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Mechanism of Angiogenesis01:10

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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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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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Positioning the cell division plane is a critical step during development and cell differentiation, particularly during mitosis when the plane is essential for determining the size of the two daughter cells. The cell division plane is perpendicular to the plane of chromosome segregation, but different types of organisms have different cell division mechanisms to suit their morphology and function. 
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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.
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由细胞性驱动的螺旋式血管生成.

Haokang Zhang1,2, Tasnif Rahman1,2, Shuhan Lu3

  • 1Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.

Science advances
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概括
此摘要是机器生成的。

科学家们使用微流体设计了右手螺旋内皮管,揭示了细胞性作为血管发育和疾病的关键. 药物诱导的细胞性变化逆转了管的手性,影响了透性.

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科学领域:

  • 生物物理学和发育生物学,专注于细胞形态发生和组织工程.

背景情况:

  • 细胞螺旋结构在发育和疾病中至关重要,但推动它们形成的机制尚不清楚.
  • 在控制工程系统中复制这些复杂的螺旋结构仍然是一个重大挑战.

研究的目的:

  • 研究工程系统中螺旋内皮管的自发出现.
  • 阐明固有的细胞性在控制这些结构的手性中的作用.
  • 探索调节性形态发生的生物力学因素.

主要方法:

  • 利用先进的微流体学来创建和观察螺旋内皮管的自发形成.
  • 在工程血管和原生小鼠血管组织中分析了奇拉性.
  • 采用小分子药物来操纵内皮细胞性,并评估对血管手性和透性的影响.
  • 开发了一个三维细胞顶点模型,以获得生物力学见解.

主要成果:

  • 证明了右手螺旋内皮管的自发出现,由固有的细胞性驱动.
  • 在小鼠血管组织中证实了一致的右手性偏差.
  • 显示,通过药物剂量取决于药物来操纵细胞性,可以逆转输管手性和改变血管透性.
  • 细胞顶点模型强调了细胞扭矩和组织流动性在性形态发生过程中的作用.

结论:

  • 揭示了由细胞性和生物力学力量控制的血管性形态发生的新奇机制.
  • 提供可控制的工程系统来研究管体生成及其对发育和疾病的影响.
  • 提供了对生物系统中管形成的基本过程的新视角.