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Bifunctional role of ephrin A1-Eph system in stimulating cell proliferation and protecting cells from cell death through the attenuation of ER stress and inflammatory responses in bovine mammary epithelial cells

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dc.contributor.authorKang, Minkyung-
dc.contributor.authorJeong, Wooyoung-
dc.contributor.authorBae, Hyocheol-
dc.contributor.authorLim, Whasun-
dc.contributor.authorBazer, Fuller W.-
dc.contributor.authorSong, Gwonhwa-
dc.date.accessioned2021-09-02T14:50:07Z-
dc.date.available2021-09-02T14:50:07Z-
dc.date.created2021-06-16-
dc.date.issued2018-03-
dc.identifier.issn0021-9541-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/77295-
dc.description.abstractStructural and functional development of themammary gland is constant in themammary gland life cycle. Ephreceptors and their ligands, ephrins, control events through cell-to-cell interactions during embryonic development, and adult tissue homeostasis; however, little information on participation of ephrin A1, a representative ligand of the Eph receptor, in the development and function of normal mammary glands is known. In this study, we demonstrated functional effects of the ephrin A1-Eph system and mechanisms of its action on bovine mammary epithelial (MAC-T) cells. The in vitro cultured MAC-T cells expressed the ephrin A1 ligand and EphA1, A2, A4, A7, and A8 among the eight members of the Eph A family. Our results revealed that ephrin A1 induced MAC-T cell cycle progression and stimulated cell proliferation with abundant expression of nucleic PCNA and cyclin D1 proteins. Additionally, ephrin A1 induced activation of intracellular signaling molecules involved in PI3 K/AKT and MAPK signaling, and the proliferation-stimulating effect of ephrin A1 was mediated by activation of these pathways. Furthermore, ephrin A1 influenced expression and activation of various ER stress-related proteins and protected MAC-T cells from stress-induced cell death. Finally, ephrin A1 alleviated LPS-induced cell death through down-regulation of inflammatory cytokines. In conclusion, the results of this study suggest that the Eph A-ephrin A1 system is a positive factor in the increase and maintenance of epithelial cells in mammary glands of cows; the signaling system contributes to development, remodeling, and functionality of normal mammary glands and could overcome mastitis in cows and other mammals.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-
dc.subjectRECEPTOR TYROSINE KINASE-
dc.subjectENDOPLASMIC-RETICULUM STRESS-
dc.subjectDAIRY-COWS-
dc.subjectGLAND DEVELOPMENT-
dc.subjectDRY PERIOD-
dc.subjectCYCLE PROGRESSION-
dc.subjectMILK-PRODUCTION-
dc.subjectAMINO-ACIDS-
dc.subjectLACTATION-
dc.subjectMORPHOGENESIS-
dc.titleBifunctional role of ephrin A1-Eph system in stimulating cell proliferation and protecting cells from cell death through the attenuation of ER stress and inflammatory responses in bovine mammary epithelial cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorSong, Gwonhwa-
dc.identifier.doi10.1002/jcp.26131-
dc.identifier.scopusid2-s2.0-85030027316-
dc.identifier.wosid000433519300071-
dc.identifier.bibliographicCitationJOURNAL OF CELLULAR PHYSIOLOGY, v.233, no.3, pp.2560 - 2571-
dc.relation.isPartOfJOURNAL OF CELLULAR PHYSIOLOGY-
dc.citation.titleJOURNAL OF CELLULAR PHYSIOLOGY-
dc.citation.volume233-
dc.citation.number3-
dc.citation.startPage2560-
dc.citation.endPage2571-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaPhysiology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.subject.keywordPlusRECEPTOR TYROSINE KINASE-
dc.subject.keywordPlusENDOPLASMIC-RETICULUM STRESS-
dc.subject.keywordPlusDAIRY-COWS-
dc.subject.keywordPlusGLAND DEVELOPMENT-
dc.subject.keywordPlusDRY PERIOD-
dc.subject.keywordPlusCYCLE PROGRESSION-
dc.subject.keywordPlusMILK-PRODUCTION-
dc.subject.keywordPlusAMINO-ACIDS-
dc.subject.keywordPlusLACTATION-
dc.subject.keywordPlusMORPHOGENESIS-
dc.subject.keywordAuthorEph A-
dc.subject.keywordAuthorephrin A1-
dc.subject.keywordAuthormammary epithelial cells-
dc.subject.keywordAuthormammary gland-
dc.subject.keywordAuthormilk production-
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