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Enhanced expression of transglutaminase 2 in anterior polar cataracts and its induction by TGF-B in vitro

DC Field Value Language
dc.contributor.author고형준-
dc.contributor.author김응권-
dc.contributor.author김찬윤-
dc.contributor.author이종복-
dc.date.accessioned2016-05-16T11:13:31Z-
dc.date.available2016-05-16T11:13:31Z-
dc.date.issued2002-
dc.identifier.issn0007-1161-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/144071-
dc.description.abstractBackground/aims: Transglutaminase activity has long been implicated in the cataract formation. However, the precise mechanism of how it is produced and involved in this process remains unclear. Here the authors sought to examine whether transglutaminase 2 (TGase 2) is expressed in lens epithelial cells from patients with anterior polar cataracts, to determine whether TGase 2 expression is induced by transforming growth factor (TGF-β) in cultured lens epithelial cells, and to determine whether TGase 2 participates in the crosslinking of fibronectin in lens epithelial cells in vitro. Methods: Lens epithelial cells from anterior polar cataracts, nuclear cataracts, and non-cataractous clear lenses were examined for the expression of TGase 2 using reverse transcription-polymerase chain reaction, western blot analysis, and immunohistochemical analysis. The modulation of extracellular TGase 2 activity by TGF-β was measured by the formation of fibronectin polymers and the incorporation of fluorescein cadaverine into extracellular matrix proteins. The effect of TGase 2 overexpression was analysed by immunofluorescence staining and western blot analysis of human lens epithelial (HLE) B-3 cells transiently transfected with TGase 2 gene. Results: The expression of TGase 2 mRNA and its protein was markedly enhanced in lens epithelial cells from patients with anterior polar cataracts. Treatment of HLE B-3 cells with TGF-β caused an increase in TGase 2 protein, its extracellular activity, and the crosslinking of fibronectin. Transient transfection of HLE B-3 cells with the TGase 2 gene led to the increased production of fibronectin monomers and polymers. Conclusions: This study shows that TGase 2 is overexpressed in lens epithelial cells from anterior polar cataracts and that TGF-β may be a causative factor in the induction of TGase 2. The enhanced expression of TGase 2 might cause the accumulation and crosslinking of the extracellular matrix proteins and might play a part in anterior polar cataract development.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1293~1298-
dc.relation.isPartOfBRITISH JOURNAL OF OPHTHALMOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAged-
dc.subject.MESHBlotting, Western-
dc.subject.MESHCadaverine/analogs & derivatives*-
dc.subject.MESHCadaverine/pharmacology-
dc.subject.MESHCataract/enzymology*-
dc.subject.MESHCell Line-
dc.subject.MESHEnzyme Inhibitors/pharmacology-
dc.subject.MESHEpithelium/drug effects-
dc.subject.MESHEpithelium/enzymology-
dc.subject.MESHFemale-
dc.subject.MESHFibronectins/metabolism-
dc.subject.MESHFluorescent Antibody Technique-
dc.subject.MESHGTP-Binding Proteins/genetics*-
dc.subject.MESHGTP-Binding Proteins/metabolism-
dc.subject.MESHGene Expression/genetics*-
dc.subject.MESHHumans-
dc.subject.MESHLens, Crystalline/drug effects-
dc.subject.MESHLens, Crystalline/enzymology*-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHRNA, Messenger/genetics-
dc.subject.MESHTransfection-
dc.subject.MESHTransforming Growth Factor beta/metabolism*-
dc.subject.MESHTransglutaminases/genetics*-
dc.subject.MESHTransglutaminases/metabolism-
dc.titleEnhanced expression of transglutaminase 2 in anterior polar cataracts and its induction by TGF-B in vitro-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Ophthalmology (안과학)-
dc.contributor.googleauthorX.H. Wan-
dc.contributor.googleauthorE. H. Lee-
dc.contributor.googleauthorH.J. Koh-
dc.contributor.googleauthorJ. Song-
dc.contributor.googleauthorE.K. Kim-
dc.contributor.googleauthorC.Y. Kim-
dc.contributor.googleauthorJ.B. Lee-
dc.contributor.googleauthorS. Y. Kim-
dc.contributor.googleauthorK. Yao-
dc.contributor.googleauthorJ. H. Lee-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00152-
dc.contributor.localIdA00831-
dc.contributor.localIdA01035-
dc.contributor.localIdA03140-
dc.relation.journalcodeJ00412-
dc.identifier.eissn1468-2079-
dc.identifier.pmid12386092-
dc.contributor.alternativeNameKoh, Hyoung Jun-
dc.contributor.alternativeNameKim, Eung Kweon-
dc.contributor.alternativeNameKim, Chan Yun-
dc.contributor.alternativeNameLee, Jong Bok-
dc.contributor.affiliatedAuthorKoh, Hyoung Jun-
dc.contributor.affiliatedAuthorKim, Eung Kweon-
dc.contributor.affiliatedAuthorKim, Chan Yun-
dc.contributor.affiliatedAuthorLee, Jong Bok-
dc.rights.accessRightsfree-
dc.citation.volume86-
dc.citation.number11-
dc.citation.startPage1293-
dc.citation.endPage1298-
dc.identifier.bibliographicCitationBRITISH JOURNAL OF OPHTHALMOLOGY, Vol.86(11) : 1293-1298, 2002-
dc.identifier.rimsid55563-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Ophthalmology (안과학교실) > 1. Journal Papers

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