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Extracellular Vesicles Derived from Induced Pluripotent Stem Cells Promote Renoprotection in Acute Kidney Injury Model

Induced pluripotent stem cells (iPSC) have been the focus of several studies due to their wide range of application, including in cellular therapy. The use of iPSC in regenerative medicine is limited by their tumorigenic potential. Extracellular vesicles (EV) derived from stem cells have been shown...

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Autores principales: Collino, Federica, Lopes, Jarlene A., Tapparo, Marta, Tortelote, Giovane G., Kasai-Brunswick, Taís H., Lopes, Gustavo M.C., Almeida, Douglas B., Skovronova, Renata, Wendt, Camila H. C., de Miranda, Kildare R., Bussolati, Benedetta, Vieyra, Adalberto, Lindoso, Rafael Soares
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072760/
https://www.ncbi.nlm.nih.gov/pubmed/32079274
http://dx.doi.org/10.3390/cells9020453
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author Collino, Federica
Lopes, Jarlene A.
Tapparo, Marta
Tortelote, Giovane G.
Kasai-Brunswick, Taís H.
Lopes, Gustavo M.C.
Almeida, Douglas B.
Skovronova, Renata
Wendt, Camila H. C.
de Miranda, Kildare R.
Bussolati, Benedetta
Vieyra, Adalberto
Lindoso, Rafael Soares
author_facet Collino, Federica
Lopes, Jarlene A.
Tapparo, Marta
Tortelote, Giovane G.
Kasai-Brunswick, Taís H.
Lopes, Gustavo M.C.
Almeida, Douglas B.
Skovronova, Renata
Wendt, Camila H. C.
de Miranda, Kildare R.
Bussolati, Benedetta
Vieyra, Adalberto
Lindoso, Rafael Soares
author_sort Collino, Federica
collection PubMed
description Induced pluripotent stem cells (iPSC) have been the focus of several studies due to their wide range of application, including in cellular therapy. The use of iPSC in regenerative medicine is limited by their tumorigenic potential. Extracellular vesicles (EV) derived from stem cells have been shown to support renal recovery after injury. However, no investigation has explored the potential of iPSC-EV in the treatment of kidney diseases. To evaluate this potential, we submitted renal tubule cells to hypoxia-reoxygenation injury, and we analyzed cell death rate and changes in functional mitochondria mass. An in vivo model of ischemia-reperfusion injury was used to evaluate morphological and functional alterations. Gene array profile was applied to investigate the mechanism involved in iPSC-EV effects. In addition, EV derived from adipose mesenchymal cells (ASC-EV) were also used to compare the potential of iPSC-EV in support of tissue recovery. The results showed that iPSC-EV were capable of reducing cell death and inflammatory response with similar efficacy than ASC-EV. Moreover, iPSC-EV protected functional mitochondria and regulated several genes associated with oxidative stress. Taken together, these results show that iPSC can be an alternative source of EV in the treatment of different aspects of kidney disease.
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spelling pubmed-70727602020-03-19 Extracellular Vesicles Derived from Induced Pluripotent Stem Cells Promote Renoprotection in Acute Kidney Injury Model Collino, Federica Lopes, Jarlene A. Tapparo, Marta Tortelote, Giovane G. Kasai-Brunswick, Taís H. Lopes, Gustavo M.C. Almeida, Douglas B. Skovronova, Renata Wendt, Camila H. C. de Miranda, Kildare R. Bussolati, Benedetta Vieyra, Adalberto Lindoso, Rafael Soares Cells Article Induced pluripotent stem cells (iPSC) have been the focus of several studies due to their wide range of application, including in cellular therapy. The use of iPSC in regenerative medicine is limited by their tumorigenic potential. Extracellular vesicles (EV) derived from stem cells have been shown to support renal recovery after injury. However, no investigation has explored the potential of iPSC-EV in the treatment of kidney diseases. To evaluate this potential, we submitted renal tubule cells to hypoxia-reoxygenation injury, and we analyzed cell death rate and changes in functional mitochondria mass. An in vivo model of ischemia-reperfusion injury was used to evaluate morphological and functional alterations. Gene array profile was applied to investigate the mechanism involved in iPSC-EV effects. In addition, EV derived from adipose mesenchymal cells (ASC-EV) were also used to compare the potential of iPSC-EV in support of tissue recovery. The results showed that iPSC-EV were capable of reducing cell death and inflammatory response with similar efficacy than ASC-EV. Moreover, iPSC-EV protected functional mitochondria and regulated several genes associated with oxidative stress. Taken together, these results show that iPSC can be an alternative source of EV in the treatment of different aspects of kidney disease. MDPI 2020-02-17 /pmc/articles/PMC7072760/ /pubmed/32079274 http://dx.doi.org/10.3390/cells9020453 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Collino, Federica
Lopes, Jarlene A.
Tapparo, Marta
Tortelote, Giovane G.
Kasai-Brunswick, Taís H.
Lopes, Gustavo M.C.
Almeida, Douglas B.
Skovronova, Renata
Wendt, Camila H. C.
de Miranda, Kildare R.
Bussolati, Benedetta
Vieyra, Adalberto
Lindoso, Rafael Soares
Extracellular Vesicles Derived from Induced Pluripotent Stem Cells Promote Renoprotection in Acute Kidney Injury Model
title Extracellular Vesicles Derived from Induced Pluripotent Stem Cells Promote Renoprotection in Acute Kidney Injury Model
title_full Extracellular Vesicles Derived from Induced Pluripotent Stem Cells Promote Renoprotection in Acute Kidney Injury Model
title_fullStr Extracellular Vesicles Derived from Induced Pluripotent Stem Cells Promote Renoprotection in Acute Kidney Injury Model
title_full_unstemmed Extracellular Vesicles Derived from Induced Pluripotent Stem Cells Promote Renoprotection in Acute Kidney Injury Model
title_short Extracellular Vesicles Derived from Induced Pluripotent Stem Cells Promote Renoprotection in Acute Kidney Injury Model
title_sort extracellular vesicles derived from induced pluripotent stem cells promote renoprotection in acute kidney injury model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072760/
https://www.ncbi.nlm.nih.gov/pubmed/32079274
http://dx.doi.org/10.3390/cells9020453
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