Expression of keratin K2e in cutaneous and oral lesions - Association with keratinocyte activation, proliferation, and keratinization

被引:53
作者
Bloor, BK
Tidman, N
Leigh, IM
Odell, E
Dogan, B
Wollina, U
Ghali, L
Waseem, A
机构
[1] Kings Coll London, Dept Craniofacial Dev, Guys Kings & St Thomass Dent Inst, Head & Neck Canc Res Program, London SE1 9RT, England
[2] Queen Mary Univ London, Ctr Cutaneous Res, Canc Res United Kingdom Skin Tumour Biol Unit, London E1 4NS, England
[3] Haydarpasa Teaching Hosp, GATA, Dept Dermatol, Istanbul, Turkey
[4] Gen Hosp Dresden Friedrichstadt, Dept Dermatol, Dresden, Germany
关键词
D O I
10.1016/S0002-9440(10)63891-6
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The cytoskeleton in keratinocytes is a complex of highly homologous structural proteins derived from two families of type I and type II polypeptides. Keratin K2e is a type II polypeptide that is expressed in epidermis late in differentiation. Here we report the influence of keratinocyte activation, proliferation, and keratinization on K2e expression in samples of cutaneous and oral lesions. The normal expression of K2e in the upper spinous and granular layers of interfollicular epidermis is increased in keloid scars but showed distinct down-regulation in psoriasis and hypertrophic scars where keratinocytes are known to undergo activation. Unlike normal and psoriatic skin, K2e expression in hypertrophic and keloid scars began in the deepest suprabasal layer. in cutaneous basal and squamous cell carcinomas, K2e was absent in most tumor islands but the overlying epidermis showed strong expression. No significant K2e expression in nonkeratinized or keratinized oral epithelia, including buccal mucosa, lateral border of tongue and gingiva was detected. in oral lichen planus K2e expression was undetectable, but in benign keratoses of lingual mucosa induction of K2e along with K1 and K10 was observed. In mild-to-moderate oral dysplasia. with orthokeratinization, K2e was highly expressed compared with parakeratinized areas but in severe dysplasia as well as in oral squamous cell carcinoma, K2e expression was undetectable. Taken together, the data suggest that Me expression in skin is sensitive to keratinocyte activation but its up-regulation in oral lesions is a reflection of the degree of orthokeratinization.
引用
收藏
页码:963 / 975
页数:13
相关论文
共 67 条
[1]   CHANGES IN KERATINOCYTE ADHESION DURING TERMINAL DIFFERENTIATION - REDUCTION IN FIBRONECTIN BINDING PRECEDES ALPHA-5-BETA-1-INTEGRIN LOSS FROM THE CELL-SURFACE [J].
ADAMS, JC ;
WATT, FM .
CELL, 1990, 63 (02) :425-435
[2]   Expression of type XVI collagen in human skin fibroblasts: Enhanced expression in fibrotic skin diseases [J].
Akagi, A ;
Tajima, S ;
Ishibashi, A ;
Yamaguchi, N ;
Nagai, Y .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 113 (02) :246-250
[3]   FILAGGRIN PRODUCTION BY CULTURED HUMAN EPIDERMAL-KERATINOCYTES AND ITS REGULATION BY RETINOIC ACID [J].
ASSELINEAU, D ;
DALE, BA ;
BERNARD, BA .
DIFFERENTIATION, 1990, 45 (03) :221-229
[4]  
Bloor BK, 1998, LAB INVEST, V78, P787
[5]   Gene expression of differentiation-specific keratins in oral epithelial dysplasia and squamous cell carcinoma [J].
Bloor, BK ;
Seddon, SV ;
Morgan, PR .
ORAL ONCOLOGY, 2001, 37 (03) :251-261
[6]   Gene expression of differentiation-specific keratins (K4, K13, K1 and K10) in oral non-dysplastic keratoses and lichen planus [J].
Bloor, BK ;
Seddon, SV ;
Morgan, PR .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2000, 29 (08) :376-384
[7]  
CLARK RAF, 1993, MECH CUTANEOUS WOUND
[8]   CHARACTERIZATION OF HUMAN CYTOKERATIN-2, AN EPIDERMAL CYTOSKELETAL PROTEIN SYNTHESIZED LATE DURING DIFFERENTIATION [J].
COLLIN, C ;
MOLL, R ;
KUBICKA, S ;
OUHAYOUN, JP ;
FRANKE, WW .
EXPERIMENTAL CELL RESEARCH, 1992, 202 (01) :132-141
[9]   SUPRABASAL MARKER PROTEINS DISTINGUISHING KERATINIZING SQUAMOUS EPITHELIA - CYTOKERATIN-2 POLYPEPTIDES OF ORAL MASTICATORY EPITHELIUM AND EPIDERMIS ARE DIFFERENT [J].
COLLIN, C ;
OUHAYOUN, JP ;
GRUND, C ;
FRANKE, WW .
DIFFERENTIATION, 1992, 51 (02) :137-148
[10]   Towards a molecular definition of keratinocyte activation after acute injury to stratified epithelia [J].
Coulombe, PA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 236 (02) :231-238