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巯基乙酸诱导的巨噬细胞表现出病毒复制增强和细菌杀伤能力降低。

Thioglycollate elicited macrophages demonstrate enhanced virus replication and depressed bacterial killing.

作者信息

Sich J J, Bubel H C, Bonventre P F

出版信息

Microbiologica. 1987 Jul;10(3):247-56.

PMID:3114595
Abstract

Thioglycollate elicited peritoneal macrophages of Balb/c mice exhibited minimal antibacterial activity against Listeria monocytogenes but were fully permissive for the replication of ectromelia virus. By comparison, resident and LPS elicited macrophages did not exhibited depressed antibacterial activity nor did they support viral replication. The thioglycollate effects were demonstrated in macrophages cultured in vitro and also in intact Balb/c mice. Mice given thioglycollate intraperitoneally and challenged by the same route suffered overwhelming virus and bacterial infections as a result of early local proliferation within peritoneal macrophages with subsequent spread to the liver. Balb/c mice challenged intravenously with similar doses of the virus of bacterial pathogen after administration of thioglycollate by the i.p. route did not succumb to either infection. Thus the ability of thioglycollate to compromise cellular host defenses against the infectious agents appears to be site specific; i.e. restricted to the peritoneal cavity where exudate macrophages and challenge inocula first come into contact.

摘要

巯基乙酸诱导的Balb/c小鼠腹腔巨噬细胞对单核细胞增生李斯特菌表现出最小的抗菌活性,但对痘苗病毒的复制完全允许。相比之下,驻留巨噬细胞和脂多糖诱导的巨噬细胞既没有表现出降低的抗菌活性,也不支持病毒复制。巯基乙酸的作用在体外培养的巨噬细胞以及完整的Balb/c小鼠中都得到了证实。腹腔注射巯基乙酸并通过相同途径进行攻击的小鼠,由于病毒和细菌在腹腔巨噬细胞内早期局部增殖并随后扩散到肝脏,从而遭受严重的病毒和细菌感染。通过腹腔注射途径给予巯基乙酸后,静脉注射相似剂量的病毒或细菌病原体进行攻击的Balb/c小鼠均未死于任何一种感染。因此,巯基乙酸损害细胞宿主对感染因子防御能力的能力似乎具有部位特异性;即仅限于渗出性巨噬细胞和攻击接种物首次接触的腹腔。

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