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心力衰竭中的肌浆网Ca2+-ATP酶2a:作用及治疗前景

SERCA2a in heart failure: role and therapeutic prospects.

作者信息

Gianni Davide, Chan Joachim, Gwathmey Judith K, del Monte Federica, Hajjar Roger J

机构信息

Cardiovascular Research Centre, Heart Failure Center, Massachusetts General Hospital, Boston, Massachusetts, USA.

出版信息

J Bioenerg Biomembr. 2005 Dec;37(6):375-80. doi: 10.1007/s10863-005-9474-z.

Abstract

Ca(2+) is a key molecule controlling several cellular processes, from fertilization to cell death, in all cell types. In excitable and contracting cells, such as cardiac myocytes, Ca(2+) controls muscle contractility. The spatial and temporal segregation of Ca(2+) concentrations are central to maintain its concentration gradients across the cells and the cellular compartments for proper function. SERCA2a is a cornerstone molecule for maintaining a balanced concentration of Ca(2+) during the cardiac cycle, since it controls the transport of Ca(2+) to the sarcoplasmic reticulum (SR) during relaxation. Alterations of the activity of this pump have been widely investigated, emphasizing its central role in the control of Ca(2+) homeostasis and consequently in the pathogenesis of the contractile defect seen with heart failure. This review focuses on the molecular characteristics of the pump, its role during the cardiac cycle and the prospects derived from the manipulation of SERCA2a for heart failure treatment.

摘要

钙离子(Ca(2+))是控制所有细胞类型中从受精到细胞死亡等多种细胞过程的关键分子。在可兴奋和收缩性细胞(如心肌细胞)中,Ca(2+)控制肌肉收缩力。Ca(2+)浓度的时空分隔对于维持其跨细胞和细胞内区室的浓度梯度以实现正常功能至关重要。肌浆网Ca(2+) - ATP酶2a(SERCA2a)是在心动周期中维持Ca(2+)平衡浓度的基石分子,因为它在舒张期控制Ca(2+)向肌浆网(SR)的转运。该泵活性的改变已得到广泛研究,强调了其在控制Ca(2+)稳态以及因此在心力衰竭时出现的收缩功能缺陷发病机制中的核心作用。本综述重点关注该泵的分子特征、其在心动周期中的作用以及通过操纵SERCA2a治疗心力衰竭的前景。

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