银屑病
车站3
转基因小鼠
下调和上调
转基因
表型
发病机制
角质形成细胞
细胞生物学
癌症研究
免疫学
生物
体外
信号转导
基因
遗传学
作者
Shigetoshi Sano,Keith Syson Chan,Steve Carbajal,John L. Clifford,Mary Peavey,Kaoru Kiguchi,Satoshi Itami,Brian J. Nickoloff,John DiGiovanni
出处
期刊:Nature Medicine
[Springer Nature]
日期:2004-12-12
卷期号:11 (1): 43-49
被引量:688
摘要
Here we report that epidermal keratinocytes in psoriatic lesions are characterized by activated Stat3. Transgenic mice with keratinocytes expressing a constitutively active Stat3 (K5.Stat3C mice) develop a skin phenotype either spontaneously, or in response to wounding, that closely resembles psoriasis. Keratinocytes from K5.Stat3C mice show upregulation of several molecules linked to the pathogenesis of psoriasis. In addition, the development of psoriatic lesions in K5.Stat3C mice requires cooperation between Stat3 activation in keratinocytes and activated T cells. Finally, abrogation of Stat3 function by a decoy oligonucleotide inhibits the onset and reverses established psoriatic lesions in K5.Stat3C mice. Thus, targeting Stat3 may be potentially therapeutic in the treatment of psoriasis.
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