首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Nitric oxide production by alveolar macrophages in response to house dust mite fecal pellets and the mite allergens, Der p 1 and Der p 2.
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Nitric oxide production by alveolar macrophages in response to house dust mite fecal pellets and the mite allergens, Der p 1 and Der p 2.

机译:肺泡巨噬细胞对室内尘螨粪便颗粒和螨过敏原产生的一氧化氮,Der p 1和Der p 2。

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BACKGROUND: Allergens are frequently found within or attached to particulate material. For example, house dust mite fecal pellets (HDMFP) contain the major mite allergens, exposure to which have been implicated in the development of asthma. Although several studies have examined the ability of purified allergens to generate inflammatory responses, few studies have investigated whether HDMFP per se, are biologically active. OBJECTIVE: Our objective was to examine the ability of whole HDMFP to stimulate nitric oxide (NO) release from alveolar macrophages. METHODS: The rat alveolar macrophage cell line, NR8383, was exposed to HDMFP, Der p 1, or Der p 2, and nitrite levels in the culture supernatants were measured with the Griess reagent. NO synthase mRNA expression was determined by RT-PCR. RESULTS: HDMFP stimulated the production of NO in a dose-dependent and time-dependent manner, with maximum NO levels measured after 48 hours of exposure. Inclusion of polymyxin B did not influence NO production, suggesting that LPS was not responsible for NO production. HDMFP-mediated NO release was down-modulated after treatment with N(G)-nitro-l-arginine methyl ester (L-NAME), dexamethasone, EDTA, and cysteine, but not heat treatment. Inducible nitric oxide synthase mRNA was observed 3 hours after HDMFP exposure, with maximum levels after 48 hours. Both purified Der p 1 and Der p 2 induced NO production, and inhibition of the cysteine protease activity of Der p 1 had little effect on NO production. CONCLUSIONS: HDMFP, Der p 1 and Der p 2 are potent inducers of NO. Neither LPS nor the enzymatic activity of Der p 1 was responsible for NO production observed.
机译:背景:过敏原经常发现于或附着在颗粒物质中。例如,屋尘螨粪便颗粒(HDMFP)含有主要的螨过敏原,接触这些过敏原可能与哮喘的发生有关。尽管有几项研究检查了纯化的过敏原产生炎症反应的能力,但很少有研究调查HDMFP本身是否具有生物学活性。目的:我们的目的是检查整个HDMFP刺激肺泡巨噬细胞释放一氧化氮(NO)的能力。方法:将大鼠肺泡巨噬细胞系NR8383暴露于HDMFP,Der p 1或Der p 2中,并使用Griess试剂测量培养上清液中的亚硝酸盐水平。通过RT-PCR确定NO合酶mRNA表达。结果:HDMFP以剂量依赖性和时间依赖性方式刺激NO的产生,在暴露48小时后测得的最大NO水平。包含多粘菌素B不会影响NO的产生,这表明LPS不负责NO的产生。用N(G)-硝基-1-精氨酸甲酯(L-NAME),地塞米松,EDTA和半胱氨酸处理后,HDMFP介导的NO释放被下调,但不进行热处理。 HDMFP暴露后3小时观察到诱导型一氧化氮合酶mRNA,48小时后达到最高水平。纯化的Der p 1和Der p 2均诱导NO生成,而抑制Der p 1的半胱氨酸蛋白酶活性对NO生成影响很小。结论:HDMFP,Der p 1和Der p 2是NO的有效诱导剂。 LPS或Der p 1的酶促活性均与观察不到的NO产生有关。

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