首页> 外文期刊>American Journal of Physiology >Integration of rapid cytosolic Ca2+ signals by mitochondria in cat ventricular myocytes.
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Integration of rapid cytosolic Ca2+ signals by mitochondria in cat ventricular myocytes.

机译:猫心室肌细胞中线粒体的快速胞质Ca2 +信号整合。

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摘要

Decoding of fast cytosolic Ca(2+) concentration ([Ca(2+)](i)) transients by mitochondria was studied in permeabilized cat ventricular myocytes. Mitochondrial [Ca(2+)] ([Ca(2+)](m)) was measured with fluo-3 trapped inside mitochondria after removal of cytosolic indicator by plasma membrane permeabilization with digitonin. Elevation of extramitochondrial [Ca(2+)] ([Ca(2+)](em)) to >0.5 microM resulted in a [Ca(2+)](em)-dependent increase in the rate of mitochondrial Ca(2+) accumulation ([Ca(2+)](em) resulting in half-maximal rate of Ca(2+) accumulation = 4.4 microM) via Ca(2+) uniporter. Ca(2+) uptake was sensitive to the Ca(2+) uniporter blocker ruthenium red and the protonophore carbonyl cyanide p-trifluoromethoxyphenylhydrazone and depended on inorganic phosphate concentration. The rates of [Ca(2+)](m) increase and recovery were dependent on the extramitochondrial [Na(+)] ([Na(+)](em)) due to Ca(2+) extrusion via mitochondrial Na(+)/Ca(2+) exchanger. The maximal rate of Ca(2+) extrusion was observed with [Na(+)](em) in the range of 20-40 mM. Rapid switching (0.25-1 Hz) of [Ca(2+)](em) between 0 and 100 microM simulated rapid beat-to-beat changes in [Ca(2+)](i) (with [Ca(2+)](i) transient duration of 100-500 ms). No [Ca(2+)](m) oscillations were observed, either under conditions of maximal rate of Ca(2+) uptake (100 microM [Ca(2+)](em), 0 [Na(+)](em)) or with maximal rate of Ca(2+) removal (0 [Ca(2+)](em), 40 mM [Na(+)](em)). The slow frequency-dependent increase of [Ca(2+)](m) argues against a rapid transmission of Ca(2+) signals between cytosol and mitochondria on a beat-to-beat basis in the heart. [Ca(2+)](m) changes elicited by continuous or pulsatile exposure to elevated [Ca(2+)](em) showed no difference in mitochondrial Ca(2+) uptake. Thus in cardiac myocytes fast [Ca(2+)](i) transients are integrated by mitochondrial Ca(2+) transport systems, resulting in a frequency-dependent net mitochondrial Ca(2+) accumulation.
机译:在通透性猫心室心肌细胞中研究了线粒体对快速胞质Ca(2+)浓度([Ca(2 +)](i)瞬态的解码。线粒体[Ca(2+)]([Ca(2 +)](m))是用指孔蛋白通过质膜透化作用除去细胞溶质指示剂后用捕获在线粒体内的fluo-3进行测定的。线粒体[Ca(2+)]([Ca(2 +)](em))升高到> 0.5 microM导致线粒体Ca(2)的速率依赖于[Ca(2 +)](em) +)累积([Ca(2 +)](em)导致Ca(2+)累积的一半最大速率= 4.4 microM)通过Ca(2+)单向端口。 Ca(2+)摄取对Ca(2+)单向阻滞剂钌红和质子体羰基氰化物对三氟甲氧基苯基hydr敏感,并取决于无机磷酸盐的浓度。 [Ca(2 +)](m)增加和恢复的速率取决于线粒体[Na(+)]([Na(+)](em)),这是由于Ca(2+)通过线粒体Na( +)/ Ca(2+)交换剂。观察到的Ca(2+)挤出的最大速率与[Na(+)](em)在20-40 mM的范围内。 [Ca(2 +)](em)在0到100 microM之间快速切换(0.25-1 Hz),模拟了[Ca(2 +)](i)的逐拍快速变化(使用[Ca(2+ )](i)持续时间为100-500毫秒)。在最大Ca(2+)吸收速率(100 microM [Ca(2 +)](em),0 [Na(+)]( em))或最大去除率(0 [Ca(2 +)](em),40 mM [Na(+)](em))。 [Ca(2 +)](m)的频率依赖性缓慢增加表明,心脏中心律不整的基础上,Ca(2+)信号在细胞质和线粒体之间快速传递。 [Ca(2 +)](m)的变化是由连续或脉动性暴露于升高的[Ca(2 +)](em)引起的,表明线粒体Ca(2+)的摄取没有差异。因此,在心肌细胞中快速的[Ca(2 +)](i)瞬变是由线粒体Ca(2+)传输系统整合的,从而导致频率依赖的线粒体Ca(2+)积累。

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