Le Gros G S, Herbert A G, Watson J D
Lymphokine Res. 1985 Summer;4(3):221-7.
The effect of sodium butyrate on lymphokine production in WEHI-3, LBRM-33, and JURKAT cells, as well as an IL-2-dependent T cell line (I) was studied. Constitutive production of IL-3 by WEHI-3 cells was enhanced by sodium butyrate and was accompanied by the growth arrest of WEHI-3 cells in the G1 phase of the cell cycle. Treatment of I cells with ConA and sodium butyrate led to an increase in IL-3 production and the initiation of IL-2 production. In contrast, the synthesis of IL-2 and IL-3 by the ConA-activated T lymphoma line LBRM-33 was coordinately inhibited by sodium butyrate. Similarly, the synthesis of IL-2 by the human T cell lymphoma JURKAT was inhibited by sodium butyrate. No cell cycle-specific effects of sodium butyrate were observed in LBRM-33 or JURKAT cells.
研究了丁酸钠对WEHI-3、LBRM-33和JURKAT细胞以及IL-2依赖的T细胞系(I)中淋巴因子产生的影响。丁酸钠增强了WEHI-3细胞组成性产生IL-3的能力,并伴随着WEHI-3细胞在细胞周期的G1期生长停滞。用刀豆蛋白A(ConA)和丁酸钠处理I细胞导致IL-3产生增加并启动IL-2产生。相反,丁酸钠协同抑制ConA激活的T淋巴瘤系LBRM-33合成IL-2和IL-3。同样,丁酸钠抑制人T细胞淋巴瘤JURKAT合成IL-2。在LBRM-33或JURKAT细胞中未观察到丁酸钠对细胞周期的特异性影响。