Witte S
J Microsc. 1979 Aug;116(3):373-84. doi: 10.1111/j.1365-2818.1979.tb00222.x.
Intravital microscopic techniques were developed in order to measure plasma proteins: (1) circulating in the streaming blood of microcirculatory vessels of the exposed rat mesentery, (2) permeating the vessel wall, and (3) moving through the perivascular interstitial tissue. By means of the ultramicrospectrophotometry, the absorbance of proteins containing aromatic amino acids at 280 nm is measured. Absolute amounts of proteins in the range of picograms are measured in a circular measuring field with a diameter of 17 micrometers. Problems of calibration and of unspecific light scattering are discussed. The scanning microfluorometry makes use of the fluorescent labelling of the plasma proteins. Interstitial tissue with a capillary vessel containing labelled proteins is measured at high speed. A motor-driven object stage synchronized with a measuring system uses scanning lines to traverse the tissue. The data are then processed by a computer. In this way we get continuous quantitative information about the dynamics of protein permeability, starting from time zero. The measuring of the fluorescence intensity and the speed of the fluorometric system are further improved by a computerized 10 kHz scanning device.
(1)在暴露的大鼠肠系膜微循环血管的流动血液中循环的血浆蛋白;(2)渗透血管壁的血浆蛋白;(3)在血管周围间质组织中移动的血浆蛋白。通过超微量分光光度法,测量含芳香族氨基酸的蛋白质在280nm处的吸光度。在直径为17微米的圆形测量区域内测量皮克级范围内蛋白质的绝对量。讨论了校准和非特异性光散射问题。扫描显微荧光测定法利用血浆蛋白的荧光标记。对含有标记蛋白的毛细血管的间质组织进行高速测量。与测量系统同步的电动载物台使用扫描线穿过组织。然后由计算机处理数据。通过这种方式,从时间零点开始,我们可以获得有关蛋白质通透性动力学的连续定量信息。荧光测量系统的荧光强度测量和速度通过计算机化的10kHz扫描装置得到进一步提高。