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Related Concept Videos

Mechanism of Angiogenesis01:10

Mechanism of Angiogenesis

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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A Novel Window into Angiogenesis-Intravital Microscopy in the AV-Loop-Model.

Ravikumar Vaghela1, Andreas Arkudas1, Daniel Gage2

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|January 21, 2023
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Researchers developed novel in vivo imaging chambers to visualize cellular processes in the arteriovenous (AV) loop model. This advancement enhances understanding of vascular development for tissue engineering applications.

Keywords:
GelMAarteriovenous loopintravital microscopytissue engineering

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Area of Science:

  • Biomedical Engineering
  • Regenerative Medicine
  • Vascular Biology

Background:

  • Current in vivo models have limitations in studying vascular development.
  • Understanding vascularization is crucial for engineered tissue constructs.
  • The arteriovenous (AV) loop model offers a platform for studying vascularization.

Purpose of the Study:

  • To develop novel in vivo imaging chambers for live visualization of cellular processes.
  • To enable detailed study of vascular development in the AV loop model.
  • To overcome limitations of existing experimental designs.

Main Methods:

  • Two types of intravital microscopy (IVM) chambers were designed and fabricated.
  • Chambers were implanted in rats using different fixation methods (skin and subcutaneous).
  • Modified gelatin hydrogel was used as a matrix, and fluorescent dyes were employed for visualization.

Main Results:

  • Chamber A supported AV loop function for two weeks, enabling leukocyte trafficking visualization.
  • Chamber B allowed examination of microvascular development in the AV loop for 21 days.
  • Microvascular outgrowth was quantified using Fiji-ImageJ software.

Conclusions:

  • The developed IVM chambers provide a unique tool for studying vascular development in the AV loop model.
  • Combining both chamber types offers a comprehensive approach to understanding vascularization.
  • This research advances the field of tissue engineering by improving in vivo study capabilities.