期刊论文详细信息
FEBS Letters
NO2‐induced expression of specific protein kinase C isoforms and generation of phosphatidylcholine‐derived diacylglycerol in cultured pulmonary artery endothelial cells
Patel, Jawaharlal M.1  Li, Yong D.1  Block, Edward R.1 
[1] Division of Pulmonary Medicine, University of Florida College of Medicine and the Veterans Affairs Medical Center, Gainesville, FL 32608-1197, USA
关键词: Nitrogen dioxide;    Protein kinase C;    Pliospholipase C;    Phospholipase D;    Diacylglycerol;    Plasma membrane;    Endothelial cell;   
DOI  :  10.1016/0014-5793(96)00550-9
学科分类:生物化学/生物物理
来源: John Wiley & Sons Ltd.
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【 摘 要 】

The present study examines whether nitrogen dioxide (NO2)-induced activation of protein kinase C (PKC) is associated with increased expression of specific PKC isoforms and/or with enhanced generation of phosphatidylcholine(PC)-derived diacylglycerol (DAG) in pulmonary artery endothelial cells (PAEC). Western blot analysis revealed that exposure to 5 ppm NO2 resulted in increased expression of PKC α and ε isoforms in both cytosol and membrane fractions in a time-dependent fashion compared with controls. A time-dependent elevated expression of PKC isoform β was observed in the cytosol fraction only of NO2-exposed cells. PKC isoform λ was not detectable in either the cytosolic or membrane fractions from control or NO2-exposed cells. Scatchard analysis of [3H]phorbol 12,13-dibutyrate (PDBu) binding showed that exposure to NO2 for 24 h increased the maximal number of binding sites (B max) from 15.2±2.3 pmollmg (control) to 42.3±5.3 pmol/mg (p < 0.01, n = 4) (NO2-exposed). Exposure to NO2 significantly increased PC specific-phospholipase C and phospholipase D activities in the plasma membrane of PAEC (p < 0.05 and p < 0.001, respectively). When [3H]myristic acid-labeled cells were exposed to NO2, significantly increased radioactivity was associated with cellular DAG. These results show for the first time that exposure of PAEC to NO2 results in elevated expression of specific PKC isoforms and in enhanced generation of cellular DAG, and the latter appears to arise largely from the hydrolysis of plasma membrane PC.

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