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Use of a chimeric adenovirus vector enhances BMP2 production and bone formation.

Use of a chimeric adenovirus vector enhances BMP2 production and bone formation. Research Abstract Details 

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  • Use of a chimeric adenovirus vector enhances BMP2 production and bone formation. Abstract Text:

    elizabeth a olmsted-davisElizabeth A Olmsted-Davis,zbigniew gugalaZbigniew Gugala,francis h gannonFrancis H Gannon,patricia yotndaPatricia Yotnda,robert e mcalhanyRobert E McAlhany,ronald w lindseyRonald W Lindsey,alan r davisAlan R Davis,

    Recombinant adenoviral vectors have potential for the treatment of a variety of musculoskeletal defects and such gene therapy systems have been a recent research focus in orthopedic surgery. In studies reported here, two different adenovirus vectors have been compared for their ability to transduce human bone marrow mesenchymal stem cells (hBM-MSCs) and elicit bone formation in vivo. Vectors consisted either of standard adenovirus type 5 (Ad5) vector or a chimeric adenovirus type 5 vector that contains an adenovirus type 35 fiber (Ad5F35), which has been recently demonstrated to bestow a different cellular tropism, and a complete cDNA encoding human bone morphogenetic 2 (BMP2). Studies were also conducted to compare the transduction efficiency of these vectors using enhanced green fluorescent protein (GFP). hBM-MSCs transduced with Ad5F35 vectors had higher levels of transgene expression than those transduced with Ad5 vectors. The results also demonstrate that hBM-MSCs lack the coxsackie-adenovirus receptor (CAR), which is responsible for cellular adsorption of Ad5. Therefore, the data suggest that Ad5 virus adsorption to hBM-MSCs is inefficient. Ad5BMP2- or Ad5F35BMP2-transduced hBM-MSCs were also compared in an in vivo heterotopic bone formation assay. Mineralized bone was radiologically identified only in muscle that received the Ad5F35BMP2 transduced hBM-MSCs. In summary, Ad5F35BMP2 can efficiently transduce hBM-MSCs leading to enhanced bone formation in vivo.

    Use of a chimeric adenovirus vector enhances BMP2 production and bone formation. Publishing Authors By Initials

    ea olmsted-davisEA Olmsted-Davis,z gugalaZ Gugala,fh gannonFH Gannon,p yotndaP Yotnda,re mcalhanyRE McAlhany,rw lindseyRW Lindsey,ar davisAR Davis,

    For similar cells: cells, cultured: tumor cells, cultured research abstracts see: cells: cells, cultured: tumor cells, cultured research

    PUBMED ID PMID:

    MEDLINE DATE:

    Use of a chimeric adenovirus vector enhances BMP2 production and bone formation. Journal Published:

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

    Journal: Human gene therapy

    VOLUME: 13

    Page Numbers: 1337-47

    Journal Abbreviation: Hum. Gene Ther.

    ISSN: 1043-0342

    DAY: 20

    MONTH: Jul

    YEAR: 2002

    Use of a chimeric adenovirus vector enhances BMP2 production and bone formation. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9008950

    Use of a chimeric adenovirus vector enhances BMP2 production and bone formation. Keywords Mesh Terms:

    KEYWORDS: Tumor Cells, Cultured

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Use of a chimeric adenovirus vector enhances BMP2 production and bone formation. Information

    Substance Name: Green Fluorescent Proteins

    Registry Number: 147336-22-9

    Grant and Affiliation Information for Use of a chimeric adenovirus vector enhances BMP2 production and bone formation.

    AFFILIATION: Center for Cell and Gene Therapy, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIAMS

    GRANT: R21AR484-01

    ACRONYM: AR

    MEDLINETA: Hum Gene Ther

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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