Williams D A, Cody S H, Gehring C A, Parish R W, Harris P J
Department of Physiology, University of Melbourne, Parkville, Victoria, Australia.
Cell Calcium. 1990 Apr;11(4):291-7. doi: 10.1016/0143-4160(90)90006-g.
Laser-scanning confocal microscopy has been used in conjunction with Fluo-3, a highly fluorescent visible wavelength probe for Ca2+, to visualize Ca2(+)-dynamics in the function of living plant cells. This combination has overcome many of the problems that have limited the use of fluorescence imaging techniques in the study of the role of cations (Ca2+ and H+) in plant cell physiology and enables these processes to be studied in single cells within intact plant tissue preparations. Maize coleoptiles respond to application of ionophores and plant growth hormones with elevations in cytosolic Ca2+ that can be resolved with a high degree of spatial resolution and can be interpreted quantitatively.
激光扫描共聚焦显微镜已与Fluo-3(一种用于Ca2+的高荧光可见波长探针)结合使用,以可视化活植物细胞功能中的Ca2(+)-动态变化。这种结合克服了许多限制荧光成像技术在研究阳离子(Ca2+和H+)在植物细胞生理学中的作用时应用的问题,并使这些过程能够在完整植物组织制备物中的单个细胞中进行研究。玉米胚芽鞘对离子载体和植物生长激素的应用会产生胞质Ca2+升高的反应,这种升高可以通过高空间分辨率解析并进行定量解释。