Hirata A, Baluk P, Fujiwara T, McDonald D M
Cardiovascular Research Institute, University of California, San Francisco 94143, USA.
Am J Physiol. 1995 Sep;269(3 Pt 1):L403-18. doi: 10.1152/ajplung.1995.269.3.L403.
The century-old histological technique of silver nitrate staining has proven to be extremely useful for visualizing endothelial cell borders and localizing endothelial gaps, but the significance of the staining is still not fully understood. To gain some insight into what silver nitrate stains, we developed a method that enabled us to use scanning electron microscopy with backscattered and secondary electron imaging to examine silver staining at endothelial cell borders of venules of the rat tracheal mucosa. We found that in normal venules, silver lines followed the smooth contour of cell borders. However, 1 min after endothelial permeability was increased by substance P, cell borders were irregular and displaced from the silver lines by as much as 4.3 microns, and the lines were accompanied by three types of silver deposits. Most common (46% of total) were annulus-shaped silver deposits that surrounded endothelial gaps. These deposits averaged 1.5 microns in width, were positioned symmetrically across cell borders, and were located at a depth of 0.3 micron beneath the luminal surface. Many endothelial gaps were partitioned into multiple pores (mean, 2.4) by fingerlike processes of endothelial cells. Surprisingly, the gaps occupied only 5.4% of the total area of the silver deposits and constituted 0.15% of the luminal surface of the leaky postcapillary venules. A second type of silver deposit (19% of total) was positioned asymmetrically with respect to the cell border and marked sites where endothelial cell margins still overlapped but appeared to be vertically separated by obliquely oriented gaps. A third type marked gaps at three-cell junctions; these were no more abundant than deposits elsewhere around the cell perimeter, suggesting that three-cell junctions were not unusually leaky sites. We conclude that silver nitrate marks endothelial cell borders and outlines endothelial cell gaps by staining an element of intercellular junctions. The annular shape of many silver deposits around gaps suggests that junctional elements in the apposing cells are separated during gap formation but are still present at the gap perimeter.
有着百年历史的硝酸银染色组织学技术已被证明在观察内皮细胞边界和定位内皮间隙方面极为有用,但该染色的意义仍未被完全理解。为了深入了解硝酸银所染之物,我们开发了一种方法,能够利用带有背散射和二次电子成像的扫描电子显微镜来检查大鼠气管黏膜小静脉内皮细胞边界处的银染情况。我们发现,在正常小静脉中,银线沿着细胞边界的平滑轮廓分布。然而,在通过P物质增加内皮通透性1分钟后,细胞边界变得不规则,与银线的距离最多偏移了4.3微米,并且这些银线伴有三种类型的银沉积物。最常见的(占总数的46%)是围绕内皮间隙的环状银沉积物。这些沉积物平均宽度为1.5微米,对称分布于细胞边界,位于管腔表面下方0.3微米深处。许多内皮间隙被内皮细胞的指状突起分隔成多个小孔(平均为2.4个)。令人惊讶的是,间隙仅占银沉积物总面积的5.4%,占渗漏性毛细血管后小静脉管腔表面的0.15%。第二种类型的银沉积物(占总数的19%)相对于细胞边界不对称定位,标记了内皮细胞边缘仍重叠但似乎被倾斜排列的间隙垂直分隔的部位。第三种类型标记了三细胞连接处的间隙;这些间隙并不比细胞周边其他部位的沉积物更丰富,这表明三细胞连接处并非异常渗漏的部位。我们得出结论,硝酸银通过对细胞间连接的一种成分进行染色来标记内皮细胞边界并勾勒出内皮细胞间隙。间隙周围许多银沉积物的环状形状表明,在间隙形成过程中,相邻细胞中的连接成分被分开,但仍存在于间隙周边。