Department of Biological Sciences, Stanford University, 94305, Stanford, CA, USA.
Planta. 1984 Mar;160(4):289-97. doi: 10.1007/BF00393409.
The interior of a new lateral organ, such as a leaf, arises from the products of periclinal divisions of sub-epidermal cells. The biophysical basis of the elongation of such a new axis is transverse (hoop) reinforcement of the cells by cellulose in the primary walls. This structural polarity is associated with transverse alignment of cortical microtubules. We have brought the histological and biophysical views together by showing that the new, periclinal, divisions are a prerequisite for a corresponding change in the orientation of the microtubular array in the daughter cells. Investigation of this relationship required development of criteria for assessing the predominant orientation of a microtubule array in a single section of known orientation. By obtaining information about the predominant orientation of microtubule arrays in the sub-epidermal cells, we were able to study structural polarity shifts which occurred as a detached leaf of Graptopetalum produced a new shoot. During organogenesis, the new polarity is seen only in cells which have divided periclinally. Following single periclinal divisions, cells are seen with microtubules in the old or new orientation or in a mixture of different orientations. Cells with more than one orientation of microtubules are probably at intermediate stages in the shift to the new polarity. Among cells which have undergone two consecutive periclinal divisions, the old polarity is no longer seen, all cells having high frequencies of microtubules in the new orientation. Such cells are either polarized in the new direction or nonpolarized. The shifts in polarity of the cells in the interior anticipate the appearance of the first leaf primordia. However, contrary to the expectations from the histological view of organogenesis, these shifts do not dominate the process. Concurrent polarity changes in the epidermis appear at least as important.
一个新的侧生器官(如叶子)的内部,是由表皮下细胞的垂周分裂产物产生的。这种新轴的伸长的生物物理基础是初生壁中纤维素对细胞的横向(箍状)加强。这种结构极性与皮层微管的横向排列有关。我们通过显示新的垂周分裂是子细胞中微管阵列方向相应变化的先决条件,将组织学和生物物理学观点结合在一起。研究这种关系需要开发评估单个已知取向切片中微管阵列主要取向的标准。通过获取关于表皮下细胞中微管阵列主要取向的信息,我们能够研究作为一个分离的Graptopetalum 叶子产生新梢时发生的结构极性转变。在器官发生过程中,新的极性仅见于垂周分裂的细胞中。在单次垂周分裂之后,可以看到微管处于旧的或新的取向,或者处于不同取向的混合物中。具有多于一种微管取向的细胞可能处于向新极性转变的中间阶段。在经历了两次连续垂周分裂的细胞中,不再看到旧的极性,所有细胞的微管都以新的取向出现高频率。这些细胞要么在新方向上极化,要么非极化。细胞极性的这种转变先于第一叶原基的出现。然而,与器官发生的组织学观点的预期相反,这些转变并没有主导这个过程。表皮中的并发极性变化似乎至少同样重要。