Preservation of phenotype in an organotypic cell culture model of a recessive keratinization defect of Norfolk terrier dogs

被引:6
作者
Barnhart, KF
Credille, KM
Ambrus, A
Dunstan, RW
机构
[1] Texas A&M Univ, Coll Vet Med, Dept Pathobiol, College Stn, TX 77843 USA
[2] Pfizer Global Res & Dev, Ann Arbor, MI USA
关键词
canine; keratin; 10; keratinization defect; organotypic cell culture; recessive inheritance;
D O I
10.1111/j.0906-6705.2005.00306.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The purpose of this study is to reproduce in vitro a recessive keratinization defect of Norfolk terrier dogs characterized by a lack of keratin 10 (K10) production. Keratinocytes from skin biopsy samples of four normal dogs and two affected dogs were cultured organotypically with growth factor-supplemented media in order to stimulate cornification. The cultured epidermis from the normal dogs closely resembled the normal epidermis in vivo and cornified. The cultured epidermis from the affected dogs displayed many phenotypic alterations identified in skin biopsies from dogs with this heritable defect. Immunohistochemistry and immunoblotting showed a marked decrease in K10 from the cultures of the affected keratinocytes, compared to that in K10 from the cultures of the normal keratinocytes. Real-time reverse transcription polymerase chain reaction quantitation showed a 31-fold decrease in K10, a 1.75-fold increase in K1 and a 136-fold increase in K2e between the affected and the normal epidermis. Organotypic keratinocytes showed a 241-fold decrease in K10, a 31-fold decrease in K1 and a 1467-fold decrease in K2e between the affected and normal cultures. Although in vitro keratin expression did not precisely simulate in vivo, the morphology of the normal and the affected epidermis was largely preserved; thus, this culture system may provide an alternative to in vivo investigations for cutaneous research involving cornification.
引用
收藏
页码:481 / 490
页数:10
相关论文
共 84 条
[61]  
Relchelt J, 2002, J CELL SCI, V115, P2639
[62]   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
[63]   A MUTATION IN THE MUCOSAL KERATIN K4 IS ASSOCIATED WITH ORAL WHITE SPONGE NEVUS [J].
RUGG, EL ;
MCLEAN, WHI ;
ALLISON, WE ;
LUNNY, DP ;
MACLEOD, RI ;
FELIX, DH ;
LANE, EB ;
MUNRO, CS .
NATURE GENETICS, 1995, 11 (04) :450-452
[64]   DENSITY-DEPENDENT MODULATION OF SYNTHESIS OF KERATIN-1 AND KERATIN-10 IN THE HUMAN KERATINOCYTE LINE HACAT AND IN RAS-TRANSFECTED TUMORIGENIC CLONES [J].
RYLE, CM ;
BREITKREUTZ, D ;
STARK, HJ ;
LEIGH, IM ;
STEINERT, PM ;
ROOP, D ;
FUSENIG, NE .
DIFFERENTIATION, 1989, 40 (01) :42-54
[65]   Severe abnormalities in the oral mucosa induced by suprabasal expression of epidermal keratin K10 in transgenic mice [J].
Santos, M ;
Bravo, A ;
López, C ;
Paramio, JM ;
Jorcano, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (38) :35371-35377
[66]   KERATIN AND KERATINIZATION [J].
SMACK, DP ;
KORGE, BP ;
JAMES, WD .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1994, 30 (01) :85-102
[67]   The molecular genetics of keratin disorders [J].
Smith, FJD .
AMERICAN JOURNAL OF CLINICAL DERMATOLOGY, 2003, 4 (05) :347-364
[68]  
Smith LT, 1999, BRIT J DERMATOL, V140, P582
[69]   Refined mapping of Naegeli-Franceschetti-Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes [J].
Sprecher, E ;
Itin, P ;
Whittock, NV ;
McGrath, JA ;
Meyer, R ;
DiGiovanna, JJ ;
Bale, SJ ;
Uitto, J ;
Richard, G .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 119 (03) :692-698
[70]   Organotypic keratinocyte cocultures in defined medium with regular epidermal morphogenesis and differentiation [J].
Stark, HJ ;
Baur, M ;
Breitkreutz, D ;
Mirancea, N ;
Fusenig, NE .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (05) :681-691