Ono T, Nakabayashi T
Department of Protozoology, Osaka University, Japan.
Parasitol Res. 1989;75(5):348-52. doi: 10.1007/BF00931129.
Gametocytogenesis induction medium (RPMI-FSC reactive medium), prepared with a mixture of the culture supernatant from anti-Plasmodium falciparum antibody-producing hybridoma cells and hybridoma cell lysate, consistently induced gametocytogenesis in cultured P. falciparum. Gametocytogenesis was induced in three strains (0662, FCB 1, and FCR-3) and one clone (R.FCR-3) as has previously been described in two other strains (Ono et al. 1986). Both caffeine (2 mM/ml) and calmodulin (5 micrograms/ml) enhanced the effects of RPMI-FSC reactive medium. Furthermore, gametocytes that appeared after treatment with RPMI-FSC reactive medium continued their development to ookinete formation in candle jar culture with Waymouth's medium.
配子体生成诱导培养基(RPMI-FSC反应性培养基)由产生抗恶性疟原虫抗体的杂交瘤细胞的培养上清液和杂交瘤细胞裂解物混合制备而成,能持续诱导培养的恶性疟原虫产生配子体。如之前在另外两个菌株中所描述的那样(Ono等人,1986年),在三个菌株(0662、FCB 1和FCR-3)和一个克隆株(R.FCR-3)中诱导出了配子体生成。咖啡因(2 mM/ml)和钙调蛋白(5微克/毫升)均可增强RPMI-FSC反应性培养基的作用。此外,用RPMI-FSC反应性培养基处理后出现的配子体在含有Waymouth培养基的烛缸培养中继续发育形成动合子。