Hafner M, Petzelt C
Institute of Cell and Tumor Biology, German Cancer Research Center, Heidelberg.
Nature. 1987;330(6145):264-6. doi: 10.1038/330264a0.
Calcium ions are important in the regulation of mitotic apparatus assembly and in the control of chromosome movement. Changes in intracellular free calcium concentration, [Ca2+]i are achieved by an intracellular calcium-transport system which is highly conserved in different cell types. A membrane-bound protein of relative molecular mass (Mr) 46,000 (46K) is part of this transport system and has been implicated in the regulation of the [Ca2+]i changes associated with the course of mitosis. A monoclonal antibody against this 46K protein inhibits Ca2+-uptake into isolated Ca2+-sequestering membranes and specifically labels membranes associated with the mitotic apparatus of sea urchin embryos. Here we investigate the relationship between the intracellular calcium transport system and mitosis by injection of this monoclonal antibody into living mitotic sea urchin embryos. We find that after injection the intracellular free calcium increases up to 10(-6) M, the mitotic apparatus is rapidly destroyed and the cell is irreversibly blocked in its development.
钙离子在有丝分裂器组装的调节以及染色体运动的控制中起着重要作用。细胞内游离钙浓度[Ca2+]i的变化是通过一个在不同细胞类型中高度保守的细胞内钙转运系统实现的。一种相对分子质量(Mr)为46,000(46K)的膜结合蛋白是这个转运系统的一部分,并与有丝分裂过程中[Ca2+]i变化的调节有关。针对这种46K蛋白的单克隆抗体可抑制钙离子摄取到分离的钙离子隔离膜中,并特异性标记与海胆胚胎有丝分裂器相关的膜。在这里,我们通过将这种单克隆抗体注射到活的有丝分裂海胆胚胎中来研究细胞内钙转运系统与有丝分裂之间的关系。我们发现注射后细胞内游离钙增加到10^(-6) M,有丝分裂器迅速被破坏,细胞在其发育过程中被不可逆地阻断。