Korbelik M, Hung J, Lam S, Palcic B
Cancer Imaging, British Columbia Cancer Research Centre, Vancouver, Canada.
Photochem Photobiol. 1990 Feb;51(2):191-6. doi: 10.1111/j.1751-1097.1990.tb01702.x.
The cellular uptake of Photofrin II (PII) was studied using fluorescence imaging and chemical extraction. The influence of serum and low density lipoproteins (LDL) was examined under a variety of experimental conditions employing cultured human cells of different origins as well as a subcutaneously SMT-F tumor implanted in mice. Results showed that serum inhibited PII uptake. In general, LDL also inhibits PII uptake with the exception of an initial increase in the first 10-30 min when the cellular concentration of PII was measured by fluorescence imaging instead of chemical extraction. Our results suggest a possible de-aggregation process occurring upon internalization or binding of PII to LDL.
使用荧光成像和化学提取方法研究了二血卟啉醚(PII)的细胞摄取情况。在多种实验条件下,采用不同来源的培养人类细胞以及小鼠皮下植入的SMT - F肿瘤,检测了血清和低密度脂蛋白(LDL)的影响。结果表明,血清会抑制PII的摄取。一般来说,LDL也会抑制PII的摄取,但当通过荧光成像而非化学提取来测量PII的细胞浓度时,在最初的10 - 30分钟内会出现初始增加的情况。我们的结果表明,PII内化或与LDL结合时可能会发生解聚过程。