TY - JOUR
T1 - Dermatophagoides farinae extract induces severe atopic dermatitis in NC/Nga mice, which is effectively suppressed by the administration of tacrolimus ointment
AU - Oshio, Tomoyuki
AU - Sasaki, Yasuharu
AU - Funakoshi-Tago, Megumi
AU - Aizu-Yokota, Eriko
AU - Sonoda, Yoshiko
AU - Matsuoka, Hiroyuki
AU - Kasahara, Tadashi
N1 - Funding Information:
We would like to thank Professor Kenjiro Matsuno, Dokkyo Medical College, for his kind advice on the histological examinations. We also thank Dr. Jean F Rigod, for English editing. This work was partly supported by the Grants-in-Aid for Scientific Research (19590075), and High-tech Research from MEXT, Japan.
PY - 2009/4
Y1 - 2009/4
N2 - Atopic dermatitis (AD) is a chronic inflammatory skin disease, which is accompanied by marked increases in the levels of inflammatory cells, including mast cells and eosinophils as well as T cells and macrophages. To investigate the expression pattern of chemokines in AD, a house dust mite, Dermatophagoides farinae extracts (DfE)-induced NC/Nga AD model was developed in mice, and this model was used to determine the expression levels of chemokines in atopic lesions using DNA microarrays and RT-PCR. When NC/Nga mice were repeatedly treated with DfE for 4 to 7 weeks on the back skin, the mRNA expression levels of CCL20/LARC, CCL24/eotaxin-2, CCL17/TARC, and CCL11/eotaxin-1 were markedly induced and lesser of CCL2/MCP-1, within the inflammatory lesion of the back skin. Immunohistochemical staining revealed the expression of these chemokines in the epidermis and dermis of DfE-treated NC/Nga mice. Interestingly, repeated application of tacrolimus ointment potently inhibited DfE-induced atopic dermatitis in NC/Nga mice concomitant with the inhibition of these changes in chemokine gene and protein expression levels particularly of CCL20/LARC, CCL17/TARC, and CCL11/eotaxin-1. These data indicate that severe atopic dermatitis induced by DfE accompanies elevated chemokine levels, and it was proposed that tacrolimus ointment is beneficial for the treatment of severe AD.
AB - Atopic dermatitis (AD) is a chronic inflammatory skin disease, which is accompanied by marked increases in the levels of inflammatory cells, including mast cells and eosinophils as well as T cells and macrophages. To investigate the expression pattern of chemokines in AD, a house dust mite, Dermatophagoides farinae extracts (DfE)-induced NC/Nga AD model was developed in mice, and this model was used to determine the expression levels of chemokines in atopic lesions using DNA microarrays and RT-PCR. When NC/Nga mice were repeatedly treated with DfE for 4 to 7 weeks on the back skin, the mRNA expression levels of CCL20/LARC, CCL24/eotaxin-2, CCL17/TARC, and CCL11/eotaxin-1 were markedly induced and lesser of CCL2/MCP-1, within the inflammatory lesion of the back skin. Immunohistochemical staining revealed the expression of these chemokines in the epidermis and dermis of DfE-treated NC/Nga mice. Interestingly, repeated application of tacrolimus ointment potently inhibited DfE-induced atopic dermatitis in NC/Nga mice concomitant with the inhibition of these changes in chemokine gene and protein expression levels particularly of CCL20/LARC, CCL17/TARC, and CCL11/eotaxin-1. These data indicate that severe atopic dermatitis induced by DfE accompanies elevated chemokine levels, and it was proposed that tacrolimus ointment is beneficial for the treatment of severe AD.
KW - Atopic dermatitis
KW - Chemokines
KW - Dermatophagoides farinae
KW - NC/Nga
KW - Tacrolimus ointment/protopic
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U2 - 10.1016/j.intimp.2008.12.013
DO - 10.1016/j.intimp.2008.12.013
M3 - Article
C2 - 19162238
AN - SCOPUS:61649125989
SN - 1567-5769
VL - 9
SP - 403
EP - 411
JO - International Immunopharmacology
JF - International Immunopharmacology
IS - 4
ER -