Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Development of the Heart01:27

Development of the Heart

3.4K
The development of the human heart, a crucial organ, commences from the mesoderm on the 18th or 19th day after fertilization. This process initiates in the cardiogenic area, a group of mesodermal cells at the embryo's head end, which evolves into elongated strands known as cardiogenic cords. These cords undergo a transformation to form hollow-centered endocardial tubes.
As the embryo undergoes lateral folding, these paired tubes approach each other, merging into a single primitive heart...
3.4K
Structure of Cardiac Muscles01:13

Structure of Cardiac Muscles

18.6K
Cardiac muscle, or myocardium, is a specialized type of muscle found exclusively in the heart. Its unique structural and functional characteristics enable the heart to perform its vital role of pumping blood throughout the body continuously and rhythmically. The cardiac muscle cells, or cardiomyocytes, possess an endomysium and perimysium but do not have an epimysium.
Compared to skeletal muscles, cardiac muscle cells are small and mostly have a single nucleus. Additionally, they are usually...
18.6K
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

636
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
636

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Mitochondrial dysfunction underlies cardiac contractility and growth defects in a zebrafish model of <i>NAA15</i>-related heart disease.

bioRxiv : the preprint server for biology·2026
Same author

Cardiovascular and Cardiometabolic Outcomes in Adults with Fetal Alcohol Spectrum Disorders: A Retrospective Cohort Study.

medRxiv : the preprint server for health sciences·2026
Same author

3D spatial organization of heterogeneous nkx2.5+ progenitors in the zebrafish heart field pre-patterns cardiovascular development.

Nature communications·2025
Same author

Dosage-sensitive <i>RBFOX2</i> autoregulation promotes cardiomyocyte differentiation by maturing the transcriptome.

bioRxiv : the preprint server for biology·2025
Same author

An organ-wide spatiotemporal transcriptomic and cellular atlas of the regenerating zebrafish heart.

Nature communications·2025
Same author

Embryonic alcohol exposure in zebrafish predisposes adults to cardiomyopathy and diastolic dysfunction.

Cardiovascular research·2024

相关实验视频

Updated: Mar 18, 2026

En Face Endocardial Cushion Preparation for Planar Morphogenesis Analysis in Mouse Embryos
08:57

En Face Endocardial Cushion Preparation for Planar Morphogenesis Analysis in Mouse Embryos

Published on: July 27, 2022

2.2K

协调心肌细胞相互作用以指导心室形态发生

Peidong Han1, Joshua Bloomekatz1, Jie Ren1

  • 1Department of Medicine, Division of Cardiology, University of California, San Diego, La Jolla, California 92093, USA.

Nature
|July 1, 2016
PubMed
概括

心肌细胞组装到心室壁中涉及Notch和Erbb2信号之间的反循环. 这一过程引导细胞定位, 确保正确的心脏结构和功能.

更多相关视频

Analysis of Cardiac Chamber Development During Mouse Embryogenesis Using Whole Mount Epifluorescence
06:27

Analysis of Cardiac Chamber Development During Mouse Embryogenesis Using Whole Mount Epifluorescence

Published on: April 17, 2019

8.2K
Analysis of Cardiomyocyte Development using Immunofluorescence in Embryonic Mouse Heart
10:56

Analysis of Cardiomyocyte Development using Immunofluorescence in Embryonic Mouse Heart

Published on: March 26, 2015

22.2K

相关实验视频

Last Updated: Mar 18, 2026

En Face Endocardial Cushion Preparation for Planar Morphogenesis Analysis in Mouse Embryos
08:57

En Face Endocardial Cushion Preparation for Planar Morphogenesis Analysis in Mouse Embryos

Published on: July 27, 2022

2.2K
Analysis of Cardiac Chamber Development During Mouse Embryogenesis Using Whole Mount Epifluorescence
06:27

Analysis of Cardiac Chamber Development During Mouse Embryogenesis Using Whole Mount Epifluorescence

Published on: April 17, 2019

8.2K
Analysis of Cardiomyocyte Development using Immunofluorescence in Embryonic Mouse Heart
10:56

Analysis of Cardiomyocyte Development using Immunofluorescence in Embryonic Mouse Heart

Published on: March 26, 2015

22.2K

科学领域:

  • 心血管生物学
  • 发育生物学
  • 细胞信号传输

背景情况:

  • 心室壁有明显的紧和状层, 对于功能至关重要.
  • 心肌壁形成的障碍会导致先天性心脏病和心肌病.
  • 胚胎心肌细胞空间组织的机制在很大程度上是未知的.

研究的目的:

  • 阐明控制斑马鱼心脏内心肌细胞组合的信号通路.
  • 了解心肌突和Erbb2信号如何相互作用以指导细胞定位和形态发生.
  • 为了揭示腹腔壁形成的细胞动态.

主要方法:

  • 在斑马鱼模型中利用先进的基因操纵和体内成像.
  • 研究了诺奇和Erbb2信号的细胞自主和非细胞自主作用.
  • 对心肌突活动对心室形态的影响进行分析.

主要成果:

  • 确定了心肌突信号抑制Erbb2信号的反循环, 防止心肌细胞发芽和化.
  • 心肌特异性Notch无活化导致心室尺寸缩小和壁壁加厚.
  • 广泛的心肌突活动导致心室扩大,
  • 激活Erbb2的心肌细胞非细胞自主激活心肌突信号.

结论:

  • 诺奇和Erbb2信号之间的新型互动细胞反过程指导心肌细胞组合.
  • 这种信号相互作用对于确定心室壁的空间尺寸和心肌质量至关重要.
  • 这些发现提供了关于组织形态和器官形式的细胞动态的见解.