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从原发性鼠肉瘤病毒(MSV)诱导的肿瘤中分离出的巨噬细胞的溶细胞活性。

Cytolytic activity of macrophages isolated from primary murine sarcoma virus (MSV)-induced tumors.

作者信息

Taniyama T, Holden H T

出版信息

Int J Cancer. 1979 Aug;24(2):151-60. doi: 10.1002/ijc.2910240205.

Abstract

Macrophages isolated from regressing or progressing tumors induced by murine sarcoma virus (MSV) were tested for cytolytic activity in a 18-h 51Cr release assay. Macrophages from the tumors of mice injected 14 days earlier with stocks of MSV-producing regressor or progressor tumors had comparable levels of cytotoxicity. However, macrophages from the progressively growing tumors, 50--65 days after the inoculation with the progressor virus, had lower levels of cytotoxicity than those from the regressing tumors (day 14). On the other hand, macrophages from progressively growing MSV tumors (day 14) in nude mice had little or no detectable cytolytic activity. In a fractionation study, using the 1-g velocity sedimentation technique, cells from regressing tumors (day 14) showed at least two peaks of cytolytic activity, one at about 4 mm/h and another at 6--7 mm/h. In contrast, none of the cell fractions of tumors from nude mice (day 14) showed cytolytic activity. Since bacterial lipopolysaccharide (LPS) has been shown to augment the cytolytic activity of primed macrophages, its effect on cells from MSV tumors was evaluated. Cytolytic activity of the cells from regressing or progr-ssing tumors that had pre-existing cytolytic activity was augmented by the addition of LPS during the assay period, but LPS treatment did not activate inactive fractions or change the distribution patterns of the cytolytic activity in fractions from 1-g velocity sedimentation.

摘要

从由鼠肉瘤病毒(MSV)诱导的消退或进展性肿瘤中分离出的巨噬细胞,在18小时的51Cr释放试验中检测其细胞溶解活性。在14天前注射产生MSV的消退型或进展型肿瘤毒株的小鼠肿瘤中的巨噬细胞,具有相当水平的细胞毒性。然而,在接种进展型病毒50 - 65天后,进展性生长肿瘤中的巨噬细胞,其细胞毒性水平低于消退性肿瘤中的巨噬细胞(第14天)。另一方面,裸鼠中进展性生长的MSV肿瘤(第14天)中的巨噬细胞几乎没有或没有可检测到的细胞溶解活性。在一项分级研究中,使用1g速度沉降技术,消退性肿瘤(第14天)的细胞显示出至少两个细胞溶解活性峰,一个在约4mm/h,另一个在6 - 7mm/h。相比之下,裸鼠肿瘤(第14天)的细胞分级均未显示出细胞溶解活性。由于已证明细菌脂多糖(LPS)可增强致敏巨噬细胞的细胞溶解活性,因此评估了其对MSV肿瘤细胞的影响。在测定期间添加LPS可增强来自已有细胞溶解活性的消退或进展性肿瘤细胞的细胞溶解活性,但LPS处理并未激活无活性分级,也未改变1g速度沉降分级中细胞溶解活性的分布模式。

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