TY - JOUR
T1 - Macrophage migration inhibitory factor is essential for eosinophil recruitment in allergen-induced skin inflammation
AU - Yoshihisa, Yoko
AU - Makino, Teruhiko
AU - Matsunaga, Kenji
AU - Honda, Ayumi
AU - Norisugi, Osamu
AU - Abe, Riichiro
AU - Shimizu, Hiroshi
AU - Shimizu, Tadamichi
N1 - Funding Information:
This research was supported by a Grant-in-Aid for Scientific Research (Nos.11670813 and 13357008) from the Japan Society for the Promotion of Science.
PY - 2011/4
Y1 - 2011/4
N2 - Macrophage migration inhibitory factor (MIF) is a pluripotent cytokine that has an essential role in the pathophysiology of experimental allergic inflammation. Recent findings suggest that MIF is involved in several allergic disorders, including atopic dermatitis (AD). In this study, the role of MIF in allergic skin inflammation was examined using a murine model of AD elicited by epicutaneous sensitization with ovalbumin (OVA). We observed the number of skin-infiltrating eosinophils to significantly increase in OVA-sensitized MIF transgenic (Tg) mice compared with their wild-type (WT) littermates. On the other hand, eosinophils were virtually absent from the skin of MIF knockout (KO) mice and failed to infiltrate their skin after repeated epicutaneous sensitization with OVA. The mRNA expression levels of eotaxin and IL-5 were significantly increased in OVA-sensitized skin sites of MIF Tg mice, but were significantly decreased in MIF KO mice in comparison with the levels in WT littermates. Eotaxin expression was induced by IL-4 stimulation in fibroblasts in MIF Tg mice, but not in MIF KO mice. These findings indicate that MIF can induce eosinophil accumulation in the skin. Therefore, the targeted inhibition of MIF might be a promising new therapeutic strategy for allergic skin diseases.
AB - Macrophage migration inhibitory factor (MIF) is a pluripotent cytokine that has an essential role in the pathophysiology of experimental allergic inflammation. Recent findings suggest that MIF is involved in several allergic disorders, including atopic dermatitis (AD). In this study, the role of MIF in allergic skin inflammation was examined using a murine model of AD elicited by epicutaneous sensitization with ovalbumin (OVA). We observed the number of skin-infiltrating eosinophils to significantly increase in OVA-sensitized MIF transgenic (Tg) mice compared with their wild-type (WT) littermates. On the other hand, eosinophils were virtually absent from the skin of MIF knockout (KO) mice and failed to infiltrate their skin after repeated epicutaneous sensitization with OVA. The mRNA expression levels of eotaxin and IL-5 were significantly increased in OVA-sensitized skin sites of MIF Tg mice, but were significantly decreased in MIF KO mice in comparison with the levels in WT littermates. Eotaxin expression was induced by IL-4 stimulation in fibroblasts in MIF Tg mice, but not in MIF KO mice. These findings indicate that MIF can induce eosinophil accumulation in the skin. Therefore, the targeted inhibition of MIF might be a promising new therapeutic strategy for allergic skin diseases.
UR - http://www.scopus.com/inward/record.url?scp=79952765250&partnerID=8YFLogxK
U2 - 10.1038/jid.2010.418
DO - 10.1038/jid.2010.418
M3 - 学術論文
C2 - 21191413
AN - SCOPUS:79952765250
SN - 0022-202X
VL - 131
SP - 925
EP - 931
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 4
ER -