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Does the Mesenchymal Stem Cell Source Influence Smooth Muscle Regeneration in Tissue-Engineered Urinary Bladders?

A variety of tissue engineering techniques utilizing different cells and biomaterials are currently being explored to construct urinary bladder walls de novo, but so far no approach is clearly superior. The aim of this study was to determine whether mesenchymal stem cells (MSCs) isolated from differ...

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Autores principales: Pokrywczynska, Marta, Jundzill, Arkadiusz, Warda, Karolina, Buchholz, Lukasz, Rasmus, Marta, Adamowicz, Jan, Bodnar, Magdalena, Marszalek, Andrzej, Helmin-Basa, Anna, Michalkiewicz, Jacek, Gagat, Maciej, Grzanka, Alina, Frontczak-Baniewicz, Malgorzata, Gastecka, Agata Magdalena, Kloskowski, Tomasz, Nowacki, Maciej, Ricordi, Camillo, Drewa, Tomasz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784518/
https://www.ncbi.nlm.nih.gov/pubmed/29338385
http://dx.doi.org/10.1177/0963689717722787
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author Pokrywczynska, Marta
Jundzill, Arkadiusz
Warda, Karolina
Buchholz, Lukasz
Rasmus, Marta
Adamowicz, Jan
Bodnar, Magdalena
Marszalek, Andrzej
Helmin-Basa, Anna
Michalkiewicz, Jacek
Gagat, Maciej
Grzanka, Alina
Frontczak-Baniewicz, Malgorzata
Gastecka, Agata Magdalena
Kloskowski, Tomasz
Nowacki, Maciej
Ricordi, Camillo
Drewa, Tomasz
author_facet Pokrywczynska, Marta
Jundzill, Arkadiusz
Warda, Karolina
Buchholz, Lukasz
Rasmus, Marta
Adamowicz, Jan
Bodnar, Magdalena
Marszalek, Andrzej
Helmin-Basa, Anna
Michalkiewicz, Jacek
Gagat, Maciej
Grzanka, Alina
Frontczak-Baniewicz, Malgorzata
Gastecka, Agata Magdalena
Kloskowski, Tomasz
Nowacki, Maciej
Ricordi, Camillo
Drewa, Tomasz
author_sort Pokrywczynska, Marta
collection PubMed
description A variety of tissue engineering techniques utilizing different cells and biomaterials are currently being explored to construct urinary bladder walls de novo, but so far no approach is clearly superior. The aim of this study was to determine whether mesenchymal stem cells (MSCs) isolated from different sources, (bone marrow [BM-MSCs] and adipose tissue [ADSCs]), differ in their potential to regenerate smooth muscles in tissue-engineered urinary bladders and to determine an optimal number of MSCs for urinary bladder smooth muscle regeneration. Forty-eight rats underwent hemicystectomy and bladder augmentation with approximately 0.8 cm(2) graft. In the first and second groups, urinary bladders were reconstructed with small intestinal submucosa (SIS) seeded with 10 × 10(6) or 4 × 10(6) ADSCs/cm(2), respectively. In the third and fourth groups, urinary bladders were augmented with SIS seeded with 10 × 10(6) or 4 × 10(6) BM-MSCs/cm(2), respectively. In the fifth group, urinary bladders were augmented with SIS without cells. The sixth group (control) was left intact. Smooth muscle regeneration was evaluated by real-time polymerase chain reaction (RT-PCR) and histological examinations. Histologically, there were no significant differences between urinary bladders augmented with ADSCs and BM-MSCs, but there was a marked increase in smooth muscle formation in bladders augmented with grafts seeded with MSCs in higher density (10 × 10(6)/cm(2)) compared to lower density (4 × 10(6)/cm(2)). Molecular analysis revealed that bladders reconstructed with ADSC-seeded grafts expressed higher levels of smooth muscle myosin heavy chain, caldesmon, and vinculin. Bladders augmented with unseeded SIS were fibrotic and devoid of smooth muscles. ADSCs and BM-MSCs have comparable smooth muscle regenerative potential, but the number of MSCs used for graft preparation significantly affects the smooth muscle content in tissue-engineered urinary bladders.
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spelling pubmed-57845182018-01-30 Does the Mesenchymal Stem Cell Source Influence Smooth Muscle Regeneration in Tissue-Engineered Urinary Bladders? Pokrywczynska, Marta Jundzill, Arkadiusz Warda, Karolina Buchholz, Lukasz Rasmus, Marta Adamowicz, Jan Bodnar, Magdalena Marszalek, Andrzej Helmin-Basa, Anna Michalkiewicz, Jacek Gagat, Maciej Grzanka, Alina Frontczak-Baniewicz, Malgorzata Gastecka, Agata Magdalena Kloskowski, Tomasz Nowacki, Maciej Ricordi, Camillo Drewa, Tomasz Cell Transplant Original Articles A variety of tissue engineering techniques utilizing different cells and biomaterials are currently being explored to construct urinary bladder walls de novo, but so far no approach is clearly superior. The aim of this study was to determine whether mesenchymal stem cells (MSCs) isolated from different sources, (bone marrow [BM-MSCs] and adipose tissue [ADSCs]), differ in their potential to regenerate smooth muscles in tissue-engineered urinary bladders and to determine an optimal number of MSCs for urinary bladder smooth muscle regeneration. Forty-eight rats underwent hemicystectomy and bladder augmentation with approximately 0.8 cm(2) graft. In the first and second groups, urinary bladders were reconstructed with small intestinal submucosa (SIS) seeded with 10 × 10(6) or 4 × 10(6) ADSCs/cm(2), respectively. In the third and fourth groups, urinary bladders were augmented with SIS seeded with 10 × 10(6) or 4 × 10(6) BM-MSCs/cm(2), respectively. In the fifth group, urinary bladders were augmented with SIS without cells. The sixth group (control) was left intact. Smooth muscle regeneration was evaluated by real-time polymerase chain reaction (RT-PCR) and histological examinations. Histologically, there were no significant differences between urinary bladders augmented with ADSCs and BM-MSCs, but there was a marked increase in smooth muscle formation in bladders augmented with grafts seeded with MSCs in higher density (10 × 10(6)/cm(2)) compared to lower density (4 × 10(6)/cm(2)). Molecular analysis revealed that bladders reconstructed with ADSC-seeded grafts expressed higher levels of smooth muscle myosin heavy chain, caldesmon, and vinculin. Bladders augmented with unseeded SIS were fibrotic and devoid of smooth muscles. ADSCs and BM-MSCs have comparable smooth muscle regenerative potential, but the number of MSCs used for graft preparation significantly affects the smooth muscle content in tissue-engineered urinary bladders. SAGE Publications 2018-01-16 2017-11 /pmc/articles/PMC5784518/ /pubmed/29338385 http://dx.doi.org/10.1177/0963689717722787 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Pokrywczynska, Marta
Jundzill, Arkadiusz
Warda, Karolina
Buchholz, Lukasz
Rasmus, Marta
Adamowicz, Jan
Bodnar, Magdalena
Marszalek, Andrzej
Helmin-Basa, Anna
Michalkiewicz, Jacek
Gagat, Maciej
Grzanka, Alina
Frontczak-Baniewicz, Malgorzata
Gastecka, Agata Magdalena
Kloskowski, Tomasz
Nowacki, Maciej
Ricordi, Camillo
Drewa, Tomasz
Does the Mesenchymal Stem Cell Source Influence Smooth Muscle Regeneration in Tissue-Engineered Urinary Bladders?
title Does the Mesenchymal Stem Cell Source Influence Smooth Muscle Regeneration in Tissue-Engineered Urinary Bladders?
title_full Does the Mesenchymal Stem Cell Source Influence Smooth Muscle Regeneration in Tissue-Engineered Urinary Bladders?
title_fullStr Does the Mesenchymal Stem Cell Source Influence Smooth Muscle Regeneration in Tissue-Engineered Urinary Bladders?
title_full_unstemmed Does the Mesenchymal Stem Cell Source Influence Smooth Muscle Regeneration in Tissue-Engineered Urinary Bladders?
title_short Does the Mesenchymal Stem Cell Source Influence Smooth Muscle Regeneration in Tissue-Engineered Urinary Bladders?
title_sort does the mesenchymal stem cell source influence smooth muscle regeneration in tissue-engineered urinary bladders?
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784518/
https://www.ncbi.nlm.nih.gov/pubmed/29338385
http://dx.doi.org/10.1177/0963689717722787
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