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Decorin modulates matrix mineralization in vitroDecorin (DCN), a member of small leucine-rich proteoglycans, is known to modulate collagen fibrillogenesis. In order to investigate the potential roles of DCN in collagen matrix mineralization, several stable osteoblastic cell clones expressing higher (sense-DCN, S-DCN) and lower (antisense-DCN, As-DCN) levels of DCN were generated and the mineralized nodules formed by these clones were characterized. In comparison with control cells, the onset of mineralization by S-DCN clones was significantly delayed; whereas it was markedly accelerated and the number of mineralized nodules was significantly increased in As-DCN clones. The timing of mineralization was inversely correlated with the level of DCN synthesis. In these clones, the patterns of cell proliferation and differentiation appeared unaffected. These results suggest that DCN may act as an inhibitor of collagen matrix mineralization, thus modulating the timing of matrix mineralization.
Document ID
20040087709
Acquisition Source
Legacy CDMS
Document Type
Reprint (Version printed in journal)
Authors
Mochida, Yoshiyuki
(Dental Research Center, University of North Carolina at Chapel Hill Chapel Hill, NC 27599-7455, United States)
Duarte, Wagner R.
Tanzawa, Hideki
Paschalis, Eleftherios P.
Yamauchi, Mitsuo
Date Acquired
August 21, 2013
Publication Date
May 23, 2003
Publication Information
Publication: Biochemical and biophysical research communications
Volume: 305
Issue: 1
ISSN: 0006-291X
Subject Category
Life Sciences (General)
Funding Number(s)
CONTRACT_GRANT: AR46505
CONTRACT_GRANT: DE10489
CONTRACT_GRANT: DE014290
Distribution Limits
Public
Copyright
Other
Keywords
NASA Discipline Musculoskeletal
Non-NASA Center

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