Mechanisms of CD26/dipeptidyl peptidase IV cytokine-dependent regulation on human activated lymphocytes

被引:44
作者
Salgado, FJ
Vela, E
Martín, M
Franco, R
Nogueira, M
Cordero, OJ
机构
[1] Univ Santiago de Compostela, Fac Biol, Dept Biochem & Mol Biol, Santiago De Compostela 15706, Spain
[2] Univ Barcelona, Dept Biochem & Mol Biol, Barcelona, Spain
[3] Univ Hosp Germans Trias & Pujol Badalona, Serv Anat Pathol, Mol Biol Lab, Barcelona, Spain
关键词
CD26; dipeptidyl peptidase IV; hydrocortisone; interleukin; 12; tumour necrosis factor-alpha;
D O I
10.1006/cyto.1999.0643
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Among the cellular pathways activated by IL-12,,ve bad previously found that both the percentage and intensity of CD26(+) cells in the PHA-stimulated T cells increased when IL-12 mas present (independently of its CD4 or CD8 phenotype). Now, we examined the molecular mechanisms of this IL-12-mediated effect. The IL-12 regulation pathway is dependent of de novo protein synthesis and independent of cytokine secretion. Our results show two transcripts for CD26 in PBMC for the first time and no regulation by ILs at this level. Furthermore, secretion of the serum forms of CD26/DPPIV were not affected by IL-12. Interestingly, assays with neutralizing mAbs against TNF-alpha suggest that this cytokine negatively modulates CD26 expression, The fact that translation and probably translocation of CD26 toward the cell surface can be regulated by IL-12 and TNF-a repeals new aspects about the control of this T,, marker. (C) 2000 Academic Press.
引用
收藏
页码:1136 / 1141
页数:6
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