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Establishment and characterization of porcine Sertoli cell line for the study of xenotransplantation

DC Field Value Language
dc.contributor.authorLee, Hak-Mo-
dc.contributor.authorOh, Byoung Chol-
dc.contributor.authorLim, Dong-Pyo-
dc.contributor.authorLee, Dong-Sup-
dc.contributor.authorCho, Jaejin-
dc.contributor.authorLee, Gene-
dc.contributor.authorLee, Jeong Ryul-
dc.date.accessioned2010-01-08T08:39:43Z-
dc.date.available2010-01-08T08:39:43Z-
dc.date.issued2007-03-27-
dc.identifier.citationXenotransplantation. 2007 Mar;14(2):112-8.en
dc.identifier.issn0908-665X (Print)-
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=17381685-
dc.identifier.urihttps://hdl.handle.net/10371/29099-
dc.description.abstractBACKGROUND: An understanding of the main mechanism that determines the ability of immune privilege related to Sertoli cells (SC) will provide clues for promoting a local tolerogenic environment. In this report, we established neonatal porcine SC line and evaluated their characteristics. METHODS: SC line was established following the transfection of primary SC (NPSC) from the testis of neonatal pig with plasmid pRNS-1 carrying genes for neomycin resistance and the SV40 large T antigen. Immunohistochemistry and RT-PCR were performed to evaluate the character of immortalized SC lines. RESULTS: Our immortalized SC line (iPS) proliferated stably and had a phenotype similar to NPSC, as indicated by the immunoexpression of follicle stimulating hormone receptor (FSHR), and mRNA expression of androgen receptor (AR), and Wilms' tumor antigen (WT1). Interestingly, NPSC and iPS expressed mRNA of complement regulatory proteins (CRP) such as membrane cofactor protein (CD46), decay accelerating factor (DAF or CD55), and protectin (CD59), but CD59 mRNA expression was negligible in iPS. CONCLUSION: These results suggest that iPS, immortalized by the introduction of SV40 T, retain their original characteristics, except for the relatively low expression of CD59, and that they may be useful for future in vitro and in vivo studies of immune privilege mechanisms related to SC.en
dc.language.isoen-
dc.publisherWiley-Blackwellen
dc.subjectAnimalsen
dc.subjectAntigens, Polyomavirus Transforming/geneticsen
dc.subjectCell Proliferationen
dc.subjectCell Transplantation/*methodsen
dc.subjectCells, Cultureden
dc.subjectComplement System Proteins/genetics/metabolismen
dc.subjectMaleen
dc.subjectPhenotypeen
dc.subjectPlasmids/geneticsen
dc.subjectRNA, Messenger/genetics/metabolismen
dc.subjectReceptors, Androgen/genetics/metabolismen
dc.subjectReceptors, FSH/genetics/metabolismen
dc.subjectSertoli Cells/*cytology/*immunology/metabolismen
dc.subjectSwineen
dc.subjectTransfectionen
dc.subjectTransplantation, Heterologous/immunology/*methodsen
dc.subjectWT1 Proteins/genetics/metabolismen
dc.subjectCell Line-
dc.titleEstablishment and characterization of porcine Sertoli cell line for the study of xenotransplantationen
dc.typeArticleen
dc.contributor.AlternativeAuthor이학모-
dc.contributor.AlternativeAuthor오병철-
dc.contributor.AlternativeAuthor임동표-
dc.contributor.AlternativeAuthor이동섭-
dc.contributor.AlternativeAuthor조재진-
dc.contributor.AlternativeAuthor이진-
dc.contributor.AlternativeAuthor이정렬-
dc.identifier.doi10.1111/j.1399-3089.2007.00366.x-
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