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Comparative pluripotent characteristics of porcine induced pluripotent stem cells generated using different viral transduction systemsopen accessComparative pluripotent characteristics of porcine induced pluripotent stem cells generated using different viral transduction systems

Other Titles
Comparative pluripotent characteristics of porcine induced pluripotent stem cells generated using different viral transduction systems
Authors
백상기이인원이연지서보경최정우김태석황보철이준희
Issue Date
Dec-2023
Publisher
사단법인 한국동물생명공학회
Keywords
induced pluripotent stem cells; Lenti-viral; pluripotency; porcine; Sendai-viral
Citation
Journal of Animal Reproduciton and Biotechnology, v.38, no.4, pp 275 - 290
Pages
16
Indexed
KCI
Journal Title
Journal of Animal Reproduciton and Biotechnology
Volume
38
Number
4
Start Page
275
End Page
290
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/69390
DOI
10.12750/JARB.38.4.275
ISSN
2671-4639
2671-4663
Abstract
Background: Porcine pluripotent stem cells (pPSCs) would provide enormous potential for agriculture and biomedicine. However, authentic pPSCs have not established yet because standards for pPSCs-specific markers and culture conditions are not clear. Therefore, the present study reports comparative pluripotency characteristics in porcine induced pluripotent stem cells (piPSCs) derived from different viral transduction and reprogramming factors [Lenti-iPSCs (OSKM), Lenti-iPSCs (OSKMNL) and Sev-iPSCs (OSKM)]. Methods: Porcine fibroblasts were induced into Lenti-iPSCs (OSKM) and Lenti-iPSCs (OSKMNL) by using Lentiviral vector and Sev-iPSCs (OSKM) by using Sendaiviral vector. Expressions of endogenous or exogenous pluripotency-associated genes, surface marker and in vitro differentiation in between Lenti-piPSCs (OSKM), Lenti-iPSCs (OSKMNL) and Sev-piPSCs (OSKM) were compared. Results: Colonial morphology of Lenti-iPSCs (OSKMNL) closely resembles the naïve mouse embryonic stem cells colony for culture, whereas Sev-iPSCs (OSKM) colony is similar to the primed hESCs. Also, the activity of AP shows a distinct different in piPSCs (AP-positive (+) Lenti-iPSCs (OSKMNL) and Sev-iPSCs (OSKM), but AP-negative (-) LentiiPSCs (OSKM)). mRNAs expression of several marker genes (OCT-3/4, NANOG and SOX2) for pluripotency was increased in Lenti-iPSCs (OSKMNL) and Sev-iPSCs (OSKM), but Sev-iPSCs (OSKM). Interestingly, SSEA-1 of surface markers was expressed only in Sev-iPSCs (OSKM), whereas SSEA-4, Tra-1-60 and Tra-1-81 were positively expressed in Lenti-iPSCs (OSKMNL). Exogenous reprogramming factors continuously expressed in Lenti-iPSCs (OSKMNL) for passage 20, whereas Sev-iPSCs (OSKM) did not express any exogenous transcription factors. Finally, only Lenti-iPSCs (OSKMNL) express the three germ layers and primordial germ cells markers in aggregated EBs. Conclusions: These results indicate that the viral transduction system of reprograming factors into porcine differentiated cells display different pluripotency characteristics in piPSCs.
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Lee, Joon Hee
농업생명과학대학 (동물생명융합학부)
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