Molecular mechanism of kallikrein-related peptidase 8/neuropsin-induced hyperkeratosis in inflamed skin

作者：Shingaki K^*; Matsuzaki S; Taniguchi M; Kubo T; Fujiwara T; Kanazawa S; Yamamoto A; Tamura H; Maeda T; Ooi K; Matsumoto K; Shiosaka S; Tohyama M

来源：British Journal of Dermatology, 2010, 163(3): 466-475.

DOI：10.1111/j.1365-2133.2010.09864.x

• differentiation
• hyperkeratosis
• kallikrein
• keratin
• keratinocyte

P>Background
Hyperkeratosis and acanthosis occur in inflamed skin. Proliferation and differentiation of keratinocytes are important processes during epidermal repair after inflammation. Neuropsin and its human homologue kallikrein-related peptidase 8 (KLK8) have been reported to be involved in epidermal proliferation and differentiation, but the involved molecular mechanisms are obscure.
Objectives
To explore the molecular mechanism of KLK8/neuropsin-induced hyperkeratosis and acanthosis in inflamed skin.
Methods
The molecular mechanism involved in KLK8/neuropsin-induced hyperkeratosis and acanthosis in inflamed skin was investigated both in vivo and in vitro using neuropsin knockout mice and KLK8 knockdown human keratinocytes. Neuropsin-related genes were identified by differential gene display. The localization and functional relationship of the molecules affected downstream of KLK8/neuropsin in normal and inflamed skin were analysed by in situ hybridization and immunohistochemistry.
Results
Hyperkeratosis and acanthosis in sodium lauryl sulphate-stimulated skin were markedly inhibited in neuropsin knockout mice. Knockdown of KLK8/neuropsin increased transcription factor activator protein-2 alpha (AP-2 alpha) expression and decreased keratin 10 expression in human keratinocytes and mouse skin, respectively. AP-2 alpha has been reported to inhibit epidermal proliferation and keratin 10 expression. Distributional analysis showed that KLK8/neuropsin was expressed in the stratum spinosum, AP-2 alpha was expressed in the stratum basale and the lower part of the stratum spinosum, and keratin 10 was expressed throughout the stratum spinosum.
Conclusions
The above findings suggest the following mechanism of events underlying KLK8/neuropsin-induced hyperkeratosis: (i) skin inflammation increases KLK8/neuropsin expression in the stratum spinosum; (ii) the released KLK8/neuropsin inhibits AP-2 alpha expression in the cells of the stratum basale and stratum spinosum; (iii) the decrease in AP-2 alpha results in cell proliferation in the stratum basale and cell differentiation in the stratum spinosum, with an increase in keratin 10 expression.

• 出版日期2010-9