Henry C B, Duling B R
Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, Virginia 22906, USA.
Am J Physiol. 1999 Aug;277(2):H508-14. doi: 10.1152/ajpheart.1999.277.2.H508.
The endothelial cell glycocalyx influences blood flow and presents a selective barrier to movement of macromolecules from plasma to the endothelial surface. In the hamster cremaster microcirculation, FITC-labeled Dextran 70 and larger molecules are excluded from a region extending almost 0.5 micrometer from the endothelial surface into the lumen. Red blood cells under normal flow conditions are excluded from a region extending even farther into the lumen. Examination of cultured endothelial cells has shown that the glycocalyx contains hyaluronan, a glycosaminoglycan which is known to create matrices with molecular sieving properties. To test the hypothesis that hyaluronan might be involved in establishing the permeation properties of the apical surface glycocalyx in vivo, hamster microvessels in the cremaster muscle were visualized using video microscopy. After infusion of one of several FITC-dextrans (70, 145, 580, and 2,000 kDa) via a femoral cannula, microvessels were observed with bright-field and fluorescence microscopy to obtain estimates of the anatomic diameters and the widths of fluorescent dextran columns and of red blood cell columns (means +/- SE). The widths of the red blood cell and dextran exclusion zones were calculated as one-half the difference between the bright-field anatomic diameter and the width of the red blood cell column or dextran column. After 1 h of treatment with active Streptomyces hyaluronidase, there was a significant increase in access of 70- and 145-kDa FITC-dextrans to the space bounded by the apical glycocalyx, but no increase in access of the red blood cells or in the anatomic diameter in capillaries, arterioles, and venules. Hyaluronidase had no effect on access of FITC-Dextrans 580 and 2,000. Infusion of a mixture of hyaluronan and chondroitin sulfate after enzyme treatment reconstituted the glycocalyx, although treatment with either molecule separately had no effect. These results suggest that cell surface hyaluronan plays a role in regulating or establishing permeation of the apical glycocalyx to macromolecules. This finding and our prior observations suggest that hyaluronan and other glycoconjugates are required for assembly of the matrix on the endothelial surface. We hypothesize that hyaluronidase creates a more open matrix, enabling smaller dextran molecules to penetrate deeper into the glycocalyx.
内皮细胞糖萼影响血流,并对大分子从血浆向内皮表面的移动形成选择性屏障。在仓鼠提睾肌微循环中,异硫氰酸荧光素标记的葡聚糖70及更大的分子被排除在从内皮表面向管腔延伸近0.5微米的区域之外。在正常血流条件下,红细胞被排除在向管腔延伸更远的区域之外。对培养的内皮细胞的研究表明,糖萼含有透明质酸,一种已知具有分子筛分特性并能形成基质的糖胺聚糖。为了验证透明质酸可能参与体内顶端表面糖萼渗透特性建立的假说,使用视频显微镜观察了仓鼠提睾肌中的微血管。通过股动脉插管注入几种异硫氰酸荧光素标记的葡聚糖(70、145、580和2000 kDa)之一后,用明场和荧光显微镜观察微血管,以获得解剖直径、荧光葡聚糖柱宽度和红细胞柱宽度的估计值(平均值±标准误)。红细胞和葡聚糖排除区的宽度计算为明场解剖直径与红细胞柱或葡聚糖柱宽度之差的一半。用活性链霉菌透明质酸酶处理1小时后,70 kDa和145 kDa的异硫氰酸荧光素标记的葡聚糖进入顶端糖萼界定空间的量显著增加,但红细胞的进入量或毛细血管、小动脉和小静脉的解剖直径没有增加。透明质酸酶对580 kDa和2000 kDa的异硫氰酸荧光素标记的葡聚糖的进入没有影响。酶处理后注入透明质酸和硫酸软骨素的混合物可重建糖萼,尽管单独用任何一种分子处理均无效果。这些结果表明,细胞表面透明质酸在调节或建立顶端糖萼对大分子的渗透性方面发挥作用。这一发现以及我们之前的观察结果表明,透明质酸和其他糖缀合物是内皮表面基质组装所必需的。我们推测,透明质酸酶会形成一个更开放的基质,使较小的葡聚糖分子能够更深地穿透糖萼。