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논문 기본 정보

자료유형
학술저널
저자정보
Jae-Won Jeon (Korea Research Institute of Bioscience and Biotechnology) Bum-Chan Park (Korea Research Institute of Bioscience and Biotechnology) Joon-Goo Jung (Korea Research Institute of Bioscience and Biotechnology) Young-Soon Jang (KAIST) Eui-Cheol Shin (KAIST) Young Woo Park (Korea Research Institute of Bioscience and Biotechnology)
저널정보
대한면역학회 Immune Network Immune Network Vol.13 No.4
발행연도
2013.8
수록면
148 - 156 (9page)

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초록· 키워드

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The PrP<SUP>C</SUP> is expressed in many types of immune cells including monocytes and macrophages, however, its function in immune regulation remains to be elucidated. In the present study, we examined a role for PrP<SUP>C</SUP> in regulation of monocyte function. Specifically, the effect of a soluble form of PrP<SUP>C</SUP> was studied in human monocytes. A recombinant fusion protein of soluble human PrP<SUP>C</SUP> fused with the Fc portion of human IgG1 (designated as soluble PrP<SUP>C</SUP>-Fc) bound to the cell surface of monocytes, induced differentiation to macrophage-like cells, and enhanced adherence and phagocytic activity. In addition, soluble PrP<SUP>C</SUP>-Fc stimulated monocytes to produce pro-inflammatory
cytokines such as TNF-α, IL-1β, and IL-6. Both ERK and NF-κB signaling pathways were activated in soluble PrP<SUP>C</SUP>-treated monocytes, and inhibitors of either pathway abrogated monocyte adherence and cytokine production. Taken together, we conclude that soluble PrP<SUP>C</SUP>-Fc enhanced adherence, phagocytosis, and cytokine production of monocytes via activation of the ERK and NF-κB signaling pathways.

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INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2016-511-001746104