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大鼠血管平滑肌细胞中诱导型一氧化氮合酶的克隆

Cloning of inducible nitric oxide synthase in rat vascular smooth muscle cells.

作者信息

Nunokawa Y, Ishida N, Tanaka S

机构信息

Suntory Institute for Biomedical Research, Osaka, Japan.

出版信息

Biochem Biophys Res Commun. 1993 Feb 26;191(1):89-94. doi: 10.1006/bbrc.1993.1188.

Abstract

We previously showed that interferon(IFN)-gamma inhibited the proliferation of rat vascular smooth muscle cells(VSMC) by generation of nitric oxide(NO) through the induction of an NO synthase(NOS). To identify the NOS in the VSMC at molecular level, we analyzed messenger RNA(mRNA) levels and primary structure of the novel NOS by cDNA cloning with application of polymerase chain reaction(PCR). mRNA of the NOS was induced and the level of induction was significantly increased by IFN-gamma in VSMC within a few hours. The amino acid sequence deduced from the cloned NOS cDNA was distinct from that of the previously reported constitutive types of NOSs, while highly similar to that of macrophage NOS. Cofactor binding regions were highly conserved among these NOSs. These findings show that the NOS is inducible and could regulate the proliferation of VSMC. Besides, this is the first report of cloning of the NOS in VSMC.

摘要

我们先前表明,干扰素(IFN)-γ 通过诱导一氧化氮合酶(NOS)生成一氧化氮(NO)来抑制大鼠血管平滑肌细胞(VSMC)的增殖。为了在分子水平上鉴定 VSMC 中的 NOS,我们通过应用聚合酶链反应(PCR)进行 cDNA 克隆来分析新型 NOS 的信使核糖核酸(mRNA)水平和一级结构。NOS 的 mRNA 被诱导,并且在数小时内,IFN-γ 显著增加了 VSMC 中 NOS 的诱导水平。从克隆的 NOS cDNA 推导的氨基酸序列与先前报道的组成型 NOS 类型不同,而与巨噬细胞 NOS 的序列高度相似。这些 NOS 之间的辅因子结合区域高度保守。这些发现表明该 NOS 是可诱导的,并且可以调节 VSMC 的增殖。此外,这是关于 VSMC 中 NOS 克隆的首次报道。

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