Establishment of the cells useful for murine interleukin-18 bioassay by introducing murine interleukin-18 receptor cDNA into human myelomonocytic KG-1 cells
We genetically engineered human myelomonocytic KG-1 cells by introducing cDNA of murine interleukin-18 receptor (MuIL-18R) and established human cells which were capable of responding to MuIL-18. These cells expressed larger number of MuIL-18R (>13,000 sites/cell) than intrinsic human IL-18 recep...
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Published in | Journal of immunological methods Vol. 217; no. 1; pp. 97 - 102 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Amsterdam
Elsevier B.V
01.08.1998
Elsevier |
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Abstract | We genetically engineered human myelomonocytic KG-1 cells by introducing cDNA of murine interleukin-18 receptor (MuIL-18R) and established human cells which were capable of responding to MuIL-18. These cells expressed larger number of MuIL-18R (>13,000 sites/cell) than intrinsic human IL-18 receptor (HuIL-18R) (<2,500 sites/cell). And the cells responded to MuIL-18 as well as to HuIL-18 in a dose-dependent manner, and produced large amounts of interferon-γ (IFN-γ). We could estimate the amount of murine IL-18 based on the amounts of IFN-γ produced by these cells. The stoichiometry was observed up to 150 ng/ml of MuIL-18. By using these cells, a large amount of MuIL-18 (448±89.2 ng/ml) was detected in sera of
Propionibacterium acnes (
P. acnes)/lipopolysaccharide (LPS)-treated endotoxic mice (the same conditions in which IL-18 was first identified). These cells provide us with a useful tool for determining the bioactivity of MuIL-18. |
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AbstractList | We genetically engineered human myelomonocytic KG-1 cells by introducing cDNA of murine interleukin-18 receptor (MuIL-18R) and established human cells which were capable of responding to MuIL-18. These cells expressed larger number of MuIL-18R (>13,000 sites/cell) than intrinsic human IL-18 receptor (HuIL-18R) (<2,500 sites/cell). And the cells responded to MuIL-18 as well as to HuIL-18 in a dose-dependent manner, and produced large amounts of interferon-γ (IFN-γ). We could estimate the amount of murine IL-18 based on the amounts of IFN-γ produced by these cells. The stoichiometry was observed up to 150 ng/ml of MuIL-18. By using these cells, a large amount of MuIL-18 (448±89.2 ng/ml) was detected in sera of
Propionibacterium acnes (
P. acnes)/lipopolysaccharide (LPS)-treated endotoxic mice (the same conditions in which IL-18 was first identified). These cells provide us with a useful tool for determining the bioactivity of MuIL-18. We genetically engineered human myelomonocytic KG-I cells by introducing cDNA of murine interleukin-18 receptor (MuIL-18R) and established human cells which were capable of responding to MuIL-18. These cells expressed larger number of MuIL-18R (> 13,000 sites/cell) than intrinsic human IL-18 receptor (HuIL-18R) (< 2,500 sites/cell). And the cells responded to MuIL-18 as well as to HuIL-18 in a dose-dependent manner, and produced large amounts of interferon-gamma (IFN-gamma). We could estimate the amount of murine IL-18 based on the amounts of IFN-gamma produced by these cells. The stoichiometry was observed up to 150 ng/ml of MuIL-18. By using these cells, a large amount of MuIL-18 (448 +/- 89.2 ng/ml) was detected in sera of Propionibacterium acnes (P. acnes)/lipopolysaccharide (LPS)-treated endotoxic mice (the same conditions in which IL-18 was first identified). These cells provide us with a useful tool for determining the bioactivity of MuIL-18. We genetically engineered human myelomonocytic KG-1 cells by introducing cDNA of murine interleukin-18 receptor (MuIL-18R) and established human cells which were capable of responding to MuIL-18. These cells expressed larger number of MuIL-18R (>13,000 sites/cell) than intrinsic human IL-18 receptor (HuIL-18R) (<2,500 sites/cell). And the cells responded to MuIL-18 as well as to HuIL-18 in a dose-dependent manner, and produced large amounts of interferon- gamma (IFN- gamma ). We could estimate the amount of murine IL-18 based on the amounts of IFN- gamma produced by these cells. The stoichiometry was observed up to 150 ng/ml of MuIL-18. By using these cells, a large amount of MuIL-18 (448 plus or minus 89.2 ng/ml) was detected in sera of Propionibacterium acnes (P. acnes) /lipopolysaccharide (LPS)-treated endotoxic mice (the same conditions in which IL-18 was first identified). These cells provide us with a useful tool for determining the bioactivity of MuIL-18. |
Author | Yamauchi, Hiroshi Mori, Tsutomu Kurimoto, Masashi Ushio, Shimpei Taniguchi, Mutsuko Nagaoka, Katsue Okura, Takanori Ohta, Tsunetaka Nukada, Yoshiyuki Ikegami, Hakuo |
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CitedBy_id | crossref_primary_10_1073_pnas_96_20_11537 crossref_primary_10_1097_00001432_200106000_00004 crossref_primary_10_1016_j_jim_2007_07_002 crossref_primary_10_1002_0471142735_im0626s44 crossref_primary_10_1038_sj_leu_2401789 crossref_primary_10_1248_bpb_29_896 |
Cites_doi | 10.1006/bbrc.1997.7099 10.4049/jimmunol.157.9.3967 10.1093/nar/18.17.5322 10.1006/cimm.1996.0272 10.1006/bbrc.1997.6665 10.1074/jbc.271.8.3967 10.1006/clin.1997.4475 10.1074/jbc.272.41.25737 10.1007/s002620050345 10.1002/eji.1830260736 10.4049/jimmunol.156.11.4274 10.1016/S0022-1759(97)00164-6 10.4049/jimmunol.158.4.1541 10.1006/bbrc.1998.8236 10.1038/378088a0 |
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Keywords | IL-18R, interleukin-18 receptor Bioassay Murine IL-18 cDNA, complementary DNA Cytokine IFNγ, interferon-γ Recombinant DNA IL-18, interleukin-18 Human cells Human Cell line Transfection Established cell line Bone marrow Biosynthesis Gamma interferon Biological receptor Genetic transfer |
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Meth. doi: 10.1016/S0022-1759(97)00164-6 contributor: fullname: Konishi – volume: 158 start-page: 1541 year: 1997 ident: 10.1016/S0022-1759(98)00098-2_BIB4 article-title: IFN-γ-inducing factor (IGIF) is a costimulatory factor on the activation of Th1 but not Th2 cells and exerts its effect independently of IL-12 publication-title: J. Immunol. doi: 10.4049/jimmunol.158.4.1541 contributor: fullname: Kohno – volume: 244 start-page: 183 year: 1998 ident: 10.1016/S0022-1759(98)00098-2_BIB5 article-title: Interleukin-18 activates the IRAK-TRAF6 pathway in mouse EL-4 cells publication-title: Biochem. Biophys. Res. Commun. doi: 10.1006/bbrc.1998.8236 contributor: fullname: Kojima – volume: 378 start-page: 88 year: 1995 ident: 10.1016/S0022-1759(98)00098-2_BIB12 article-title: Cloning of a new cytokine that induces IFN-γ production by T cells publication-title: Nature doi: 10.1038/378088a0 contributor: fullname: Okamura |
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Snippet | We genetically engineered human myelomonocytic KG-1 cells by introducing cDNA of murine interleukin-18 receptor (MuIL-18R) and established human cells which... We genetically engineered human myelomonocytic KG-I cells by introducing cDNA of murine interleukin-18 receptor (MuIL-18R) and established human cells which... |
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SubjectTerms | Animal cells Animals Bioassay Biological and medical sciences Biological Assay Cell cultures. Hybridization. Fusion Cytokine DNA, Complementary - genetics Endotoxemia - blood Endotoxemia - chemically induced Endotoxemia - immunology Fundamental and applied biological sciences. Psychology Genetic Vectors Human cells Humans Interferon-gamma - biosynthesis Interleukin-18 - analysis Interleukin-18 - metabolism Interleukin-18 Receptor alpha Subunit Lipopolysaccharides - toxicity Mice Mice, Inbred C57BL Molecular and cellular biology Monocytes - metabolism Murine IL-18 Propionibacterium acnes Protein Binding Receptors, Interleukin - genetics Receptors, Interleukin - metabolism Receptors, Interleukin-18 Recombinant DNA Recombinant Fusion Proteins - metabolism Signal Transduction Tumor Cells, Cultured |
Title | Establishment of the cells useful for murine interleukin-18 bioassay by introducing murine interleukin-18 receptor cDNA into human myelomonocytic KG-1 cells |
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