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实验性射血分数保留心力衰竭中线粒体肌丝磷酸化和功能障碍。

Deranged myofilament phosphorylation and function in experimental heart failure with preserved ejection fraction.

机构信息

Department of Cardiovascular Physiology, Ruhr University, MA 3/56, D-44780 Bochum, Germany.

出版信息

Cardiovasc Res. 2013 Mar 1;97(3):464-71. doi: 10.1093/cvr/cvs353. Epub 2012 Dec 4.

Abstract

AIMS

Heart failure (HF) with preserved ejection fraction (HFpEF) is a major cause of morbidity and mortality. Key alterations in HFpEF include increased left ventricular (LV) stiffness and abnormal relaxation. We hypothesized that myofilament protein phosphorylation and function are deranged in experimental HFpEF vs. normal myocardium. Such alterations may involve the giant elastic protein titin, which contributes decisively to LV stiffness.

METHODS AND RESULTS

LV tissue samples were procured from normal dogs (CTRL) and old dogs with hypertension-induced LV hypertrophy and diastolic dysfunction (OHT/HFpEF). We quantified the expression and phosphorylation of myofilament proteins, including all-titin and site-specific titin phosphorylation, and assessed the expression/activity of major protein kinases (PKs) and phosphatases (PPs), myofilament calcium sensitivity (pCa(50)), and passive tension (F(passive)) of isolated permeabilized cardiomyocytes. In OHT vs. CTRL hearts, protein kinase-G (PKG) activity was decreased, whereas PKCα activity and PP1/PP2a expression were increased. Cardiac MyBPC, TnT, TnI and MLC2 were less phosphorylated and pCa(50) was increased in OHT vs. CTRL. The titin N2BA (compliant) to N2B (stiff) isoform-expression ratio was lowered in OHT. Hypophosphorylation in OHT was detected for all-titin and at serines S4010/S4099 within titin-N2Bus, whereas S11878 within proline, glutamate, valine, and lysine (PEVK)-titin was hyperphosphorylated. Cardiomyocyte F(passive) was elevated in OHT, but could be normalized by PKG or PKA, but not PKCα, treatment.

CONCLUSIONS

This patient-mimicking HFpEF model is characterized by titin stiffening through altered isoform composition and phosphorylation, both contributing to increased LV stiffness. Hypophosphorylation of myofilament proteins and increased calcium sensitivity suggest that functional impairment at the sarcomere level may be an early event in HFpEF.

摘要

目的

射血分数保留的心力衰竭(HFpEF)是发病率和死亡率的主要原因。HFpEF 的主要改变包括左心室(LV)僵硬和异常松弛。我们假设,在实验性 HFpEF 与正常心肌相比,肌丝蛋白磷酸化和功能异常。这种改变可能涉及巨大的弹性蛋白 titin,它对 LV 僵硬有决定性的贡献。

方法和结果

从正常狗(CTRL)和高血压引起的 LV 肥厚和舒张功能障碍的老年狗(OHT/HFpEF)中获取 LV 组织样本。我们量化了肌丝蛋白的表达和磷酸化,包括全 titin 和 titin 特定位点的磷酸化,并评估了主要蛋白激酶(PKs)和磷酸酶(PPs)、肌丝钙敏感性(pCa(50))和分离的通透化心肌细胞的被动张力(F(passive))的表达/活性。在 OHT 与 CTRL 心脏相比,蛋白激酶-G(PKG)活性降低,而 PKCα 活性和 PP1/PP2a 表达增加。心脏 MyBPC、TnT、TnI 和 MLC2 的磷酸化减少,pCa(50)在 OHT 中增加。OHT 中的 titin N2BA(顺应性)到 N2B(僵硬)同工型表达比例降低。OHT 中检测到全 titin 和 titin-N2Bus 中的丝氨酸 S4010/S4099 的低磷酸化,而 proline、glutamate、valine 和 lysine (PEVK)-titin 中的 S11878 则发生高磷酸化。OHT 中的心肌细胞 F(passive)升高,但可通过 PKG 或 PKA 但不是 PKCα 治疗来正常化。

结论

这种模拟患者的 HFpEF 模型的特点是 titin 通过改变同工型组成和磷酸化而变硬,这两者都导致 LV 僵硬增加。肌丝蛋白的低磷酸化和钙敏感性增加表明,在 HFpEF 中,肌节水平的功能障碍可能是早期事件。

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