Behr S R, Kraemer F B
J Exp Med. 1986 Oct 1;164(4):1362-7. doi: 10.1084/jem.164.4.1362.
Lipoprotein lipase (LPL) activity was measured in the media of cultured mouse peritoneal macrophages that were isolated after the intraperitoneal injection of inflammatory agents in order to yield a variety of states of activation. Fully activated macrophages obtained from Corynebacterium parvum-injected mice secreted very low levels of LPL when compared to unstimulated macrophages, while inflammatory and primed macrophages had increased LPL secretion. When inflammatory macrophages were incubated with conditioned medium obtained from fully activated macrophages, LPL secretion decreased in a time- and dose-dependent fashion. The factor(s) secreted by fully activated macrophages that inhibited LPL secretion was shown to be thermolabile and distinct from tumor necrosis factor. These results demonstrate that activation dramatically alters macrophage LPL secretion.
为了产生多种激活状态,在腹腔注射炎性介质后分离培养的小鼠腹腔巨噬细胞培养基中测量脂蛋白脂肪酶(LPL)活性。与未刺激的巨噬细胞相比,从小棒状杆菌注射小鼠获得的完全激活的巨噬细胞分泌的LPL水平非常低,而炎性巨噬细胞和致敏巨噬细胞的LPL分泌增加。当炎性巨噬细胞与从完全激活的巨噬细胞获得的条件培养基一起孵育时,LPL分泌以时间和剂量依赖性方式减少。完全激活的巨噬细胞分泌的抑制LPL分泌的因子显示为热不稳定的,且与肿瘤坏死因子不同。这些结果表明,激活显著改变巨噬细胞LPL分泌。