Yao Yu-mei, Hu Shen-jiang, Huang Yuan-wei, Yang Chun-hu, Sun Jian, Zhu Zhao-hui, Wu Tao
Department of Cardiology, the First Affiliated Hospital, Zhejiang University Medical College, Hangzhou 310003, China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005 Dec;27(6):767-71.
To explore the effects of tumor necrosis factor alpha (TNFalpha) on the expression of phospholamban (PLB) and sarco (endo) plasmic reticulum Ca(2+)-ATPase (SERCA2a) and concentration of intracellular free calcium in myocardiocytes.
The neonatal rat myocardiocytes were randomly divided into 6 groups: treatment with different concentrations of TNFalpha (1,10,30,50,and 70 microg/L, respectively) and without TNFalpha (control). The mRNA and protein expression of PLB and SERCA2a were detected with one-step reverse transcription-polymerase chain reaction and Western blotting. The changes of intracellular free calcium concentration ([Ca2+]i) in cultured single neonatal rat cardiomyocyte were determined with Fluo-3/AM loading by laser scanning confocal microscopy. RESULTS TNFalpha significantly increased the expression of PLB mRNA and protein in a dose-dependent fashion. The ratio of PLB/beta-actin mRNA in myocardiocytes incubated with 10,30,50, and 70 microg/L TNFalpha significantly increased by 66%, 106%, 141%, and 189% compared with control (P < 0.05), and protein levels significantly increased by 30%, 48%, 73%, and 114% respectively compared with control (P < 0.001), but there was no significant difference in PLB mRNA expression between the group treated with 1 microg/L TNFalpha and control group. TNFalpha had no effect on the expression of mRNA and protein of SERCA2a. TNFalpha (50 microg/L) incubated with cell for 24 hours diminished delta[Ca2+]i of single neonatal rat cardiomyocyte about 33% stimulated by isoproterenol (P < 0.01), but had no effect on delta [Ca2+]i of cardiomyocyte without isoproterenol stimulation.
TNFalpha can increase the expression of PLB and decrease delta[Ca2+]i in cardiomyocytes, which may be related with its negative inotropic effects on cardiomyocytes.
探讨肿瘤坏死因子α(TNFα)对心肌细胞中受磷蛋白(PLB)和肌浆(内质)网Ca²⁺-ATP酶(SERCA2a)表达及细胞内游离钙浓度的影响。
将新生大鼠心肌细胞随机分为6组:分别用不同浓度的TNFα(1、10、30、50和70μg/L)处理以及不用TNFα处理(对照组)。采用一步法逆转录-聚合酶链反应和蛋白质印迹法检测PLB和SERCA2a的mRNA和蛋白质表达。用Fluo-3/AM负载,通过激光扫描共聚焦显微镜测定培养的单个新生大鼠心肌细胞内游离钙浓度([Ca²⁺]i)的变化。结果TNFα以剂量依赖性方式显著增加PLB的mRNA和蛋白质表达。与对照组相比,用10、30、50和70μg/L TNFα孵育的心肌细胞中PLB/β-肌动蛋白mRNA的比值分别显著增加66%、106%、141%和189%(P<0.05),蛋白质水平分别显著增加30%、48%、73%和114%(P<0.001),但用1μg/L TNFα处理的组与对照组之间PLB mRNA表达无显著差异。TNFα对SERCA2a的mRNA和蛋白质表达无影响。用50μg/L TNFα与细胞孵育24小时,可使异丙肾上腺素刺激的单个新生大鼠心肌细胞的Δ[Ca²⁺]i降低约33%(P<0.01),但对无异丙肾上腺素刺激的心肌细胞的Δ[Ca²⁺]i无影响。
TNFα可增加心肌细胞中PLB的表达并降低Δ[Ca²⁺]i,这可能与其对心肌细胞的负性变力作用有关。