Shear stress activation of nitric oxide synthase and increased nitric oxide levels in human red blood cells

被引:75
作者
Ulker, Pinar [2 ]
Yaras, Nazmi [3 ]
Yalcin, Ozlem [4 ]
Celik-Ozenci, Ciler [5 ]
Johnson, Paul C. [4 ]
Meiselman, Herbert J. [6 ]
Baskurt, Oguz K. [1 ]
机构
[1] Koc Univ, Sch Med, TR-34450 Istanbul, Turkey
[2] Akdeniz Univ, Fac Med, Dept Physiol, TR-07058 Antalya, Turkey
[3] Akdeniz Univ, Fac Med, Dept Biophys, TR-07058 Antalya, Turkey
[4] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[5] Akdeniz Univ, Fac Med, Dept Histol & Embryol, TR-07058 Antalya, Turkey
[6] Univ So Calif, Keck Sch Med, Dept Physiol & Biophys, Los Angeles, CA 90033 USA
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2011年 / 24卷 / 04期
关键词
Nitric oxide synthase; Erythrocyte; Shear stress; Activation; Intracellular calcium; FLUORESCENT INDICATORS; S-NITROSOHEMOGLOBIN; HUMAN-ERYTHROCYTES; ENDOTHELIAL-CELLS; MECHANISMS; FLOW; DICHLOROFLUORESCIN; STIMULATION; OXYGENATION; RELEASE;
D O I
10.1016/j.niox.2011.03.003
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
Red blood cells (RBC) play an important role in the balance between generation and scavenging of nitric oxide (NO) and hence its local bioavailability and influence on vasomotor control. Previous studies have reported increased NO levels in RBC suspensions subsequent to exposure to shear forces; the present study was designed to further investigate changes in intracellular NO concentration and possible mechanisms involved for RBC exposed to well-controlled shear forces. Attached human RBC were subjected to shear stresses up to 0.1 Pa in a parallel-plate flow channel; fluorescent methods were used to monitor changes in intracellular NO and calcium concentrations. Intracellular NO concentration, estimated by the fluorescence level of 4-amino-5-methylamino-2',7'-difluorofluorescein diacetate (OAF-FM), increased sharply within 30 s following the application of shear stress between 0.013 and 0.1 Pa. This increase was only partially prevented by the absence of L-arginine and by the presence of L-N-acetyl-methyl-arginine (L-NAME), strongly suggesting that this response was in part related to the activation of NO-synthase (NOS) enzyme. The increase in intracellular NO concentration under shear stress was also inhibited by calcium chelation in the suspending medium, indicating the role of calcium entry for NOS activation. Increases of intracellular calcium concentrations under the same shearing conditions were demonstrated by monitoring Fluo-3/AM fluorescence in RBC exposed to shear stress. Serine 1177 phosphorylated NOS protein, the activated form of the enzyme determined by immunohistochemistry, was found to be significantly increased following the exposure of RBC to 0.1 Pa shear stress for 1 min. These data confirm that RBC possess a NOS enzyme that is actively synthesizing NO and activated by effective shear forces. The data also suggest that there may be additional (e.g., non-enzymatic) NO generating mechanisms in RBC that are also enhanced under shear stress. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:184 / 191
页数:8
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