Sairenji T, Spiro R C, Humphreys R E
Hematol Oncol. 1984 Oct-Dec;2(4):381-9. doi: 10.1002/hon.2900020408.
The aim of this study was to test whether EBV induction by TPA or n-butyrate was related directly to hyperexpression of Ii, an electrophoretically invariant, 35 000 dalton, HLA-DR antigen-associated glycoprotein which is abundantly detected in EBV freshly transformed cells and is enhanced by EBV superinfection of lymphoblastoid cell lines. P3HR-1 lymphoblasts were treated with n-butyrate or TPA in variable doses and durations. The augmented expression of Ii, EBV antigens (EA and VCA), DNA synthesis, and cell growth and viability were monitored. n-Butyrate induced hyperexpression of Ii at 2 days with a maximal effective dose of 4 mM, induced EBV antigens (EA and VCA) in 36 per cent of the cells at 2 days, inhibited DNA synthesis and cell growth, and was not cytolytic at 48 h when Ii induction was maximal. TPA did not induce hyperexpression of Ii, induced EBV antigens (EA) in 30 per cent of the cells at 4 days, did not inhibit DNA synthesis and cell growth, and was not cytolytic in the time course and doses studied. Ii expression, therefore, did not appear to be an obligatory consequence of EBV antigen induction. Ii induction might be related to an effect of EBV inducers on cellular DNA synthesis, or on control of the cell cycle, or directly upon Ii gene regulation.
本研究的目的是测试佛波酯(TPA)或正丁酸盐诱导EB病毒(EBV)是否与Ii的过表达直接相关,Ii是一种电泳不变的、35000道尔顿的、与HLA-DR抗原相关的糖蛋白,在EBV新转化的细胞中大量检测到,并且在淋巴母细胞系被EBV超感染后会增强。用不同剂量和持续时间的正丁酸盐或TPA处理P3HR-1淋巴母细胞。监测Ii、EBV抗原(EA和VCA)的表达增加、DNA合成以及细胞生长和活力。正丁酸盐在2天时诱导Ii过表达,最大有效剂量为4 mM,在2天时诱导36%的细胞产生EBV抗原(EA和VCA),抑制DNA合成和细胞生长,并且在48小时Ii诱导达到最大值时无细胞毒性。TPA不诱导Ii过表达,在4天时诱导30%的细胞产生EBV抗原(EA),不抑制DNA合成和细胞生长,在所研究的时间进程和剂量下无细胞毒性。因此,Ii表达似乎不是EBV抗原诱导的必然结果。Ii诱导可能与EBV诱导剂对细胞DNA合成、细胞周期控制的影响有关,或者直接与Ii基因调控有关。