Novel mechanisms of T-cell and dendritic cell activation revealed by profiling of psoriasis on the 63,100-element oligonucleotide array

被引:238
作者
Zhou, XH
Krueger, JG
Kao, MCJ
Lee, E
Du, FH
Menter, A
Wong, WH
Bowcock, AM
机构
[1] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[2] Harvard Univ, Dept Biostat, Boston, MA 02115 USA
[3] Rockefeller Univ, Invest Dermatol Lab, New York, NY 10021 USA
[4] Baylor Univ, Med Ctr, Dept Internal Med, Div Dermatol, Dallas, TX 75246 USA
[5] Harvard Univ, Dept Stat, Cambridge, MA 02138 USA
[6] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[7] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
关键词
immune signaling; promoter analysis; chemokines; gene expression;
D O I
10.1152/physiolgenomics.00157.2002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A global picture of gene expression in the common immune-mediated skin disease, psoriasis, was obtained by interrogating the full set of Affymetrix GeneChips with psoriatic and control skin samples. We identified 1,338 genes with potential roles in psoriasis pathogenesis/maintenance and revealed many perturbed biological processes. A novel method for identifying transcription factor binding sites was also developed and applied to this dataset. Many of the identified sites are known to be involved in immune response and proliferation. An in-depth study of immune system genes revealed the presence of many regulating cytokines and chemokines within involved skin, and markers of dendritic cell ( DC) activation in uninvolved skin. The combination of many CCR7+ T cells, DCs, and regulating chemokines in psoriatic lesions, together with the detection of DC activation markers in nonlesional skin, strongly suggests that the spatial organization of T cells and DCs could sustain chronic T-cell activation and persistence within focal skin regions.
引用
收藏
页码:69 / 78
页数:10
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