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Updated: Apr 18, 2026

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HUVEC Tube-formation Assay to Evaluate the Impact of Natural Products on Angiogenesis
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NO-dependent proliferation and migration induced by Vitamin D in HUVEC
Pamela Pittarella1, Diletta F Squarzanti2, Claudio Molinari2
1Innovative Research Laboratory for Wound Healing, Health Sciences Department, University of Eastern Piedmont "A. Avogadro", Via Solaroli 17, 28100 Novara, Italy.
The Journal of Steroid Biochemistry and Molecular Biology
|January 24, 2015
Summary
Vitamin D (Vit. D) promotes human endothelial cell proliferation and migration via nitric oxide (NO) production. This finding supports Vitamin D
Area of Science:
- Endocrinology
- Cell Biology
- Cardiovascular Research
Background:
- Vitamin D (Vit. D) plays crucial roles beyond bone health, impacting extraskeletal organs.
- Emerging evidence suggests beneficial cardiovascular effects of Vit. D, potentially mediated by endothelial nitric oxide (NO) pathways.
Purpose of the Study:
- To investigate the impact of Vit. D on human endothelial cell (EC) proliferation and migration.
- To elucidate the role of nitric oxide (NO) production in mediating these Vit. D effects.
Main Methods:
- Utilized human umbilical vein endothelial cells (HUVEC) in a 3D matrix model.
- Assessed cell proliferation and migration with and without Vit. D administration.
- Investigated the involvement of the Vitamin D Receptor (VDR) ligand ZK159222 and the eNOS inhibitor L-NAME.
Main Results:
- Vit. D significantly enhanced HUVEC proliferation and migration in the 3D matrix.
- These pro-proliferative and pro-migratory effects were dependent on nitric oxide (NO) production.
- Inhibition of endothelial nitric oxide synthase (eNOS) by L-NAME abrogated Vit. D-induced effects and MMP-2 expression.
Conclusions:
- Vit. D promotes endothelial cell proliferation and migration through an NO-dependent mechanism.
- These findings highlight Vit. D's role in angiogenesis.
- Suggests potential therapeutic applications for Vit. D in tissue repair and wound healing.
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