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Protective effects of guggulsterone against colitis are associated with the suppression of TREM-1 and modulation of macrophages

DC Field Value Language
dc.contributor.author김원호-
dc.contributor.author김태일-
dc.contributor.author박기청-
dc.contributor.author박수정-
dc.contributor.author천재희-
dc.contributor.author김승원-
dc.date.accessioned2018-08-28T17:28:54Z-
dc.date.available2018-08-28T17:28:54Z-
dc.date.issued2018-
dc.identifier.issn0193-1857-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/162662-
dc.description.abstractTriggering receptor expressed on myeloid cells 1 (TREM-1)-expressing intestinal macrophages are significantly increased in the colons of patients with inflammatory bowel disease (IBD). We focused here on the effects of guggulsterone on macrophage modulation in colitis as a potential therapeutic molecule in human IBD and explore the underlying mechanisms. Gene expression in macrophages was examined and wound-healing assay using HT-29 cells was performed. Colitis in wild-type and IL-10-, Toll-like receptor 4 (TLR4)-, and myeloid differentiation primary response 88 (MyD88)-deficient mice was induced via the administration of 2,4,6-trinitrobenzene sulfonic acid (TNBS) into the colon. In both in vitro and in vivo experiments, guggulsterone suppressed intestinal inflammation amplified by TREM-1 stimulation, in which the suppression of NF-kappaB, activating protein-1, and proteasome pathways was involved. In the TNBS-induced colitis model, guggulsterone reduced disease activity index scores and TREM-1 expression, stimulated IL-10 production, and improved survival in wild-type mice. These effects were not observed in IL-10-, TLR4-, and MyD88-deficient mice. Guggulsterone also suppressed M1 polarization, yet induced the M2 phenotype in macrophages from IBD patients as well as from mice. These findings indicate that guggulsterone blocks the hyperactivation of macrophages via TREM-1 suppression and induces M2 polarization via IL-10 mediated by the TLR4 signaling pathway. Furthermore, this study provides a new rationale for the therapeutic potential of guggulsterone in the treatment of IBD. NEW & NOTEWORTHY We found that guggulsterone attenuates triggering receptor expressed on myeloid cells 1 (TREM-1)-mediated hyperactivation of macrophages and polarizes macrophages toward the M2 phenotype. This was mediated by IL-10 and partly Toll-like receptor 4 signaling pathways. Overall, these data support that guggulsterone as a natural plant sterol modulates macrophage phenotypes in colitis, which may be of novel therapeutic importance in inflammatory bowel disease treatment.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherAmerican Physiological Society-
dc.relation.isPartOfAMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleProtective effects of guggulsterone against colitis are associated with the suppression of TREM-1 and modulation of macrophages-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Internal Medicine-
dc.contributor.googleauthorXiumei Che-
dc.contributor.googleauthorKi Cheong Park-
dc.contributor.googleauthorSoo Jung Park-
dc.contributor.googleauthorYou Hyun Kang-
dc.contributor.googleauthorHyun A Jin-
dc.contributor.googleauthorJoo Wan Kim-
dc.contributor.googleauthorDong Hyuk Seo-
dc.contributor.googleauthorDae Kyu Kim-
dc.contributor.googleauthorTae Il Kim-
dc.contributor.googleauthorWon Ho Kim-
dc.contributor.googleauthorSeung Won Kim-
dc.contributor.googleauthorJae Hee Cheon-
dc.identifier.doi10.1152/ajpgi.00027.2018-
dc.contributor.localIdA00774-
dc.contributor.localIdA01079-
dc.contributor.localIdA01449-
dc.contributor.localIdA01539-
dc.contributor.localIdA04030-
dc.relation.journalcodeJ00104-
dc.identifier.eissn1522-1547-
dc.identifier.pmid29543509-
dc.identifier.urlhttps://www.physiology.org/doi/10.1152/ajpgi.00027.2018-
dc.subject.keywordM2 macrophage-
dc.subject.keywordguggulsterone-
dc.subject.keywordinflammatory bowel disease-
dc.subject.keywordinterleukin-10-
dc.subject.keywordtriggering receptor expressed on myeloid cells 1-
dc.contributor.alternativeNameKim, Won Ho-
dc.contributor.alternativeNameKim, Tae Il-
dc.contributor.alternativeNamePark, Ki Cheong-
dc.contributor.alternativeNamePark, Soo Jung-
dc.contributor.alternativeNameCheon, Jae Hee-
dc.contributor.affiliatedAuthorKim, Won Ho-
dc.contributor.affiliatedAuthorKim, Tae Il-
dc.contributor.affiliatedAuthorPark, Ki Cheong-
dc.contributor.affiliatedAuthorPark, Soo Jung-
dc.contributor.affiliatedAuthorCheon, Jae Hee-
dc.citation.volume315-
dc.citation.number1-
dc.citation.startPageg128-
dc.citation.endPageg139-
dc.identifier.bibliographicCitationAMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, Vol.315(1) : g128-g139, 2018-
dc.identifier.rimsid60241-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Others (기타) > 1. Journal Papers

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