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来自巨型黏液虫轴突分离出的轴浆非线粒体细胞器的ATP依赖性钙积累。

ATP-dependent calcium accumulation by non-mitochondrial organelles of axoplasm isolated from Myxicola giant axons.

作者信息

Ortiz O E, Sjodin R A, Boyne A

出版信息

Biochim Biophys Acta. 1985 Mar 28;814(1):13-22. doi: 10.1016/0005-2736(85)90414-6.

Abstract

Axoplasm from freshly isolated Myxicola giant axons was mixed with small volumes of 'artificial axoplasm' containing 45Ca and either CaEGTA/EGTA or CaDTPA/DTPA buffers giving various nominal values of [Ca2+]. The axoplasm samples were centrifuged at 100 000 X g for 30 min to form a pellet and the percentage of 45Ca bound to the pellet was determined. The fraction of bound calcium rose with increasing values of [Ca2+] along an S-shaped curve. Carbonyl cyanide p-trifluoromethoxyphenylhydrazone (FCCP) was used to reveal the presence of mitochondrial Ca uptake. At physiological values of [Ca2+], around 100 nM, Ca uptake was insensitive to FCCP. As [Ca2+] was elevated, increasing sensitivity to FCCP was noted above [Ca2+] = 0.5 microM. At low values of [Ca2+], including the physiological range, Ca binding was significantly reduced by vanadate and quercetin, agents known to inhibit Ca uptake mediated by Ca2+-activated ATPase reactions. Inhibition of Ca binding by these agents was approximately 50% at physiological values of [Ca2+]. ATP depletion decreased the percentage of Ca binding by the pellet at physiological [Ca2+]. The results suggest that about 50% of the Ca buffering by particulate matter in axoplasm is via organelles requiring intact Ca2+-ATPase reaction at physiological values of [Ca2+].

摘要

将刚分离出的黏液虫巨型轴突的轴浆与少量含有45Ca以及CaEGTA/EGTA或CaDTPA/DTPA缓冲液的“人工轴浆”混合,这些缓冲液可给出不同的[Ca2+]标称值。将轴浆样品在100000×g下离心30分钟以形成沉淀,并测定结合到沉淀上的45Ca的百分比。结合钙的比例随着[Ca2+]值的增加沿S形曲线上升。羰基氰化物对三氟甲氧基苯腙(FCCP)用于揭示线粒体钙摄取的存在。在[Ca2+]的生理值(约100 nM)时,钙摄取对FCCP不敏感。随着[Ca2+]升高,在[Ca2+]=0.5 microM以上观察到对FCCP的敏感性增加。在包括生理范围在内的低[Ca2+]值时,钒酸盐和槲皮素可显著降低钙结合,这两种物质已知可抑制由Ca2+激活的ATP酶反应介导的钙摄取。在[Ca2+]的生理值时,这些物质对钙结合的抑制约为50%。ATP耗竭降低了在生理[Ca2+]下沉淀结合钙的百分比。结果表明,轴浆中颗粒物质对钙的缓冲作用约50%是通过在[Ca2+]生理值时需要完整Ca2+-ATP酶反应的细胞器实现的。

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