Koopdonk-Kool J M, Van Noorden C J
Academic Medical Center, University of Amsterdam, Laboratory of Cell Biology and Histology, The Netherlands.
Acta Histochem. 1995 Oct;97(4):409-19. doi: 10.1016/S0065-1281(11)80066-8.
A quantitative histochemical assay has been developed for measurement of endogenous substrate concentrations in cryostat sections using a colorimetric visualization technique. Model sections of frozen gelatin solutions with known concentrations of glucose-6-phosphate (G6P) were sandwiched with a second cryostat section containing glucose-6-phosphate dehydrogenase (G6PDH) and all other compounds (with the exception of G6P) that are necessary for the demonstration of G6PDH activity with a tetrazolium salt method. After 60 min of incubation, G6P was converted with concomitant formazan production. The amount of formazan generated was measured cytophotometrically and used as a parameter of the G6P concentration in the first section. A calibration graph was obtained with a high correlation coefficient, allowing the conversion of mean integrated absorbance values into absolute substrate concentrations. The method was highly reproducible, and the recovery of G6P was 85 +/- 4% irrespective section thickness (4-20 microns) and G6P concentration (0.08-1.6 mM) in the sections. The sensitivity of the tetrazolium-linked method appeared to be 100 microM in 20 microns thick sections. This sensitivity enables the measurement of physiological substrate concentrations in tissue sections. Spatial resolution was approximately 150 microns, indicating a relatively high rate of diffusion of G6P during the reaction. The model study shows that the method described here allows the quantitative determination of substrate concentrations in tissue sections. These endogenous substrate concentrations are necessary for the calculation of local metabolic fluxes when determined in combination with local enzyme activities and kinetics, thus giving a more accurate reflection of in situ metabolic heterogeneity of tissues.
已开发出一种定量组织化学测定法,用于使用比色可视化技术测量低温恒温器切片中的内源性底物浓度。将含有已知浓度葡萄糖-6-磷酸(G6P)的冷冻明胶溶液的模型切片与另一个低温恒温器切片夹在一起,该切片含有葡萄糖-6-磷酸脱氢酶(G6PDH)以及用四唑盐法显示G6PDH活性所需的所有其他化合物(G6P除外)。孵育60分钟后,G6P被转化并伴随生成甲臜。通过细胞光度法测量生成的甲臜量,并将其用作第一切片中G6P浓度的参数。获得了具有高相关系数的校准曲线,可将平均积分吸光度值转换为绝对底物浓度。该方法具有高度可重复性,无论切片厚度(4-20微米)和切片中G6P浓度(0.08-1.6 mM)如何,G6P的回收率均为85±4%。在20微米厚的切片中,四唑连接法的灵敏度似乎为100 microM。这种灵敏度能够测量组织切片中的生理底物浓度。空间分辨率约为150微米,表明反应过程中G6P的扩散速率相对较高。模型研究表明此处描述的方法可对组织切片中的底物浓度进行定量测定。当与局部酶活性和动力学结合测定时,这些内源性底物浓度对于计算局部代谢通量是必要的,从而能更准确地反映组织原位代谢异质性。