Turco J, Winkler H H
Department of Microbiology and Immunology, University of South Alabama College of Medicine, Mobile 36688-0002.
Infect Immun. 1993 Oct;61(10):4317-25. doi: 10.1128/iai.61.10.4317-4325.1993.
The ability of tumor necrosis factor alpha (TNF-alpha) alone and in combination with gamma interferon (IFN-gamma) to inhibit the growth of interferon-sensitive and -resistant Rickettsia prowazekii strains in mouse L929 cells was examined, and the possible role of the nitric oxide synthase pathway in the suppression of rickettsial growth induced by TNF-alpha, IFN-gamma, or both cytokines was evaluated. TNF-alpha inhibited the growth of strains Madrid E (IFN-gamma sensitive and alpha/beta interferon [IFN-alpha/beta] sensitive) and Breinl (IFN-gamma sensitive and IFN-alpha/beta resistant), but not that of strain 83-2P (IFN-gamma resistant and IFN-alpha/beta resistant), in L929 cells. Inhibition of the growth of the Madrid E strain in L929 cells treated with TNF-alpha and IFN-gamma in combination was greater than that observed with either TNF-alpha or IFN-gamma alone. Similarly, inhibition of the growth of the Breinl strain in L929 cells treated with both cytokines was greater than that observed with TNF-alpha alone; however, it did not differ significantly from the inhibition observed with IFN-gamma alone. Although strain 83-2P was resistant to TNF-alpha or IFN-gamma alone, its growth was inhibited in L929 cells treated with TNF-alpha and IFN-gamma in combination. Nitrite production was measured in mock-infected and infected L929 cell cultures, and the nitric oxide synthase inhibitors NG-methyl-L-arginine (NGMA) and aminoguanidine were used to evaluate the role of the nitric oxide synthase pathway in cytokine-induced inhibition of rickettsial growth. Nitrite production was induced in mock-infected or R. prowazekii-infected L929 cell cultures treated with IFN-gamma plus TNF-alpha, but not in mock-infected cultures that were untreated or treated with IFN-gamma or TNF-alpha alone. Nitrite production was also not induced in untreated, R. prowazekii-infected cultures; however, in some instances, it was induced in infected cultures treated with IFN-gamma or TNF-alpha alone. Nitrite production was blocked by NGMA or aminoguanidine, and these compounds markedly relieved the synergistic inhibitory effect of IFN-gamma plus TNF-alpha on the growth of strain 83-2P in L929 cells. In contrast, NGMA did not alleviate the inhibition of the growth of the Madrid E strain in L929 cells treated with IFN-gamma or TNF-alpha alone; however, it slightly and variably relieved the inhibition of the growth of the Madrid E strain in L929 cells treated with IFN-gamma and TNF-alpha in combination.(ABSTRACT TRUNCATED AT 400 WORDS)
研究了单独的肿瘤坏死因子α(TNF-α)以及其与γ干扰素(IFN-γ)联合使用时,对小鼠L929细胞中干扰素敏感和耐药的普氏立克次体菌株生长的抑制能力,并评估了一氧化氮合酶途径在TNF-α、IFN-γ或两种细胞因子诱导的立克次体生长抑制中的可能作用。TNF-α抑制了马德里E株(对IFN-γ敏感且对α/β干扰素[IFN-α/β]敏感)和布雷因尔株(对IFN-γ敏感且对IFN-α/β耐药)在L929细胞中的生长,但未抑制83-2P株(对IFN-γ耐药且对IFN-α/β耐药)的生长。在L929细胞中,TNF-α和IFN-γ联合处理对马德里E株生长的抑制作用大于单独使用TNF-α或IFN-γ时的观察结果。同样,两种细胞因子联合处理对L929细胞中布雷因尔株生长的抑制作用大于单独使用TNF-α时的观察结果;然而,与单独使用IFN-γ时的抑制作用相比,差异不显著。尽管83-2P株对单独的TNF-α或IFN-γ耐药,但在TNF-α和IFN-γ联合处理的L929细胞中其生长受到抑制。在未感染和感染立克次体的L929细胞培养物中测量了亚硝酸盐的产生,并使用一氧化氮合酶抑制剂NG-甲基-L-精氨酸(NGMA)和氨基胍来评估一氧化氮合酶途径在细胞因子诱导的立克次体生长抑制中的作用。在用IFN-γ加TNF-α处理的未感染或普氏立克次体感染的L929细胞培养物中诱导了亚硝酸盐的产生,但在未处理或单独用IFN-γ或TNF-α处理的未感染培养物中未诱导。在未处理的普氏立克次体感染培养物中也未诱导亚硝酸盐的产生;然而,在某些情况下,单独用IFN-γ或TNF-α处理的感染培养物中诱导了亚硝酸盐的产生。NGMA或氨基胍可阻断亚硝酸盐的产生,并且这些化合物显著减轻了IFN-γ加TNF-α对L929细胞中83-2P株生长的协同抑制作用。相比之下,NGMA并未减轻单独用IFN-γ或TNF-α处理的L929细胞中马德里E株生长的抑制作用;然而,它略微且可变地减轻了IFN-γ和TNF-α联合处理的L929细胞中马德里E株生长的抑制作用。(摘要截短至400字)