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驻留、诱导及免疫激活的小鼠腹腔巨噬细胞的趋化性。

Chemotaxis of resident, elicited and immunologically activated murine peritoneal macrophages.

作者信息

Staer A F, Rhodes J M, Bennedsen J, Olesen Larsen S

出版信息

Acta Pathol Microbiol Immunol Scand C. 1983 Apr;91(2):117-21.

PMID:6880746
Abstract

The in vitro chemotactic response of peritoneal macrophages fourteen days after immunization with BCG was greater than that of macrophages from control mice. Peritoneal macrophages from mice treated with other agents which enhance bactericidal activity, and macrophages induced with proteose-peptone were less responsive to chemotactic stimuli than resident macrophages. The addition of PPD or PHA lymphokines to the peritoneal cells from BCG injected mice depressed the chemotactic response, but increased unstimulated migration. PPD had no effect on the migration of resident macrophages, but PHA lymphokines depressed the chemotactic activity of these cells.

摘要

用卡介苗免疫14天后,腹膜巨噬细胞的体外趋化反应大于对照小鼠的巨噬细胞。用其他增强杀菌活性的药物处理的小鼠的腹膜巨噬细胞,以及用蛋白胨诱导的巨噬细胞对趋化刺激的反应比驻留巨噬细胞小。向注射卡介苗小鼠的腹膜细胞中添加PPD或PHA淋巴细胞因子会抑制趋化反应,但会增加未刺激的迁移。PPD对驻留巨噬细胞的迁移没有影响,但PHA淋巴细胞因子会抑制这些细胞的趋化活性。

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