Pesacreta Thomas C
Microscopy Center, University of Louisiana Lafayette, P.O. Box 42451, Lafayette, Louisiana 70504 USA
Am J Bot. 2015 Sep;102(9):1422-33. doi: 10.3732/ajb.1500179. Epub 2015 Sep 7.
Primary vascular tissues of angiosperm and gymnosperm roots have significant anatomical differences. In gymnosperms, lack of protophloem sieve elements indicates a lengthy parenchymatous pathway for nutrient transport to the root apical meristem (RAM). Because F-actin is an essential component of transport in parenchyma cells, the distribution of F-actin was determined and compared among roots of several angiosperm and gymnosperm species.
Roots were chemically fixed and sectioned by hand to enable rapid production of many sections for labeling F-actin with phalloidin.
In angiosperm and gymnosperm root tips, relative intensity of F-actin labeling was highest in primary vascular tissues. Parenchyma cells in and around protophloem tended to have more F-actin while cells in cortical and protoxylem tissues tended to have less. In gymnosperms, phloem parenchyma was intensely labeled for several millimeters distal to the root apical meristem (RAM), and the F-actin is mostly composed of bundles that lie parallel to the root longitudinal axis. This orientation differed from the multidirectional arrangement of F-actin filaments in cortical cells. In angiosperms, intense F-actin labeling of pericycle and phloem parenchyma cells occurred around the first mature sieve elements.
F-actin is concentrated in the vascular cylinder, commonly in primary phloem parenchyma. In gymnosperms, the absence of sieve elements suggests that cytoplasmic streaming has a role in some aspect of phloem transport or unloading. In angiosperms, the region of intense F-actin labeling in the phloem parenchyma is limited to the extreme terminal portion of primary phloem where unloading of the earliest mature sieve elements occurs.
被子植物和裸子植物根的初生维管组织在解剖学上存在显著差异。在裸子植物中,缺乏原生韧皮部筛管分子表明营养物质向根尖分生组织(RAM)运输的薄壁组织途径较长。由于F-肌动蛋白是薄壁细胞运输的重要组成部分,因此测定并比较了几种被子植物和裸子植物根中F-肌动蛋白的分布。
对根进行化学固定并手工切片,以便快速制作许多切片,用鬼笔环肽标记F-肌动蛋白。
在被子植物和裸子植物根尖中,F-肌动蛋白标记的相对强度在初生维管组织中最高。原生韧皮部及其周围的薄壁细胞往往有更多的F-肌动蛋白,而皮层和原生木质部组织中的细胞则较少。在裸子植物中,在根尖分生组织(RAM)远端几毫米处,韧皮部薄壁组织被强烈标记,且F-肌动蛋白大多由与根纵轴平行的束状结构组成。这种取向不同于皮层细胞中F-肌动蛋白丝的多方向排列。在被子植物中,在第一个成熟筛管分子周围,中柱鞘和韧皮部薄壁细胞有强烈的F-肌动蛋白标记。
F-肌动蛋白集中在维管束中,通常在初生韧皮部薄壁组织中。在裸子植物中,筛管分子的缺失表明胞质环流在韧皮部运输或卸载的某些方面起作用。在被子植物中,韧皮部薄壁组织中F-肌动蛋白强烈标记的区域仅限于初生韧皮部的最末端部分,即最早成熟筛管分子卸载的部位。