Sarin A, Saxena R K
Laboratory of Immunology, School of Life Sciences, Jawaharlal Nehru, University, New Delhi, India.
Asian Pac J Allergy Immunol. 1988 Dec;6(2):88-94.
Effects of interleukin-2 (IL-2) on the natural killer (NK) activities of BALB/c mouse and Wistar rat spleen cells were compared. While mouse spleen cells cultured alone rapidly lost NK activity, co-culture with IL-2 resulted in a marked enhancement of NK activity. In contrast, the levels of NK activity of rat spleen cells cultured alone increased and remained high for 3 days and declined thereafter. Addition of human recombinant IL-2 or purified rat IL-2 did not influence the NK levels in rat spleen cell bulk cultures. Both IL-2 preparations were however biologically active as shown by their capacities to induced proliferation in rat spleen cells. Rat spleen cells suppressed the IL-2 activation of mouse spleen cells in a dose dependent manner, indicating a suppressor influence generated by rat spleen cells. Culture supernatants of rat spleen cells cultured with or without IL-2 for 3 or 5 days could also suppress the mouse spleen NK activation in response to IL-2. The suppressor activity could be concentrated on a 5K MW cut-off Amicon filter indicating that the molecular weight of the factor is more than 5000. These results indicate that a suppressor of IL-2 induced NK activation of mouse spleen cells is released by cultured rat spleen cells.
比较了白细胞介素-2(IL-2)对BALB/c小鼠和Wistar大鼠脾细胞自然杀伤(NK)活性的影响。单独培养的小鼠脾细胞会迅速丧失NK活性,而与IL-2共培养则导致NK活性显著增强。相反,单独培养的大鼠脾细胞的NK活性水平会升高,并在3天内保持较高水平,之后下降。添加人重组IL-2或纯化的大鼠IL-2对大鼠脾细胞大量培养物中的NK水平没有影响。然而,两种IL-2制剂都具有生物学活性,这可通过它们诱导大鼠脾细胞增殖的能力来证明。大鼠脾细胞以剂量依赖性方式抑制小鼠脾细胞的IL-2激活,表明大鼠脾细胞产生了抑制作用。用或不用IL-2培养3天或5天的大鼠脾细胞的培养上清液也可抑制小鼠脾细胞对IL-2的NK激活。抑制活性可浓缩在截留分子量为5000的Amicon滤膜上,表明该因子的分子量大于5000。这些结果表明,培养的大鼠脾细胞可释放一种抑制IL-2诱导的小鼠脾细胞NK激活的因子。