Holdaway-Clarke T. L., Feijo J. A., Hackett G. R., Kunkel J. G., Hepler P. K.
Biology Department, Morrill Science Center, University of Massachusetts, Amherst, Massachusetts 01003.
Plant Cell. 1997 Nov;9(11):1999-2010. doi: 10.1105/tpc.9.11.1999.
Ratio images of cytosolic Ca2+ (Ca2+i) in growing, fura-2-dextran-loaded Lilium longiflorum pollen tubes taken at 3- to 5-sec intervals showed that the tip-focused [Ca2+]i gradient oscillates with the same period as growth. Similarly, measurement of the extracellular inward current, using a noninvasive ion-selective vibrating probe, indicated that the tip-directed extracellular Ca2+ (Ca2+o) current also oscillates with the same period as growth. Cross-correlation analysis revealed that whereas the [Ca2+]i gradient oscillates in phase with growth, the influx of Ca2+o lags by ~11 sec. Ion influx thus appears to follow growth, with the effect that the rate of growth at a given point determines the magnitude of the ion influx ~11 sec later. To explain the phase delay in the extracellular inward current, there must be a storage of Ca2+ for which we consider two possibilities: either the inward current represents the refilling of intracellular stores (capacitative calcium entry), or it represents the binding of the ion within the cell wall domain.
以3至5秒的间隔拍摄的、用fura - 2 - 葡聚糖加载的麝香百合花粉管生长过程中胞质Ca2+(Ca2+i)的比率图像显示,尖端聚焦的[Ca2+]i梯度与生长具有相同的振荡周期。同样,使用非侵入性离子选择性振动探针测量细胞外内向电流表明,尖端定向的细胞外Ca2+(Ca2+o)电流也与生长具有相同的振荡周期。互相关分析表明,虽然[Ca2+]i梯度与生长同步振荡,但Ca2+o的流入滞后约11秒。因此,离子流入似乎跟随生长,结果是在给定点的生长速率决定了约11秒后离子流入的大小。为了解释细胞外内向电流中的相位延迟,必须存在Ca2+的储存,对此我们考虑两种可能性:要么内向电流代表细胞内储存的再填充(容量性钙内流),要么它代表离子在细胞壁区域内的结合。