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Human endothelial cell growth and phenotypic expression on three dimensional poly(lactide-co-glycolide) sintered microsphere scaffolds for bone tissue engineering.

Human endothelial cell growth and phenotypic expression on three dimensional poly(lactide-co-glycolide) sintered microsphere scaffolds for bone tissue engineering. Research Abstract Details 

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  • Human endothelial cell growth and phenotypic expression on three dimensional poly(lactide-co-glycolide) sintered microsphere scaffolds for bone tissue engineering. Abstract Text:

    ehsan jabbarzadehEhsan Jabbarzadeh,tao jiangTao Jiang,meng dengMeng Deng,lakshmi s nairLakshmi S Nair,yusuf m khanYusuf M Khan,cato t laurencinCato T Laurencin,ehsan jabbarzadehEhsan Jabbarzadeh,tao jiangTao Jiang,meng dengMeng Deng,lakshmi s nairLakshmi S Nair,yusuf m khanYusuf M Khan,cato t laurencinCato T Laurencin,

    Bone tissue engineering offers promising alternatives to repair and restore tissues. Our laboratory has employed poly(lactide-co-glycolide) PLAGA microspheres to develop a three dimensional (3-D) porous bioresorbable scaffold with a biomimetic pore structure. Osseous healing and integration with the surrounding tissue depends in part on new blood vessel formation within the porous structure. Since endothelial cells play a key role in angiogenesis (formation of new blood vessels from pre-existing vasculature), the purpose of this study was to better understand human endothelial cell attachment, viability, growth, and phenotypic expression on sintered PLAGA microsphere scaffold. Scanning electron microscopy (SEM) examination showed cells attaching to the surface of microspheres and bridging the pores between the microspheres. Cell proliferation studies indicated that cell number increased during early stages and reached a plateau between days 10 and 14. Immunofluorescent staining for actin showed that cells were proliferating three dimensionally through the scaffolds while staining for PECAM-1 (platelet endothelial cell adhesion molecule) displayed typical localization at cell-cell contacts. Gene expression analysis showed that endothelial cells grown on PLAGA scaffolds maintained their normal characteristic phenotype. The cell proliferation and phenotypic expression were independent of scaffold pore architecture. These results demonstrate that PLAGA sintered microsphere scaffolds can support the growth and biological functions of human endothelial cells. The insights from this study should aid future studies aimed at enhancing angiogenesis in three dimensional tissue engineered scaffolds.

    Human endothelial cell growth and phenotypic expression on three dimensional poly(lactide-co-glycolide) sintered microsphere scaffolds for bone tissue engineering. Publishing Authors By Initials

    e jabbarzadehE Jabbarzadeh,t jiangT Jiang,m dengM Deng,ls nairLS Nair,ym khanYM Khan,ct laurencinCT Laurencin,e jabbarzadehE Jabbarzadeh,t jiangT Jiang,m dengM Deng,ls nairLS Nair,ym khanYM Khan,ct laurencinCT Laurencin,

    For similar abstracts research abstracts see: abstracts research

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    Human endothelial cell growth and phenotypic expression on three dimensional poly(lactide-co-glycolide) sintered microsphere scaffolds for bone tissue engineering. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Biotechnology and bioengineering

    VOLUME: 98

    Page Numbers: 1094-102

    Journal Abbreviation: Biotechnol. Bioeng.

    ISSN: 0006-3592

    DAY: 1

    MONTH: Dec

    YEAR: 2007

    Human endothelial cell growth and phenotypic expression on three dimensional poly(lactide-co-glycolide) sintered microsphere scaffolds for bone tissue engineering. Information

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    LANGUAGE: eng

    NlmUniqueID: 7502021

    Human endothelial cell growth and phenotypic expression on three dimensional poly(lactide-co-glycolide) sintered microsphere scaffolds for bone tissue engineering. Keywords Mesh Terms:

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    Grant and Affiliation Information for Human endothelial cell growth and phenotypic expression on three dimensional poly(lactide-co-glycolide) sintered microsphere scaffolds for bone tissue engineering.

    AFFILIATION: Department of Orthopaedic Surgery, University of Virginia, 400 Ray C. Hunt Drive, Suite 330, Charlottesville, Virginia 22903, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIAMS

    GRANT: R01-AR052536

    ACRONYM: AR

    MEDLINETA: Biotechnol Bioeng

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