REAL

Ferritin prevents calcification and osteoblastic differentiation of vascular smooth muscle cells

Zarjou, Abolfazl and Jeney, Viktória and Arosio, Paolo and Poli, Maura and Antal-Szalmás, Péter and Agarwal, Anupam and Balla, György and Balla, József (2009) Ferritin prevents calcification and osteoblastic differentiation of vascular smooth muscle cells. Journal of the American Society of Nephrology, 20 (6). pp. 1254-1263. ISSN 1046-6673

[img] Text
2009_Zarjou_Ferritin_prevents.pdf
Restricted to Registered users only

Download (416kB)

Abstract

Vascular calcification plays a role in the pathogenesis of atherosclerosis, diabetes, and chronic kidney disease. Human aortic smooth muscle cells (HSMCs) undergo mineralization in response to elevated levels of inorganic phosphate (Pi) in an active and well-regulated process. This process involves increased activity of alkaline phosphatase and increased expression of core binding factor α-1, a bone-specific transcription factor, with the subsequent induction of osteocalcin. Mounting evidence suggests an essential role for the heme oxygenase 1 (HO-1)/ferritin system to maintain homeostasis of vascular function. We examined whether induction of HO-1 and ferritin alters mineralization of HSMCs provoked by high Pi. Upregulation of the HO-1/ferritin system inhibited HSMC calcification and osteoblastic differentiation. Of the products of the system, only ferritin and, to a lesser extent, biliverdin were responsible for the inhibition. Ferritin heavy chain and ceruloplasmin, which both possess ferroxidase activity, inhibited calcification; a site-directed mutant of ferritin heavy chain, which lacked ferroxidase activity, failed to inhibit calcification. In addition, osteoblastic transformation of HSMCs provoked by elevated Pi (assessed by upregulation of core binding factor α-1, osteocalcin, and alkaline phosphatase activity) was diminished by ferritin/ferroxidase activity. We conclude that induction of the HO-1/ferritin system prevents Pi-mediated calcification and osteoblastic differentiation of human smooth muscle cells mainly via the ferroxidase activity of ferritin.

Item Type: Article
Subjects: R Medicine / orvostudomány > RZ Other systems of medicine / orvostudomány egyéb területei
Depositing User: Dr. József Balla
Date Deposited: 14 Sep 2017 13:24
Last Modified: 14 Sep 2017 13:24
URI: http://real.mtak.hu/id/eprint/62457

Actions (login required)

View Item View Item