INTERFERONS INDUCE XANTHINE DEHYDROGENASE GENE-EXPRESSION IN L929 CELLS

被引:51
作者
FALCIANI, F
GHEZZI, P
TERAO, M
CAZZANIGA, G
GARATTINI, E
机构
[1] MARIO NEGRI INST PHARMACOL RES, CTR DANIELA & CATULLA BORGOMAINERIO, MOLEC BIOL UNIT, I-20157 MILAN, ITALY
[2] MARIO NEGRI INST PHARMACOL RES, NEUROIMMUNOL LAB, I-20157 MILAN, ITALY
关键词
D O I
10.1042/bj2851001
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
Human interferon-alpha A/D (BglII) (IFN-alpha A/D) and mouse interferon-gamma (IFN-gamma) are shown to induce xanthine dehydrogenase (XD) mRNA in L929 fibroblastic cells. XD mRNA accumulation after IFN-alpha, A/D treatment is relatively fast, being already evident after 4 h and reaching its maximum after 24 h. IFN-alpha A/D is active in inducing XD mRNA at 0.1 unit/ml and it is maximally active at 10(3) units/ml. The half-life of the XD message is unaffected by IFN-alpha A/D treatment, whereas the transcriptional activity of the XD gene and the concentrations of XD heterogeneous nuclear RNA are increased by 2- and 6-fold respectively. The effect of IFN-alpha A/D on XD mRNA is insensitive to cycloheximide, suggesting that protein synthesis de novo is not required. Experiments conducted with specific inhibitors suggest that protein kinase C, cyclic AMP and arachidonic acid metabolites derived from lipoxygenase or cycloxygenase do not act as second-messenger molecules in the induction of XD mRNA by IFN-alpha A/D. XD mRNA is also induced in NIH3T3 fibroblastic cells, but not in F9 teratocarcinoma or B 1 6 melanoma cells after treatment with IFN-alpha A/D. NIH3T3 are the only cells so far tested that have detectable XD and xanthine oxidase activities under basal conditions and after IFN-alpha A/D treatment, although their responsiveness to the cytokine is much less than that observed in L929 cells.
引用
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页码:1001 / 1008
页数:8
相关论文
共 46 条
[1]   INHIBITION OF THE CELLULAR-RESPONSE TO INTERFERONS BY PRODUCTS OF THE ADENOVIRUS TYPE-5 E1A ONCOGENE [J].
ACKRILL, AM ;
FOSTER, GR ;
LAXTON, CD ;
FLAVELL, DM ;
STARK, GR ;
KERR, IM .
NUCLEIC ACIDS RESEARCH, 1991, 19 (16) :4387-4393
[2]   MOLECULAR-CLONING OF INTERFERON RECEPTORS - A SHORT REVIEW [J].
AGUET, M .
BRITISH JOURNAL OF HAEMATOLOGY, 1991, 79 :6-8
[3]  
BENECH P, 1985, NUCLEIC ACIDS RES, V13, P1267
[4]   STRUCTURE OF 2 FORMS OF THE INTERFERON-INDUCED (2-'-5-') OLIGO-A SYNTHETASE OF HUMAN-CELLS BASED ON CDNAS AND GENE-SEQUENCES [J].
BENECH, P ;
MORY, Y ;
REVEL, M ;
CHEBATH, J .
EMBO JOURNAL, 1985, 4 (09) :2249-2256
[5]   REGULATION OF A TRANSFECTED HUMAN CLASS-II MAJOR HISTOCOMPATIBILITY COMPLEX GENE IN HUMAN-FIBROBLASTS [J].
BOSS, JM ;
STROMINGER, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (23) :9139-9143
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   PURIFICATION AND CHARACTERIZATION OF MOUSE-LIVER XANTHINE-OXIDASE [J].
CARPANI, G ;
RACCHI, M ;
GHEZZI, P ;
TERAO, M ;
GARATTINI, E .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1990, 279 (02) :237-241
[8]   ENHANCER-LIKE INTERFERON RESPONSIVE SEQUENCES OF THE HUMAN AND MURINE (2'-5') OLIGOADENYLATE SYNTHETASE GENE PROMOTERS [J].
COHEN, B ;
PERETZ, D ;
VAIMAN, D ;
BENECH, P ;
CHEBATH, J .
EMBO JOURNAL, 1988, 7 (05) :1411-1419
[10]  
DELLACORTE E, 1968, BIOCHEM J, V108, P349