Subcellular localization of hematoporphyrin derivative in bladder tumor cells in culture

• Published in: Photochemistry and photobiology Vol. 51; no. 4; p. 451
• Main Authors: Shulok, J R, Wade, M H, Lin, C W
• Format: Journal Article
• Language: English
• Published: United States 01.04.1990
• Subjects: Cell Line; Hematoporphyrin Derivative; Hematoporphyrins - metabolism; Humans; Microscopy, Fluorescence; Radiation-Sensitizing Agents - metabolism; Tumor Cells, Cultured - cytology; Tumor Cells, Cultured - metabolism; Urinary Bladder Neoplasms
• ISSN: 0031-8655
• DOI: 10.1111/j.1751-1097.1990.tb01736.x

Mitochondria have been implicated as a primary subcellular site of porphyrin localization and photodestruction. However, other organelles including the cell membrane, lysosomes and nucleus have been shown to be damaged by hematoporphyrin derivative (HpD) photosensitized destruction as well. In this study we attempted to follow the translocation of the fluorescent components of HpD in human bladder tumor cells (MGH-U1) in culture to determine whether specific subcellular localization occurs over time. Following a 30 min exposure to HpD the cellular fluorescence was examined immediately and 1, 2, 4, and 24 h after HpD removal using fluorescence microscopy and an interactive laser cytometer. The in vitro translocation of dye appeared to be fairly rapid with fluorescence present at the cell membrane and later (1-2 h) within a perinuclear area of the cytoplasm. To determine whether HpD had become concentrated into a specific subcellular organelle, these fluorescence distribution patterns were compared with fluorescent marker dyes specific for mitochondria, endoplasmic reticulum and other membranous organelles. The HpD fluorescence did not appear to be as discrete as the dyes specific for mitochondria or endoplasmic reticulum but appeared similar to the diffuse cytomembrane stain. Finally, the interaction between the fluorescent components of HpD and the cellular constituents was evaluated using a "fluorescence redistribution after photobleaching" technique. The results indicated that the mean lateral diffusion for HpD in MGH-U1 cells was 1.05 x 10(-8) cm2/s, a rate closer to that of lipid diffusion (10(-8)) than that of protein diffusion (10(-10)).