Background and Objective: The purpose of this study was to compare the diff
erential susceptibility to photodynamic therapy (PDT) mediated damage in hu
man U-105MG glioma cells and CB-157MN meningioma cells in vitro using B-ami
nolevulinic acid (ALA) as photosensitizer, and to determine if growth facto
rs would enhance PDT-mediated damage of these cells.
Study Design/Materials and Methods: U105MG or CH-157MN cells were irradiate
d with polychromatic light in the presence of ALA. A Xenon lamp (150 W) was
used as the light source. For the study on the effect of growth factor on
ALA-PDT, cells were cultured in serum free medium for 24 hours. Epidermal g
rowth factor (EGF), basic fibroblast growth factor (bFGF), or platelet deri
ved growth factor BE (PDGF-BB) was added to achieve a final concentration o
f 50 ng/ml. 30 minutes later, cells were incubated with ALA (100 mu g/ml) f
or 24 hours, washed, and irradiated with light (11 J/cm(2)). MTT tetrazoliu
m assays were performed 24 hours after light irradiation.
Results: The inhibition of metabolic cellular function in U-105MG cells by
ALA depended on both light energy density and ALA concentration. The suscep
tibility to ALA-PDT was profoundly lower for CH-157MN meningioma cells than
U-105MG glioma cells. When incubated with ALA (100 mu g/ml), U-105MG cells
exhibited an LD50 around 8 J/cm(2) of light irradiation, whereas that of C
H-157MN cells was more than 25 J/cm(2). EGF, bFGF, or PDGF-BB did not have
any effects on the susceptibility of these two cell lines to ALA-PDT.
Conclusion: ALA-PDT was more effective in killing U-105MG glioma cells than
CH-157MN meningioma cells. The differential susceptibility was likely due
to differential accumulation of PpIX in these cells. EGF, bFGF, or PDGF-BB
did not have stimulatory or inhibitory effect on the efficiency of ALA-PDT.
(C) 1999 Wiley-Liss, Inc.