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The AdLMP-1 transfection in two different cells; AF cells, chondrocytes as potential cell therapy candidates for disc degeneration.

DC Field Value Language
dc.contributor.author구성욱-
dc.date.accessioned2015-05-19T16:44:55Z-
dc.date.available2015-05-19T16:44:55Z-
dc.date.issued2008-
dc.identifier.issn0001-6268-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/106871-
dc.description.abstractBACKGROUND: LMP-1 is known to increase proteoglycan production through the upregulating the BMPs and it is also known that BMP-2 acts on anulus fibrosus cells and chondrocytes to increase proteoglycan production. METHOD: We carried out an experiment, the effect of AdLMP-1 transfection on AF cells and chondrocytes in the production of sulfated-glycosaminoglycans, mRNA expression (aggrecan, type I, II collagen, LMP-1, BMP-2, and BMP-7), and immunofluorescence staining. AF cells and chondrocytes were grown in monolayer and treated for 6 days with AdLMP1-green fluorescence protein (GFP) (10, 20, and 30 multiplicity of infection [MOI]). After 6 days, the sGAG content in the media was quantified using 1,9-dimethylmethylene blue staining. The mRNA expression was measured with real-time PCR after 20 MOI infection of AdLMP1-GFP. The each cells treated with 20 MOI infection of AdGFP was used as a control group for the mRNA expression. The each cell group was immunofluorescence stained with each antibodies in the chamber slide at 3 x 10(4) cells/chamber. FINDINGS: 1) The sGAG production was maximum in 20 MOI AdLMP1-GFP infection on the AdLMP-1 treatment for both of AF cells and chondrocytes. 2) The mRNA expression of aggrecan, type I collagen, type II collagen, LMP-1, BMP-2, and BMP-7 is increased in both AF cells and chondrocytes in 20 MOI AdLMP1-GFP infection. 3) On the immunofluorescence staining results, the positive immunofluorescence stained cell numbers are increased after 20 MOI AdLMP1-GFP infection concordant with upregulation of mRNA expression. CONCLUSIONS: The AdLMP-1 treatments in AF cells and chondrocytes may be useful for cell transplantation therapy in disc degeneration-
dc.description.statementOfResponsibilityopen-
dc.format.extent803~810-
dc.relation.isPartOfACTA NEUROCHIRURGICA-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdaptor Proteins, Signal Transducing-
dc.subject.MESHAggrecans/genetics-
dc.subject.MESHBone Morphogenetic Protein 2-
dc.subject.MESHBone Morphogenetic Protein 7-
dc.subject.MESHBone Morphogenetic Proteins/metabolism-
dc.subject.MESHCell Transplantation*-
dc.subject.MESHChondrocytes/metabolism*-
dc.subject.MESHChondrocytes/pathology-
dc.subject.MESHChondrocytes/transplantation*-
dc.subject.MESHCollagen Type I/genetics-
dc.subject.MESHCollagen Type II/genetics-
dc.subject.MESHCytoskeletal Proteins-
dc.subject.MESHGene Expression Regulation/genetics-
dc.subject.MESHGenetic Therapy/methods*-
dc.subject.MESHGlycosaminoglycans/metabolism-
dc.subject.MESHHumans-
dc.subject.MESHIntervertebral Disc/metabolism*-
dc.subject.MESHIntervertebral Disc/pathology-
dc.subject.MESHIntracellular Signaling Peptides and Proteins/genetics*-
dc.subject.MESHLIM Domain Proteins-
dc.subject.MESHPolymerase Chain Reaction-
dc.subject.MESHRNA, Messenger/genetics-
dc.subject.MESHSpinal Diseases/therapy*-
dc.subject.MESHTransfection/methods*-
dc.subject.MESHTransforming Growth Factor beta/metabolism-
dc.titleThe AdLMP-1 transfection in two different cells; AF cells, chondrocytes as potential cell therapy candidates for disc degeneration.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurosurgery (신경외과학)-
dc.contributor.googleauthorKuh SU-
dc.contributor.googleauthorZhu Y-
dc.contributor.googleauthorLi J-
dc.contributor.googleauthorTsai KJ-
dc.contributor.googleauthorFei Q-
dc.contributor.googleauthorHutton WC-
dc.contributor.googleauthorYoon ST-
dc.identifier.doi10.1007/s00701-008-1617-7-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00196-
dc.relation.journalcodeJ00018-
dc.identifier.eissn0942-0940-
dc.identifier.pmid18618069-
dc.identifier.urlhttp://link.springer.com/article/10.1007/s00701-008-1617-7-
dc.subject.keywordProteoglycan-
dc.subject.keywordAnulus fibrosus cell-
dc.subject.keywordChondrocyte-
dc.subject.keywordAdLMP-1-
dc.contributor.alternativeNameKuh, Sung Uk-
dc.contributor.affiliatedAuthorKuh, Sung Uk-
dc.rights.accessRightsnot free-
dc.citation.volume150-
dc.citation.number8-
dc.citation.startPage803-
dc.citation.endPage810-
dc.identifier.bibliographicCitationACTA NEUROCHIRURGICA, Vol.150(8) : 803-810, 2008-
dc.identifier.rimsid50901-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurosurgery (신경외과학교실) > 1. Journal Papers

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