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Related Concept Videos

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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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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Development of Blood Vessels01:07

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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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Procedure for the Development of Multi-depth Circular Cross-sectional Endothelialized Microchannels-on-a-chip
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Advances in on-chip vascularization.

Kristina Haase1, Roger D Kamm1,2,3

  • 1Department of Mechanical Engineering, MIT, Cambridge, MA, USA.

Regenerative Medicine
|March 21, 2017
PubMed
Summary
This summary is machine-generated.

Microfluidics enables advanced in vitro models for studying blood vessels and organ development. These microfluidic systems offer precise control for applications in drug screening and regenerative medicine.

Keywords:
angiogenesismicrofluidicsmicrovasculatureorgan-on-a-chippermeabilityregenerative medicinetissue-engineeringvasculogenesis

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Area of Science:

  • Biomedical Engineering
  • Microfluidics
  • Tissue Engineering

Background:

  • Microfluidics is crucial for studying microvasculature, organ-on-chip models, and microtissue engineering.
  • Microfluidic systems precisely control geometrical, biochemical, and mechanical factors to simulate in vivo conditions.

Purpose of the Study:

  • To review the generation and application of in vitro vascular networks using microfluidic technology.
  • To highlight the potential of microfluidics in drug screening and regenerative medicine.

Main Methods:

  • Generation of in vitro vascular networks via endothelial-lined patterned channels or self-assembled networks.
  • Application of microfluidic techniques for rapid perfusion in tissue and organ-mimicking models.
  • Integration with tuneable hydrogels for enhanced functionality.

Main Results:

  • Microfluidic approaches effectively mimic in vivo conditions, controlling shear and interstitial flow.
  • Both patterned and self-assembled vascular networks are suitable for studying angiogenesis, vasculogenesis, and cancer metastasis.
  • Successful in vivo implantation of microfluidic-generated vascular networks has been demonstrated.

Conclusions:

  • Microfluidics provides a powerful platform for creating complex in vitro vascular models.
  • This technology holds significant promise for accelerating drug discovery and advancing regenerative medicine through prevascularized tissue development.