Title :
Cardiomyocyte Apoptosis Were Inhibited by Anti-Fas Ribozyme
Author :
Zhu, Xiao-gang ; Zheng, Shi-Ying ; Dong Jiang ; Ge, Jin-Feng
Author_Institution :
Dept. of Anesthesiology, First Affiliated Hosp. of Suzhou Univ., Suzhou, China
Abstract :
We investigate the effects of anti-Fas ribozyme on Fas expression and apoptosis in primary cultured Neonatal mouse ventricular myocytes. Neonatal mouse ventricular myocytes were isolated by using collagenase irrigation. A hammerhead ribozyme targeting the Fas mRNA was constructed, and transfected into Neonatal mouse ventricular myocytes via Effectene. Then Fas expression in Neonatal mouse ventricular myocytes was detected by RT-PCR and western blotting.After being treated with anti-Fas antibody (JO2), myocytes viability was measured with MTT assay. Caspase-3 proteolytic activity was detected, and cell apoptosis was measured according to Annexin V-FITC apoptosis detection kit. Fas expressed in primary mouse myocytes.Fas expression in myocytes transfected with anti-Fas ribozyme was decreased remarkably and correlated with the resistance to Fas-mediated apoptosis as determined by flow cytometry and caspase-3 proteolytic activity. Anti-Fas ribozyme can remarkably decrease the Fas expression in mouse myocytes, thus inhibit Fasmediated apoptosis in myocytes. It is suggested that anti-Fas ribozyme could significantly increase the resistance of transplanted myocytes to apoptosis and improve the survival of transplanted myocytes.
Keywords :
biochemistry; cardiology; cellular biophysics; enzymes; molecular biophysics; Fas expression; Fas mRNA; MTT assay; RT-PCR; anti-Fas antibody; anti-Fas ribozyme; cardiomyocyte apoptosis; caspase-3 proteolytic activity; effectene; flow cytometry; hammerhead ribozyme; primary cultured neonatal mouse ventricular myocytes; western blotting; Birth disorders; Cardiology; Cells (biology); DNA; Hospitals; Mice; Pediatrics; Proteins; RNA; Sequences;
Conference_Titel :
Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
Conference_Location :
Chengdu
Print_ISBN :
978-1-4244-4712-1
Electronic_ISBN :
2151-7614
DOI :
10.1109/ICBBE.2010.5514718