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Odz4上调窦房结特异性基因以促进分化为心脏起搏器样细胞。

Odz4 upregulates SAN-specific genes to promote differentiation into cardiac pacemaker-like cells.

作者信息

Dong Anqi, Yoshizumi Masao, Kokubo Hiroki

机构信息

Department of Physiology and Biophysics, Hiroshima University, Japan.

Department of Physical Therapy, Tohto University, Chiba, Japan.

出版信息

FEBS Lett. 2025 Feb;599(3):299-315. doi: 10.1002/1873-3468.15036. Epub 2024 Oct 27.

Abstract

Cardiac arrhythmias stemming from abnormal sinoatrial node (SAN) function can lead to sudden death. Developing a biological pacemaker device for treating sick sinus syndrome (SSS) could offer a potential cure. Understanding SAN differentiation is crucial, yet its regulatory mechanism remains unclear. We reanalyzed published RNA-seq data and identified Odz4 as a SAN-specific candidate. In situ hybridization revealed Odz4 expression in the cardiac crescent and throughout the cardiac conduction system (CCS). To assess the role of Odz4 in CCS differentiation, we utilized a Tet-Off inducible system for its intracellular domain (ICD). Embryonic bodies (EBs) exogenously expressing Odz4-ICD exhibited an increased propensity to develop into pacemaker-like cells with enhanced automaticity and upregulated expression of SAN-specific genes. CellChat and GO analyses unveiled SAN-specific enrichment of ligand-receptor sets, especially Ptn-Ncl, and extracellular matrix components in the group exogenously expressing Odz4-ICD. Our findings underscore the significance of Odz4 in SAN development and offer fresh insights into biological pacemaker establishment.

摘要

源自异常窦房结(SAN)功能的心律失常可导致猝死。开发一种用于治疗病态窦房结综合征(SSS)的生物起搏器装置可能提供一种潜在的治疗方法。了解SAN分化至关重要,但其调控机制仍不清楚。我们重新分析了已发表的RNA测序数据,并确定Odz4为SAN特异性候选基因。原位杂交显示Odz4在心脏新月区和整个心脏传导系统(CCS)中表达。为了评估Odz4在CCS分化中的作用,我们利用Tet-Off诱导系统研究其细胞内结构域(ICD)。外源性表达Odz4-ICD的胚胎体(EBs)表现出更高的倾向发展为具有增强自律性和上调SAN特异性基因表达的起搏器样细胞。CellChat和基因本体(GO)分析揭示了在外源性表达Odz4-ICD的组中配体-受体集,特别是Ptn-Ncl和细胞外基质成分的SAN特异性富集。我们的研究结果强调了Odz4在SAN发育中的重要性,并为生物起搏器的建立提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8444/11808419/44aa1558c42e/FEB2-599-299-g002.jpg

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