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pubmed-article:8987171pubmed:dateCreated1997-2-19lld:pubmed
pubmed-article:8987171pubmed:abstractTextThe effects of two inhibitors, fluoride (F-) and zinc (Zn2+), were studied on the formation of mineral by matrix vesicles (MV) in an in vitro system. Kinetically, mineral formation by MV incubated in a synthetic cartilage lymph (SCL) is characterized by three phases: a lag period, a period of rapid uptake, and finally a period of slow uptake. Zn2+ at > or = 5 microM completely inhibited MV mineralization; at < or = 1 microM, it had little effect on rate of ion uptake, but delayed conversion of an OCP-like intermediate into hydroxyapatite (OHAp). F- at > or = 10 microM reduced the rate of rapid uptake by MV and caused the OCP-like precursor to convert to OHAp. When synthetic OCP was seeded into SCL, mineralization ensued and OHAp became the dominant phase. With Zn2+ present, OCP-like features persisted longer; with F-, the OCP-like features were lost more rapidly. When ACP was seeded into SCL, OHAp formed; Zn2+ at < or = 1 microM caused OCP-like mineral to form. Our findings indicate that Zn2+ stabilizes a noncrystalline precursor in MV regulating the length of the lag period; Zn2+ also favors the formation of an OCP-like intermediate whose growth accounts for the rapid uptake phase. This OCP-like phase appears to nucleate formation of OHAp by MV.lld:pubmed
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pubmed-article:8987171pubmed:authorpubmed-author:WuthierR ERElld:pubmed
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pubmed-article:8987171pubmed:authorpubmed-author:SauerG RGRlld:pubmed
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pubmed-article:8987171pubmed:volume65lld:pubmed
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pubmed-article:8987171pubmed:pagination57-65lld:pubmed
pubmed-article:8987171pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:8987171pubmed:year1997lld:pubmed
pubmed-article:8987171pubmed:articleTitleThe influence of trace elements on calcium phosphate formation by matrix vesicles.lld:pubmed
pubmed-article:8987171pubmed:affiliationDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia 29208, USA.lld:pubmed
pubmed-article:8987171pubmed:publicationTypeJournal Articlelld:pubmed
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pubmed-article:8987171pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed