Olsson G M, Rungby J, Rundquist I, Brunk U T
Department of Pathology, Linköping University, Sweden.
Virchows Arch B Cell Pathol Incl Mol Pathol. 1989;56(4):263-9. doi: 10.1007/BF02890025.
The ability of living mouse peritoneal macrophages to retain the lysosomotropic photosensitizer acridine orange (AO) within their secondary lysosomes was studied with a novel cytofluorometric method. During exposure to blue light, cellular AO fluorescence turned from a red granular pattern to that of diffuse green. The resulting change in total fluorescence intensity versus time - a primary decline due to red fluorescence bleaching and a secondary recovery due to the spectral shift - was interpreted as the result of leakage of AO from the lysosomal vacuome. The hypothesis that this time course should be affected by changes in lysosomal membrane stability was tested by labilizing the lysosomes by exposure of cultured macrophages to either hypotonic medium or silver lactate. In hypotonic medium, the ability to retain AO decreased continuously. Exposure to low concentrations of silver lactate (10 microM) also decreased AO retention time. We suggest that this method could be used, within appropriate experimental conditions, to evaluate lysosomal membrane stability in living cells.
采用一种新型细胞荧光测定法,研究了活体小鼠腹膜巨噬细胞将溶酶体亲和性光敏剂吖啶橙(AO)保留在其次级溶酶体内的能力。在蓝光照射期间,细胞AO荧光从红色颗粒状模式转变为弥漫性绿色模式。总荧光强度随时间的变化结果——由于红色荧光漂白导致的一次下降和由于光谱偏移导致的二次恢复——被解释为AO从溶酶体腔室泄漏的结果。通过将培养的巨噬细胞暴露于低渗介质或乳酸银中来破坏溶酶体,从而检验了这一过程应受溶酶体膜稳定性变化影响的假设。在低渗介质中,保留AO的能力持续下降。暴露于低浓度的乳酸银(10微摩尔)也会缩短AO保留时间。我们认为,在适当的实验条件下,该方法可用于评估活细胞中的溶酶体膜稳定性。