Berg K
Department of Biophysics, Institute for Cancer Research, Montebello, Oslo, Norway.
Biochim Biophys Acta. 1992 Jun 10;1135(2):147-53. doi: 10.1016/0167-4889(92)90130-4.
Several porphyrins, including tetra(4-sulfonatophenyl)porphine, sensitize cells to photoinactivation. The treatment leads to an accumulation of cells in mitosis, directly or indirectly due to a perturbation of the mitotic spindle. The present work relates to the target for this mode of action. Cells incubated with tetra(4-sulfonatophenyl)porphine were exposed to light and the microtubules were quantified 30 min after light exposure. The amount of microtubules decreased with increasing fluences. The reduction in the amount of microtubules after light exposure was enhanced by prior treatment with nocodazole (1 microgram/ml for 20 min) or low temperature (1 degree C for 60 min). When nocodazole was combined with the photochemical treatment the extent of the inhibition of microtubule formation was dose-dependent only for the lowest fluences applied. Additional light exposure did not further reduce the amount of microtubules 30 min after light exposure. The results presented indicate that the unpolymerized fraction of tubulin is the target for photochemical inhibition of microtubule formation.
包括四(4-磺酸苯基)卟啉在内的几种卟啉可使细胞对光灭活敏感。这种处理会导致细胞在有丝分裂中积累,这是由于有丝分裂纺锤体受到干扰而直接或间接造成的。目前的工作涉及这种作用方式的靶点。用四(4-磺酸苯基)卟啉孵育的细胞经光照处理,在光照30分钟后对微管进行定量分析。微管的数量随着光通量的增加而减少。用诺考达唑(1微克/毫升,处理20分钟)或低温(1℃,处理60分钟)预处理可增强光照后微管数量的减少。当诺考达唑与光化学处理联合使用时,微管形成的抑制程度仅在应用的最低光通量下呈剂量依赖性。额外的光照在光照30分钟后并未进一步减少微管的数量。所呈现的结果表明,微管蛋白的未聚合部分是光化学抑制微管形成的靶点。