Nicholls David G, Chalmers Susan
Buck Institute for Age Research, Novato, California 94945, USA.
J Bioenerg Biomembr. 2004 Aug;36(4):277-81. doi: 10.1023/B:JOBB.0000041753.52832.f3.
The extraordinary capacity of isolated mitochondria to accumulate Ca(2+) has been established for more than 40 years. The distinct kinetics of the independent uptake and efflux pathways accounts for the dual functionality of the transport process to either modulate matrix free Ca(2+) concentrations or to act as temporary stores of large amounts of Ca(2+) in the presence of phosphate. One puzzle has been the nature of the matrix calcium phosphate complex, since matrix free Ca(2+) seems to be buffered in the region of 1-5 microM in the presence of phosphate while millimolar Ca(2+) remains soluble in in vitro media. The key seems to be the elevated matrix pH and the third-power relationship of the PO(4)(3-) concentration with pH. Taking this into account we may now finally have a model that explains the major features of physiological mitochondrial Ca(2+) transport.
孤立线粒体积累Ca(2+)的非凡能力已被确认超过40年。独立摄取和外流途径的独特动力学解释了运输过程的双重功能,即调节基质游离Ca(2+)浓度或在有磷酸盐存在时充当大量Ca(2+)的临时储存库。一个谜题是基质磷酸钙复合物的性质,因为在有磷酸盐存在的情况下,基质游离Ca(2+)似乎在1-5 microM区域被缓冲,而毫摩尔级的Ca(2+)在体外培养基中仍可溶。关键似乎在于升高的基质pH值以及PO(4)(3-)浓度与pH值的三次方关系。考虑到这一点,我们现在最终可能有一个模型来解释生理性线粒体Ca(2+)运输的主要特征。