6533b85afe1ef96bd12b8ae6

RESEARCH PRODUCT

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

Jutta G. EbertUte Gödtel-armbrustAngelika B. Reske-kunzUlrich FörstermannRalf RossIngolf Gath

subject

LipopolysaccharideMyogenesisGlucose uptakeSkeletal muscleCell BiologyBiologyBiochemistryMolecular biologyCaveolin 3chemistry.chemical_compoundGastrocnemius musclemedicine.anatomical_structurechemistryBiochemistrymedicineInterferon gammaMolecular BiologyC2C12medicine.drug

description

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 γ. 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.

https://doi.org/10.1042/bj3400723