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中性粒细胞在己烯雌酚和锶89对痤疮丙酸杆菌激活巨噬细胞作用中的参与情况。

Neutrophil involvement in effects of diethylstilbestrol and strontium 89 on macrophage activation by Propionibacterium acnes.

作者信息

Ackermann M F, Morahan P S

机构信息

Department of Microbiology and Immunology, Medical College of Pennsylvania, Philadelphia 19129.

出版信息

Int J Immunopharmacol. 1988;10(1):7-13. doi: 10.1016/0192-0561(88)90144-0.

Abstract

We have recently demonstrated that diethylstilbestrol (DES) significantly suppresses macrophage (M phi) activation by Propionibacterium acnes. Because the initial activation of M phi by P. acnes appears to involve the close interaction of the killed bacteria with inflammatory neutrophils (PMN) and resident M phi in the peritoneal cavity, we investigated whether the DES inhibition of M phi activation was associated with inhibition of the PMN response. Our data demonstrate that treatment of mice with DES did not interfere with the acute inflammatory peritoneal PMN influx 5 h after P. acnes injection. DES treatment also did not affect development of the early (day 4) tumor cytotoxic activity of P. acnes activated M phi; this M phi activity has been shown to be mediated by the acute PMN influx. DES treatment, however, did reduce M phi activation as evidenced by alterations in other markers typically associated with M phi activation by P. acnes, including the characteristic reductions in alkaline phosphodiesterase (APD) ectoenzyme activity and the total RNA synthesis, as well as the characteristic persistence of the peritoneal PMN response seen on days 4 and 7 after P. acnes injection. In addition, M phi activity 7 days after P. acnes injection was inhibited in DES treated mice, as evidenced by reduced antitumor activity, and alteration of the markers mentioned above. As a second approach to elucidate the involvement of the acute and persistent PMN response in the M phi activation process, we depleted mice of circulating PMN by treatment of mice with 89Sr before administration of P. acnes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们最近证明,己烯雌酚(DES)能显著抑制痤疮丙酸杆菌对巨噬细胞(M phi)的激活。由于痤疮丙酸杆菌对M phi的初始激活似乎涉及被杀死的细菌与炎症中性粒细胞(PMN)以及腹腔内常驻M phi的密切相互作用,我们研究了DES对M phi激活的抑制是否与PMN反应的抑制有关。我们的数据表明,用DES处理小鼠不会干扰痤疮丙酸杆菌注射后5小时急性炎症性腹腔PMN的流入。DES处理也不会影响痤疮丙酸杆菌激活的M phi早期(第4天)肿瘤细胞毒性活性的发展;这种M phi活性已被证明是由急性PMN流入介导的。然而,DES处理确实降低了M phi的激活,这可通过其他通常与痤疮丙酸杆菌激活M phi相关的标志物的改变来证明,包括碱性磷酸二酯酶(APD)外切酶活性和总RNA合成的特征性降低,以及痤疮丙酸杆菌注射后第4天和第7天观察到的腹腔PMN反应的特征性持续存在。此外,在DES处理的小鼠中,痤疮丙酸杆菌注射后7天的M phi活性受到抑制,这可通过抗肿瘤活性降低以及上述标志物的改变来证明。作为阐明急性和持续性PMN反应在M phi激活过程中所起作用的第二种方法,我们在给予痤疮丙酸杆菌之前用89Sr处理小鼠,以耗尽循环中的PMN。(摘要截短于250字)

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