Role of Toll-like receptor 4 in cardiomyocyte apoptosis induced by hypoxia-reoxygenation in newborn rats
Yongping Zheng, Yun Wang, Chengyao Wang, Zongze Zhang, Yanlin Wang
Abstract
Yongping Zheng, Yun Wang, Chengyao Wang, Zongze Zhang, Yanlin Wang
Abstract
Objective To evaluate the role of Toll-like receptor 4 (TLR4) in cardiomyocyte apoptosis induced by hypoxia-reoxygenation (H/R) in newborn rats. Methods Cardiomyocytes obtained from newborn Sprague-Dawley rats, aged 1-3 days, were primarily cultured in DMEM culture medium supplemented with 20% fetal bovine serum and divided into 4 groups (n=10 each) using a random number table: control group (group C), H/R group, negative control group (con-siRNA group) and TLR4-siRNA group.Cardiomyocytes were routinely cultured for 24 h in group C. Cardiomyocytes were subjected to hypoxia for 2 h followed by 4 h of reoxygenation in group H/R.Cardiomyocytes were transfected with siRNA and TLR4-siRNA at the final concentration of 80 nmol/L in con-siRNA group and TLR4-siRNA group, respectively.After successful establishment of H/R injury model, the cell survival rate was measured by MTT assay, flow cytometry was used to detect apoptosis in cardiomyocytes, the expression of TLR4 mRNA was determined by real-time polymerase chain reaction, and the expression of TLR4, Bcl-2, Bax and caspase-3 was detected by Western blot.The apoptosis rate was calculated. Results Compared with group C, the cell survival rate was significantly decreased, the expression of TLR4 protein and mRNA, caspase-3 and Bax was up-regulated, the apoptosis rate was increased and the expression of Bcl-2 was down-regulated in the other three groups (P<0.01). Compared with H/R and con-siRNA groups, the cell survival rate was significantly increased, the expression of TLR4 protein and mRNA, caspase-3 and Bax was down-regulated, the apoptosis rate was decreased and the expression of Bcl-2 was up-regulated in group TLR4-siRNA (P<0.01). Conclusion TLR4 is involved in cardiomyocyte apoptosis induced by H/R in newborn rats. Key words: Toll-like receptor 4; RNA, small interfering; Myocytes, cardiac; Anoxia; Apoptosis
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Objective To evaluate the role of Toll-like receptor 4 (TLR4) in cardiomyocyte apoptosis induced by hypoxia-reoxygenation (H/R) in newborn rats. Methods Cardiomyocytes obtained from newborn Sprague-Dawley rats, aged 1-3 days, were primarily cultured in DMEM culture medium supplemented with 20% fetal bovine serum and divided into 4 groups (n=10 each) using a random number table: control group (group C), H/R group, negative control group (con-siRNA group) and TLR4-siRNA group.Cardiomyocytes were routinely cultured for 24 h in group C. Cardiomyocytes were subjected to hypoxia for 2 h followed by 4 h of reoxygenation in group H/R.Cardiomyocytes were transfected with siRNA and TLR4-siRNA at the final concentration of 80 nmol/L in con-siRNA group and TLR4-siRNA group, respectively.After successful establishment of H/R injury model, the cell survival rate was measured by MTT assay, flow cytometry was used to detect apoptosis in cardiomyocytes, the expression of TLR4 mRNA was determined by real-time polymerase chain reaction, and the expression of TLR4, Bcl-2, Bax and caspase-3 was detected by Western blot.The apoptosis rate was calculated. Results Compared with group C, the cell survival rate was significantly decreased, the expression of TLR4 protein and mRNA, caspase-3 and Bax was up-regulated, the apoptosis rate was increased and the expression of Bcl-2 was down-regulated in the other three groups (P<0.01). Compared with H/R and con-siRNA groups, the cell survival rate was significantly increased, the expression of TLR4 protein and mRNA, caspase-3 and Bax was down-regulated, the apoptosis rate was decreased and the expression of Bcl-2 was up-regulated in group TLR4-siRNA (P<0.01). Conclusion TLR4 is involved in cardiomyocyte apoptosis induced by H/R in newborn rats. Key words: Toll-like receptor 4; RNA, small interfering; Myocytes, cardiac; Anoxia; Apoptosis
Key concepts: Apoptosis, Andrology, Molecular biology, Western blot, Hypoxia (environmental), Flow cytometry, Transfection, TLR4