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通过γ干扰素在体内激活巨噬细胞,以在体外杀死溶组织内阿米巴滋养体。

In vivo activation of macrophages by IFN-gamma to kill Entamoeba histolytica trophozoites in vitro.

作者信息

Ghadirian E, Denis M

机构信息

Montreal General Hospital Research Institute, Quebec, Canada.

出版信息

Parasite Immunol. 1992 Jul;14(4):397-404. doi: 10.1111/j.1365-3024.1992.tb00014.x.

Abstract

To determine the role of interferon-gamma (IFN-gamma) in the activation of macrophages to kill Entamoeba histolytica trophozoites in vitro, C57BL/6 mice were injected with various doses of recombinant IFN-gamma (rIFN-gamma) by either the intravenous, intraperitoneal or intramuscular routes. Mice were treated with doses of rIFN-gamma ranging from 10(1) to 10(5) units. Twenty hours later, peritoneal macrophages were harvested from the treated animals. Macrophage monolayers were prepared and their in vitro cytotoxic activity against a virulent strain of E. hystolytica (IP:0682:1) was determined. Amoebicidal activity was determined by counting the number of dead trophozoites by Trypan Blue exclusion in cultures containing macrophages and amoebic trophozoites which were incubated together for 4 h. Both intravenous and intraperitoneal treatment resulted in the recovery of macrophages from the peritoneal cavity which exhibited amoebicidal activity in vitro. Peritoneal macrophages harvested from mice that had been treated intraperitoneally or intravenously with rIFN-gamma, however, showed significantly more amoebicidal activity in comparison to macrophages harvested from animals treated intramuscularly. There was a dose dependent relationship between the concentration of rIFN-gamma used to activate macrophages in vivo and the number of dead trophozoites in vitro. In addition, these results confirm our previous observations that treatment in vitro with rIFN-gamma can activate murine peritoneal macrophages to kill amoebic trophozoites.

摘要

为了确定γ干扰素(IFN-γ)在激活巨噬细胞以体外杀伤溶组织内阿米巴滋养体中的作用,通过静脉、腹腔或肌肉途径给C57BL/6小鼠注射不同剂量的重组γ干扰素(rIFN-γ)。给小鼠使用的rIFN-γ剂量范围为10¹至10⁵单位。20小时后,从接受治疗的动物体内收获腹腔巨噬细胞。制备巨噬细胞单层,并测定其对溶组织内阿米巴毒力菌株(IP:0682:1)的体外细胞毒性活性。通过在含有巨噬细胞和阿米巴滋养体且一起孵育4小时的培养物中用台盼蓝排除法计数死亡滋养体的数量来确定杀阿米巴活性。静脉和腹腔治疗均导致从腹腔中回收在体外表现出杀阿米巴活性的巨噬细胞。然而,与从肌肉注射治疗的动物中收获的巨噬细胞相比,从经腹腔或静脉注射rIFN-γ治疗的小鼠中收获的腹腔巨噬细胞表现出明显更强的杀阿米巴活性。用于体内激活巨噬细胞的rIFN-γ浓度与体外死亡滋养体的数量之间存在剂量依赖关系。此外,这些结果证实了我们之前的观察结果,即体外使用rIFN-γ治疗可激活小鼠腹腔巨噬细胞以杀伤阿米巴滋养体。

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