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相关概念视频

Mechanism of Angiogenesis01:10

Mechanism of Angiogenesis

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Blood vessel formation starts early during embryonic development, around day 7. In the extraembryonic yolk sac, mesodermal precursor cells called hemangioblast proliferate and differentiate into angioblast. Angioblasts express vascular endothelial growth factor receptor 2 or VEGFR2, which binds VEGF-A, a proangiogenic factor, guiding blood vessel formation. VEGF signaling promotes angioblasts to form a blood island in the developing embryo. Angioblasts further differentiate, giving rise to...
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Development of the Heart01:27

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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...
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Development of Blood Vessels01:07

Development of Blood Vessels

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The development of the vascular system in a fetus is a complex and intricate process that begins as early as 15 to 16 days post-conception. This process starts outside the embryo, specifically in the mesoderm of the yolk sac, chorion, and connecting stalk. Approximately two days later, the formation of blood vessels occurs within the embryo itself.
The initial formation of this system is facilitated by the small amount of yolk present in the ovum and yolk sac. Blood vessels originate from...
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Regulation of Angiogenesis and Blood Supply01:24

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Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl...
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内肌心发芽的尖端细胞指定冠状动脉的冠状动脉化

Elena Cano1,2,3,4,5, Jennifer Schwarzkopf1,2,3, Masatoshi Kanda6,7

  • 1Integrative Vascular Biology Laboratory (E.C., J.S., I.H., H.G.), Max-Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.

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|August 2, 2024
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概括

冠状动脉由尖端细胞形成,这一过程对于心脏血管化和修复至关重要. 这条尖端细胞到动脉通路从发育到成年时保持不变,并在缺血性心脏病中重新激活.

关键词:
血管新生是因为血管新生.动脉 动脉 动脉 动脉冠状动脉血管 冠状动脉血管心脏内脏的内脏.它们的内皮质 (endothelium).

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En Face Endocardial Cushion Preparation for Planar Morphogenesis Analysis in Mouse Embryos
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科学领域:

  • 心血管生物学 心血管生物学
  • 发育生物学 发展生物学
  • 内皮细胞生物学 内皮细胞生物学

背景情况:

  • 冠状动脉的模式对心脏功能至关重要,但人们对其了解甚少.
  • 内皮细胞协调和动脉静脉特异性的机制尚不清楚.
  • 对于针对缺血性心脏病的治疗方法,知识至关重要.

研究的目的:

  • 划分发育和成熟的冠状动脉内皮的转录状态.
  • 调查冠状动脉血管新生发芽的起源和机制.
  • 评估内皮细胞状态在发育,疾病和物种的保护.

主要方法:

  • 单细胞转录和组织学验证.
  • 遗传谱系的追踪和3D成像.
  • 来自小鼠和人类胚胎心脏的转录组数据的整合.

主要成果:

  • 冠状动脉起源于具有尖端细胞表型的细胞.
  • 确定了不同的心脏内和心下尖端细胞种群.
  • 尖端细胞到动脉的特异性是一个保存的机制,从发育到成年时代存在,并对损伤做出反应.

结论:

  • 一个尖端细胞到动脉的规范机制驱动了整个生命的冠状动脉.
  • 在缺血性损伤后,这种机制在成人心脏中被重新激活.
  • 不同的发芽程序调节了动脉和静脉冠状动脉的形成.