In vitro induced pluripotency from urine-derived cells in porcine.

Methods: The UDCs were reprogrammed in vitro using human or murine octamer-binding transcription factor 4 (OCT4), SRY-box2 (SOX2), Kruppel-like factor 4 (KLF4), and C-MYC, and cultured with basic fibroblast growth factor (bFGF) supplementation. To characterize the putative porcine iPSCs three clonal lineages were submitted to immunocytochemistry for alkaline phosphatase (AP), OCT4, SOX2, NANOG, TRA1 81 and SSEA 1 detection. Endogenous transcripts related to the pluripotency (OCT4, SOX2 and NANOG) were analyzed via reverse transcription quantitative real-time polymerase chain reaction in different time points during the culture, and all three lineages formed embryoid bodies (EBs) when cultured in suspension without bFGF supplementation. Results: The UDCs were isolated from swine urine samples and when at passage 2 submitted to in vitro reprogramming. Colonies of putative iPSCs were obtained only from UDCs transduced with the murine factors (mOSKM), but not from human factors (hOSKM). Three clonal lineages were isolated and further cultured for at least 28 passages, all the lineages were positive for AP detection, the OCT4, SOX2, NANOG markers, albeit the immunocytochemical analysis also revealed heterogeneous phenotypic profiles among lineages and passages for NANOG and SSEA1, similar results were observed in the abundance of the endogenous transcripts related to pluripotent state. All the clonal lineages when cultured in suspension without bFGF were able to form EBs expressing ectoderm and mesoderm layers transcripts. Conclusion: For the first time UDCs were isolated in the swine model and reprogrammed into a pluripotent-like state, enabling new numerous applications in both human or veterinary regenerative medicine.

Saved in:
Bibliographic Details
Main Authors: RECCHIA, K., MACHADO, L. S., BOTIGELLI, R. C., PIERI, N. C. G., BARBOSA, G., CASTRO, R. V. G. de, MARQUES, M. G., PESSÔA, L. V. de F., FANTINATO NETO, P., MEIRELLES, F. V., SOUZA, A. F. de, MARTINS, S. M. M. K., BRESSAN, F. F.
Other Authors: KAIANA RECCHIA, Universidade de São Paulo; LUCAS SIMÕES MACHADO, Universidade de São Paulo; RAMON CESAR BOTIGELLI, Universidade Estadual Paulista; NAIRA CAROLINE GODOY PIERI, Universidade de São Paulo; GABRIELA BARBOSA, Universidade de São Paulo; RAQUEL VASCONCELOS GUIMARÃES DE CASTRO, Universidade de São Paulo; MARIANA GROKE MARQUES, CNPSA; LAÍS VICARI DE FIGUEIREDO PESSÔA, Universidade de São Paulo; PAULO FANTINATO NETO, Universidade de São Paulo; FLÁVIO VIEIRA MEIRELLES, Universidade de São Paulo; ALINE FERNANDA DE SOUZA, Universidade de São Paulo; SIMONE MARIA MASSAMI KITAMURA MARTINS, Universidade de São Paulo; FABIANA FERNANDES BRESSAN, Universidade de São Paulo.
Format: Artigo de periódico biblioteca
Language:Ingles
English
Published: World Journal of Stem Cells, v. 14, n. 3, p. 231-244, 2022. 2022-12-21
Subjects:Células-tronco, Pluripotência, IPSC, Noninvasive, Pluripotency, Reprogramming, Suíno, Urina, Induced pluripotent stem cells, Urine, Swine,
Online Access:http://www.alice.cnptia.embrapa.br/alice/handle/doc/1150134
https://doi.org/10.4252/wjsc.v14.i3.231
Tags: Add Tag
No Tags, Be the first to tag this record!
id dig-alice-doc-1150134
record_format koha
spelling dig-alice-doc-11501342022-12-21T12:01:45Z In vitro induced pluripotency from urine-derived cells in porcine. RECCHIA, K. MACHADO, L. S. BOTIGELLI, R. C. PIERI, N. C. G. BARBOSA, G. CASTRO, R. V. G. de MARQUES, M. G. PESSÔA, L. V. de F. FANTINATO NETO, P. MEIRELLES, F. V. SOUZA, A. F. de MARTINS, S. M. M. K. BRESSAN, F. F. KAIANA RECCHIA, Universidade de São Paulo; LUCAS SIMÕES MACHADO, Universidade de São Paulo; RAMON CESAR BOTIGELLI, Universidade Estadual Paulista; NAIRA CAROLINE GODOY PIERI, Universidade de São Paulo; GABRIELA BARBOSA, Universidade de São Paulo; RAQUEL VASCONCELOS GUIMARÃES DE CASTRO, Universidade de São Paulo; MARIANA GROKE MARQUES, CNPSA; LAÍS VICARI DE FIGUEIREDO PESSÔA, Universidade de São Paulo; PAULO FANTINATO NETO, Universidade de São Paulo; FLÁVIO VIEIRA MEIRELLES, Universidade de São Paulo; ALINE FERNANDA DE SOUZA, Universidade de São Paulo; SIMONE MARIA MASSAMI KITAMURA MARTINS, Universidade de São Paulo; FABIANA FERNANDES BRESSAN, Universidade de São Paulo. Células-tronco Pluripotência IPSC Noninvasive Pluripotency Reprogramming Suíno Urina Induced pluripotent stem cells Urine Swine Methods: The UDCs were reprogrammed in vitro using human or murine octamer-binding transcription factor 4 (OCT4), SRY-box2 (SOX2), Kruppel-like factor 4 (KLF4), and C-MYC, and cultured with basic fibroblast growth factor (bFGF) supplementation. To characterize the putative porcine iPSCs three clonal lineages were submitted to immunocytochemistry for alkaline phosphatase (AP), OCT4, SOX2, NANOG, TRA1 81 and SSEA 1 detection. Endogenous transcripts related to the pluripotency (OCT4, SOX2 and NANOG) were analyzed via reverse transcription quantitative real-time polymerase chain reaction in different time points during the culture, and all three lineages formed embryoid bodies (EBs) when cultured in suspension without bFGF supplementation. Results: The UDCs were isolated from swine urine samples and when at passage 2 submitted to in vitro reprogramming. Colonies of putative iPSCs were obtained only from UDCs transduced with the murine factors (mOSKM), but not from human factors (hOSKM). Three clonal lineages were isolated and further cultured for at least 28 passages, all the lineages were positive for AP detection, the OCT4, SOX2, NANOG markers, albeit the immunocytochemical analysis also revealed heterogeneous phenotypic profiles among lineages and passages for NANOG and SSEA1, similar results were observed in the abundance of the endogenous transcripts related to pluripotent state. All the clonal lineages when cultured in suspension without bFGF were able to form EBs expressing ectoderm and mesoderm layers transcripts. Conclusion: For the first time UDCs were isolated in the swine model and reprogrammed into a pluripotent-like state, enabling new numerous applications in both human or veterinary regenerative medicine. 2022-12-21T12:01:45Z 2022-12-21T12:01:45Z 2022-12-21 2022 Artigo de periódico http://www.alice.cnptia.embrapa.br/alice/handle/doc/1150134 https://doi.org/10.4252/wjsc.v14.i3.231 Ingles en openAccess World Journal of Stem Cells, v. 14, n. 3, p. 231-244, 2022.
institution EMBRAPA
collection DSpace
country Brasil
countrycode BR
component Bibliográfico
access En linea
databasecode dig-alice
tag biblioteca
region America del Sur
libraryname Sistema de bibliotecas de EMBRAPA
language Ingles
English
topic Células-tronco
Pluripotência
IPSC
Noninvasive
Pluripotency
Reprogramming
Suíno
Urina
Induced pluripotent stem cells
Urine
Swine
Células-tronco
Pluripotência
IPSC
Noninvasive
Pluripotency
Reprogramming
Suíno
Urina
Induced pluripotent stem cells
Urine
Swine
spellingShingle Células-tronco
Pluripotência
IPSC
Noninvasive
Pluripotency
Reprogramming
Suíno
Urina
Induced pluripotent stem cells
Urine
Swine
Células-tronco
Pluripotência
IPSC
Noninvasive
Pluripotency
Reprogramming
Suíno
Urina
Induced pluripotent stem cells
Urine
Swine
RECCHIA, K.
MACHADO, L. S.
BOTIGELLI, R. C.
PIERI, N. C. G.
BARBOSA, G.
CASTRO, R. V. G. de
MARQUES, M. G.
PESSÔA, L. V. de F.
FANTINATO NETO, P.
MEIRELLES, F. V.
SOUZA, A. F. de
MARTINS, S. M. M. K.
BRESSAN, F. F.
In vitro induced pluripotency from urine-derived cells in porcine.
description Methods: The UDCs were reprogrammed in vitro using human or murine octamer-binding transcription factor 4 (OCT4), SRY-box2 (SOX2), Kruppel-like factor 4 (KLF4), and C-MYC, and cultured with basic fibroblast growth factor (bFGF) supplementation. To characterize the putative porcine iPSCs three clonal lineages were submitted to immunocytochemistry for alkaline phosphatase (AP), OCT4, SOX2, NANOG, TRA1 81 and SSEA 1 detection. Endogenous transcripts related to the pluripotency (OCT4, SOX2 and NANOG) were analyzed via reverse transcription quantitative real-time polymerase chain reaction in different time points during the culture, and all three lineages formed embryoid bodies (EBs) when cultured in suspension without bFGF supplementation. Results: The UDCs were isolated from swine urine samples and when at passage 2 submitted to in vitro reprogramming. Colonies of putative iPSCs were obtained only from UDCs transduced with the murine factors (mOSKM), but not from human factors (hOSKM). Three clonal lineages were isolated and further cultured for at least 28 passages, all the lineages were positive for AP detection, the OCT4, SOX2, NANOG markers, albeit the immunocytochemical analysis also revealed heterogeneous phenotypic profiles among lineages and passages for NANOG and SSEA1, similar results were observed in the abundance of the endogenous transcripts related to pluripotent state. All the clonal lineages when cultured in suspension without bFGF were able to form EBs expressing ectoderm and mesoderm layers transcripts. Conclusion: For the first time UDCs were isolated in the swine model and reprogrammed into a pluripotent-like state, enabling new numerous applications in both human or veterinary regenerative medicine.
author2 KAIANA RECCHIA, Universidade de São Paulo; LUCAS SIMÕES MACHADO, Universidade de São Paulo; RAMON CESAR BOTIGELLI, Universidade Estadual Paulista; NAIRA CAROLINE GODOY PIERI, Universidade de São Paulo; GABRIELA BARBOSA, Universidade de São Paulo; RAQUEL VASCONCELOS GUIMARÃES DE CASTRO, Universidade de São Paulo; MARIANA GROKE MARQUES, CNPSA; LAÍS VICARI DE FIGUEIREDO PESSÔA, Universidade de São Paulo; PAULO FANTINATO NETO, Universidade de São Paulo; FLÁVIO VIEIRA MEIRELLES, Universidade de São Paulo; ALINE FERNANDA DE SOUZA, Universidade de São Paulo; SIMONE MARIA MASSAMI KITAMURA MARTINS, Universidade de São Paulo; FABIANA FERNANDES BRESSAN, Universidade de São Paulo.
author_facet KAIANA RECCHIA, Universidade de São Paulo; LUCAS SIMÕES MACHADO, Universidade de São Paulo; RAMON CESAR BOTIGELLI, Universidade Estadual Paulista; NAIRA CAROLINE GODOY PIERI, Universidade de São Paulo; GABRIELA BARBOSA, Universidade de São Paulo; RAQUEL VASCONCELOS GUIMARÃES DE CASTRO, Universidade de São Paulo; MARIANA GROKE MARQUES, CNPSA; LAÍS VICARI DE FIGUEIREDO PESSÔA, Universidade de São Paulo; PAULO FANTINATO NETO, Universidade de São Paulo; FLÁVIO VIEIRA MEIRELLES, Universidade de São Paulo; ALINE FERNANDA DE SOUZA, Universidade de São Paulo; SIMONE MARIA MASSAMI KITAMURA MARTINS, Universidade de São Paulo; FABIANA FERNANDES BRESSAN, Universidade de São Paulo.
RECCHIA, K.
MACHADO, L. S.
BOTIGELLI, R. C.
PIERI, N. C. G.
BARBOSA, G.
CASTRO, R. V. G. de
MARQUES, M. G.
PESSÔA, L. V. de F.
FANTINATO NETO, P.
MEIRELLES, F. V.
SOUZA, A. F. de
MARTINS, S. M. M. K.
BRESSAN, F. F.
format Artigo de periódico
topic_facet Células-tronco
Pluripotência
IPSC
Noninvasive
Pluripotency
Reprogramming
Suíno
Urina
Induced pluripotent stem cells
Urine
Swine
author RECCHIA, K.
MACHADO, L. S.
BOTIGELLI, R. C.
PIERI, N. C. G.
BARBOSA, G.
CASTRO, R. V. G. de
MARQUES, M. G.
PESSÔA, L. V. de F.
FANTINATO NETO, P.
MEIRELLES, F. V.
SOUZA, A. F. de
MARTINS, S. M. M. K.
BRESSAN, F. F.
author_sort RECCHIA, K.
title In vitro induced pluripotency from urine-derived cells in porcine.
title_short In vitro induced pluripotency from urine-derived cells in porcine.
title_full In vitro induced pluripotency from urine-derived cells in porcine.
title_fullStr In vitro induced pluripotency from urine-derived cells in porcine.
title_full_unstemmed In vitro induced pluripotency from urine-derived cells in porcine.
title_sort in vitro induced pluripotency from urine-derived cells in porcine.
publisher World Journal of Stem Cells, v. 14, n. 3, p. 231-244, 2022.
publishDate 2022-12-21
url http://www.alice.cnptia.embrapa.br/alice/handle/doc/1150134
https://doi.org/10.4252/wjsc.v14.i3.231
work_keys_str_mv AT recchiak invitroinducedpluripotencyfromurinederivedcellsinporcine
AT machadols invitroinducedpluripotencyfromurinederivedcellsinporcine
AT botigellirc invitroinducedpluripotencyfromurinederivedcellsinporcine
AT pierincg invitroinducedpluripotencyfromurinederivedcellsinporcine
AT barbosag invitroinducedpluripotencyfromurinederivedcellsinporcine
AT castrorvgde invitroinducedpluripotencyfromurinederivedcellsinporcine
AT marquesmg invitroinducedpluripotencyfromurinederivedcellsinporcine
AT pessoalvdef invitroinducedpluripotencyfromurinederivedcellsinporcine
AT fantinatonetop invitroinducedpluripotencyfromurinederivedcellsinporcine
AT meirellesfv invitroinducedpluripotencyfromurinederivedcellsinporcine
AT souzaafde invitroinducedpluripotencyfromurinederivedcellsinporcine
AT martinssmmk invitroinducedpluripotencyfromurinederivedcellsinporcine
AT bressanff invitroinducedpluripotencyfromurinederivedcellsinporcine
_version_ 1756028931357540352