Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13294
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dc.contributor.authorSrisomboon Y.
dc.contributor.authorPoonyachoti S.
dc.contributor.authorDeachapunya C.
dc.date.accessioned2021-04-05T03:23:08Z-
dc.date.available2021-04-05T03:23:08Z-
dc.date.issued2017
dc.identifier.issn10467408
dc.identifier.other2-s2.0-85018643426
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13294-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85018643426&doi=10.1111%2faji.12694&partnerID=40&md5=a23dacb15a155ec8658f7667e2b2e2b6
dc.description.abstractProblem: β-defensins are important innate chemical barriers that protect the endometrium from pathogen invasion. The effects of soy isoflavones, genistein and daidzein, on the expression and secretion of porcine β-defensins (PBD) in endometrial epithelial cells were investigated under normal or poly I:C-stimulated conditions. Method of study: Primary cultured porcine endometrial epithelial (PE) cells were pretreated with genistein or daidzein followed by poly I:C inoculation. During treatment, the culture media were analyzed for PBD 1-4 secretion by ELISA and the total RNA for PBD gene expression by quantitative RT-PCR. Results: Porcine endometrial epithelial cells constitutively expressed PBD 1-4 and secreted PBD-1, PBD-2, and PBD-4. Genistein and daidzein enhanced PBD-2 expression and PBD-2 and PBD-3 secretion. These compounds also potentiated PBD-2 and PBD-3 expression and secretion which were upregulated by poly I:C. Conclusion: Soy isoflavones, genistein and daidzein, could be potentially used for promoting the innate host defense of endometrium against infection. © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
dc.subjectbeta defensin
dc.subjectbeta defensin 1
dc.subjectbeta defensin 2
dc.subjectbeta defensin 3
dc.subjectbeta defensin 4
dc.subjectdaidzein
dc.subjectgenistein
dc.subjectmessenger RNA
dc.subjectpolyinosinic polycytidylic acid
dc.subjectantiinfective agent
dc.subjectbeta defensin
dc.subjectdaidzein
dc.subjectgenistein
dc.subjectisoflavone derivative
dc.subjectpolyinosinic polycytidylic acid
dc.subjectanimal cell
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectdrug effect
dc.subjectdrug response
dc.subjectendometrium cell
dc.subjectenzyme linked immunosorbent assay
dc.subjectfemale
dc.subjectgene expression
dc.subjectinoculation
dc.subjectnonhuman
dc.subjectpig
dc.subjectprimary cell culture
dc.subjectpriority journal
dc.subjectprotein secretion
dc.subjectprotein synthesis
dc.subjectquantitative analysis
dc.subjectreal time polymerase chain reaction
dc.subjectupregulation
dc.subjectanimal
dc.subjectcell culture
dc.subjectcytology
dc.subjectendometrium
dc.subjectepithelium cell
dc.subjectgene expression regulation
dc.subjectgenetics
dc.subjectimmunology
dc.subjectinnate immunity
dc.subjectmetabolism
dc.subjectsoybean
dc.subjectAnimals
dc.subjectAnti-Bacterial Agents
dc.subjectbeta-Defensins
dc.subjectCells, Cultured
dc.subjectEndometrium
dc.subjectEpithelial Cells
dc.subjectFemale
dc.subjectGene Expression Regulation
dc.subjectGenistein
dc.subjectImmunity, Innate
dc.subjectIsoflavones
dc.subjectPoly I-C
dc.subjectSoybeans
dc.subjectSwine
dc.titleSoy isoflavones enhance β-defensin synthesis and secretion in endometrial epithelial cells with exposure to TLR3 agonist polyinosinic-polycytidylic acid
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationAmerican Journal of Reproductive Immunology. Vol 78, No.4 (2017)
dc.identifier.doi10.1111/aji.12694
Appears in Collections:Scopus 1983-2021

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