Izzard C S, Lochner L R
J Cell Sci. 1980 Apr;42:81-116. doi: 10.1242/jcs.42.1.81.
The formatin of close contacts and focal contacts (ca. 30 nm and 10-15 nm separation distance respectively) has been studied during the movement of chick heart fibroblasts on planar substrates using interference-reflexion microscopy, and evaluated in the context of spreading and net movement. During spreading the overall advance of the margin of the close contact is steady, punctuated by periods in which it remains stationary, and only 5% of the time is spent withdrawing in contrast to the extreme leading edge. The close contact advances only where a lamellipodium has first extended free of the substrate (greater than or equal to 100 nm separation distance) ahead of the existing close contact. The new close contact is formed by the lamellipodium lowering to the substrate either progressively from its base forward or distally in patches which later join with the main close contact. New focal contacts are formed successively ahead of existing ones, either by microspikes or lamellipodia contacting the substrate locally ahead of the close contact, or within the close contact usually immediately, but not more than 1-2 microns, behind its margin. Examining the cell margin alternately with interference-reflexion and differential-interference contrast showed that the formation of the focal contact was preceded in 90% of the cases by the development of a linear structure in the form of a microspike (as expected), a short projection (< 2 microns long) of the lamellipodium, or a fibre within the lamellipodium, each of which could be traced to the cytoplasmic fibre typically associated with the focal contact. Stress fibres subsequently developed centripetally from these initial fibres. The different forms of the linear structure which preceded the focal contact were interchangeable, giving rise to one another, and we have evaluated that the structure common to each is probably a short bundle of microfilaments. The following features indicate that the close contact plays a primary role in marginal spreading: it is lost when spreading ceases; it is reformed when spreading resumes but only under the newly spread area; the advance of the margin of the thicker leading lamella closely follows that of the close contact; the advance of both can occur ahead of and is thus independent of existing focal contacts and associated stress fibres. We propose that the close contact provides the adhesion required to transmit to the substrate the forces involved in the forward movements of the marginal cytoplasm. The continual formation of focal contacts and stress fibres at the margin is consistent with their role, suggested by others, in drawing the bulk of the cell forward. These evaluations are discussed in the context of the form and distribution of contractile proteins in the cell margin. A primary role of the lamellipodia and microspikes in extending the cell margin and forming new adhesions, preparatory to further cytoplasmic movement, is established by this work.
利用干涉反射显微镜研究了鸡心脏成纤维细胞在平面基质上移动过程中紧密接触和粘着斑(分别约为30纳米和10 - 15纳米的分离距离)的形成,并在铺展和净移动的背景下进行了评估。在铺展过程中,紧密接触边缘的整体推进是稳定的,其间会有保持静止的时期,与极端前沿相比,只有5%的时间用于回撤。紧密接触仅在片状伪足在现有紧密接触前方首次伸展离开基质(分离距离大于或等于100纳米)的地方前进。新的紧密接触是由片状伪足从其基部向前逐渐下降到基质上形成的,或者是在片状伪足的远端以斑块形式下降,这些斑块随后与主要的紧密接触相连。新的粘着斑在现有粘着斑前方相继形成,要么是通过微刺或片状伪足在紧密接触前方局部接触基质形成,要么是在紧密接触内通常紧邻其边缘但不超过1 - 2微米的位置形成。交替使用干涉反射和微分干涉对比观察细胞边缘表明,在90%的情况下,粘着斑的形成之前会出现微刺(如预期)形式的线性结构、片状伪足的短突起(< 2微米长)或片状伪足内的纤维,每一种都可以追溯到典型的与粘着斑相关的细胞质纤维。应力纤维随后从这些初始纤维向心发展。粘着斑之前的线性结构的不同形式是可互换的,相互产生,我们评估每种结构共有的结构可能是一小束微丝。以下特征表明紧密接触在边缘铺展中起主要作用:铺展停止时紧密接触消失;铺展恢复时紧密接触重新形成,但仅在新铺展的区域下方;较厚的前沿片状伪足边缘的推进紧密跟随紧密接触的推进;两者的推进都可以在现有粘着斑和相关应力纤维之前发生,因此是独立的。我们提出紧密接触提供了将边缘细胞质向前运动所涉及的力传递到基质所需的粘附力。边缘粘着斑和应力纤维的持续形成与其他人提出的它们在拉动细胞主体向前的作用是一致的。这些评估在细胞边缘收缩蛋白的形式和分布的背景下进行了讨论。这项工作确立了片状伪足和微刺在扩展细胞边缘和形成新粘附方面的主要作用,为进一步的细胞质运动做准备。