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激动剂诱发的人血小板胞质pH值和钙浓度变化:在生理碳酸氢盐条件下的研究

Agonist-evoked changes in cytosolic pH and calcium concentration in human platelets: studies in physiological bicarbonate.

作者信息

Sage S O, Jobson T M, Rink T J

机构信息

Physiological Laboratory, University of Cambridge.

出版信息

J Physiol. 1990 Jan;420:31-45. doi: 10.1113/jphysiol.1990.sp017900.

DOI:10.1113/jphysiol.1990.sp017900
PMID:2109061
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1190037/
Abstract
  1. Cytosolic pH (pHi) and calcium concentration ([Ca2+]i) have been investigated in the presence and absence of physiological HCO3- in human platelets co-loaded with the fluorescent indicators BCECF and Fura-2. Basal pHi and changes evoked by butyrate, thrombin, platelet activating factor (PAF), ADP and phorbol ester were investigated, as were the effects of removing external Na+. 2. In the presence of physiological HCO3- and CO2, basal pHi was 7.02 +/- 0.04 compared with 7.15 +/- 0.05 in the absence of HCO3-. Estimated cytosolic buffering power was reduced from 35.6 +/- 3.0 to 14.5 +/- 0.4 mM/pH unit by the omission of HCO3-. 3. Thrombin evoked an immediate acidification of 0.03 +/- 0.01 pH units in the presence of HCO3- and 0.07 +/- 0.01 pH units in its absence. The acidifications were followed by a slow alkalinization. The final pHi was 0.10 +/- 0.01 units above basal in the presence of HCO3- and 0.08 +/- 0.02 units above basal in the absence of HCO3-. The initial acidification was significantly greater in the absence of HCO3-. The subsequent increase in pHi was similar in the presence and absence of this ion, but the calculated loss of proton equivalents was greater in the presence of HCO3-. 4. Replacement of extracellular Na+ with N-methyl-D-glucamine resulted in a fall in basal pHi and abolished recovery from thrombin-evoked acidification in both the presence and absence of HCO3-. 5. In the presence of HCO3-, PAF and ADP evoked an intracellular acidification similar to that caused by thrombin. However, with PAF and ADP, the subsequent recovery in pHi was slow and did not rise above basal levels. Phorbol dibutyrate, an activator of protein kinase C, evoked a similar elevation in pHi of 0.04 +/- 0.01 units over 3 min in the presence and absence of HCO3-. 6. Stopped-flow fluorimetric measurements were made of both BCECF and Fura-2 fluorescence in the presence of HCO3-. In the presence and absence of external Ca2+, thrombin-evoked rises in [Ca2+]i peaked before any cytoplasmic alkalinization occurred. ADP evoked rapid elevations in [Ca2+]i, but caused no alkalinization.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在同时装载荧光指示剂2',7'-双(2-羧乙基)-5(6)-羧基荧光素(BCECF)和氟罗-2(Fura-2)的人血小板中,研究了在有和没有生理浓度碳酸氢根(HCO₃⁻)存在的情况下的胞质pH(pHi)和钙浓度([Ca²⁺]i)。研究了基础pHi以及丁酸盐、凝血酶、血小板活化因子(PAF)、二磷酸腺苷(ADP)和佛波酯引起的变化,以及去除细胞外钠离子的影响。2. 在有生理浓度HCO₃⁻和二氧化碳存在的情况下,基础pHi为7.02±0.04,而在没有HCO₃⁻时为7.15±0.05。通过省略HCO₃⁻,估计的胞质缓冲能力从35.6±3.0降低到14.5±0.4 mM/pH单位。3. 在有HCO₃⁻存在时,凝血酶引起立即酸化0.03±0.01 pH单位,在没有HCO₃⁻时为0.07±0.01 pH单位。酸化之后是缓慢的碱化。在有HCO₃⁻存在时,最终pHi比基础值高0.10±0.01单位,在没有HCO₃⁻时比基础值高0.08±0.02单位。在没有HCO₃⁻时,初始酸化明显更大。在有和没有这种离子存在的情况下,随后pHi的升高相似,但在有HCO₃⁻存在时计算出的质子当量损失更大。4. 用N-甲基-D-葡糖胺替代细胞外钠离子导致基础pHi下降,并消除了在有和没有HCO₃⁻存在时凝血酶引起的酸化后的恢复。5. 在有HCO₃⁻存在时,PAF和ADP引起的细胞内酸化与凝血酶引起的相似。然而,对于PAF和ADP,随后pHi的恢复缓慢且未升至基础水平以上。蛋白激酶C的激活剂佛波二丁酯在有和没有HCO₃⁻存在的情况下,在3分钟内引起pHi类似的升高0.04±0.01单位。6. 在有HCO₃⁻存在的情况下,对BCECF和Fura-2荧光进行了停流荧光测量。在有和没有细胞外Ca²⁺存在的情况下,凝血酶引起的[Ca²⁺]i升高在任何细胞质碱化发生之前达到峰值。ADP引起[Ca²⁺]i快速升高,但未引起碱化。(摘要截断于400字)

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Changes in cytoplasmic pH and in membrane potential in thrombin-stimulated human platelets.凝血酶刺激的人血小板中细胞质pH值和膜电位的变化。
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Removal of extraplatelet Na+ eliminates indomethacin-sensitive secretion from human platelets stimulated by epinephrine, ADP, and thrombin.去除血小板外的钠离子可消除肾上腺素、二磷酸腺苷(ADP)和凝血酶刺激的人血小板中对吲哚美辛敏感的分泌。
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