Meerpohl H G, Bauknecht T
Prostaglandins. 1986 May;31(5):961-72. doi: 10.1016/0090-6980(86)90026-2.
The data presented show different effects of prostaglandins on proliferation and cytotoxic effector functions of murine bone-marrow derived mononuclear cells. Colony stimulating factor (CSF)-dependent proliferation of colony forming unit-cells (CFU c) was inhibited by PGE1, PGE2 and PGB2. Lymphokine induced cytotoxicity and antibody mediated cytotoxicity (ADCC) of monocytes and macrophages were also affected by PG. We conclude that PGE2 may regulate macrophage mediated tumorcell-lysis mainly at the induction phase. If these processes function in vivo, one would therefore expect high affinity binding sites for PGE2 on macrophages. The existence of a receptor for PGE2 one murine bone marrow derived macrophages is described.
所呈现的数据表明,前列腺素对小鼠骨髓来源的单核细胞的增殖和细胞毒性效应功能具有不同影响。集落刺激因子(CSF)依赖的集落形成单位细胞(CFU-c)的增殖受到PGE1、PGE2和PGB2的抑制。前列腺素也影响单核细胞和巨噬细胞的淋巴因子诱导的细胞毒性以及抗体介导的细胞毒性(ADCC)。我们得出结论,PGE2可能主要在诱导阶段调节巨噬细胞介导的肿瘤细胞裂解。因此,如果这些过程在体内起作用,人们会预期巨噬细胞上存在PGE2的高亲和力结合位点。本文描述了小鼠骨髓来源的巨噬细胞上PGE2受体的存在。