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小鼠骨骼肌中的一氧化氮合酶II与小窝蛋白3相关。

NO synthase II in mouse skeletal muscle is associated with caveolin 3.

作者信息

Gath I, Ebert J, Gödtel-Armbrust U, Ross R, Reske-Kunz A B, Förstermann U

机构信息

Department of Pharmacology, Johannes Gutenberg University, Obere Zahlbacher Strasse 67, D-55101 Mainz, Germany.

出版信息

Biochem J. 1999 Jun 15;340 ( Pt 3)(Pt 3):723-8.

Abstract

The inducible-type NO synthase (NOS II; iNOS) is constitutively expressed in slow-twitch skeletal muscle fibres of guinea-pigs [Gath, Closs, Gödtel-Armbrust, Schmitt, Nakane, Wessler and Förstermann (1996) FASEB J. 10, 1614-1620]. Here we studied the expression of NOS II in skeletal muscle of wild-type and NOS II-deficient mice and investigated the molecular basis for the membrane association of this NOS in muscle. A basal expression of NOS II mRNA and protein was detected in skeletal muscle from untreated wild-type mice; expression increased when mice were treated with bacterial lipopolysaccharide (LPS). No NOS II was found in any tissue of untreated or LPS-treated NOS II-deficient mice. Immunoprecipitation experiments were performed with homogenates of gastrocnemius muscle from untreated or LPS-treated wild-type mice. A NOS II-specific antibody precipitated caveolin 3 in all homogenates investigated, the effect being most pronounced in skeletal muscle from LPS-treated animals. Conversely, an antibody against caveolin 3 co-precipitated NOS II in muscle homogenates. Similarly, a weak co-precipitation of NOS II and caveolin 3 was seen in homogenates of untreated murine C2C12 myotubes; co-precipitation was markedly enhanced in cells stimulated with LPS/interferon gamma. The association of NOS II with caveolin 3 might have implications for the regulation of contraction of, and/or glucose uptake by, slow-twitch muscle fibres.

摘要

诱导型一氧化氮合酶(NOS II;iNOS)在豚鼠的慢肌纤维中组成性表达[Gath、Closs、Gödtel-Armbrust、Schmitt、Nakane、Wessler和Förstermann(1996年)《美国实验生物学会联合会杂志》10,1614 - 1620]。在此,我们研究了野生型和NOS II缺陷型小鼠骨骼肌中NOS II的表达,并探讨了该NOS在肌肉中与膜结合的分子基础。在未处理的野生型小鼠的骨骼肌中检测到了NOS II mRNA和蛋白的基础表达;当用细菌脂多糖(LPS)处理小鼠时,表达增加。在未处理或LPS处理的NOS II缺陷型小鼠的任何组织中均未发现NOS II。用未处理或LPS处理的野生型小鼠的腓肠肌匀浆进行免疫沉淀实验。一种NOS II特异性抗体在所有研究的匀浆中沉淀出小窝蛋白3,在LPS处理动物的骨骼肌中这种作用最为明显。相反,一种抗小窝蛋白3的抗体在肌肉匀浆中共沉淀出NOS II。同样,在未处理的小鼠C2C12肌管匀浆中也观察到了NOS II和小窝蛋白3的弱共沉淀;在用LPS/干扰素γ刺激的细胞中,共沉淀明显增强。NOS II与小窝蛋白3的结合可能对慢肌纤维的收缩调节和/或葡萄糖摄取有影响。

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