Schultz R M, Pavlidis N A, Stylos W A, Chirigos M A
Science. 1978 Oct 20;202(4365):320-1. doi: 10.1126/science.694537.
Exogenously added prostaglandins E1 and E2, but not F2alpha, inhibited the tumoricidal activity of interferon-activated macrophages of mice. A role for adenosine 3',5'-monophosphate (cyclic AMP) in modulating macrophage functional activity was suggested because prostaglandins of the E series increase intracellular concentrations of cyclic AMP in macrophages and because treatment of interferon-activated macrophages with dibutyryl cyclic AMP consistently inhibits expression of cytotoxicity. Since the activated macrophage releases high concentrations of prostaglandin E2, it is postulated that this prostaglandin could act locally in negative feedback inhibition to limit cell activities.
外源性添加的前列腺素E1和E2(而非F2α)抑制了小鼠干扰素激活巨噬细胞的杀肿瘤活性。由于E系列前列腺素可提高巨噬细胞内3',5'-单磷酸腺苷(环磷酸腺苷)的浓度,且用二丁酰环磷酸腺苷处理干扰素激活的巨噬细胞会持续抑制细胞毒性的表达,因此提示环磷酸腺苷在调节巨噬细胞功能活性中发挥作用。鉴于活化的巨噬细胞会释放高浓度的前列腺素E2,推测这种前列腺素可能通过局部负反馈抑制作用来限制细胞活性。