Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Ohkawara, T. et al.

Ohkawara, Takeda, Miyashita, Nishiwaki, Nakayama, Taniguchi, Yoshiki, Takana, Imamura, Sugiyama, Asaka, Nishihira,

Regulation of Toll-like receptor 4 expression in mouse colon by macrophage migration inhibitory factor.

Recent studies have indicated that macrophage migration inhibitory factor (MIF) and Toll-like receptor (TLR) play an important role in the regulation of innate immune responses. In this study, we investigated the effect of MIF on the expression of TLR4, a receptor that recognizes lipopolysaccharide, in colon using MIF-deficient mice. TLR4 mRNA expression in the colon tissues was determined by northern blot analysis. Western blot analysis and immunohistochemistry in the colon tissues were performed to evaluate the expression of TLR4 protein. The expressions of TLR4 mRNA and protein were remarkably down-regulated in colon tissues of MIF-deficient mice compared with wild-type mice and up-regulated by treatment with recombinant MIF. Immunohistochemical study revealed the presence of TLR4-positive staining in mononuclear cells in the lamina propria and intraepithelial mononuclear cells as well as weak staining in epithelial cells and crypts in colon tissues of wild-type mice. In contrast, MIF-deficient mice did not show TLR4-positive staining in the colonic mucosa. In MIF-deficient mice injected with recombinant mouse MIF (rMIF), TLR4-positive staining cells were observed in colon tissues similar to the findings in wild-type mice. Administration of dextran sulfate sodium (DSS) up-regulated the expression of TLR4 in the colons of WT mice but not in those of MIF-deficient mice. Furthermore, pretreatment with rMIF up-regulated the expression of TLR4 in response to DSS in MIF-deficient mice. Our results suggest that MIF affects the expression of TLR4 in mouse colon under both normal and colitic conditions.[1]

References

Regulation of Toll-like receptor 4 expression in mouse colon by macrophage migration inhibitory factor. Ohkawara, T., Takeda, H., Miyashita, K., Nishiwaki, M., Nakayama, T., Taniguchi, M., Yoshiki, T., Takana, J., Imamura, M., Sugiyama, T., Asaka, M., Nishihira, J. Histochem. Cell Biol. (2006) [Pubmed]

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