Shear stress-induced pH increase in plasma is mediated by a decrease in PCO2:: The increase in pH enhances shear stress-induced P-selectin expression in platelets

被引:6
作者
Chung, Ka-Young [1 ]
Lim, Kyung-Min [1 ]
Chung, Seung-Min [1 ]
Lee, Moo-Yeol [1 ]
Noh, Ji-Yoon [1 ]
Bae, Ok-Nam [1 ]
Chung, Jin-Ho [1 ]
机构
[1] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
关键词
shear stress; platelet; pH; P-selectin; P-CO2; bicarbonate;
D O I
10.1080/09537100500437711
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To investigate shear stress-induced platelet activation, the cone-plate viscometer or the Couette rotational viscometer has been widely used. In a previous report, it was shown that shearing platelet-rich plasma using a Couette rotational viscometer could lead to an increase in pH by CO2 release. However, any clear mechanism has not been provided. In this study, we examined whether shearing cell free plasma only using a cone-plate viscometer can also induce pH increase and studied the underlying mechanism of shear-induced pH increase by directly measuring total CO2 (T-CO2) and CO2 tension (P-CO2). When human plasma was sheared using a cone-plate viscometer, the pH of the human plasma increased time- and shear rate-dependently. Although T-CO2 of human plasma was not affected, P-CO2 was decreased by shearing, indicating that the decreased P-CO2 is associated with a pH increase of plasma. In addition, the pH of bicarbonate-containing suspension buffer was also shown to be increased by shearing; suggesting that the platelet studies using suspension buffers containing bicarbonate could be affected similarly. The effects of pH changes on shear stress-induced platelet activation were also investigated in the same in vitro systems. While shear stress-induced platelet aggregation was not affected by the pH changes, P-selectin expression was significantly increased in accordance with the pH increase. In conclusion, shear stress using a cone-plate viscometer induces pH increase in plasma or bicarbonate-containing suspension buffer through a P-CO2 decrease and the pH changes alone can contribute to platelet activation by enhancing shear stress-induced P-selectin expression.
引用
收藏
页码:127 / 133
页数:7
相关论文
共 37 条
  • [1] BROWN CH, 1975, J LAB CLIN MED, V86, P462
  • [2] DJALDETTI M, 1979, ARCH SURG-CHICAGO, V114, P707
  • [3] PLATELETS ROLL ON STIMULATED ENDOTHELIUM IN-VIVO - AN INTERACTION MEDIATED BY ENDOTHELIAL P-SELECTIN
    FRENETTE, PS
    JOHNSON, RC
    HYNES, RO
    WAGNER, DD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) : 7450 - 7454
  • [4] MECHANISMS OF DISEASE - THE PATHOGENESIS OF CORONARY-ARTERY DISEASE AND THE ACUTE CORONARY SYNDROMES .1.
    FUSTER, V
    BADIMON, L
    BADIMON, JJ
    CHESEBRO, JH
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (04) : 242 - 250
  • [5] PHYSICAL AND CHEMICAL EFFECTS OF RED-CELLS IN THE SHEAR-INDUCED AGGREGATION OF HUMAN PLATELETS
    GOLDSMITH, HL
    BELL, DN
    BRAOVAC, S
    STEINBERG, A
    MCINTOSH, F
    [J]. BIOPHYSICAL JOURNAL, 1995, 69 (04) : 1584 - 1595
  • [6] Shear stress induces iNOS expression in cultured smooth muscle cells: role of oxidative stress
    Gosgnach, W
    Messika-Zeitoun, D
    Gonzalez, W
    Philipe, M
    Michel, JB
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2000, 279 (06): : C1880 - C1888
  • [7] Distinct mechanisms of platelet aggregation as a consequence of different shearing flow conditions
    Goto, S
    Ikeda, Y
    Saldívar, E
    Ruggeri, ZM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (02) : 479 - 486
  • [8] Goto S, 2000, INT ANGIOL, V19, P147
  • [9] Platelet activation in flowing blood passing growing arterial thrombi
    Hagberg, IA
    Roald, HE
    Lyberg, T
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (07) : 1331 - 1336
  • [10] INFLUENCE OF PH, TEMPERATURE, AND CALCIUM ON PLATELET-AGGREGATION - MAINTENANCE OF ENVIRONMENTAL PH AND PLATELET-FUNCTION FOR IN-VITRO STUDIES IN PLASMA STORED AT 37 DEGREES C
    HAN, P
    ARDLIE, NG
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1974, 26 (03) : 373 - 389