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Related Concept Videos

Cells Coordinate Growth and Proliferation02:36

Cells Coordinate Growth and Proliferation

Cell size is a significant factor impacting cellular design, function, and fitness. There exists some internal coordination by which cells double their masses before division, thus, achieving homeostasis. Coordination between cell growth and proliferation depends on the checkpoints in between cell cycle phases. Loss of coordination or failure in the checkpoint mechanism can drive the cell to uncontrolled growth and loss of cellular function. Like dividing cells that coordinate cellular growth,...
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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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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...
Regulation of Hematopoietic Stem Cells01:01

Regulation of Hematopoietic Stem Cells

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Cells Coordinate Growth and Proliferation02:36

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Cell size is a significant factor impacting cellular design, function, and fitness. There exists some internal coordination by which cells double their masses before division, thus, achieving homeostasis. Coordination between cell growth and proliferation depends on the checkpoints in between cell cycle phases. Loss of coordination or failure in the checkpoint mechanism can drive the cell to uncontrolled growth and loss of cellular function. Like dividing cells that coordinate cellular growth,...
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Role of Hematopoietic Growth Factors

Hematopoietic growth factors are molecules that regulate the differentiation rate of hematopoietic stem cells (HSCs). Erythropoietin (EPO), primarily produced by the kidneys, plays a crucial role in erythrocyte production. When oxygen levels in the blood are low, EPO is released into the bloodstream, reaching the bone marrow, where it stimulates HSCs to differentiate and mature into erythrocytes, which are vital for oxygen transport.
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Related Experiment Video

Updated: Jun 30, 2026

Strategic Endothelial Cell Tube Formation Assay: Comparing Extracellular Matrix and Growth Factor Reduced Extracellular Matrix
08:46

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Published on: August 14, 2016

Basic fibroblast growth factor increases tissue factor expression in circulating monocytes and in vascular wall.

D Corseaux1, T Meurice, I Six

  • 1Laboratoire d'Hématologie, Centre Hospitalier Régional Universitaire and Faculté de Médecine, Lille, France.

Circulation
|April 26, 2000
PubMed
Summary

Basic fibroblast growth factor (bFGF) increases tissue factor (TF) expression in monocytes and vascular cells in rabbits. This effect is notable in normal rabbits and less pronounced in hypercholesterolemic ones, requiring further investigation into thrombosis risk.

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Last Updated: Jun 30, 2026

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Area of Science:

  • Vascular Biology
  • Hemostasis
  • Endocrinology

Background:

  • Basic fibroblast growth factor (bFGF) is known to promote vascular repair and angiogenesis.
  • bFGF can induce tissue factor (TF) in vitro, a key initiator of thrombogenesis.
  • The role of bFGF-induced TF in angiogenesis warrants investigation.

Purpose of the Study:

  • To investigate whether systemic bFGF administration induces TF expression in monocytes and vascular cells.
  • To compare TF expression in normal and hypercholesterolemic rabbits following bFGF administration.

Main Methods:

  • TF expression was studied in normal and cholesterol-fed rabbits.
  • Animals received intravenous bFGF or saline injections.
  • TF expression in monocytes and aortic sections was assessed via immunohistochemistry.

Main Results:

  • bFGF administration significantly increased monocyte TF expression in both normal and hypercholesterolemic rabbits.
  • TF expression was lower in hypercholesterolemic rabbits compared to normal rabbits.
  • bFGF induced strong TF expression in the vascular wall of normal rabbits and weak expression in hypercholesterolemic rabbits.

Conclusions:

  • Systemic bFGF administration markedly increases TF expression in circulating monocytes and the vascular wall.
  • The effect of bFGF on TF expression is more pronounced in normal rabbits than in hypercholesterolemic rabbits.
  • The clinical significance of bFGF-induced TF expression regarding in vivo thrombosis requires further study.