Role of Bone-Type Tissue-Nonspecific Alkaline Phosphatase and PHOSPO1 in Vascular Calcification

Author(s): Yuri V. Bobryshev, Alexander N. Orekhov, Igor Sobenin, Dimitry A. Chistiakov

Journal Name: Current Pharmaceutical Design

Volume 20 , Issue 37 , 2014


Become EABM
Become Reviewer
Call for Editor

Abstract:

Matrix vesicle (MV)-mediated mineralization is important for bone ossification. However, under certain circumstances such as atherosclerosis, mineralization may occur in the arterial wall. Bone-type tissue-nonspecific alkaline phosphatase (TNAP) hydrolyzes inorganic pyrophosphate (PPi) and generates inorganic phosphate (Pi), which is essential for MV-mediated hydroxyapatite formation. MVs contain another phosphatase, PHOSPHO1, that serves as an additional supplier of Pi. Activation of bone-type tissue-nonspecific alkaline phosphatase (TNAP) in vascular smooth muscle cells precedes vascular calcification. By degrading PPi, TNAP plays a procalcific role changing the Pi/PPi ratio toward mineralization. A pathologic role of bone-type TNAP and PHOSPHO1 make them to be attractive targets for cardiovascular therapy.

Keywords: Arterial calcification, atherosclerosis, vascular smooth muscle cells, mineralizing matrix vesicles, bone-type tissue-nonspecific alkaline phosphatise, PHOSPO1.

Rights & PermissionsPrintExport Cite as

Article Details

VOLUME: 20
ISSUE: 37
Year: 2014
Page: [5821 - 5828]
Pages: 8
DOI: 10.2174/1381612820666140212193011
Price: $65

Article Metrics

PDF: 44