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Immobilized rhBMP-2/succinylated type I atelocollagen gene expression of intracellular signaling molecules on ST2 cells.

Immobilized rhBMP-2/succinylated type I atelocollagen gene expression of intracellular signaling molecules on ST2 cells. Research Abstract Details 

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  • Immobilized rhBMP-2/succinylated type I atelocollagen gene expression of intracellular signaling molecules on ST2 cells. Abstract Text:

    hidetsugu tsujigiwaHidetsugu Tsujigiwa,hitoshi nagatsukaHitoshi Nagatsuka,you jin leeYou Jin Lee,phuu pwint hanPhuu Pwint Han,mehmet gunduzMehmet Gunduz,racquel z legerosRacquel Z Legeros,masahisa inoueMasahisa Inoue,masao yamadaMasao Yamada,noriyuki nagaiNoriyuki Nagai,

    Recombinant human bone morphogenetic protein-2 (rhBMP-2) chemically-bonded to succinylated type I atelocollagen, a biomaterial carrier with a porous structure, was reported to augment cellular activity of ST2 cells. The Smad protein family has been suggested to play an important role in the intracellular signaling pathway of BMP by its binding to receptors on target cells. However, there has been no study analyzing the downstream genes of the rhBMP-2 induced intracellular signal transduction pathway. The purpose of this study was to examine the effect of immobilized rhBMP-2 on gene expression of intracellular signaling molecules on ST2 cells. Our study showed two expression patterns of downstream genes of rhBMP-2 intracellular signal transduction pathway. In the first pattern, BMPR-IA, Smad 1, and Smad 5 genes showed high basic expression before the addition of rhBMP, and the high level of gene expression continued for long period and decreased in the late stage when rhBMP-2 was immobilized. In the second pattern, Smad 6, Smad 7, and Smad 8 genes showed low basic expression before the addition of rhBMP-2 and a continuous increase from the beginning was followed by a decrease in the late stage when rhBMP-2 was immobilized. Our results also showed that intracellular signaling continued for prolonged period when rhBMP-2 was immobilized to succinylated type I atelocollagen. This study indicated that immobilizing rhBMP-2 is an efficient method to increase bone induction.

    Immobilized rhBMP-2/succinylated type I atelocollagen gene expression of intracellular signaling molecules on ST2 cells. Publishing Authors By Initials

    h tsujigiwaH Tsujigiwa,h nagatsukaH Nagatsuka,yj leeYJ Lee,pp hanPP Han,m gunduzM Gunduz,rz legerosRZ Legeros,m inoueM Inoue,m yamadaM Yamada,n nagaiN Nagai,

    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

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    Immobilized rhBMP-2/succinylated type I atelocollagen gene expression of intracellular signaling molecules on ST2 cells. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of biomedical materials research. Part A

    VOLUME: 77

    Page Numbers: 507-11

    Journal Abbreviation:

    ISSN: 1549-3296

    DAY: 1

    MONTH: Jun

    YEAR: 2006

    Immobilized rhBMP-2/succinylated type I atelocollagen gene expression of intracellular signaling molecules on ST2 cells. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101234237

    Immobilized rhBMP-2/succinylated type I atelocollagen gene expression of intracellular signaling molecules on ST2 cells. Keywords Mesh Terms:

    KEYWORDS: Transforming Growth Factor beta

    MESH TERMS: physiology

    Chemical & Substance for Abstract: Immobilized rhBMP-2/succinylated type I atelocollagen gene expression of intracellular signaling molecules on ST2 cells. Information

    Substance Name: Collagen

    Registry Number: 9007-34-5

    Grant and Affiliation Information for Immobilized rhBMP-2/succinylated type I atelocollagen gene expression of intracellular signaling molecules on ST2 cells.

    AFFILIATION: Department of Virology, Graduate School of Medicine and Dentistry, Okayama University, Okayama, Japan.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Biomed Mater Res A

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