CCL27 and CCL17 are chemokines believed to be involved in the process of establishing the inflammatory infiltrate, characteristic for the various inflammatory skin diseases. The skin-specific CCL27 binds the chemokine receptor-10 (CCR10), and CCL17 is a chemokine receptor-4 (CCR4) ligand. The purpose of our study was to characterize the expression of CCL27 and CCL17 in the inflammatory skin diseases: psoriasis, atopic dermatitis (AD) and acute allergic contact dermatitis (ACD) induced in nickel-sensitive individuals. Surprisingly, our studies revealed a markedly decreased CCL27 mRNA and protein expression in psoriatic lesions compared with non-lesional psoriatic skin. A minor CCL17 mRNA increase was measured in lesional psoriatic skin. No alterations were found in AD. In ACD, we found a pronounced (90-fold) raise in CCL17 mRNA and a 50-fold increase in CCL17 protein compared with normal skin. A kinetic ACD study of CCL17 expression showed the highest mean value 24 h after hapten application. Furthermore, we found the mRNA levels of CCR10 and CCR4 paralleling the results of their corresponding ligands. Overall, our principal findings were a distinct decrease in CCL27 in lesional psoriatic skin and a marked upregulation of CCL17 in ACD. These findings underscore the differential cutaneous T-cell recruitment in different inflammatory diseases.
机构:
Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Gudjonsson, Johann E.
Ding, Jun
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Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Stat Genet, Sch Publ Hlth, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Ding, Jun
Johnston, Andrew
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Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Johnston, Andrew
Tejasvi, Trilokraj
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Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Tejasvi, Trilokraj
Guzman, Andrew M.
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Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Guzman, Andrew M.
Nair, Rajan P.
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Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Nair, Rajan P.
Voorhees, John J.
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Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Voorhees, John J.
Abecasis, Goncalo R.
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Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Stat Genet, Sch Publ Hlth, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
机构:
Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Gudjonsson, Johann E.
Ding, Jun
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机构:
Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Stat Genet, Sch Publ Hlth, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Ding, Jun
Johnston, Andrew
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Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Johnston, Andrew
Tejasvi, Trilokraj
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Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Tejasvi, Trilokraj
Guzman, Andrew M.
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Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Guzman, Andrew M.
Nair, Rajan P.
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Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Nair, Rajan P.
Voorhees, John J.
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Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA
Voorhees, John J.
Abecasis, Goncalo R.
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机构:
Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Stat Genet, Sch Publ Hlth, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI 48109 USA