Please use this identifier to cite or link to this item: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1129085
Full metadata record
DC FieldValueLanguage
dc.contributor.authorDUARTE, F. B.
dc.contributor.authorBRÍGIDO, M. de M.
dc.contributor.authorMELO, E. de O.
dc.contributor.authorBÁO, S. N.
dc.contributor.authorMARTINS, C. F.
dc.date.accessioned2025-05-13T15:47:34Z-
dc.date.available2025-05-13T15:47:34Z-
dc.date.created2021-01-08
dc.date.issued2022
dc.identifier.citationAnimal Biotechnology, v. 33, n. 6, p. 1014-1024, 2022.
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/1129085-
dc.descriptionCells from different origins behave differently regarding the incorporation of exogenous DNA and formation of transgenic cells. Milk production of recombinant antibody may benefit from efficient transfection protocols to produce transgenic animals. In this context, the objective of this study was to verify the transfection potential of bovine mesenchymal stemcells from Wharton’s jelly (MSC-WJ) and adipose tissue (MSC-AT), comparing co-transfection protocols with vectors pBC1-anti-CD3 and pEF-NEO-GFP, using transfection reagents Lipofectamine LTX with Plus Reagent or Xfect. Skin fibroblasts (FIB) were used as the control group. Forty-eight hours after transfection, neomycin was added and cells cultured for 2 weeks. Treated cells were submitted to fluorescence microscopy, flow cytometry, and PCR evaluations. Wharton’s jelly cells were sensitive to treatments and started necrosis. In theflow cytometry assay, the median fluorescence was higher in adipocytes than fibroblasts, forboth the Xfect (20.057 ± 1.620,7 and 10.601 ± 702,86, respectively, p < 0.05) and LTX(19.590 ± 113,84 and 10.518 ± 442,65, respectively, p < 0.05). These results, associated withevaluation of epifluorescence, demonstrated that adipocytes presented a better response to transfection than other cells, independent of the kit used. Performing PCR on co-transfectedcells demonstrated the presence of anti-CD3, making this approach feasible for future experiments.
dc.language.isoeng
dc.rightsopenAccess
dc.subjectPBC1
dc.subjectHumanized anti-CD3
dc.subjectMonoclonal antibody
dc.titleStrategies for transfection of bovine mesenchymal stem cells with pBC1-anti- CD3 vector.
dc.typeArtigo de periódico
dc.subject.nalthesaurusTransfection
riaa.ainfo.id1129085
riaa.ainfo.lastupdate2025-05-13
dc.contributor.institutionFERNANDA BORGES DUARTE, UNIVERSIDADE DE BRASÍLIA; MARCELO DE MACEDO BRÍGIDO, UNIVERSIDADE DE BRASÍLIA; EDUARDO DE OLIVEIRA MELO, CENARGEN; SÔNIA NAIR BÁO, UNIVERSIDADE DE BRASÍLIA; CARLOS FREDERICO MARTINS, CPAC.
Appears in Collections:Artigo em periódico indexado (CENARGEN)

Files in This Item:
File SizeFormat 
document.pdf8.69 kBAdobe PDFView/Open
Show simple item record

FacebookTwitterDeliciousLinkedInGoogle BookmarksMySpace