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Chemokine bioactivity of RANTES in endometriotic and normal endometrial stromal cells and peritoneal fluid.

Chemokine bioactivity of RANTES in endometriotic and normal endometrial stromal cells and peritoneal fluid. Research Abstract Details 

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  • Chemokine bioactivity of RANTES in endometriotic and normal endometrial stromal cells and peritoneal fluid. Abstract Text:

    d hornungD Hornung,f bentzienF Bentzien,d wallwienerD Wallwiener,l kieselL Kiesel,r n taylorR N Taylor,

    Endometriotic lesions secrete chemokines that recruit immune cells into the peritoneal cavity. The accumulation of these immune cells, especially activated macrophages and T lymphocytes, is thought to mediate inflammatory symptoms associated with endometriosis. Previous studies have demonstrated that RANTES (regulated on activation, normal T cell expressed and secreted) is synthesized by endometriotic stromal cells and circulates in peritoneal fluid, commensurate with the stage of endometriosis. In the current studies, we used the human monocytic cell line, U937, to assay chemotactic activity in cell culture conditioned media and peritoneal fluid from patients with endometriosis and normal controls. We demonstrated expression of the human RANTES receptors CCR-1 and CCR-5 in U937 cells and peritoneal macrophages. Over a range of 0-1000 pg/ml recombinant human RANTES had a direct, linear effect on monocyte migration. Conditioned media and peritoneal fluid induced dose-dependent effects on monocyte migration that were correlated with concentrations of immunoreactive RANTES (as measured by enzyme-linked immunosorbent assay) and the severity of endometriosis. Heat denaturation of the RANTES protein or addition of anti-human RANTES antibodies neutralized the chemoattractant effects of conditioned media and peritoneal fluid. RANTES stimulation of monocyte recruitment may be an important pathogenetic target for the treatment of infertility and pain associated with endometriosis.

    Chemokine bioactivity of RANTES in endometriotic and normal endometrial stromal cells and peritoneal fluid. Publishing Authors By Initials

    d hornungD Hornung,f bentzienF Bentzien,d wallwienerD Wallwiener,l kieselL Kiesel,rn taylorRN Taylor,

    For similar cells: cells, cultured: cell line: cell line, tumor: u937 cells research abstracts see: cells: cells, cultured: cell line: cell line, tumor: u937 cells research

    PUBMED ID PMID:

    MEDLINE DATE:

    Chemokine bioactivity of RANTES in endometriotic and normal endometrial stromal cells and peritoneal fluid. Journal Published:

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

    Journal: Molecular human reproduction

    VOLUME: 7

    Page Numbers: 163-8

    Journal Abbreviation: Mol. Hum. Reprod.

    ISSN: 1360-9947

    DAY: 19

    MONTH: Feb

    YEAR: 2001

    Chemokine bioactivity of RANTES in endometriotic and normal endometrial stromal cells and peritoneal fluid. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9513710

    Chemokine bioactivity of RANTES in endometriotic and normal endometrial stromal cells and peritoneal fluid. Keywords Mesh Terms:

    KEYWORDS: U937 Cells

    MESH TERMS: immunology

    Chemical & Substance for Abstract: Chemokine bioactivity of RANTES in endometriotic and normal endometrial stromal cells and peritoneal fluid. Information

    Substance Name: Receptors, Chemokine

    Registry Number: 0

    Grant and Affiliation Information for Chemokine bioactivity of RANTES in endometriotic and normal endometrial stromal cells and peritoneal fluid.

    AFFILIATION: Department of Obstetrics and Gynecology, 72076 Tübingen, Germany.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NICHD

    GRANT: U54-HD37321

    ACRONYM: HD

    MEDLINETA: Mol Hum Reprod

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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