Pu R, Robinson K R
Department of Biological Sciences, Purdue University, West Lafayette, IN 47907-1392, USA.
J Cell Sci. 1998 Nov;111 ( Pt 21):3197-207. doi: 10.1242/jcs.111.21.3197.
The predicted existence of cytoplasmic Ca2+ gradients during the photopolarization of the zygotes of the brown algae, Pelvetia and Fucus, has proved to be difficult to establish, and the downstream targets of the putative gradients are not known. We have used quantitative microinjection of the long excitation wavelength Ca2+ indicator, Calcium Crimson, and of antibodies against calmodulin to investigate these matters in the zygotes and early embryos of Pelvetia. We found that there is a window of cytoplasmic Calcium Crimson concentration that gives an adequate signal above autofluorescence yet allows normal development of the zygotes. As Calcium Crimson is not a ratiometric indicator, we injected other zygotes with a Ca2+-insensitive dye, rhodamine B, and imaged the cells at the same time that Calcium Crimson-injected cells were imaged. Ratios were calculated by dividing the averaged pixel values of Calcium Crimson images by the averaged pixel values of corresponding rhodamine B images. By this method, we observed the formation of a cytoplasmic Ca2+ gradient within one hour of the exposure of the cells to unilateral blue light during the photosensitive period. The region of high Ca2+ was localized to and predictive of the site of future rhizoid formation. We validated this somewhat indirect method by applying it to the growing rhizoid, where the existence of a tip-localized Ca2+ gradient is well established. The method clearly revealed the known gradient. The injection of ungerminated zygotes with antibodies made against Dictyostelium calmodulin inhibited germination, and this inhibition was abolished if the calmodulin antibodies were coinjected with an excess of purified maize calmodulin. Likewise, the growth of the rhizoids was inhibited by calmodulin antibody injections. The fungus-derived calmodulin antagonist, ophiobolin A, which has previously been shown to be a potent inhibitor of germination, also inhibited rhizoidal growth. Our results provide evidence that a cytoplasmic Ca2+ gradient is present during photopolarization and that calmodulin acts as a mediator of Ca2+ gradients throughout the early developmental processes of germination and rhizoidal growth in Pelvetia compressa.
在褐藻鹿角菜和墨角藻的合子光极化过程中,预测存在的细胞质Ca2+梯度已被证明难以确立,而且假定梯度的下游靶点也尚不清楚。我们使用长激发波长的Ca2+指示剂钙 Crimson以及抗钙调蛋白抗体进行定量显微注射,以研究鹿角菜合子和早期胚胎中的这些问题。我们发现存在一个细胞质钙 Crimson浓度窗口,该窗口能在自发荧光之上给出足够的信号,同时又能使合子正常发育。由于钙 Crimson不是比率型指示剂,我们向其他合子注射了一种对Ca2+不敏感的染料罗丹明B,并在对注射了钙 Crimson的细胞成像的同时对这些细胞进行成像。通过将钙 Crimson图像的平均像素值除以相应罗丹明B图像的平均像素值来计算比率。通过这种方法,我们观察到在感光期细胞暴露于单侧蓝光后一小时内形成了细胞质Ca2+梯度。高Ca2+区域定位于并可预测未来假根形成部位。我们将此方法应用于生长中的假根,验证了这种 somewhat间接的方法,在假根中尖端定位的Ca2+梯度的存在已得到充分证实。该方法清楚地揭示了已知的梯度。向未萌发的合子注射针对盘基网柄菌钙调蛋白制备的抗体可抑制萌发,如果将钙调蛋白抗体与过量纯化的玉米钙调蛋白共同注射,则这种抑制作用会被消除。同样,向假根注射钙调蛋白抗体也会抑制其生长。先前已证明是一种有效萌发抑制剂的真菌衍生钙调蛋白拮抗剂蛇孢菌素A也会抑制假根生长。我们的结果提供了证据,表明在光极化过程中存在细胞质Ca2+梯度,并且钙调蛋白在鹿角菜压缩体萌发和假根生长的整个早期发育过程中作为Ca2+梯度的介质发挥作用。