett, RR ;
Swope, VB ;
Harriger, MD ;
Hoath, SB ;
Boyce, ST .
WOUND REPAIR AND REGENERATION, 1999, 7 (04) :226-237
[37]   Enhanced vascularization of cultured skin substitutes genetically modified to overexpress vascular endothelial growth factor [J].
Supp, DM ;
Supp, AP ;
Bell, SM ;
Boyce, ST .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 114 (01) :5-13
[38]   Expression of insulin-like growth factor I by cultured skin substitutes does not replace the physiologic requirement for insulin in vitro [J].
Swope, VB ;
Supp, AP ;
Greenhalgh, DG ;
Warden, GD ;
Boyce, ST .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 116 (05) :650-657
[39]   INVITRO AND POSTTRANSPLANTATION DIFFERENTIATION OF HUMAN KERATINOCYTES GROWN ON THE HUMAN TYPE-IV COLLAGEN FILM OF A BILAYERED DERMAL SUBSTITUTE [J].
TINOIS, E ;
TIOLLIER, J ;
GAUCHERAND, M ;
DUMAS, H ;
TARDY, M ;
THIVOLET, J .
EXPERIMENTAL CELL RESEARCH, 1991, 193 (02) :310-319
[40]  
Vicanova J, 1998, J Investig Dermatol Symp Proc, V3, P114