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Elevation of transforming growth factor beta (TGFbeta) and its downstream mediators in subcutaneous foreign body capsule tissue.

Elevation of transforming growth factor beta (TGFbeta) and its downstream mediators in subcutaneous foreign body capsule tissue. Research Abstract Details 

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  • Elevation of transforming growth factor beta (TGFbeta) and its downstream mediators in subcutaneous foreign body capsule tissue. Abstract Text:

    allen g liAllen G Li,matthew j quinnMatthew J Quinn,yasmin siddiquiYasmin Siddiqui,michael d woodMichael D Wood,isaac f federiukIsaac F Federiuk,heather m dumanHeather M Duman,w kenneth wardW Kenneth Ward,

    Foreign body encapsulation represents a chronic fibrotic response and has been a major obstacle that reduces the useful life of implanted biomedical devices. The precise mechanism underlying such an encapsulation is still unknown. We hypothesized that, considering its central role in many other fibrotic conditions, transforming growth factor beta (TGFbeta) may play an important role during the formation of foreign body capsule (FBC). In the present study, we implanted mock sensors in rats subcutaneously and excised FBC samples at day 7, 21, and 48-55 postimplantation. The most abundant TGFbeta isoform in all tissues was TGFbeta1, which was expressed minimally in control tissue. The expression of both TGFbeta1 RNA and protein was significantly increased in FBC tissues at all time points, with the highest level in day 7 FBC. The number of cells stained for phosphorylated Smad2, an indication of activated TGFbeta signaling, paralleled the expression of TGFbeta. A similar dynamic change was also observed in the numbers of FBC myofibroblasts, which in response to TGFbeta, differentiate from quiescent fibroblasts and synthesize collagen. Type I collagen, the most prominent downstream target of TGFbeta in fibrosis, was found in abundance in the FBC, especially during the latter time periods. We suggest that TGFbeta plays an important role in the FBC formation. Inhibition of TGFbeta signaling could be a promising strategy in the prevention of FBC formation, thereby extending the useful life of subcutaneous implants.

    Elevation of transforming growth factor beta (TGFbeta) and its downstream mediators in subcutaneous foreign body capsule tissue. Publishing Authors By Initials

    ag liAG Li,mj quinnMJ Quinn,y siddiquiY Siddiqui,md woodMD Wood,if federiukIF Federiuk,hm dumanHM Duman,wk wardWK Ward,

    For similar peptides: intercellular signaling peptides and proteins: cytokines: transforming growth factor beta: transforming growth factor beta1 research abstracts see: peptides: intercellular signaling peptides and proteins: cytokines: transforming growth factor beta: transforming growth factor beta1 research

    PUBMED ID PMID:

    MEDLINE DATE:

    Elevation of transforming growth factor beta (TGFbeta) and its downstream mediators in subcutaneous foreign body capsule tissue. Journal Published:

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

    Journal: Journal of biomedical materials research. Part A

    VOLUME: 82

    Page Numbers: 498-508

    Journal Abbreviation:

    ISSN: 1549-3296

    DAY: 3

    MONTH: Aug

    YEAR: 2007

    Elevation of transforming growth factor beta (TGFbeta) and its downstream mediators in subcutaneous foreign body capsule tissue. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101234237

    Elevation of transforming growth factor beta (TGFbeta) and its downstream mediators in subcutaneous foreign body capsule tissue. Keywords Mesh Terms:

    KEYWORDS: Transforming Growth Factor beta1

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Elevation of transforming growth factor beta (TGFbeta) and its downstream mediators in subcutaneous foreign body capsule tissue. Information

    Substance Name: Transforming Growth Factor beta1

    Registry Number: 0

    Grant and Affiliation Information for Elevation of transforming growth factor beta (TGFbeta) and its downstream mediators in subcutaneous foreign body capsule tissue.

    AFFILIATION: Department of Dermatology, Oregon Health and Science University, Portland, Oregon 97239, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIBIB

    GRANT: R01 EB000743

    ACRONYM: EB

    MEDLINETA: J Biomed Mater Res A

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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