TAXOL PROTECTS AGAINST CALCIUM-MEDIATED DEATH OF DIFFERENTIATED RAT PHEOCHROMOCYTOMA CELLS

被引:26
作者
BURKE, WJ
RAGHU, G
STRONG, R
机构
[1] AUDIE L MURPHY MEM VET ADM MED CTR, CTR GERIATR RES EDUC & CLIN 182, SAN ANTONIO, TX 78284 USA
[2] ST LOUIS UNIV, SCH MED, DEPT NEUROL, ST LOUIS, MO USA
[3] ST LOUIS UNIV, SCH MED, DEPT MED, ST LOUIS, MO 63104 USA
[4] ST LOUIS UNIV, SCH MED, DEPT ANAT, ST LOUIS, MO USA
[5] VET ADM MED CTR, ST LOUIS, MO 63125 USA
[6] UNIV TEXAS, HLTH SCI CTR, DEPT CELLULAR & STRUCT BIOL, SAN ANTONIO, TX 78284 USA
[7] UNIV TEXAS, HLTH SCI CTR, DEPT PHARMACOL, SAN ANTONIO, TX 78284 USA
关键词
TAXOL; CALCIUM-MEDIATED CELL DEATH; PC12; CELLS; NERVE GROWTH FACTOR;
D O I
10.1016/0024-3205(94)90074-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Elevated levels of intraneuronal calcium may contribute to neuronal death in both Alzheimer's disease and stroke. In part, this neuronal death may be due to calcium-induced disruption of microtubules and inhibition of axonal transport. Taxol stabilizes microtubules to disaggregation. To determine whether taxol could protect against calcium-mediated neuron eel death, a test system was established using a nerve growth factor-differentiated rat pheochromocytoma cell line (PC12 cells). PC12 cells were cultured with nerve growth factor to induce a neuronal phenotype. After 15 days, the cells were exposed to taxol, the calcium ionophore, A23187, or taxol plus ionophore for up to 24 h. Taxol alone reduced cell survival in a concentration dependent manner. At a concentration of 50 nM survival was reduced to between 63% and 84% of control after 4 h of exposure. The ionophore (1 mu M) variably reduced cell survival to between 10 and 55% at 4h. However, when taxol was added to the ionophore the cell survival was significantly increased by 1.5 to 4-fold. The protective effect of taxol lasted up to 24h. We conclude that taxol has a protective effect on calcium-mediated neurotoxicity. Drugs targeting underlying cellular mechanisms involved in calcium-mediated neuronal death may lead to successful therapy for Alzheimer's disease and stroke.
引用
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页码:PL313 / PL319
页数:7
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