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小鼠巨噬细胞系中一氧化氮合酶与精氨酸琥珀酸合成酶的共诱导。对一氧化氮产生调节的意义。

Coinduction of nitric oxide synthase and argininosuccinate synthetase in a murine macrophage cell line. Implications for regulation of nitric oxide production.

作者信息

Nussler A K, Billiar T R, Liu Z Z, Morris S M

机构信息

Department of Surgery, University of Pittsburgh School of Medicine, Pennsylvania 15261.

出版信息

J Biol Chem. 1994 Jan 14;269(2):1257-61.

PMID:7507106
Abstract

In macrophages and other cell types, bacterial lipopolysaccharide and certain cytokines stimulate nitric oxide (NO) production via expression of the inducible isoform of nitric oxide synthase (NOS). Citrulline, which is the coproduct of NOS-catalyzed metabolism of arginine, can be recycled to arginine by the action of argininosuccinate synthetase and argininosuccinate lyase, which are present at high levels in hepatocytes and renal tubular cells but normally at very low levels in other cell types such as macrophages. The present study demonstrates that lipopolysaccharide and interferon-gamma, which induce NOS in the murine macrophage cell line RAW 264.7, also coinduce activity and mRNA for argininosuccinate synthetase, which is limiting for arginine synthesis. Argininosuccinate lyase activity and mRNA abundance are unaffected. Induction of argininosuccinate synthetase is not blocked by NG-monomethyl-L-arginine, a potent inhibitor of NOS, indicating that argininosuccinate synthetase induction is not the consequence of depleting cellular arginine levels by NOS. Because plasma levels of arginine are limiting for NO synthesis, enhanced cellular capacity to regenerate arginine from citrulline could play a significant role in regulating NO production, especially under conditions where the inducible isoform of NOS is expressed.

摘要

在巨噬细胞和其他细胞类型中,细菌脂多糖和某些细胞因子通过诱导型一氧化氮合酶(NOS)的表达刺激一氧化氮(NO)的产生。瓜氨酸是NOS催化精氨酸代谢的副产物,可通过精氨琥珀酸合成酶和精氨琥珀酸裂解酶的作用再循环为精氨酸,这两种酶在肝细胞和肾小管细胞中含量很高,但在其他细胞类型如巨噬细胞中通常含量很低。本研究表明,在小鼠巨噬细胞系RAW 264.7中诱导NOS的脂多糖和干扰素-γ,也共同诱导精氨琥珀酸合成酶的活性和mRNA,而精氨琥珀酸合成酶是精氨酸合成的限速酶。精氨琥珀酸裂解酶的活性和mRNA丰度不受影响。精氨琥珀酸合成酶的诱导不受NOS的有效抑制剂NG-单甲基-L-精氨酸的阻断,这表明精氨琥珀酸合成酶的诱导不是NOS消耗细胞内精氨酸水平的结果。由于血浆中精氨酸水平是NO合成的限制因素,增强细胞从瓜氨酸再生精氨酸的能力可能在调节NO产生中起重要作用,特别是在诱导型NOS表达的情况下。

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