McCann M C, Stacey N J, Wilson R, Roberts K
Department of Cell Biology, John Innes Institute, Norwich, UK.
J Cell Sci. 1993 Dec;106 ( Pt 4):1347-56. doi: 10.1242/jcs.106.4.1347.
When round cells from a carrot cell suspension culture are diluted into fresh medium without auxin, the cells elongate to almost 50 times their original diameter within three days. This process of elongation is accompanied by changes in both the composition and the orientation of cell wall polymers. We have obtained information on the orientation of wall polymers in elongating cells by two complementary techniques, one using microscopy and one spectroscopy. Images obtained by the fast-freeze, deep-etch, rotary-shadowed replica technique show that walls of round carrot cells have no net orientation of cellulose microfibrils, and that many thin fibres can be seen cross-linking microfibrils. Walls of elongated carrot cells, in contrast, show a marked net orientation of microfibrils at right angles to the axis of elongation. Fourier Transform Infrared (FTIR) spectra obtained from defined areas of single cell walls show that walls of round carrot cells contain more protein, esters and phenolics in a given area (10 microns x 10 microns) than walls of elongated carrot cells, that contain proportionally more carbohydrate. The orientation of particular functional groups, with respect to the direction of elongation of the cell, can be determined by inserting a polariser into the path of the infrared beam, before it passes through a cell wall sample mounted on the stage of the microscope accessory. In the walls of elongated cells, ester bands, amide bands characteristic of proteins, and stretching frequencies in the carbohydrate region of the spectrum all show a net orientation transverse to the long axis of the cells. In the walls of round carrot cells, however, there is no such net orientation of polymers. Spectra obtained from 25 microns-thick fresh sections of the etiolated stem of a carrot seedling show that different wall components are polarised in different tissue types. These techniques have therefore enabled us to define differences in both the composition and the architecture of walls of elongating cells at the level of a single cell, and to suggest that polymers not previously thought to be ordered, such as pectin and protein, are strictly oriented in some wall types.
当将胡萝卜细胞悬浮培养物中的圆形细胞稀释到不含生长素的新鲜培养基中时,细胞在三天内伸长至几乎为其原始直径的50倍。这种伸长过程伴随着细胞壁聚合物的组成和取向的变化。我们通过两种互补技术获得了伸长细胞中壁聚合物取向的信息,一种使用显微镜技术,另一种使用光谱技术。通过快速冷冻、深度蚀刻、旋转阴影复型技术获得的图像显示,圆形胡萝卜细胞的壁没有纤维素微纤丝的净取向,并且可以看到许多细纤维交联微纤丝。相比之下,伸长的胡萝卜细胞的壁在与伸长轴成直角的方向上显示出微纤丝明显的净取向。从单个细胞壁的特定区域获得的傅里叶变换红外(FTIR)光谱表明,在给定区域(10微米×10微米)内,圆形胡萝卜细胞的壁比伸长的胡萝卜细胞的壁含有更多的蛋白质、酯和酚类物质,而伸长的胡萝卜细胞壁含有比例更高的碳水化合物。通过在红外光束穿过安装在显微镜附件载物台上的细胞壁样品之前,在光束路径中插入偏振器,可以确定特定官能团相对于细胞伸长方向的取向。在伸长细胞的壁中,酯带、蛋白质特有的酰胺带以及光谱碳水化合物区域的伸缩频率都显示出与细胞长轴横向的净取向。然而,在圆形胡萝卜细胞的壁中,聚合物没有这样的净取向。从胡萝卜幼苗黄化茎25微米厚的新鲜切片获得的光谱表明,不同的壁成分在不同的组织类型中是偏振的。因此,这些技术使我们能够在单个细胞水平上定义伸长细胞的壁在组成和结构上的差异,并表明以前认为无序的聚合物,如果胶和蛋白质,在某些壁类型中是严格取向的。