Induction of gametocytogenesis in Plasmodium falciparum by the culture supernatant of hybridoma cells producing anti-P. falciparum antibody.

Biken journal Pub Date : 1986-12-01
T Ono, T Nakai, T Nakabayashi
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Abstract

There have been many unsuccessful attempts to induce gametocytogenesis in vitro. In the present experiment, however, we found that RPMI-CS medium and RPMI-FS medium prepared by dissolving powdered RPMI 1640 medium in the culture supernatants of hybridoma cells, hybrid line D21 and 219.5, respectively, that produce anti-P. falciparum antibody induced gametocytogenesis. Gametocytogenesis was consistently observed from 3 days after addition of these media. The culture supernatant of anti-P. falciparum antibody producing hybridoma cells did not induce gametocytogenesis in the absence of RPMI 1640 medium. RPMI-MS medium, prepared by dissolving powdered RPMI 1640 medium in the culture supernatant of myeloma cells, SP2/O-Ag 14, which was used as a control, induced a few gametocytes.

产生抗p的杂交瘤细胞培养上清液诱导恶性疟原虫配子细胞发生。恶性疟原虫抗体。
在体外诱导配子细胞发生的实验中,有许多失败的尝试。在本实验中,我们发现RPMI- cs培养基和RPMI- fs培养基分别在杂交瘤细胞D21和219.5的培养上清液中溶解RPMI- 1640粉末状培养基制备的RPMI- cs培养基和RPMI- fs培养基产生抗p。恶性疟原虫抗体诱导配子细胞发生。在添加这些培养基3天后,配子细胞发生的情况一致。抗p的培养上清。在没有RPMI 1640培养基的情况下,产生恶性疟原虫抗体的杂交瘤细胞不能诱导配子细胞发生。将粉末状RPMI 1640培养基溶解于骨髓瘤细胞SP2/O-Ag 14培养上清中制备的RPMI- ms培养基可诱导少量配子细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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