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心肌细胞微区中的机械转导与代谢

Mechanotransduction and Metabolism in Cardiomyocyte Microdomains.

作者信息

Pasqualini Francesco S, Nesmith Alexander P, Horton Renita E, Sheehy Sean P, Parker Kevin Kit

机构信息

Disease Biophysics Group, Wyss Institute for Biologically Inspired Engineering, School of Engineering and Applied Sciences, Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA; Institute for Regenerative Medicine (IREM), Wyss Translational Center, University and ETH Zurich, Zurich, Switzerland.

Disease Biophysics Group, Wyss Institute for Biologically Inspired Engineering, School of Engineering and Applied Sciences, Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.

出版信息

Biomed Res Int. 2016;2016:4081638. doi: 10.1155/2016/4081638. Epub 2016 Dec 4.

Abstract

Efficient contractions of the left ventricle are ensured by the continuous transfer of adenosine triphosphate (ATP) from energy production sites, the mitochondria, to energy utilization sites, such as ionic pumps and the force-generating sarcomeres. To minimize the impact of intracellular ATP trafficking, sarcomeres and mitochondria are closely packed together and in proximity with other ultrastructures involved in excitation-contraction coupling, such as t-tubules and sarcoplasmic reticulum junctions. This complex microdomain has been referred to as the intracellular energetic unit. Here, we review the literature in support of the notion that cardiac homeostasis and disease are emergent properties of the hierarchical organization of these units. Specifically, we will focus on pathological alterations of this microdomain that result in cardiac diseases through energy imbalance and posttranslational modifications of the cytoskeletal proteins involved in mechanosensing and transduction.

摘要

左心室的有效收缩通过三磷酸腺苷(ATP)从能量产生部位(线粒体)持续转移至能量利用部位(如离子泵和产生力量的肌节)来确保。为了将细胞内ATP运输的影响降至最低,肌节和线粒体紧密排列在一起,并与参与兴奋 - 收缩偶联的其他超微结构(如横小管和肌浆网连接点)相邻。这种复杂的微区被称为细胞内能量单位。在此,我们回顾文献以支持以下观点:心脏稳态和疾病是这些单位层次组织的涌现特性。具体而言,我们将关注该微区的病理改变,这些改变通过能量失衡以及参与机械传感和转导的细胞骨架蛋白的翻译后修饰导致心脏疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96e1/5164897/fe914d1997a1/BMRI2016-4081638.001.jpg

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