Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5888880 | Bone | 2016 | 12 Pages |
Abstract
The importance of matrix vesicles (MVs) has been repeatedly highlighted in the formation of cartilage, bone, and dentin since their discovery in 1967. These nano-vesicular structures, which are found in the extracellular matrix, are believed to be one of the sites of mineral nucleation that occurs in the organic matrix of the skeletal tissues. In the more recent years, there have been numerous reports on the observation of MV-like particles in calcified vascular tissues that could be playing a similar role. Therefore, here, we review the characteristics MVs possess that enable them to participate in mineral deposition. Additionally, we outline the content of skeletal tissue- and soft tissue-derived MVs, and discuss their key mineralisation mediators that could be targeted for future therapeutic use.
Keywords
ADPSmall Integrin-Binding LIgand N-linked GlycoproteinMEPERGDPPIRUNX2RANKLMGPVICVDAC1GPiGRPANXVSMCTGM2OPNOPGNPP1ECMPhosphotidylcholineTNAPLPSJnkNeutral sphingomyelinase 2PSSnSMase2ASARMc-Jun N-terminal kinaseSmall interfering RNAsiRNAAdenosine TriphosphateATPadenosine diphosphateArginine-Glycine-Aspartic AcidTissue-nonspecific alkaline phosphataseAnnexinOsteoprotegerinOsteopontinApoptotic bodychronic kidney diseaseTransglutaminase 2SiblingValve interstitial cellVascular smooth muscle cellRunt-related transcription factor 2PhosphatephosphatidylethanolaminePhosphatidylserinePhosphatidylserine synthasematrix extracellular phosphoglycoproteinLysophosphatidylserineMatrix vesiclesExtracellular matrixMatrix vesicleBMPMineralisationMechanismsMicroRNAMiRNACKDHydroxyapatiteMatrix Gla proteinBone morphogenetic proteinPyrophosphateVoltage-dependent anion channel 1Vascular calcificationcholine kinaseglycosylphosphatidylinositolPitreceptor activator of nuclear factor kappa-B ligand
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Authors
L. Cui, D.A. Houston, C. Farquharson, V.E. MacRae,