Casley-Smith J R
Experientia. 1976 Jan 15;32(1):1-12. doi: 10.1007/BF01932595.
The structure and function of blood capillaries, as related to permeability, depends on tight, close and (in injured vessels) open junctional regions, small vesicles, vacuoles (in injured vessels) and fenestrae. The basement membrane presents a hindrance to the larger macromolecules, at high flow rates, but not to small molecules. The connective tissue channels are probably the paths by which macromolecules, and most of the small ones, pass from the arterial-limbs to the venous ones, and to the lymphatics. In some regions these channels are grouped in special systems: the prelymphatics. The initial lymphatics take up material via open junctions, which close during tissue-compression. The collecting lymphatics retain the lymph because they do not have open junctions. In the close junctional regions the motive force for water flow is the result of Starling's forces; diffusion is very important for other small molecules. The small vesicles transport macromolecules slowly by Brownian motion, as may the vacuoles, but possibly these latter are moved actively. There is much evidence that colloids can develop high effective osmotic pressures even across pores much larger than their molecules, and that proteins can be dragged up a concentration gradient by the resultant fluid flow. On the basis of this, hypotheses have been developed about the functioning of venous-limb fenestrae and the initial lymphatics, for which there is much theoretical, in vitro, and in vivo evidence. Thus, in fenestrated regions there is held to be a large local circulation through the tissues, of which a quantitatively small, but qualitatively vital, part goes to the lymphatics. Material is considered usually to enter these latter because of the relative concentration of the lymph. It is becoming increasingly evident that in the study of the microvasculature, as with other systems, there is much to be gained by quantifying fine structural observations and by combining and contrasting this data, via physical laws, with that obtained by other methods where the characteristics of whole organs and regions are studied. Thus one can obtain interrelated information, which is not possible by either method alone, and which gives us a vital, comprehensive, perspective of the ways in which whole systems function, and how different systems interact. In this paper I shall show how this approach has yielded much that is new about the functioning of different kinds of blood capillaries, of the tissue channels, of the whole lymphatic system, and of the ways they affect each other.
毛细血管的结构和功能,与通透性相关,取决于紧密、闭合以及(在受损血管中)开放的连接区域、小泡、液泡(在受损血管中)和窗孔。基底膜在高流速时对较大的大分子构成阻碍,但对小分子则不然。结缔组织通道可能是大分子以及大多数小分子从动脉端流向静脉端并进入淋巴管的路径。在某些区域,这些通道聚集成特殊系统:即前淋巴管。初始淋巴管通过开放连接摄取物质,这些连接在组织受压时关闭。集合淋巴管保留淋巴,因为它们没有开放连接。在紧密连接区域,水流的动力是斯塔林力的结果;扩散对其他小分子非常重要。小泡通过布朗运动缓慢运输大分子,液泡可能也是如此,但后者可能是主动移动的。有大量证据表明,胶体即使在比其分子大得多的孔隙中也能产生高有效渗透压,并且蛋白质可以被由此产生的流体流动沿浓度梯度向上拖动。基于此,已经提出了关于静脉端窗孔和初始淋巴管功能的假说,对此有许多理论、体外和体内证据。因此,在有窗孔的区域,认为存在通过组织的大量局部循环,其中数量上少但质量上至关重要的一部分进入淋巴管。通常认为物质进入后者是由于淋巴的相对浓度。越来越明显的是,在微血管系统的研究中,与其他系统一样,通过对精细结构观察进行量化,并通过物理定律将这些数据与通过研究整个器官和区域特征的其他方法获得的数据进行组合和对比,可以获得很多收获。这样就可以获得相互关联的信息,这是单独使用任何一种方法都无法实现的,并且能让我们从整体系统功能以及不同系统如何相互作用的角度获得至关重要、全面的认识。在本文中,我将展示这种方法如何产生了许多关于不同类型毛细血管、组织通道、整个淋巴系统及其相互影响方式的新认识。