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A comparison of three cell types as potential candidates for intervertebral disc therapy: annulus fibrosus cells, chondrocytes, and bone marrow derived cells

DC Field Value Language
dc.contributor.author구성욱-
dc.date.accessioned2015-04-24T16:36:12Z-
dc.date.available2015-04-24T16:36:12Z-
dc.date.issued2009-
dc.identifier.issn1297-319X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/103824-
dc.description.abstractOBJECTIVES: Candidate cell types for disc cell transplantation therapy include anulus fibrosus (AF) cells, chondrocytes, and bone marrow derived cells (BMDCs). We compared the disc matrix production in these three types of cells, before and after stimulation with rhBMP-2. There is no study extant that compares these three cell types to determine the best candidate for the disc cell therapy. METHODS: AF cells, chondrocytes, and BMDCs (iliac crest and femur) were isolated and grown in monolayer. They were treated for 3 days with rhBMP-2. After 3 days, proteoglycan (sGAG) content in the media was quantified. The results were normalized by cell numbers. The mRNA expression of aggrecan, type I collagen, and type II collagen was measured using real-time PCR. Each cell type was also cultured in chamber slides and immunostained for aggrecan, type I collagen, and type II collagen after 3 days of treatment with rhBMP-2. RESULTS: (1) Without rhBMP-2 the chondrocytes produced more proteoglycan (sGAG) as compared to the other two cell types (AF cells and BMDCs). After stimulation with rhBMP-2 the chondrocytes produce even more proteoglycan than the other two cell types. (2) As compared to the other two cell types, in terms of mRNA expression, the chondrocytes expressed more aggrecan, type I collagen, and type II collagen before stimulation with rhBMP-2. After rhBMP-2 stimulation, the chondrocytes expressed even more aggrecan, type I collagen, and type II collagen in proportion to the concentration of rhBMP-2. For the BMDCs there were no changes in type I and II collagen. (3) rhBMP-2 stimulation produced increases in the protein levels of aggrecan, type I and II collagen in all three types of cells. CONCLUSIONS: On balance, according to these results, it would seem that chondrocytes are the best candidate for the disc cell therapy-
dc.description.statementOfResponsibilityopen-
dc.format.extent70~74-
dc.relation.isPartOfJOINT BONE SPINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAggrecans/genetics-
dc.subject.MESHAggrecans/metabolism-
dc.subject.MESHAnimals-
dc.subject.MESHBone Marrow Cells/cytology*-
dc.subject.MESHBone Marrow Cells/metabolism-
dc.subject.MESHBone Morphogenetic Protein 2-
dc.subject.MESHBone Morphogenetic Proteins/pharmacology-
dc.subject.MESHCartilage, Articular/cytology-
dc.subject.MESHCartilage, Articular/drug effects-
dc.subject.MESHCell Transplantation/methods*-
dc.subject.MESHCells, Cultured-
dc.subject.MESHChondrocytes/cytology*-
dc.subject.MESHChondrocytes/metabolism-
dc.subject.MESHCollagen Type I/genetics-
dc.subject.MESHCollagen Type I/metabolism-
dc.subject.MESHCollagen Type II/genetics-
dc.subject.MESHCollagen Type II/metabolism-
dc.subject.MESHDose-Response Relationship, Drug-
dc.subject.MESHExtracellular Matrix Proteins/biosynthesis-
dc.subject.MESHExtracellular Matrix Proteins/drug effects-
dc.subject.MESHFemale-
dc.subject.MESHGene Expression/drug effects-
dc.subject.MESHGlycosaminoglycans/biosynthesis-
dc.subject.MESHIntervertebral Disc/cytology*-
dc.subject.MESHIntervertebral Disc/metabolism-
dc.subject.MESHIntervertebral Disc Displacement/pathology-
dc.subject.MESHIntervertebral Disc Displacement/therapy*-
dc.subject.MESHRNA, Messenger/metabolism-
dc.subject.MESHRabbits-
dc.subject.MESHRecombinant Proteins/pharmacology-
dc.subject.MESHTransforming Growth Factor beta/pharmacology-
dc.titleA comparison of three cell types as potential candidates for intervertebral disc therapy: annulus fibrosus cells, chondrocytes, and bone marrow derived cells-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurosurgery (신경외과학)-
dc.contributor.googleauthorSung Uk Kuh-
dc.contributor.googleauthorYerun Zhu-
dc.contributor.googleauthorJun Li-
dc.contributor.googleauthorKai-Jow Tsai-
dc.contributor.googleauthorQinming Fei-
dc.contributor.googleauthorWilliam C. Hutton-
dc.contributor.googleauthorTim S. Yoon-
dc.identifier.doi10.1016/j.jbspin.2008.02.021-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00196-
dc.relation.journalcodeJ01216-
dc.identifier.eissn1778-7254-
dc.identifier.pmid18955010-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S1297319X08002236-
dc.subject.keywordProteoglycans-
dc.subject.keywordAnulus fibrosus cells-
dc.subject.keywordChondrocytes-
dc.subject.keywordBone marrow derived cells-
dc.contributor.alternativeNameKuh, Sung Uk-
dc.contributor.affiliatedAuthorKuh, Sung Uk-
dc.citation.volume76-
dc.citation.number1-
dc.citation.startPage70-
dc.citation.endPage74-
dc.identifier.bibliographicCitationJOINT BONE SPINE, Vol.76(1) : 70-74, 2009-
dc.identifier.rimsid36719-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurosurgery (신경외과학교실) > 1. Journal Papers

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