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脂多糖激活的小鼠巨噬细胞中精氨酸酶与一氧化氮合酶的共诱导

Co-induction of arginase and nitric oxide synthase in murine macrophages activated by lipopolysaccharide.

作者信息

Wang W W, Jenkinson C P, Griscavage J M, Kern R M, Arabolos N S, Byrns R E, Cederbaum S D, Ignarro L J

机构信息

Mental Retardation Research Center, University of California, Los Angeles 90024-1759, USA.

出版信息

Biochem Biophys Res Commun. 1995 May 25;210(3):1009-16. doi: 10.1006/bbrc.1995.1757.

Abstract

In view of studies showing that not only nitric oxide synthase (NOS) activity but arginase activity is induced in rodent macrophages by lipopolysaccharide (LPS), the objective of this study was to investigate the co-induction of these two enzymes and to ascertain whether common mechanisms are involved. RAW 264.7 cells were activated by 2 micrograms LPS/ml and incubated for up to 48 hr. Inducible NOS (iNOS) and inducible arginase II (AII) activities were monitored, respectively, by measuring NO2-/NO3- accumulation in cell culture media and formation of urea (as CO2) from L-arginine by cell lysates. AII activity increased linearly up to at least 48 hr, whereas NO2-/NO3- formation reached a plateau well before 48 hr. Immunoprecipitation experiments revealed that AII accounted for 90-100% of arginase activity in LPS-activated macrophages. The inhibitor of NF-kappa B activation, pyrrolidine dithiocarbamate, inhibited the induction of iNOS but not AII. Moreover, whereas IFN-gamma caused iNOS induction, AII induction was nearly abolished by IFN-gamma, perhaps by inhibiting transcription of the AII gene. These observations indicate that co-induction of iNOS and AII occurs by distinct transcriptional mechanisms, AII induction could diminish NO production by decreasing L-arginine availability, and IFN-gamma can prevent AII induction.

摘要

鉴于有研究表明,脂多糖(LPS)不仅能诱导啮齿动物巨噬细胞中的一氧化氮合酶(NOS)活性,还能诱导精氨酸酶活性,本研究的目的是调查这两种酶的共同诱导情况,并确定是否涉及共同机制。RAW 264.7细胞用2微克/毫升LPS激活,并孵育长达48小时。分别通过测量细胞培养基中NO2-/NO3-的积累以及细胞裂解物中L-精氨酸形成尿素(以CO2形式)来监测诱导型NOS(iNOS)和诱导型精氨酸酶II(AII)的活性。AII活性至少在48小时内呈线性增加,而NO2-/NO3-的形成在48小时之前就达到了平台期。免疫沉淀实验表明,AII在LPS激活的巨噬细胞中占精氨酸酶活性的90 - 100%。NF-κB激活抑制剂吡咯烷二硫代氨基甲酸盐抑制iNOS的诱导,但不抑制AII。此外,虽然IFN-γ导致iNOS诱导,但IFN-γ几乎消除了AII的诱导,这可能是通过抑制AII基因的转录实现的。这些观察结果表明,iNOS和AII的共同诱导是通过不同的转录机制发生的,AII的诱导可能通过降低L-精氨酸的可用性来减少NO的产生,并且IFN-γ可以阻止AII的诱导。

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