Gogvadze Vladimir, Walter Patrick B, Ames Bruce N
Department of Molecular and Cell Biology, University of California, Berkeley, California 94720, USA.
Arch Biochem Biophys. 2002 Feb 15;398(2):198-202. doi: 10.1006/abbi.2001.2721.
Isolated mitochondria loaded with Ca(2+) and then exposed to Fe(2+) show a transient release of Ca(2+). The magnitude of this response depends on the Ca(2+) loading and the kinetics of the response depends on the concentration of added Fe(2+). We investigated the Fe(2+)-induced Ca(2+) release mechanism by measuring mitochondrial Ca(2+) uptake in the presence of Fe(2+). The presence of Fe(2+) inhibits Ca(2+) uptake two times. Since mitochondria can cycle Ca(2+) across their inner membrane, the suppression of Ca(2+) uptake, but not release, results in an elevation of the extramitochondrial Ca(2+), thereby varying the steady state. The transient release of Ca(2+) initially observed from mitochondria appears to occur via the electroneutral 2H(+)/Ca(2+)-exchange mechanism, since it can be markedly decreased by cyclosporin A and does not involve lipid peroxidation. When Fe(2+) accumulation is completed, reuptake of released Ca(2+) into mitochondria resumes. Finally, we propose that Fe(2+) either inhibits Ca(2+) entry at the uniporter or is transported by it into the matrix.
装载有Ca(2+)的分离线粒体,随后暴露于Fe(2+)时,会出现Ca(2+)的瞬时释放。这种反应的幅度取决于Ca(2+)的装载量,而反应动力学则取决于添加的Fe(2+)的浓度。我们通过在存在Fe(2+)的情况下测量线粒体Ca(2+)摄取来研究Fe(2+)诱导的Ca(2+)释放机制。Fe(2+)的存在会抑制Ca(2+)摄取两次。由于线粒体可以使其内膜两侧的Ca(2+)循环,对Ca(2+)摄取而非释放的抑制会导致线粒体外Ca(2+)升高,从而改变稳态。最初从线粒体观察到的Ca(2+)瞬时释放似乎是通过电中性的2H(+)/Ca(2+)-交换机制发生的,因为它可被环孢菌素A显著降低且不涉及脂质过氧化。当Fe(2+)积累完成后,释放的Ca(2+)重新摄取回线粒体的过程恢复。最后,我们提出Fe(2+)要么在单向转运体处抑制Ca(2+)进入,要么被单向转运体转运到基质中。