Open Access
Article
Matrix vesicles: structure, composition, formation and function in calcification
Roy E Wuthier1,Guy F Lipscomb1
1
Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA. uthierr@bellsouth.net
DOI: 10.2741/3887 Volume 16 Issue 8, pp.2812-2902
Published: 01 June 2011
(This article belongs to the Special Issue The biomineralization process: mechanism, problems, perspectives)
Abstract

Matrix vesicles (MVs) induce calcification during endochondral bone formation. Experimental methods for structural, compositional, and functional analysis of MVs are reviewed. MV proteins, enzymes, receptors, transporters, regulators, lipids and electrolytes are detailed. MV formation is considered from both structural and biochemical perspectives. Confocal imaging of Ca(2+) and H(+) were used to depict how living chondrocytes form MVs. Biochemical studies revealed that coordinated mitochondrial Ca(2+) and Pi metabolism produce MVs containing a nucleational complex (NC) of amorphous calcium phosphate, phosphatidylserine and annexin A5--all critical to the mechanism of mineral nucleation. Reconstitution of the NC and modeling with unilamellar vesicles reveal how the NC transforms into octacalcium phosphate, regulated by Mg(2+), Zn(2+) and annexin A5. Extravasation of intravesicular mineral is mediated by phospholipases and tissue-nonspecific alkaline phosphatase (TNAP). In the extravesicular matrix, hydroxyapatite crystal propagation is enhanced by cartilage collagens and TNAP, which destroys inhibitory PPi, and by metalloproteases that degrade proteoglycans. Other proteins also modulate mineral formation. Recent findings from single and multiple gene knockouts of TNAP, NPP1, ANK, PHOSPHO1, and Annexin A5 are reviewed.

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Roy E Wuthier, Guy F Lipscomb. Matrix vesicles: structure, composition, formation and function in calcification. Frontiers in Bioscience-Landmark. 2011. 16(8); 2812-2902.