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Priming Mesenchymal Stem Cells with Endothelial Growth Medium Boosts Stem Cell Therapy for Systemic Arterial Hypertension

Systemic arterial hypertension (SAH), a clinical syndrome characterized by persistent elevation of arterial pressure, is often associated with abnormalities such as microvascular rarefaction, defective angiogenesis, and endothelial dysfunction. Mesenchymal stem cells (MSCs), which normally induce an...

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Autores principales: de Oliveira, Lucas Felipe, Almeida, Thalles Ramos, Ribeiro Machado, Marcus Paulo, Cuba, Marilia Beatriz, Alves, Angélica Cristina, da Silva, Marcos Vinícius, Rodrigues Júnior, Virmondes, Dias da Silva, Valdo José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537741/
https://www.ncbi.nlm.nih.gov/pubmed/26300922
http://dx.doi.org/10.1155/2015/685383
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author de Oliveira, Lucas Felipe
Almeida, Thalles Ramos
Ribeiro Machado, Marcus Paulo
Cuba, Marilia Beatriz
Alves, Angélica Cristina
da Silva, Marcos Vinícius
Rodrigues Júnior, Virmondes
Dias da Silva, Valdo José
author_facet de Oliveira, Lucas Felipe
Almeida, Thalles Ramos
Ribeiro Machado, Marcus Paulo
Cuba, Marilia Beatriz
Alves, Angélica Cristina
da Silva, Marcos Vinícius
Rodrigues Júnior, Virmondes
Dias da Silva, Valdo José
author_sort de Oliveira, Lucas Felipe
collection PubMed
description Systemic arterial hypertension (SAH), a clinical syndrome characterized by persistent elevation of arterial pressure, is often associated with abnormalities such as microvascular rarefaction, defective angiogenesis, and endothelial dysfunction. Mesenchymal stem cells (MSCs), which normally induce angiogenesis and improve endothelial function, are defective in SAH. The central aim of this study was to evaluate whether priming of MSCs with endothelial growth medium (EGM-2) increases their therapeutic effects in spontaneously hypertensive rats (SHRs). Adult female SHRs were administered an intraperitoneal injection of vehicle solution (n = 10), MSCs cultured in conventional medium (DMEM plus 10% FBS, n = 11), or MSCs cultured in conventional medium followed by 72 hours in EGM-2 (pMSC, n = 10). Priming of the MSCs reduced the basal cell death rate in vitro. The administration of pMSCs significantly induced a prolonged reduction (10 days) in arterial pressure, a decrease in cardiac hypertrophy, an improvement in endothelium-dependent vasodilation response to acetylcholine, and an increase in skeletal muscle microvascular density compared to the vehicle and MSC groups. The transplanted cells were rarely found in the hearts and kidneys. Taken together, our findings indicate that priming of MSCs boosts stem cell therapy for the treatment of SAH.
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spelling pubmed-45377412015-08-23 Priming Mesenchymal Stem Cells with Endothelial Growth Medium Boosts Stem Cell Therapy for Systemic Arterial Hypertension de Oliveira, Lucas Felipe Almeida, Thalles Ramos Ribeiro Machado, Marcus Paulo Cuba, Marilia Beatriz Alves, Angélica Cristina da Silva, Marcos Vinícius Rodrigues Júnior, Virmondes Dias da Silva, Valdo José Stem Cells Int Research Article Systemic arterial hypertension (SAH), a clinical syndrome characterized by persistent elevation of arterial pressure, is often associated with abnormalities such as microvascular rarefaction, defective angiogenesis, and endothelial dysfunction. Mesenchymal stem cells (MSCs), which normally induce angiogenesis and improve endothelial function, are defective in SAH. The central aim of this study was to evaluate whether priming of MSCs with endothelial growth medium (EGM-2) increases their therapeutic effects in spontaneously hypertensive rats (SHRs). Adult female SHRs were administered an intraperitoneal injection of vehicle solution (n = 10), MSCs cultured in conventional medium (DMEM plus 10% FBS, n = 11), or MSCs cultured in conventional medium followed by 72 hours in EGM-2 (pMSC, n = 10). Priming of the MSCs reduced the basal cell death rate in vitro. The administration of pMSCs significantly induced a prolonged reduction (10 days) in arterial pressure, a decrease in cardiac hypertrophy, an improvement in endothelium-dependent vasodilation response to acetylcholine, and an increase in skeletal muscle microvascular density compared to the vehicle and MSC groups. The transplanted cells were rarely found in the hearts and kidneys. Taken together, our findings indicate that priming of MSCs boosts stem cell therapy for the treatment of SAH. Hindawi Publishing Corporation 2015 2015-08-02 /pmc/articles/PMC4537741/ /pubmed/26300922 http://dx.doi.org/10.1155/2015/685383 Text en Copyright © 2015 Lucas Felipe de Oliveira et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
de Oliveira, Lucas Felipe
Almeida, Thalles Ramos
Ribeiro Machado, Marcus Paulo
Cuba, Marilia Beatriz
Alves, Angélica Cristina
da Silva, Marcos Vinícius
Rodrigues Júnior, Virmondes
Dias da Silva, Valdo José
Priming Mesenchymal Stem Cells with Endothelial Growth Medium Boosts Stem Cell Therapy for Systemic Arterial Hypertension
title Priming Mesenchymal Stem Cells with Endothelial Growth Medium Boosts Stem Cell Therapy for Systemic Arterial Hypertension
title_full Priming Mesenchymal Stem Cells with Endothelial Growth Medium Boosts Stem Cell Therapy for Systemic Arterial Hypertension
title_fullStr Priming Mesenchymal Stem Cells with Endothelial Growth Medium Boosts Stem Cell Therapy for Systemic Arterial Hypertension
title_full_unstemmed Priming Mesenchymal Stem Cells with Endothelial Growth Medium Boosts Stem Cell Therapy for Systemic Arterial Hypertension
title_short Priming Mesenchymal Stem Cells with Endothelial Growth Medium Boosts Stem Cell Therapy for Systemic Arterial Hypertension
title_sort priming mesenchymal stem cells with endothelial growth medium boosts stem cell therapy for systemic arterial hypertension
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537741/
https://www.ncbi.nlm.nih.gov/pubmed/26300922
http://dx.doi.org/10.1155/2015/685383
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