Recently, Vitamin D (Vit. D) has gained importance in cellular functions of a wide range of extraskeletal organs and target tissues, other than bone. In particular, Vit. D has displayed important beneficial effects in the cardiovascular system. Although little is known about the mechanism by which this response is exerted, a Vit. D-induced eNOS-dependent nitric oxide (NO) production in endothelial cells (EC) has been reported. The aim of this study was to evaluate whether Vit. D administration could affect human EC proliferation and/or migration through NO production. For this purpose, HUVEC (human umbilical vein endothelial cells) were used to evaluate Vit. D effects on cell proliferation and migration in a 3D matrix. Experiments were also performed in the presence of the specific VDR ligand ZK159222 and eNOS inhibitor L-NAME. This study demonstrated that Vit. D can promote both HUVEC proliferation and migration in a 3D matrix. These effects were NO dependent, since HUVEC proliferation and migration were abrogated along with Vit. D induced MMP-2 expression by inhibiting eNOS activity by L-NAME. These findings support the role of Vit. D in the angiogenic process, suggesting new applications for Vit. D in tissue repair and wound healing.

NO-dependent proliferation and migration induced by Vitamin D in HUVEC / P. Pittarella, D.F. Squarzanti, C. Molinari, M. Invernizzi, F. Uberti, F. Reno'. - In: JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY. - ISSN 0960-0760. - 149:(2015 May), pp. 35-42. [10.1016/j.jsbmb.2014.12.012]

NO-dependent proliferation and migration induced by Vitamin D in HUVEC

D.F. Squarzanti
Secondo
;
F. Reno'
Ultimo
2015

Abstract

Recently, Vitamin D (Vit. D) has gained importance in cellular functions of a wide range of extraskeletal organs and target tissues, other than bone. In particular, Vit. D has displayed important beneficial effects in the cardiovascular system. Although little is known about the mechanism by which this response is exerted, a Vit. D-induced eNOS-dependent nitric oxide (NO) production in endothelial cells (EC) has been reported. The aim of this study was to evaluate whether Vit. D administration could affect human EC proliferation and/or migration through NO production. For this purpose, HUVEC (human umbilical vein endothelial cells) were used to evaluate Vit. D effects on cell proliferation and migration in a 3D matrix. Experiments were also performed in the presence of the specific VDR ligand ZK159222 and eNOS inhibitor L-NAME. This study demonstrated that Vit. D can promote both HUVEC proliferation and migration in a 3D matrix. These effects were NO dependent, since HUVEC proliferation and migration were abrogated along with Vit. D induced MMP-2 expression by inhibiting eNOS activity by L-NAME. These findings support the role of Vit. D in the angiogenic process, suggesting new applications for Vit. D in tissue repair and wound healing.
No
English
endothelial cell; vitamin D; nitric oxide; matrix metalloproteinase-2; cell migration
Settore BIO/15 - Biologia Farmaceutica
Articolo
Esperti anonimi
Pubblicazione scientifica
mag-2015
Elsevier
149
35
42
8
Pubblicato
Periodico con rilevanza internazionale
miur
MIUR
Aderisco
info:eu-repo/semantics/article
NO-dependent proliferation and migration induced by Vitamin D in HUVEC / P. Pittarella, D.F. Squarzanti, C. Molinari, M. Invernizzi, F. Uberti, F. Reno'. - In: JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY. - ISSN 0960-0760. - 149:(2015 May), pp. 35-42. [10.1016/j.jsbmb.2014.12.012]
reserved
Prodotti della ricerca::01 - Articolo su periodico
6
262
Article (author)
Periodico con Impact Factor
P. Pittarella, D.F. Squarzanti, C. Molinari, M. Invernizzi, F. Uberti, F. Reno'
File in questo prodotto:
File Dimensione Formato  
NO-dependent proliferation and migration induced by Vitamin D in HUVEC.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 1.49 MB
Formato Adobe PDF
1.49 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1020227
Citazioni
  • ???jsp.display-item.citation.pmc??? 10
  • Scopus 27
  • ???jsp.display-item.citation.isi??? 25
social impact