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通过发育靶向心肌细胞的表观遗传调控以实现心力衰竭后治疗性心脏再生。

Targeting Epigenetic Regulation of Cardiomyocytes through Development for Therapeutic Cardiac Regeneration after Heart Failure.

机构信息

College of Science, Technology, Engineering, Arts, and Mathematics, Alvernia University, Reading, PA 19607, USA.

出版信息

Int J Mol Sci. 2022 Oct 6;23(19):11878. doi: 10.3390/ijms231911878.

Abstract

Cardiovascular diseases are the leading cause of death globally, with no cure currently. Therefore, there is a dire need to further understand the mechanisms that arise during heart failure. Notoriously, the adult mammalian heart has a very limited ability to regenerate its functional cardiac cells, cardiomyocytes, after injury. However, the neonatal mammalian heart has a window of regeneration that allows for the repair and renewal of cardiomyocytes after injury. This specific timeline has been of interest in the field of cardiovascular and regenerative biology as a potential target for adult cardiomyocyte repair. Recently, many of the neonatal cardiomyocyte regeneration mechanisms have been associated with epigenetic regulation within the heart. This review summarizes the current and most promising epigenetic mechanisms in neonatal cardiomyocyte regeneration, with a specific emphasis on the potential for targeting these mechanisms in adult cardiac models for repair after injury.

摘要

心血管疾病是全球范围内的主要死亡原因,目前尚无治愈方法。因此,我们迫切需要进一步了解心力衰竭过程中出现的机制。众所周知,成年哺乳动物心脏在受伤后,其功能性心肌细胞(心肌细胞)的再生能力非常有限。然而,新生哺乳动物心脏有一个再生窗口,允许在受伤后修复和更新心肌细胞。这一时间表在心血管和再生生物学领域引起了人们的兴趣,因为它可能成为成年心肌细胞修复的潜在靶点。最近,许多新生儿心肌细胞再生机制与心脏内的表观遗传调控有关。本综述总结了目前最有前途的新生儿心肌细胞再生的表观遗传机制,并特别强调了在成年心脏模型中针对这些机制进行损伤后修复的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ef/9569953/c86d4937aadb/ijms-23-11878-g001.jpg

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