Keratin 15 expression in stratified epithelia: Downregulation in activated keratinocytes

被引:163
作者
Waseem, A
Dogan, B
Tidman, N
Alam, Y
Purkis, P
Jackson, S
Lalli, A
Machesney, M
Leigh, IM
机构
[1] UMDS, Guys Hosp, Head & Neck Canc Res Programme, Div Dent, London, England
[2] UMDS, Guys Hosp, Head & Neck Canc Res Programme, Div Biochem, London, England
[3] UMDS, Guys Hosp, Head & Neck Canc Res Programme, Div Mol Biol, London, England
[4] Royal London Hosp, ICRF Skin Tumor Biol Unit, London E1 1BB, England
基金
英国惠康基金;
关键词
hyperproliferation; hypertrophic scar; in situ hybridization; psoriasis;
D O I
10.1046/j.1523-1747.1999.00535.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Keratin 15 (K15) is a type I keratin without a defined type II partner whose expression in epidermal diseases has not been investigated. In this study we have used LHK15, a monoclonal antibody raised against the last 17 amino acids of the K15 polypeptide, to show that K15 is expressed primarily in the basal keratinocytes of stratified tissues, including the fetal epidermis and fetal nail. Although K15 in normal hair follicles was virtually absent from hair bulbs, it was expressed by a subset of keratinocytes in the outer root sheath. By comparison, K14 expression was found throughout the outer root sheath of hair follicles; however, when both K14 alleles were naturally ablated, the expression of K15 was also observed throughout the outer root sheath of the follicles. Expression of K15 mRNA was assessed by in situ hybridization and corroborated the data from immunostaining. An increase in K15 mRNA and protein expression in hair follicles from the K14 ablated epidermis suggested an upregulation of the K15 gene in the absence of the K14 protein. In organotypical cultures where differentiating keratinocytes expressed markers of activated phenotype, i.e., K6 and K16, expression of K15 was undetectable. The expression of K15 mRNA and protein was also downregulated in two hyperproliferating situations, psoriasis and hypertrophic scars. Because keratinocytes in psoriasis and hypertrophic scars are activated, we conclude that K15 expression is not compatible with keratinocyte activation and the K15 gene is downregulated to maintain the activated phenotype.
引用
收藏
页码:362 / 369
页数:8
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