Sparagna G C, Gunter K K, Sheu S S, Gunter T E
Department of Biophysics, University of Rochester School of Medicine and Dentistry, New York 14642, USA.
J Biol Chem. 1995 Nov 17;270(46):27510-5. doi: 10.1074/jbc.270.46.27510.
A controversy in the field of bioenergetics has been whether mitochondria are capable of sequestering enough Ca2+ from cytosolic Ca2+ pulses to raise their intramitochondrial free Ca2+ level ([Ca2+]m). This is significant because an increase in [Ca2+]m has been linked to an increase in cellular metabolic rate through various mechanisms. To resolve this question, we exposed isolated liver mitochondria to physiological type pulses of Ca2+ produced using a pulse-generating system (Sparagna, G. C., Gunter, K. K., and Gunter, T. E. (1994) Anal. Biochem. 219, 96-103). We then measured the resulting mitochondrial Ca2+ uptake. The uniporter was previously thought to be the only specific Ca2+ uptake mechanism in mitochondria. Our studies have uncovered an additional uptake mechanism, the rapid mode of uptake or RaM, which functions at the beginning of each pulse and allows mitochondria to sequester a considerable amount of Ca2+ from short pulses. We have shown that the RaM is reset by decreasing the [Ca2+] between pulses for a very short time, making this uptake mode ideally suited for Ca2+ sequestration from Ca2+ pulse sequences. With rapid Ca2+ uptake occurring at the beginning of each pulse, liver mitochondria may be able to sequester sufficient Ca2+ from a short sequence of pulses to activate the cellular metabolic rate.
生物能量学领域一直存在的一个争议是,线粒体是否有能力从细胞质Ca2+脉冲中隔离足够的Ca2+,以提高其线粒体内游离Ca2+水平([Ca2+]m)。这一点很重要,因为通过各种机制,[Ca2+]m的增加与细胞代谢率的提高有关。为了解决这个问题,我们将分离的肝线粒体暴露于使用脉冲发生系统产生的生理性Ca2+脉冲中(Sparagna, G. C., Gunter, K. K., and Gunter, T. E. (1994) Anal. Biochem. 219, 96 - 103)。然后我们测量了由此产生的线粒体Ca2+摄取量。之前认为单向转运体是线粒体中唯一特定的Ca2+摄取机制。我们的研究发现了另一种摄取机制,即快速摄取模式或RaM,它在每个脉冲开始时起作用,并使线粒体能够从短脉冲中隔离相当数量的Ca2+。我们已经表明,通过在脉冲之间的极短时间内降低[Ca2+],RaM可以重置,这使得这种摄取模式非常适合从Ca2+脉冲序列中隔离Ca2+。由于在每个脉冲开始时都会发生快速Ca2+摄取,肝线粒体也许能够从短脉冲序列中隔离足够的Ca2+,以激活细胞代谢率。