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重组γ干扰素对培养的正常人角质形成细胞上II类抗原的表达和生物合成具有不同的调节作用。

Recombinant gamma interferon differentially regulates class II antigen expression and biosynthesis on cultured normal human keratinocytes.

作者信息

Basham T Y, Nickoloff B J, Merigan T C, Morhenn V B

出版信息

J Interferon Res. 1985 Winter;5(1):23-32. doi: 10.1089/jir.1985.5.23.

DOI:10.1089/jir.1985.5.23
PMID:3921630
Abstract

Recombinant gamma interferon induces class II antigen (HLA-DR) biosynthesis and expression on normal cultured human keratinocytes. HLA-DR expression was not induced on keratinocytes by recombinant alpha or beta interferons in a similar dose range nor by Con A or PHA. HLA-DR (L243) expression, as determined by FACS analysis, was detected as early as 1-2 days after addition of r-IFN-gamma to the cultures and was maximal after 4-8 days. Keratinocytes were analyzed for expression of another class II antigen, HLA-DC (Leu-10). Little or no expression of Leu-10 (DC) was detectable on these cells although Fc receptors for the IgG1 isotype were increased. These data indicate a unique role for gamma interferon in the differential regulation of keratinocyte class II antigen biosynthesis and expression. Induction of HLA-DR on keratinocytes may be functionally important in expanding the number of antigen presenting cells in the skin for the induction of an immune response and/or targeting these keratinocytes for cytolysis.

摘要

重组γ干扰素可诱导II类抗原(HLA - DR)的生物合成,并使其在正常培养的人角质形成细胞上表达。在相似剂量范围内,重组α或β干扰素、刀豆蛋白A(Con A)或植物血凝素(PHA)均不能诱导角质形成细胞表达HLA - DR。通过荧光激活细胞分选术(FACS)分析确定,早在向培养物中添加重组γ干扰素后1 - 2天即可检测到HLA - DR(L243)的表达,4 - 8天后表达量达到最大。分析角质形成细胞中另一种II类抗原HLA - DC(Leu - 10)的表达情况。尽管IgG1同种型的Fc受体增加,但在这些细胞上几乎检测不到Leu - 10(DC)的表达。这些数据表明γ干扰素在角质形成细胞II类抗原生物合成和表达的差异调节中具有独特作用。角质形成细胞上HLA - DR的诱导在扩大皮肤中抗原呈递细胞数量以诱导免疫反应和/或将这些角质形成细胞靶向细胞溶解方面可能具有重要功能。

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Recombinant gamma interferon differentially regulates class II antigen expression and biosynthesis on cultured normal human keratinocytes.重组γ干扰素对培养的正常人角质形成细胞上II类抗原的表达和生物合成具有不同的调节作用。
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