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Human mesenchymal stromal cells transplanted into mice stimulate renal tubular cells and enhance mitochondrial function

Mesenchymal stromal cells (MSCs) are renoprotective and drive regeneration following injury, although cellular targets of such an effect are still ill-defined. Here, we show that human umbilical cord (UC)-MSCs transplanted into mice stimulate tubular cells to regain mitochondrial mass and function,...

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Autores principales: Perico, Luca, Morigi, Marina, Rota, Cinzia, Breno, Matteo, Mele, Caterina, Noris, Marina, Introna, Martino, Capelli, Chiara, Longaretti, Lorena, Rottoli, Daniela, Conti, Sara, Corna, Daniela, Remuzzi, Giuseppe, Benigni, Ariela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754365/
https://www.ncbi.nlm.nih.gov/pubmed/29042548
http://dx.doi.org/10.1038/s41467-017-00937-2
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author Perico, Luca
Morigi, Marina
Rota, Cinzia
Breno, Matteo
Mele, Caterina
Noris, Marina
Introna, Martino
Capelli, Chiara
Longaretti, Lorena
Rottoli, Daniela
Conti, Sara
Corna, Daniela
Remuzzi, Giuseppe
Benigni, Ariela
author_facet Perico, Luca
Morigi, Marina
Rota, Cinzia
Breno, Matteo
Mele, Caterina
Noris, Marina
Introna, Martino
Capelli, Chiara
Longaretti, Lorena
Rottoli, Daniela
Conti, Sara
Corna, Daniela
Remuzzi, Giuseppe
Benigni, Ariela
author_sort Perico, Luca
collection PubMed
description Mesenchymal stromal cells (MSCs) are renoprotective and drive regeneration following injury, although cellular targets of such an effect are still ill-defined. Here, we show that human umbilical cord (UC)-MSCs transplanted into mice stimulate tubular cells to regain mitochondrial mass and function, associated with enhanced microtubule-rich projections that appear to mediate mitochondrial trafficking to create a reparative dialogue among adjacent tubular cells. Treatment with UC-MSCs in mice with cisplatin-induced acute kidney injury (AKI) regulates mitochondrial biogenesis in proximal tubuli by enhancing PGC1α expression, NAD(+) biosynthesis and Sirtuin 3 (SIRT3) activity, thus fostering antioxidant defenses and ATP production. The functional role of SIRT3 in tubular recovery is highlighted by data that in SIRT3-deficient mice with AKI, UC-MSC treatment fails to induce renoprotection. These data document a previously unrecognized mechanism through which UC-MSCs facilitate renal repair, so as to induce global metabolic reprogramming of damaged tubular cells to sustain energy supply.
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spelling pubmed-57543652018-01-12 Human mesenchymal stromal cells transplanted into mice stimulate renal tubular cells and enhance mitochondrial function Perico, Luca Morigi, Marina Rota, Cinzia Breno, Matteo Mele, Caterina Noris, Marina Introna, Martino Capelli, Chiara Longaretti, Lorena Rottoli, Daniela Conti, Sara Corna, Daniela Remuzzi, Giuseppe Benigni, Ariela Nat Commun Article Mesenchymal stromal cells (MSCs) are renoprotective and drive regeneration following injury, although cellular targets of such an effect are still ill-defined. Here, we show that human umbilical cord (UC)-MSCs transplanted into mice stimulate tubular cells to regain mitochondrial mass and function, associated with enhanced microtubule-rich projections that appear to mediate mitochondrial trafficking to create a reparative dialogue among adjacent tubular cells. Treatment with UC-MSCs in mice with cisplatin-induced acute kidney injury (AKI) regulates mitochondrial biogenesis in proximal tubuli by enhancing PGC1α expression, NAD(+) biosynthesis and Sirtuin 3 (SIRT3) activity, thus fostering antioxidant defenses and ATP production. The functional role of SIRT3 in tubular recovery is highlighted by data that in SIRT3-deficient mice with AKI, UC-MSC treatment fails to induce renoprotection. These data document a previously unrecognized mechanism through which UC-MSCs facilitate renal repair, so as to induce global metabolic reprogramming of damaged tubular cells to sustain energy supply. Nature Publishing Group UK 2017-10-17 /pmc/articles/PMC5754365/ /pubmed/29042548 http://dx.doi.org/10.1038/s41467-017-00937-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Perico, Luca
Morigi, Marina
Rota, Cinzia
Breno, Matteo
Mele, Caterina
Noris, Marina
Introna, Martino
Capelli, Chiara
Longaretti, Lorena
Rottoli, Daniela
Conti, Sara
Corna, Daniela
Remuzzi, Giuseppe
Benigni, Ariela
Human mesenchymal stromal cells transplanted into mice stimulate renal tubular cells and enhance mitochondrial function
title Human mesenchymal stromal cells transplanted into mice stimulate renal tubular cells and enhance mitochondrial function
title_full Human mesenchymal stromal cells transplanted into mice stimulate renal tubular cells and enhance mitochondrial function
title_fullStr Human mesenchymal stromal cells transplanted into mice stimulate renal tubular cells and enhance mitochondrial function
title_full_unstemmed Human mesenchymal stromal cells transplanted into mice stimulate renal tubular cells and enhance mitochondrial function
title_short Human mesenchymal stromal cells transplanted into mice stimulate renal tubular cells and enhance mitochondrial function
title_sort human mesenchymal stromal cells transplanted into mice stimulate renal tubular cells and enhance mitochondrial function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754365/
https://www.ncbi.nlm.nih.gov/pubmed/29042548
http://dx.doi.org/10.1038/s41467-017-00937-2
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