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Angiogenesis

© Cell Signaling Technology. All Rights Reserved.
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Pathway Description:

Angiogenesis is defined as the physiological process by which new blood vessels are formed from pre-existing blood vessels. It is a critical process that enables development, skeletal muscle hypertrophy, menstruation, pregnancy, and wound healing, but which also contributes to pathological conditions including neovascular disorders (eg, retinopathy), rheumatoid arthritis, psoriasis, AIDS/Kaposi sarcoma, and cancer (tumorigenesis). Angiogenesis is a complex and highly ordered process that relies upon extensive signaling networks both among and within endothelial cells (ECs), their associated mural cells (vascular smooth muscle cells [VSMCs] and pericytes) and other cell types (eg, immune cells).

Vascular endothelial growth factor (VEGF) is a family of proteins that are required for angiogenesis. There are multiple isoforms of VEGF, including VEGF-A, VEGF-B, VEGF-C, and VEGF-D, each playing a major role in different angiogenic contexts ranging from embryonic to lymphatic angiogenesis. VEGF-A is the principal mediator of angiogenesis. Alternative splicing produces 4 main VEGF-A isoforms of different lengths-121, 165, 189, and 206 amino acids long-which display varying affinities for heparan sulfate proteoglycans (HSPG). The balance between freely diffusible and HSPG-bound VEGF-A results in a gradient, leading to the formation of a pioneering tip cell-an endothelial cell that responds to angiogenic signaling. The tip cell creates the leading edge of the angiogenic sprout and eventually vascular branching through various steps of cell migration. The branches first expand with site-specific metabolic demands and is then subdivided into arteries, capillaries, veins, and lymphatic vessels, a process mediated by the Notch-Gridlock, Ephrin-B2/EphB4, and Sonic Hedgehog (SHH) pathways. With further vessel maturation and hemodynamic changes, ECs secrete platelet-derived growth factor (PDGF)-B to recruit pericytes and VSMCs. These mural cells, via expression of angiopoietin-1 (ANG-1), bind to ECs, resulting in TGF-β activation and extracellular matrix (ECM) deposition, thereby stabilizing the growing vascular bed. Downstream effectors-including phosphatidylinositol-3 kinase (PI3K), Src kinase, focal adhesion kinase (FAK), p38 mitogen-activated protein kinase (p38 MAPK), Smad2/3, and phospholipase C gamma (PLCγ)/Erk1/2-promote EC survival, vascular permeability, and migratory/proliferative phenotypes. Positive and negative transcriptional regulation of these moieties via microRNAs (miRNAs) further influence postnatal angiogenesis. Specifically, miR-126 has been shown to play a vital role, as deletion leads to defective vessel formation and embryonic lethality.

Pathological and physiological angiogenesis share many similarities in terms of signaling events and the resulting changes to cell function and behavior and, therefore, may be novel therapeutic options to combat disease. However, a key difference is that pathological vessel development is not terminated upon adequate tissue perfusion. Such uncontrolled, disorganized, unresolved growth precludes advancement of novel angiogenesis-disrupting agents.

Selected Reviews:

We would like to thank Diane Bielenberg, PhD, Harvard Medical School, Boston Children’s Hospital, Boston, MA for reviewing this diagram.

created September 2008

revised September 2018

Acetylase
Metabolic Enzyme
Adaptor
Methyltransferase or G-protein
Apoptosis/Autophagy Regulator
Phosphatase
Cell Cycle Regulator
Protein Complex
Deacetylase or Cytoskeletal Protein
Receptor
Growth Factor/Cytokine/Development Protein
Transcription Factor or Translation Factor
GTPase/GAP/GEF
Ubiquitin/SUMO Ligase or Deubiquitinase
Kinase
Other
 
Direct Stimulatory Modification
Direct Stimulatory Modification
Transcriptional Stimulatory Modification
Transcriptional Stimulation
Direct Inhibitory Modification
Direct Inhibitory Modification
Transcriptional Inhibition
Transcriptional Inhibition
Multistep Stimulatory Modification
Multistep Stimulatory Modification
Joining of Subunits
Joining of Subunits
Multistep Inhibitory Modification
Multistep Inhibitory Modification
Translocation
Translocation
Tentative Stimulatory Modification
Tentative Stimulatory Modification
Separation of Subunits or Cleavage Products
Separation of Subunits or Cleavage Products
Tentative Inhibitory Modification
Tentative Inhibitory Modification