Höfte Herman, Voxeur Aline
Institut Jean-Pierre Bourgin, INRA, Centre National pour la Recherche Scientifique, AgroParisTech, Université Paris-Saclay, RD10, 78026, Versailles Cedex, France.
Institut Jean-Pierre Bourgin, INRA, Centre National pour la Recherche Scientifique, AgroParisTech, Université Paris-Saclay, RD10, 78026, Versailles Cedex, France.
Curr Biol. 2017 Sep 11;27(17):R865-R870. doi: 10.1016/j.cub.2017.05.025.
Plants are able to generate large leaf surfaces that act as two-dimensional solar panels with a minimum investment in building material, thanks to a hydrostatic skeleton. This requires high intracellular pressures (up to 1 MPa), which depend on the presence of strong cell walls. The walls of growing cells (also called primary walls), are remarkably able to reconcile extreme tensile strength (up to 100 MPa) with the extensibility necessary for growth. All walled organisms are confronted with this dilemma - the need to balance strength and extensibility - and bacteria, fungi and plants have evolved independent solutions to cope. In this Primer, we discuss how plant cells have solved this problem, allowing them to support often very large increases in volume and to develop a broad variety of shapes (Figure 1A,B,D). This shape variation reflects the targeted deposition of wall material combined with local variations in cell-wall extensibility, processes that remain incompletely understood. Once the cell has reached its final size, it can lay down secondary wall layers, the composition and architecture of which are optimized to exert specific functions in different cell types (Figure 1E-G). Such functions include: providing mechanical support, for instance, for fibre cells in tree trunks or grass internodes; impermeabilising and strengthening vascular tissue to resist the negative pressure of the transpiration stream; increasing the surface area of the plasma membrane to facilitate solute exchange between cells (Figure 1C); or allowing important elastic deformation, for instance, to support the opening and closing of stomates. Specialized secondary walls, such as those constituting seed mucilage, are stored in a dehydrated form in seedcoat epidermis cells and show rapid swelling upon hydration of the seed. Other walls, in particular in reserve tissues, can accommodate large amounts of storage polysaccharides, which can be easily mobilized as a carbon source. Here we will discuss some general principles underlying wall architecture and wall growth that have emerged from recent studies, as well as future questions for investigation (Box 1).
借助流体静力骨骼,植物能够生成大的叶表面,这些叶表面充当二维太阳能板,只需投入最少的建筑材料。这需要高的细胞内压力(高达1兆帕),而这取决于坚固细胞壁的存在。正在生长的细胞的壁(也称为初生壁)能够显著地将极高的抗张强度(高达100兆帕)与生长所需的可扩展性协调起来。所有有细胞壁的生物体都面临这个两难境地——需要平衡强度和可扩展性——细菌、真菌和植物已经进化出独立的解决方案来应对。在本入门文章中,我们将讨论植物细胞是如何解决这个问题的,使它们能够支持通常非常大的体积增加,并发育出各种各样的形状(图1A、B、D)。这种形状变化反映了细胞壁材料的定向沉积以及细胞壁可扩展性的局部变化,而这些过程仍未完全被理解。一旦细胞达到其最终大小,它就可以沉积次生壁层,其次生壁层的组成和结构经过优化,以在不同细胞类型中发挥特定功能(图1E - G)。这些功能包括:提供机械支撑,例如为树干或草节间的纤维细胞提供支撑;使维管组织不透水并增强其强度,以抵抗蒸腾流的负压;增加质膜的表面积,以促进细胞间的溶质交换(图1C);或者允许重要的弹性变形,例如支持气孔的开闭。专门的次生壁,如构成种子黏液的那些次生壁,以脱水形式储存在种皮表皮细胞中,并在种子吸水时迅速膨胀。其他细胞壁,特别是在贮藏组织中的细胞壁,可以容纳大量的贮藏多糖,这些多糖可以很容易地作为碳源被调动。在这里,我们将讨论近期研究中出现的细胞壁结构和细胞壁生长的一些一般原则,以及未来有待研究的问题(方框1)。