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采用灵敏的夹心酶免疫测定法检测外周血单个核细胞体外产生人白细胞介素1α和白细胞介素1β的情况。

In vitro production of human interleukin 1 alpha and interleukin 1 beta by peripheral blood mononuclear cells examined by sensitive sandwich enzyme immunoassay.

作者信息

Tanaka K, Ishikawa E, Ohmoto Y, Hirai Y

机构信息

Department of Biochemistry, Medical College of Miyazaki, Japan.

出版信息

Eur J Immunol. 1987 Oct;17(10):1527-30. doi: 10.1002/eji.1830171024.

Abstract

The in vitro production of human interleukin 1 alpha (hIL 1 alpha) and interleukin 1 beta (hIL 1 beta) by peripheral blood mononuclear cells was examined by sensitive sandwich enzyme immunoassays which could discriminate hIL 1 alpha and hIL 1 beta without cross-reaction with human IL2. In culture supernatants of mononuclear cells, two components were detected by sandwich enzyme immunoassay for hIL 1 alpha or hIL 1 beta. The molecular weight of one component was shown to be equal to that of recombinant hIL 1 alpha or hIL 1 beta by gel filtration. The elution volume of the other component corresponded to a molecular weight of about 30,000. The sum of the two components for both hIL 1 alpha and hIL 1 beta in culture supernatants of peripheral blood mononuclear cells from healthy subjects increased 1.7 to 38-fold by Escherichia coli lipopolysaccharide. The sum of the two components for hIL 1 beta was 13 to 97-fold larger than that for hIL 1 alpha.

摘要

通过敏感的夹心酶免疫测定法检测外周血单个核细胞体外产生人白细胞介素1α(hIL-1α)和白细胞介素1β(hIL-1β),该方法能够区分hIL-1α和hIL-1β,且与人IL-2无交叉反应。在单核细胞的培养上清液中,通过hIL-1α或hIL-1β的夹心酶免疫测定法检测到两种成分。通过凝胶过滤显示,其中一种成分的分子量与重组hIL-1α或hIL-1β的分子量相等。另一种成分的洗脱体积对应于约30,000的分子量。健康受试者外周血单个核细胞培养上清液中hIL-1α和hIL-1β的两种成分总和因大肠杆菌脂多糖而增加了1.7至38倍。hIL-1β的两种成分总和比hIL-1α的总和大13至97倍。

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