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Proprotein convertase 5/6a is associated with bone morphogenetic protein-2-induced squamous cell differentiation

DC FieldValueLanguage
dc.contributor.author윤주헌-
dc.contributor.author이민구-
dc.contributor.author이상남-
dc.date.accessioned2016-02-04T11:21:50Z-
dc.date.available2016-02-04T11:21:50Z-
dc.date.issued2015-
dc.identifier.issn1044-1549-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/140259-
dc.description.abstractSquamous metaplasia in airway epithelium is a pathological process arising from abnormal remodeling/repair responses to injury. Proteolytic maturation of many growth and differentiation factors involved in tissue remodeling is controlled by proprotein convertases (PCs). However, the role of these convertases in airway remodeling remains poorly understood. Using a retinoic acid deficiency-induced squamous metaplasia model of cultured human nasal epithelial cells (HNECs), we observed a significant increase in the expression of PC5/6A, a PC member, and bone morphogenetic protein-2 (BMP-2), a candidate substrate for PC5/6A. Specific lentiviral short hairpin RNA-mediated PC5/6A knockdown decreased BMP-2 expression and maturation, decreased expression of squamous cell markers, and increased expression of ciliated cell markers. Decanoyl-Arg-Val-Lys-Arg-chloromethylketone (Dec-RVKR-CMK), a PC inhibitor, and LDN-193189, a BMP receptor inhibitor, suppressed squamous differentiation, promoted mucociliary differentiation, and down-regulated the BMP-2/Smad1/5/8/p38 signaling pathways. Dec-RVKR-CMK also decreased expression of PC5/6A, but not furin, another PC member, suggesting the involvement of PC5/6A in squamous differentiation of HNECs. Overexpression of PC5/6A and BMP-2 in the human nasal epithelial cell line RPMI-2650 demonstrated that PC5/6A can activate BMP-2. Under retinoic acid-sufficient culture conditions for mucociliary differentiation of HNECs, short-term expression of PC5/6A by the adenovirus system and addition of exogenous BMP-2 induced squamous differentiation. Furthermore, PC5/6A and BMP-2 were highly expressed in metaplastic squamous epithelium of human nasal polyps. Taken together, PC5/6A is involved in squamous differentiation of HNECs, possibly through up-regulation of the BMP-2/pSmad1/5/8/p38 signaling pathway, pointing to a potential therapeutic target for the prevention of chronic airway diseases that exhibit squamous metaplasia.-
dc.description.statementOfResponsibilityopen-
dc.format.extent749~761-
dc.relation.isPartOfAMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHBone Morphogenetic Protein 2/physiology*-
dc.subject.MESHCell Differentiation*-
dc.subject.MESHCells, Cultured-
dc.subject.MESHEpithelial Cells/physiology*-
dc.subject.MESHHumans-
dc.subject.MESHNasal Mucosa/cytology-
dc.subject.MESHProprotein Convertase 5/physiology*-
dc.subject.MESHSmad Proteins/metabolism-
dc.subject.MESHTretinoin/metabolism-
dc.titleProprotein convertase 5/6a is associated with bone morphogenetic protein-2-induced squamous cell differentiation-
dc.typeArticle-
dc.contributor.collegeResearcher Institutes (부설 연구소)-
dc.contributor.department생체방어연구센터-
dc.contributor.googleauthorSang-Nam Lee-
dc.contributor.googleauthorDa-Hyung Lee-
dc.contributor.googleauthorMin Goo Lee-
dc.contributor.googleauthorJoo-Heon Yoon-
dc.identifier.doi10.1165/rcmb.2014-0029OC-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA02604-
dc.contributor.localIdA02781-
dc.contributor.localIdA02813-
dc.relation.journalcodeJ00113-
dc.identifier.eissn1535-4989-
dc.identifier.pmid25350918-
dc.identifier.urlhttp://www.atsjournals.org/doi/abs/10.1165/rcmb.2014-0029OC#.VlKnfE0ViUk-
dc.subject.keywordairway remodeling-
dc.subject.keywordbone morphogenetic protein-2-
dc.subject.keywordcultured human nasal epithelial cells-
dc.subject.keywordproprotein convertase 5/6A-
dc.subject.keywordsquamous differentiation-
dc.contributor.alternativeNameYoon, Joo Heon-
dc.contributor.alternativeNameLee, Min Goo-
dc.contributor.alternativeNameLee, Sang Nam-
dc.contributor.affiliatedAuthorYoon, Joo Heon-
dc.contributor.affiliatedAuthorLee, Min Goo-
dc.contributor.affiliatedAuthorLee, Sang Nam-
dc.rights.accessRightsnot free-
dc.citation.volume52-
dc.citation.number6-
dc.citation.startPage749-
dc.citation.endPage761-
dc.identifier.bibliographicCitationAMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, Vol.52(6) : 749-761, 2015-
Appears in Collections:
5. Research Institutes (연구소) > Research Center for Human Natural Defense System (생체방어연구센터) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers

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