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Osteogenic potential of five different recombinant human bone morphogenetic protein adenoviral vectors in the rat.

Osteogenic potential of five different recombinant human bone morphogenetic protein adenoviral vectors in the rat. Research Abstract Details 

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  • Osteogenic potential of five different recombinant human bone morphogenetic protein adenoviral vectors in the rat. Abstract Text:

    j z liJ Z Li,h liH Li,t sasakiT Sasaki,d holmanD Holman,b beresB Beres,r j dumontR J Dumont,d d pittmanD D Pittman,g r hankinsG R Hankins,g a helmG A Helm,j z liJ Z Li,h liH Li,t sasakiT Sasaki,d holmanD Holman,b beresB Beres,r j dumontR J Dumont,d d pittmanD D Pittman,g r hankinsG R Hankins,g a helmG A Helm,

    Bone morphogenetic protein (BMP) adenoviral vectors for the induction of osteogenesis are being developed for the treatment of bone pathology. However, it is still unknown which BMP adenoviral vector has the highest potential to stimulate bone formation in vivo. In this study, the osteogenic activities of recombinant human BMP-2, BMP-4, BMP-6, BMP-7, and BMP-9 adenoviruses were compared in vitro, in athymic nude rats, and in Sprague-Dawley rats. In vitro osteogenic activity was assessed by measuring the alkaline phosphatase activity in C2C12 cells transduced by the various BMP vectors. The alkaline phosphatase activity induced by 2 x 10(5) PFU/well of BMP viral vector was 4890 x 10(-12) U/well for ADCMVBMP-9, 302 x 10(-12) U/well for ADCMVBMP-4, 220 x 10(-12) U/well for ADCMVBMP-6, 45 x 10(-12) U/well for ADCMVBMP-2, and 0.43 x 10(-12) U/well for ADCMVBMP-7. The average volume of new bone induced by 10(7) PFU of BMP vector in athymic nude rats was 0.37+/-0.03 cm(3) for ADCMVBMP-2, 0.89+/-0.07 cm(3) for ADCMVBMP-4, 1.02+/-0.07 cm(3) for ADCMVBMP-6, 0.24+/-0.05 cm(3) for ADCMVBMP-7, and 0.63+/-0.07 cm(3) for ADCMVBMP-9. In immunocompetent Sprague-Dawley rats, no bone formation was demonstrated in the ADCMVBMP-2, ADCMVBMP-4, and ADCMVBMP-7 groups. ADCMVBMP-6 at a viral dose of 10(8) PFU induced 0.10+/-0.03 cm(3) of new bone, whereas ADCMVBMP-9 at a lower viral dose of 10(7) PFU induced more bone, with an average volume of 0.29+/-0.01 cm(3).

    Osteogenic potential of five different recombinant human bone morphogenetic protein adenoviral vectors in the rat. Publishing Authors By Initials

    jz liJZ Li,h liH Li,t sasakiT Sasaki,d holmanD Holman,b beresB Beres,rj dumontRJ Dumont,dd pittmanDD Pittman,gr hankinsGR Hankins,ga helmGA Helm,jz liJZ Li,h liH Li,t sasakiT Sasaki,d holmanD Holman,b beresB Beres,rj dumontRJ Dumont,dd pittmanDD Pittman,gr hankinsGR Hankins,ga helmGA Helm,

    For similar peptides: intercellular signaling peptides and proteins: cytokines: transforming growth factor beta research abstracts see: peptides: intercellular signaling peptides and proteins: cytokines: transforming growth factor beta research

    PUBMED ID PMID:

    MEDLINE DATE:

    Osteogenic potential of five different recombinant human bone morphogenetic protein adenoviral vectors in the rat. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Gene therapy

    VOLUME: 10

    Page Numbers: 1735-43

    Journal Abbreviation: Gene Ther.

    ISSN: 0969-7128

    DAY: 19

    MONTH: Sep

    YEAR: 2003

    Osteogenic potential of five different recombinant human bone morphogenetic protein adenoviral vectors in the rat. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9421525

    Osteogenic potential of five different recombinant human bone morphogenetic protein adenoviral vectors in the rat. Keywords Mesh Terms:

    KEYWORDS: Transforming Growth Factor beta

    MESH TERMS: methods

    Chemical & Substance for Abstract: Osteogenic potential of five different recombinant human bone morphogenetic protein adenoviral vectors in the rat. Information

    Substance Name: Alkaline Phosphatase

    Registry Number: EC 3.1.3.1

    Grant and Affiliation Information for Osteogenic potential of five different recombinant human bone morphogenetic protein adenoviral vectors in the rat.

    AFFILIATION: Molecular Neurosurgery Lab, Department of Neurosurgery, University of Virginia Health System, Charlottesville, VA 22908, USA.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NIAMS

    GRANT: R01 AR46488-01A2

    ACRONYM: AR

    MEDLINETA: Gene Ther

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