CONSTITUTIVE IL-2 EXPRESSION IN HTLV-I-INFECTED LEUKEMIC T-CELL LINES

被引:0
作者
FARCET, JP [1 ]
LEBARGY, F
LAVIGNAC, C
GAULARD, P
DAUTRY, A
GAZZOLO, L
ROMEO, PH
VAINCHENKER, W
机构
[1] HOP HENRI MONDOR, INSERM, U139, F-94010 CRETEIL, FRANCE
[2] HOP HENRI MONDOR, ANAT PATHOL LAB, F-94010 CRETEIL, FRANCE
[3] INST PASTEUR, CNRS, UA 361, UNITE GENET SOMAT, F-75724 PARIS 15, FRANCE
[4] FAC MED ALEXIS CARREL, UCBC,CNRS,UMR 30, IMMUNOL VIROL MOLEC & CELLULAIRE LAB, F-69372 LYONS 2, FRANCE
关键词
IL-2; HTLV-I; CELL LINES;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
An IL-2 autocrine growth circuit has been proposed as a major mechanism in HTLV-I-related leukaemogenesis. We have developed a polymerase chain reaction combined with reverse transcription RT-PCR to detect IL-2 transcripts and a sensitive immunostaining method for IL-2 protein. Combination of these two methods with in situ hybridization demonstrated that most cells of the T cell line IARC 301.5, whose proliferation is stimulated by autocrine IL-2, constitutively synthesize IL-2. This pattern was also found in the HTLV-I T cell lines HUT, MT2 and C 8166/45, and in the HTLV-I-negative T cell lines Jurkat and HSB2 but not MOLT4. Four non-lymphoid cell lines and cultured fibroblasts were negative, in agreement with the T cell specificity of IL-2 synthesis. Hence, most T cell lines tested, whether HTLV-I-infected or not, constitutively synthesize IL-2, suggesting a possible common feature of leukaemic T cell lines. The presence of IL-2 transcript and protein in most cells of the reacting cell lines is consistent with an autocrine process possibly involved at some stage in acquiring growth autonomy.
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页码:415 / 421
页数:7
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