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Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

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 hydroxylase and factor...
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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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Multivesicular bodies (MVBs) are mature endosomes that sort ubiquitinated proteins and then fuse with lysosomes to degrade the sorted proteins. Epidermal growth factor (EGF) and its receptor (EGFR) form a complex that can be internalized through endocytosis, sorted into an MVB, and later degraded.
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Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
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Related Experiment Video

Updated: Jun 18, 2026

A Simple Bioassay for the Evaluation of Vascular Endothelial Growth Factors
09:04

A Simple Bioassay for the Evaluation of Vascular Endothelial Growth Factors

Published on: March 15, 2016

VEGF receptor trafficking in angiogenesis.

Alice Scott1, Harry Mellor

  • 1Department of Biochemistry, University of Bristol, School of Medical Sciences, University Walk, Bristol BS8 1TD, UK.

Biochemical Society Transactions
|November 14, 2009
PubMed
Summary

Cellular sensitivity to stimulation is controlled by receptor trafficking. Vascular Endothelial Growth Factor Receptor 2 (VEGFR2) trafficking via the endosomal pathway is critical for angiogenic signaling and cellular events.

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Signaling Pathways

Background:

  • Intracellular receptor trafficking regulates cellular sensitivity and signaling balance.
  • Vascular Endothelial Growth Factor Receptor 2 (VEGFR2) is a key pro-angiogenic receptor tyrosine kinase (RTK).
  • VEGFR2 shares signaling pathways with other RTKs but exhibits distinct intracellular trafficking.

Purpose of the Study:

  • To investigate the unique intracellular trafficking of VEGFR2.
  • To understand how angiogenic regulators influence VEGFR2 trafficking.
  • To elucidate the role of endosomal pathways in VEGFR2-mediated angiogenic signaling.

Main Methods:

  • Analysis of receptor sorting and endosomal pathways.
  • Investigating VEGFR2 complex formation with angiogenic regulators.

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Last Updated: Jun 18, 2026

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  • Studying the impact of regulated trafficking on signaling.
  • Main Results:

    • VEGFR2 trafficking differs significantly from other RTKs.
    • Angiogenic regulators modulate VEGFR2 trafficking through the endosomal pathway.
    • Regulated VEGFR2 trafficking has significant consequences for angiogenic signaling.

    Conclusions:

    • The endosomal pathway is crucial for connecting VEGFR2 signaling to cellular events.
    • Intracellular trafficking is a key determinant of VEGFR2 function in angiogenesis.
    • Targeting VEGFR2 trafficking may offer therapeutic strategies for angiogenesis-related diseases.