Hook W A, Dougherty S F, Oppenheim J J
Infect Immun. 1974 May;9(5):903-8. doi: 10.1128/iai.9.5.903-908.1974.
Concanavalin A (Con A) and phytohemagglutinin (PHA) released histamine from hamster mast cells incubated in a serum-free medium. Concentrations of Con A and PHA approximating those optimal for transforming lymphocytes also released maximal amounts of histamine without apparent cytotoxicity. Higher concentrations of mitogen inhibited both lymphocyte transformation and histamine release. Incubation at 37 C for 15 min released histamine, although longer times were more effective. Supernatants from cultured hamster splenocytes stimulated with Con A also released histamine from added mast cells. However, the effect could be inhibited by the addition of 0.1 M methyl alpha-D-mannoside or by passing the spleen cell culture supernatants through Sephadex G-75 to remove Con A. This mitogen-induced release of mast cell histamine is therefore not mediated by a lymphokine but probably results from a direct interaction of mitogens with receptors on mast cells.
刀豆球蛋白A(Con A)和植物血凝素(PHA)可使在无血清培养基中孵育的仓鼠肥大细胞释放组胺。与淋巴细胞转化最佳浓度相近的Con A和PHA浓度也能释放出最大量的组胺,且无明显细胞毒性。更高浓度的促有丝分裂原会抑制淋巴细胞转化和组胺释放。在37℃孵育15分钟可释放组胺,不过孵育时间延长效果更佳。用Con A刺激培养的仓鼠脾细胞所得到的上清液也能使添加的肥大细胞释放组胺。然而,添加0.1Mα-D-甲基甘露糖苷或使脾细胞培养上清液通过葡聚糖凝胶G-75以去除Con A,可抑制这种作用。因此,这种促有丝分裂原诱导的肥大细胞组胺释放不是由淋巴因子介导的,可能是促有丝分裂原与肥大细胞上的受体直接相互作用的结果。