Gaburjakova J, Gaburjakova M
Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences, Bratislava, Slovak Republic.
Acta Physiol (Oxf). 2008 Jul;193(3):219-27. doi: 10.1111/j.1748-1716.2008.01837.x. Epub 2008 Jan 17.
Two or more RYR2 channels reconstituted into a bilayer lipid membrane (BLM) can open and close either independently (single gating) or simultaneously (coupled gating). The coupled gating phenomenon has been suggested as an attractive candidate for a termination mechanism of Ca2+ release from the sarcoplasmic reticulum, required for periodic contraction and relaxation of cardiac muscle.
Using the method of reconstitution of a channel into the BLM, we investigated the potential effect of luminal Ca2+on the stability of the interaction between coupled RYR2 channels isolated from the rat heart. We introduced a new parameter - the coupling stability - for each detected simultaneous opening and closing and further averaged values for experiments performed under identical conditions.
We found that the coupling stability during simultaneous opening of RYR2 channels was significantly lower in comparison with the simultaneous closing under the same experimental conditions. Furthermore, high concentration of luminal Ca2+ (53 mmol L(-1)) as well as the absence of luminal Ca2+ noticeably destabilized functional coupling between coupled RYR2 channels during opening, in contrast to lower tested concentrations (8-20 mmol L(-1)).
We provide experimental evidence that the strength of interaction between coupled RYR2 channels depends on the functional state of the channels. Furthermore, we show, for the first time, the regulation role of luminal Ca2+ in the inter-RYR2 functional coupling in the rat heart.
重构到双层脂质膜(BLM)中的两个或更多个兰尼碱受体2(RYR2)通道可以独立地(单门控)或同时地(耦合门控)打开和关闭。耦合门控现象被认为是肌浆网Ca2+释放终止机制的一个有吸引力的候选者,而肌浆网Ca2+释放是心肌周期性收缩和舒张所必需的。
使用将通道重构到BLM中的方法,我们研究了腔内Ca2+对从大鼠心脏分离的耦合RYR2通道之间相互作用稳定性的潜在影响。对于每次检测到的同时打开和关闭,我们引入了一个新参数——耦合稳定性,并对在相同条件下进行的实验的进一步平均值进行了计算。
我们发现,在相同实验条件下,RYR2通道同时打开期间的耦合稳定性明显低于同时关闭期间的耦合稳定性。此外,与较低测试浓度(8 - 20 mmol L(-1))相比,高浓度的腔内Ca2+(53 mmol L(-1))以及腔内无Ca2+明显破坏了耦合RYR2通道打开期间的功能耦合。
我们提供了实验证据,证明耦合RYR2通道之间相互作用的强度取决于通道的功能状态。此外,我们首次展示了腔内Ca2+在大鼠心脏中RYR2之间功能耦合中的调节作用。