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Nox Family NADPH Oxidases in Mechano-Transduction: Mechanisms and Consequences
被引:65
作者:
Brandes, Ralf P.
[1
]
Weissmann, Norbert
[2
]
Schroeder, Katrin
[1
]
机构:
[1] Goethe Univ Frankfurt, Inst Kardiovaskulare Physiol, D-60590 Frankfurt, Germany
[2] Univ Giessen, Lung Ctr, D-35390 Giessen, Germany
关键词:
STIMULATES SUPEROXIDE-PRODUCTION;
NITRIC-OXIDE SYNTHASE;
LAMINAR SHEAR-STRESS;
OXIDATIVE STRESS;
NAD(P)H OXIDASE;
ENDOTHELIAL-CELLS;
DISTURBED FLOW;
ANGIOTENSIN-II;
MOLECULAR-MECHANISMS;
MEDIATED ACTIVATION;
D O I:
10.1089/ars.2013.5414
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Significance: The majority of cells in a multi-cellular organism are continuously exposed to ever-changing physical forces. Mechano-transduction links these events to appropriate reactions of the cells involving stimulation of signaling cascades, reorganization of the cytoskeleton and alteration of gene expression. Recent Advances: Mechano-transduction alters the cellular redox balance and the formation of reactive oxygen species (ROS). Nicotine amide adenine dinucleotide reduced form (NADPH) oxidases of the Nox family are prominent ROS generators and thus, contribute to this stress-induced ROS formation. Critical Issues: Different types and patterns of mechano-stress lead to Nox-dependent ROS formation and Nox-mediated ROS formation contributes to cellular responses and adaptation to physical forces. Thereby, Nox enzymes can mediate vascular protection during physiological mechano-stress. Despite this, over-activation and induction of Nox enzymes and a subsequent substantial increase in ROS formation also promotes oxidative stress in pathological situations like disturbed blood flow or extensive stretch. Future Directions: Individual protein targets of Nox-mediated redox-signaling will be identified to better understand the specificity of Nox-dependent ROS signaling in mechano-transduction. Nox-inhibitors will be tested to reduce cellular activation in response to mechano-stimuli. Antioxid. Redox Signal. 20, 887-898.
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页码:887 / 898
页数:12
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