scholarly journals Potentiation by tumour necrosis factor-α of calcium signals induced by bradykinin and carbachol in human tracheal smooth muscle cells

1995 ◽  
Vol 114 (1) ◽  
pp. 4-5 ◽  
Author(s):  
Yassine Amrani ◽  
Nadine Martinet ◽  
Christian Bronner
Keyword(s):  
Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Tumour Necrosis Factor ◽  
Tumour Necrosis ◽  
Muscle Cells ◽  
Tracheal Smooth Muscle ◽  
Tumour Necrosis Factor Α ◽  
Calcium Signals ◽  
Factor Α ◽  
Necrosis Factor

scholarly journals Tumour necrosis factor α activates a p22phox-based NADH oxidase in vascular smooth muscle

1998 ◽  
Vol 329 (3) ◽  
pp. 653-657 ◽  
Author(s):  
W. Gilles DE KEULENAER ◽  
R. Wayne ALEXANDER ◽  
Masuko USHIO-FUKAI ◽  
Nobukazu ISHIZAKA ◽  
K. Kathy GRIENDLING
Keyword(s):  
Smooth Muscle ◽  
Vascular Smooth Muscle ◽  
Nadph Oxidase ◽  
Smooth Muscle Cells ◽  
Tumour Necrosis ◽  
Nadh Oxidase ◽  
Tumour Necrosis Factor Α ◽  
Tnf Α ◽  
Factor Α ◽  
Necrosis Factor

Increasing experimental evidence suggests that non-phagocytic cells express a potent superoxide (O2-•)-producing NADH oxidase that might be related to the phagocytic NADPH oxidase. Here we show that the cytokine tumour necrosis factor α (TNF-α) activates, in a time- and dose-dependent manner, a O2-•-producing NADH oxidase in cultured rat aortic smooth-muscle cells. Dose-response experiments for NADH showed an upward shift of the curve for TNF-α-treated cells, suggesting that TNF-α increased the amount of available enzyme. Using the anti-sense transfection technique, we further demonstrate that the molecular identity of this oxidase includes p22phox (the α subunit of cytochrome b558 and part of the electron transfer component of the phagocytic NADPH oxidase), which we recently cloned from a rat vascular smooth-muscle cell cDNA library. In addition, prolonged treatment with TNF-α increased p22phox mRNA expression without affecting p22phox mRNA stability, and only when transcriptional activity was intact. These findings identify a p22phox-containing NADH oxidase as a source for cytokine-induced free radical production in vascular smooth-muscle cells and clarify some of the mechanisms involved in the regulation of vascular oxidase activity.

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