Neurodegenerative disorders are characterized by a massive loss of nerve cells. The neuronal cell death is accompanied by an increased
cholesterol release and conversion of
cholesterol into the polar metabolite,
24-hydroxycholesterol (24-OH-Chol), appears to be an important mechanism in the central nervous system for eliminating
cholesterol from the brain. We tested the influence of 24-OH-Chol on SH-SY5Y human
neuroblastoma cells by recording cell morphology,
Trypan blue exclusion, LDH-release into the culture medium, intracellular
calcium and
reactive oxygen species (ROS). The exposure of SH-SY5Y human
neuroblastoma cells to 50 microM 24-OH-Chol led to a 90% loss in cell viability within 30 h, the LDH-release into the medium increased rapidly after 24 h, and after 24 to 30 h we found an elevation in intracellular
calcium. These results show that, in a physiological concentration range, 24-OH-Chol damages neuronal cells, thus we speculate that this
oxysterol may be involved in the etiology of
neurodegenerative disease.