CONSTRUCTION OF BAXα HIGH EXPRESSING PC-12 CELL LINE AND THE MECHANISMS OF (-)CLAUSENAMIDE IN INHIBITING APOPTOSIS
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Abstract
AIM PC12 cells with high expression of Baxα were used to study the antiapoptotic effects of (-)clausenamide.METHODS The Baxα cDNA was first subcloned from pBluescript SK to eukaryotic vector pcDNA3. The pcDNA3-Baxα was transformed into PC12 cells. PC12 cells with high expression of Baxα were subjected to neurotoxin 6-hydroxydopamine 100 μmol.L-1 to induce apoptosis.RESULTS The Baxα expressing PC-12 cells has a higher apoptosis percentage compared with the vector transfected controls(49.96% vs 32.9%). (-)Clausenamide(0.1~10 μmol*L-1) was shown to significantly decrease the apoptotic cells measured by flowcytometry method. (-)Clausenamide(0.1~1.0 μmol.L-1) also improved the compromised mitochondrial membrane potential. CONCLUSION These findings suggest that (-)clausenamide may save the cells from apoptosis and provide a clue to the therapy of neurodegenerative diseases.
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