Department of Biophysics, Second Military Medical University, No. 800 Xiangyin Road, 200433, Shanghai, People's Republic of China.
J Physiol Sci. 2010 Mar;60(2):85-94. doi: 10.1007/s12576-009-0070-6. Epub 2009 Dec 9.
intracellular Ca(2+) handling by the sarcoplasmic reticulum (SR) plays a crucial role in the pathogenesis of heart failure (HF). Despite extensive effort, the underlying causes of abnormal SR Ca(2+) handling in HF have not been clarified. To determine whether the diastolic SR Ca(2+) leak along with reduced Ca(2+) reuptake is required for decreased contractility, we investigated the cytosolic Ca(2+) transients and SR Ca(2+) content and assessed the expression of ryanodine receptor (RyR2), FK506 binding protein (FKBP12.6), SR-Ca(2+) ATPase (SERCA2a), and L-type Ca(2+) channel (LTCC) using an SD-rat model of chronic HF. We found that the cytosolic Ca(2+) transients were markedly reduced in amplitude in HF myocytes (DeltaF/F(0) = 12.3 +/- 0.8) compared with control myocytes (DeltaF/F(0) = 17.7 +/- 1.2, P < 0.01), changes paralleled by a significant reduction in the SR Ca(2+) content (HF: DeltaF/F(0) = 12.4 +/- 1.1, control: DeltaF/F(0) = 32.4 +/- 1.9, P < 0.01). Moreover, we demonstrated that the expression of FKBP12.6 associated with RyR2, SERCA2a, and LTCC was significantly reduced in rat HF. These results provide evidence for phosphorylation-induced detachment of FKBP12.6 from RyRs and down-regulation of SERCA2a and LTCC in HF. We conclude that diastolic SR Ca(2+) leak (due to dissociation of FKBP12.6 from RyR2) along with reduced SR Ca(2+) uptake (due to down-regulation of SERCA2a) and defective E-C coupling (due to down-regulation of LTCC) could contribute to HF.
肌浆网(SR)的细胞内 Ca(2+) 处理在心力衰竭(HF)的发病机制中起着至关重要的作用。尽管进行了广泛的研究,但 HF 中异常 SR Ca(2+) 处理的根本原因仍未阐明。为了确定舒张期 SR Ca(2+) 渗漏是否伴随着 Ca(2+) 摄取减少而导致收缩力降低,我们使用 SD 大鼠慢性 HF 模型研究了胞浆 Ca(2+) 瞬变和 SR Ca(2+) 含量,并评估了肌质网 Ca(2+) 通道(RyR2)、FK506 结合蛋白(FKBP12.6)、SR-Ca(2+)ATP 酶(SERCA2a)和 L 型 Ca(2+) 通道(LTCC)的表达。我们发现 HF 心肌细胞的胞浆 Ca(2+) 瞬变幅度明显降低(DeltaF/F(0) = 12.3 +/- 0.8),与对照心肌细胞(DeltaF/F(0) = 17.7 +/- 1.2,P < 0.01)相比,SR Ca(2+) 含量也显著降低(HF:DeltaF/F(0) = 12.4 +/- 1.1,对照:DeltaF/F(0) = 32.4 +/- 1.9,P < 0.01)。此外,我们还证明 FKBP12.6 与 RyR2、SERCA2a 和 LTCC 的表达在大鼠 HF 中显著降低。这些结果为 FKBP12.6 与 RyR2 分离引起的舒张期 SR Ca(2+) 渗漏以及 HF 中 SERCA2a 和 LTCC 下调提供了证据。我们得出结论,舒张期 SR Ca(2+) 渗漏(由于 FKBP12.6 与 RyR2 分离)、SR Ca(2+) 摄取减少(由于 SERCA2a 下调)和 E-C 偶联缺陷(由于 LTCC 下调)可能导致 HF。