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dc.contributor.authorPatel, Jessal
dc.contributor.authorBourne, Lucie E
dc.contributor.authorDavies, Bethan K
dc.contributor.authorArnett, Timothy R
dc.contributor.authorMacRae, Vicky E
dc.contributor.authorWheeler-Jones, Caroline P D
dc.contributor.authorOrriss, Isabel R
dc.date.accessioned2019-12-07T01:09:38Z
dc.date.available2019-12-07T01:09:38Z
dc.date.issued2019-07-01
dc.identifier.citationPatel , J , Bourne , L E , Davies , B K , Arnett , T R , MacRae , V E , Wheeler-Jones , C P D & Orriss , I R 2019 , ' Differing calcification processes in cultured vascular smooth muscle cells and osteoblasts ' , Experimental Cell Research , vol. 380 , no. 1 , pp. 100-113 . https://doi.org/10.1016/j.yexcr.2019.04.020
dc.identifier.issn1090-2422
dc.identifier.otherORCID: /0000-0001-6450-8418/work/66039452
dc.identifier.urihttp://hdl.handle.net/2299/21970
dc.description© 2019 Published by Elsevier Inc.
dc.description.abstractArterial medial calcification (AMC) is the deposition of calcium phosphate mineral, often as hydroxyapatite, inthe medial layer of the arteries. AMC shares some similarities to skeletal mineralisation and has been associatedwith the transdifferentiation of vascular smooth muscle cells (VSMCs) towards an osteoblast-like phenotype. Thisstudy used primary mouse VSMCs and calvarial osteoblasts to directly compare the established and widely usedin vitromodels of AMC and bone formation. Significant differences were identified between osteoblasts andcalcifying VSMCs. First, osteoblasts formed large mineralised bone nodules that were associated with widespreaddeposition of an extracellular collagenous matrix. In contrast, VSMCs formed small discrete regions of calcifi-cation that were not associated with collagen deposition and did not resemble bone. Second, calcifying VSMCsdisplayed a progressive reduction in cell viability over time (≤7-fold), with a 50% increase in apoptosis,whereas osteoblast and control VSMCs viability remained unchanged. Third, osteoblasts expressed high levels ofalkaline phosphatase (TNAP) activity and TNAP inhibition reduced bone formation by to 90%. TNAP activity incalcifying VSMCs was∼100-fold lower than that of bone-forming osteoblasts and cultures treated withβ-gly-cerophosphate, a TNAP substrate, did not calcify. Furthermore, TNAP inhibition had no effect on VSMC calci-fication. Although, VSMC calcification was associated with increased mRNA expression of osteoblast-relatedgenes (e.g. Runx2, osterix, osteocalcin, osteopontin), the relative expression of these genes was up to 40-foldlower in calcifying VSMCs versus bone-forming osteoblasts. In summary, calcifying VSMCsin vitrodisplay somelimited osteoblast-like characteristics but also differ in several key respects: 1) their inability to form collagen-containing bone; 2) their lack of reliance on TNAP to promote mineral deposition; and, 3) the deleterious effectof calcification on their viability.en
dc.format.extent14
dc.format.extent5538166
dc.language.isoeng
dc.relation.ispartofExperimental Cell Research
dc.subjectAlkaline phosphatase
dc.subjectBone formation
dc.subjectOsteoblast
dc.subjectVSMC
dc.subjectVascular calcification
dc.subjectCell Biology
dc.titleDiffering calcification processes in cultured vascular smooth muscle cells and osteoblastsen
dc.contributor.institutionDepartment of Clinical and Pharmaceutical Sciences
dc.contributor.institutionSchool of Life and Medical Sciences
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85064685361&partnerID=8YFLogxK
rioxxterms.versionofrecord10.1016/j.yexcr.2019.04.020
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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