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心脏内稳态中的线粒体类核:心脏疾病中线粒体与细胞核的双向信号传递

Mitochondrial nucleoid in cardiac homeostasis: bidirectional signaling of mitochondria and nucleus in cardiac diseases.

机构信息

Botnar Research Centre, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Old Road, University of Oxford, Oxford, OX3 7LD, UK.

Department of Pathology and Laboratory Medicine, Regenerative Medicine Research, University of Cincinnati College of Medicine, 231 Albert Sabin Way, CincinnatiCincinnati, OH, 45267-0529, USA.

出版信息

Basic Res Cardiol. 2021 Aug 14;116(1):49. doi: 10.1007/s00395-021-00889-1.

Abstract

Metabolic function and energy production in eukaryotic cells are regulated by mitochondria, which have been recognized as the intracellular 'powerhouses' of eukaryotic cells for their regulation of cellular homeostasis. Mitochondrial function is important not only in normal developmental and physiological processes, but also in a variety of human pathologies, including cardiac diseases. An emerging topic in the field of cardiovascular medicine is the implication of mitochondrial nucleoid for metabolic reprogramming. This review describes the linear/3D architecture of the mitochondrial nucleoid (e.g., highly organized protein-DNA structure of nucleoid) and how it is regulated by a variety of factors, such as noncoding RNA and its associated R-loop, for metabolic reprogramming in cardiac diseases. In addition, we highlight many of the presently unsolved questions regarding cardiac metabolism in terms of bidirectional signaling of mitochondrial nucleoid and 3D chromatin structure in the nucleus. In particular, we explore novel techniques to dissect the 3D structure of mitochondrial nucleoid and propose new insights into the mitochondrial retrograde signaling, and how it regulates the nuclear (3D) chromatin structures in mitochondrial diseases.

摘要

真核细胞的代谢功能和能量产生受线粒体调节,线粒体被认为是真核细胞的细胞内“动力工厂”,调节细胞内环境稳定。线粒体功能不仅在正常发育和生理过程中很重要,而且在多种人类疾病中也很重要,包括心脏病。心血管医学领域的一个新兴课题是线粒体基因组对代谢重编程的影响。本综述描述了线粒体基因组的线性/3D 结构(例如基因组的高度组织化蛋白-DNA 结构)以及它如何受到多种因素的调节,如非编码 RNA 及其相关的 R 环,以实现心脏疾病中的代谢重编程。此外,我们还强调了许多关于心脏代谢的目前尚未解决的问题,包括线粒体基因组和核内 3D 染色质结构的双向信号传递。特别地,我们探索了剖析线粒体基因组 3D 结构的新方法,并提出了线粒体逆行信号的新见解,以及它如何调节线粒体疾病中的核(3D)染色质结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3022/8364536/67be2a97fe50/395_2021_889_Fig1_HTML.jpg

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