Insulin induces the expression of FGF2 but does not synergize with it during angiogenesis

Lakshmi Surekha Krishnapati1, Surendra Ghaskadbi1

  • 1Developmental Biology Group, MACS-Agharkar Research Institute, Pune 411 004, India.

Microvascular Research
|November 10, 2015
PubMed

Insights

This study investigated the interplay between insulin, fibroblast growth factor-2 (FGF-2), and vascular endothelial growth factor (VEGF) in blood vessel formation. Researchers found no evidence of a combined effect of insulin and FGF-2 on angiogenesis.

Area of Science:

  • Biomedical research
  • Molecular biology
  • Cardiovascular science

Background:

  • Cardiovascular and ischemic diseases are linked to diabetes mellitus, often caused by blocked blood vessels.
  • Current treatments involve growth factors, gene therapy, and stem cells.
  • Vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (FGF-2) promote blood vessel growth but are elevated with insulin therapy, suggesting a potential link.

Purpose of the Study:

  • To investigate the potential synergistic effect between insulin and FGF-2 in angiogenesis.
  • To explore the combinatorial effects of insulin, FGF-2, and VEGF on blood vessel formation.

Main Methods:

  • Chick embryonic chorioallantoic membrane (CAM) assay for morphological and histological analysis.
  • Semi-quantitative reverse transcriptase PCR (RT-PCR) to analyze angiogenesis regulatory gene expression.

Main Results:

  • Morphological and histological examination using the CAM assay indicated no synergistic effect between insulin and FGF-2.
  • Gene expression analysis confirmed the absence of a combinatorial effect between insulin and FGF-2.
  • The CAM assay also demonstrated no combined effect of insulin, FGF-2, and VEGF on angiogenesis.

Conclusions:

  • Insulin and FGF-2 do not appear to have a synergistic role in promoting angiogenesis.
  • The study suggests a lack of combinatorial effect between insulin, FGF-2, and VEGF in blood vessel formation.

Related Concept Videos

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...
4.0K
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...
7.6K
Insulin: The Receptor and Signaling Pathways01:28

Insulin: The Receptor and Signaling Pathways

Insulin action is mediated through a receptor tyrosine kinase, akin to the IGF-1 receptor. The number of receptors per cell varies significantly, from 40 on erythrocytes to 300,000 on adipocytes and hepatocytes. The insulin receptor consists of linked α/β subunit dimers, forming a heterotetramer glycoprotein with two extracellular α subunits and two β subunits spanning the membrane. The α subunits inhibit the inherent tyrosine kinase activity of the β subunits, but...
6.0K
Hormones Regulating Blood Glucose01:16

Hormones Regulating Blood Glucose

Insulin is released by beta cells of the pancreas when blood glucose levels are high. It facilitates glucose absorption and utilization in insulin-dependent cells with insulin receptors on their plasma membranes. Insulin promotes glucose uptake by increasing the number of glucose transport proteins in the cell membrane, allowing glucose to enter the cell. As a result, glucose utilization and ATP production are enhanced.
In addition to accelerating glucose uptake and utilization, insulin has...
8.5K
Insulin Secretory Vesicles01:05

Insulin Secretory Vesicles

Insulin secretory vesicles release insulin to stimulate blood glucose uptake and regulate carbohydrate metabolism. When the blood glucose levels increase, glucose enters the pancreatic β-islet cells through glucose transporters. Once inside, glucose is metabolized through glycolysis, the citric acid cycle, and the electron transport chain, producing ATP. This increase in ATP concentration closes ATP-sensitive potassium channels, leading to depolarization of the membrane and the opening of...
7.4K
TGF - β Signaling Pathway01:16

TGF - β Signaling Pathway

The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors...
10.9K