Masaki D I, Tanna S M, Hokama Y
Res Commun Chem Pathol Pharmacol. 1978 Oct;22(1):205-8.
Spleen cells from the BDF1 generation of DBA male X C57Bl/6 female matings sensitized with sheep erythrocytes (SRBC) were exposed to various concentrations of ARA, PGE2, and PGF2alpha for 90 minutes in vitro at 37 degrees C. Following exposure these sensitized spleen cells were then examined in the hemolytic plaque assay. No changes were demonstrated in the number of plaque forming cells (PFC) with 0.1 microgram/ml of ARA treatment. However, an increase in the number of PFC occurred with increasing concentrations of ARA. A significant increase (p less than 0.01) in PFC (59%) was shown with 10.0 microgram/ml of ARA. PGE2 treatment at 10.0 and 100.0 microgram/ml showed no evidence of increase, but a slight decrease (10%) was shown with 100.0 microgram/ml. On the other hand, exposure to PGF2alpha showed a significant increase (p less than 0.05) in PFC at the 10.0 microgram/ml (35%) and the 100.0 microgram/ml (29% levels, respectively. The data suggest that both ARA and PGF2alpha enhanced PFC formation.
用绵羊红细胞(SRBC)致敏的DBA雄性与C57Bl/6雌性杂交的BDF1代的脾细胞,于37℃在体外暴露于不同浓度的花生四烯酸(ARA)、前列腺素E2(PGE2)和前列腺素F2α(PGF2α)90分钟。暴露后,这些致敏的脾细胞随后在溶血空斑试验中进行检测。用0.1微克/毫升的ARA处理时,空斑形成细胞(PFC)的数量未显示变化。然而,随着ARA浓度的增加,PFC的数量增加。用10.0微克/毫升的ARA时,PFC显著增加(p小于0.01)(增加59%)。用10.0和100.0微克/毫升的PGE2处理未显示增加的迹象,但用100.0微克/毫升时显示略有下降(10%)。另一方面,暴露于PGF2α时,在10.0微克/毫升(增加35%)和100.0微克/毫升(分别增加29%)时,PFC显著增加(p小于0.05)。数据表明,ARA和PGF2α均增强了PFC的形成。