• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

第二心脏场发育中的转录途径。

Transcriptional pathways in second heart field development.

作者信息

Black Brian L

机构信息

Cardiovascular Research Institute and Department of Biochemistry and Biophysics, Mail Code 2240, University of California, San Francisco, California 94158-2517, USA.

出版信息

Semin Cell Dev Biol. 2007 Feb;18(1):67-76. doi: 10.1016/j.semcdb.2007.01.001. Epub 2007 Jan 17.

DOI:10.1016/j.semcdb.2007.01.001
PMID:17276708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1855211/
Abstract

The heart is the first organ to form and function during vertebrate development and is absolutely essential for life. The left ventricle is derived from the classical primary or first heart field (FHF), while the right ventricle and outflow tract are derived from a distinct second heart field (SHF). The recent discovery of the SHF has raised several fundamental and important questions about how the two heart fields are integrated into a single organ and whether unique molecular programs control the development of the two heart fields. This review briefly highlights the contributions of the SHF to the developing and mature heart and then focuses primarily on our current understanding of the transcriptional pathways that function in the development of the SHF and its derivatives.

摘要

心脏是脊椎动物发育过程中第一个形成并开始发挥功能的器官,对生命至关重要。左心室源自经典的原代或第一心脏区域(FHF),而右心室和流出道则源自一个不同的第二心脏区域(SHF)。SHF的最新发现引发了几个关于两个心脏区域如何整合为一个单一器官以及是否有独特的分子程序控制两个心脏区域发育的基本且重要的问题。本综述简要强调了SHF对发育中和成熟心脏的贡献,然后主要聚焦于我们目前对在SHF及其衍生物发育中起作用的转录途径的理解。

相似文献

1
Transcriptional pathways in second heart field development.第二心脏场发育中的转录途径。
Semin Cell Dev Biol. 2007 Feb;18(1):67-76. doi: 10.1016/j.semcdb.2007.01.001. Epub 2007 Jan 17.
2
Single-Cell Transcriptomics Reveals Chemotaxis-Mediated Intraorgan Crosstalk During Cardiogenesis.单细胞转录组学揭示了心脏发生过程中化学趋性介导的器官内串扰。
Circ Res. 2019 Aug 2;125(4):398-410. doi: 10.1161/CIRCRESAHA.119.315243. Epub 2019 Jun 21.
3
Chamber identity programs drive early functional partitioning of the heart.腔室识别程序驱动心脏的早期功能分区。
Nat Commun. 2015 Aug 26;6:8146. doi: 10.1038/ncomms9146.
4
Isl1 is a direct transcriptional target of Forkhead transcription factors in second-heart-field-derived mesoderm.Isl1是第二心脏场来源的中胚层中叉头转录因子的直接转录靶点。
Dev Biol. 2009 Oct 15;334(2):513-22. doi: 10.1016/j.ydbio.2009.06.041. Epub 2009 Jul 4.
5
Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome.哺乳动物心脏发育的遗传途径:小鼠基因组操作的最新进展
Semin Cell Dev Biol. 2007 Feb;18(1):77-83. doi: 10.1016/j.semcdb.2006.11.011. Epub 2006 Nov 24.
6
Analysis of Cripto expression during mouse cardiac myocyte differentiation.小鼠心肌细胞分化过程中Cripto表达的分析。
Int J Dev Biol. 2013;57(9-10):793-7. doi: 10.1387/ijdb.130072jd.
7
Chamber formation and morphogenesis in the developing mammalian heart.发育中的哺乳动物心脏中的腔室形成与形态发生。
Dev Biol. 2000 Jul 15;223(2):266-78. doi: 10.1006/dbio.2000.9753.
8
The formation of the embryonic mouse heart: heart fields and myocardial cell lineages.胚胎鼠心脏的形成:心脏区域和心肌细胞谱系。
Ann N Y Acad Sci. 2010 Feb;1188:15-24. doi: 10.1111/j.1749-6632.2009.05078.x.
9
Mef2c is a direct transcriptional target of ISL1 and GATA factors in the anterior heart field during mouse embryonic development.在小鼠胚胎发育过程中,Mef2c是前心脏区域中ISL1和GATA因子的直接转录靶点。
Development. 2004 Aug;131(16):3931-42. doi: 10.1242/dev.01256. Epub 2004 Jul 14.
10
The right ventricle, outflow tract, and ventricular septum comprise a restricted expression domain within the secondary/anterior heart field.右心室、流出道和室间隔在次级/前心脏区域内构成一个受限的表达域。
Dev Biol. 2005 Nov 1;287(1):134-45. doi: 10.1016/j.ydbio.2005.08.041. Epub 2005 Sep 26.

引用本文的文献

1
Heart Morphogenesis Requires Smyd1b for Proper Incorporation of the Second Heart Field in Zebrafish.心脏形态发生需要Smyd1b来正确整合斑马鱼的第二心脏场。
Genes (Basel). 2025 Jan 4;16(1):52. doi: 10.3390/genes16010052.
2
The molecular mechanisms of cardiac development and related diseases.心脏发育及相关疾病的分子机制。
Signal Transduct Target Ther. 2024 Dec 23;9(1):368. doi: 10.1038/s41392-024-02069-8.
3
A Retinoic Acid:YAP1 signaling axis controls atrial lineage commitment.视黄酸:YAP1信号轴控制心房谱系定向分化。
bioRxiv. 2024 Jul 12:2024.07.11.602981. doi: 10.1101/2024.07.11.602981.
4
Myocardial Matrix Hydrogels Mitigate Negative Remodeling and Improve Function in Right Heart Failure Model.心肌基质水凝胶减轻右心衰竭模型中的负性重塑并改善功能。
JACC Basic Transl Sci. 2024 Mar 6;9(3):322-338. doi: 10.1016/j.jacbts.2024.01.006. eCollection 2024 Mar.
5
Right Ventricle and Epigenetics: A Systematic Review.右心室与表观遗传学:系统综述。
Cells. 2023 Nov 23;12(23):2693. doi: 10.3390/cells12232693.
6
The multi-lineage transcription factor ISL1 controls cardiomyocyte cell fate through interaction with NKX2.5.多能转录因子 ISL1 通过与 NKX2.5 的相互作用控制心肌细胞的命运。
Stem Cell Reports. 2023 Nov 14;18(11):2138-2153. doi: 10.1016/j.stemcr.2023.09.014. Epub 2023 Oct 19.
7
Single-cell transcriptomic profiling unveils dysregulation of cardiac progenitor cells and cardiomyocytes in a mouse model of maternal hyperglycemia.单细胞转录组谱分析揭示了母体高血糖症小鼠模型中心脏祖细胞和心肌细胞的失调。
Commun Biol. 2022 Aug 15;5(1):820. doi: 10.1038/s42003-022-03779-x.
8
Concomitant genetic defects potentiate the adverse impact of prenatal alcohol exposure on cardiac outflow tract maturation.同时存在的遗传缺陷会增强产前酒精暴露对心脏流出道成熟的不利影响。
Birth Defects Res. 2022 Feb;114(3-4):105-115. doi: 10.1002/bdr2.1968. Epub 2021 Dec 3.
9
The Spatiotemporal Expression of Notch1 and Numb and Their Functional Interaction during Cardiac Morphogenesis.Notch1 和 Numb 的时空表达及其在心脏形态发生中的功能相互作用。
Cells. 2021 Aug 25;10(9):2192. doi: 10.3390/cells10092192.
10
Epigenetics and Heart Development.表观遗传学与心脏发育
Front Cell Dev Biol. 2021 May 6;9:637996. doi: 10.3389/fcell.2021.637996. eCollection 2021.

本文引用的文献

1
An Nkx2-5/Bmp2/Smad1 negative feedback loop controls heart progenitor specification and proliferation.一个Nkx2-5/Bmp2/Smad1负反馈回路控制心脏祖细胞的特化和增殖。
Cell. 2007 Mar 9;128(5):947-59. doi: 10.1016/j.cell.2007.01.042.
2
Ciona intestinalis as a model for cardiac development.玻璃海鞘作为心脏发育的模型。
Semin Cell Dev Biol. 2007 Feb;18(1):16-26. doi: 10.1016/j.semcdb.2006.12.007. Epub 2006 Dec 20.
3
Multipotent embryonic isl1+ progenitor cells lead to cardiac, smooth muscle, and endothelial cell diversification.多能胚胎isl1+祖细胞可导致心脏、平滑肌和内皮细胞多样化。
Cell. 2006 Dec 15;127(6):1151-65. doi: 10.1016/j.cell.2006.10.029. Epub 2006 Nov 22.
4
Gene regulatory networks in the evolution and development of the heart.心脏进化与发育中的基因调控网络。
Science. 2006 Sep 29;313(5795):1922-7. doi: 10.1126/science.1132292.
5
Making or breaking the heart: from lineage determination to morphogenesis.塑造或破坏心脏:从谱系确定到形态发生。
Cell. 2006 Sep 22;126(6):1037-48. doi: 10.1016/j.cell.2006.09.003.
6
Cardioblast-intrinsic Tinman activity controls proper diversification and differentiation of myocardial cells in Drosophila.成 cardioblast 细胞内在的 Tinman 活性控制果蝇心肌细胞的正确多样化和分化。
Development. 2006 Oct;133(20):4073-83. doi: 10.1242/dev.02586. Epub 2006 Sep 20.
7
Forkhead transcription factors, Foxc1 and Foxc2, are required for the morphogenesis of the cardiac outflow tract.叉头转录因子Foxc1和Foxc2是心脏流出道形态发生所必需的。
Dev Biol. 2006 Aug 15;296(2):421-36. doi: 10.1016/j.ydbio.2006.06.012. Epub 2006 Jun 8.
8
Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling.Fgf8在流出道形成和重塑中所需的组织特异性作用。
Development. 2006 Jun;133(12):2419-33. doi: 10.1242/dev.02367.
9
MEF2C is required for the normal allocation of cells between the ventricular and sinoatrial precursors of the primary heart field.MEF2C是原肠心脏场的心室和窦房结前体细胞正常分配所必需的。
Dev Dyn. 2006 Jul;235(7):1809-21. doi: 10.1002/dvdy.20828.
10
Left and right ventricular contributions to the formation of the interventricular septum in the mouse heart.小鼠心脏中左、右心室对室间隔形成的贡献。
Dev Biol. 2006 Jun 15;294(2):366-75. doi: 10.1016/j.ydbio.2006.02.045. Epub 2006 May 3.