Blomeyer Christoph A, Bazil Jason N, Stowe David F, Dash Ranjan K, Camara Amadou K S
Department of Anesthesiology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI, 48109, USA.
J Bioenerg Biomembr. 2016 Jun;48(3):175-88. doi: 10.1007/s10863-016-9644-1. Epub 2016 Jan 27.
The manner in which mitochondria take up and store Ca(2+) remains highly debated. Recent experimental and computational evidence has suggested the presence of at least two modes of Ca(2+) uptake and a complex Ca(2+) sequestration mechanism in mitochondria. But how Mg(2+) regulates these different modes of Ca(2+) uptake as well as mitochondrial Ca(2+) sequestration is not known. In this study, we investigated two different ways by which mitochondria take up and sequester Ca(2+) by using two different protocols. Isolated guinea pig cardiac mitochondria were exposed to varying concentrations of CaCl2 in the presence or absence of MgCl2. In the first protocol, A, CaCl2 was added to the respiration buffer containing isolated mitochondria, whereas in the second protocol, B, mitochondria were added to the respiration buffer with CaCl2 already present. Protocol A resulted first in a fast transitory uptake followed by a slow gradual uptake. In contrast, protocol B only revealed a slow and gradual Ca(2+) uptake, which was approximately 40 % of the slow uptake rate observed in protocol A. These two types of Ca(2+) uptake modes were differentially modulated by extra-matrix Mg(2+). That is, Mg(2+) markedly inhibited the slow mode of Ca(2+) uptake in both protocols in a concentration-dependent manner, but not the fast mode of uptake exhibited in protocol A. Mg(2+) also inhibited Na(+)-dependent Ca(2+) extrusion. The general Ca(2+) binding properties of the mitochondrial Ca(2+) sequestration system were reaffirmed and shown to be independent of the mode of Ca(2+) uptake, i.e. through the fast or slow mode of uptake. In addition, extra-matrix Mg(2+) hindered Ca(2+) sequestration. Our results indicate that mitochondria exhibit different modes of Ca(2+) uptake depending on the nature of exposure to extra-matrix Ca(2+), which are differentially sensitive to Mg(2+). The implications of these findings in cardiomyocytes are discussed.
线粒体摄取和储存Ca(2+)的方式仍存在激烈争论。最近的实验和计算证据表明,线粒体中至少存在两种Ca(2+)摄取模式以及一种复杂的Ca(2+)螯合机制。但Mg(2+)如何调节这些不同的Ca(2+)摄取模式以及线粒体Ca(2+)螯合尚不清楚。在本研究中,我们通过两种不同的方案研究了线粒体摄取和螯合Ca(2+)的两种不同方式。将分离的豚鼠心脏线粒体在有或无MgCl2的情况下暴露于不同浓度的CaCl2。在第一个方案A中,将CaCl2添加到含有分离线粒体的呼吸缓冲液中,而在第二个方案B中,将线粒体添加到已含有CaCl2的呼吸缓冲液中。方案A首先导致快速短暂摄取,随后是缓慢逐渐摄取。相比之下,方案B仅显示出缓慢逐渐的Ca(2+)摄取,约为方案A中观察到的缓慢摄取速率的40%。这两种Ca(2+)摄取模式受到线粒体外Mg(2+)的不同调节。也就是说,Mg(2+)以浓度依赖性方式显著抑制两种方案中Ca(2+)的缓慢摄取模式,但不抑制方案A中表现出的快速摄取模式。Mg(2+)还抑制Na(+)依赖性Ca(2+)外流。线粒体Ca(2+)螯合系统的一般Ca(2+)结合特性得到重申,并显示与Ca(2+)摄取模式无关,即通过快速或缓慢摄取模式。此外,线粒体外Mg(2+)阻碍Ca(2+)螯合。我们的结果表明,线粒体根据暴露于线粒体外Ca(2+)的性质表现出不同的Ca(2+)摄取模式,这些模式对Mg(2+)的敏感性不同。讨论了这些发现对心肌细胞的影响。