Freedman R I, Zeira M, Dirksen E R
J Submicrosc Cytol. 1983 Jan;15(1):97-100.
Ciliated cortices isolated from rabbit trachea or oviduct can be reactivated with MgATP (2.4 mM, approx). We analyzed the effects of varying concentrations (0.1-100 mM) of Ca2+ and Mn2+ on the number of cortices which reactivated, as a percentage of the controls. Although reactivation can be inhibited at approximately 10(-2) M cation, we believe that this inhibition might be the result of decreasing MgATP due to competition by Ca2+ and Mn2+ for ATP cation binding sites, rather than cation interactions with the axoneme proper. In addition, whole isolated ciliated cells were obtained from trachea or oviduct by a simple, one step pronase digestion. These cells were incubated with the calcium ionophore A23187 in the presence of 2 mM Ca2+. Inhibition of ciliary activity in 50% of the cells did not occur until about 60 min of incubation. It is believed that what we have observed is cell toxicity rather than a direct effect on the cilia.
从兔气管或输卵管分离出的纤毛皮层可用大约2.4 mM的MgATP重新激活。我们分析了不同浓度(0.1 - 100 mM)的Ca2+和Mn2+对重新激活的皮层数量的影响,以对照组的百分比表示。尽管在大约10(-2) M阳离子浓度下重新激活可被抑制,但我们认为这种抑制可能是由于Ca2+和Mn2+与ATP阳离子结合位点竞争导致MgATP减少的结果,而不是阳离子与轴丝本身的相互作用。此外,通过简单的一步链霉蛋白酶消化从气管或输卵管获得了完整的分离纤毛细胞。这些细胞在2 mM Ca2+存在下与钙离子载体A23187一起孵育。直到孵育约60分钟后,50%的细胞的纤毛活性才受到抑制。据信,我们观察到的是细胞毒性而非对纤毛的直接影响。