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Subcutaneous and Visceral Adipose-Derived Mesenchymal Stem Cells: Commonality and Diversity

Adipose-derived mesenchymal stem cells (ASCs) are considered to be a useful tool for regenerative medicine, owing to their capabilities in differentiation, self-renewal, and immunomodulation. These cells have become a focus in the clinical setting due to their abundance and easy isolation. However,...

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Autores principales: Ritter, Andreas, Friemel, Alexandra, Roth, Susanne, Kreis, Nina-Naomi, Hoock, Samira Catharina, Safdar, Babek Khan, Fischer, Kyra, Möllmann, Charlotte, Solbach, Christine, Louwen, Frank, Yuan, Juping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830091/
https://www.ncbi.nlm.nih.gov/pubmed/31640218
http://dx.doi.org/10.3390/cells8101288
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author Ritter, Andreas
Friemel, Alexandra
Roth, Susanne
Kreis, Nina-Naomi
Hoock, Samira Catharina
Safdar, Babek Khan
Fischer, Kyra
Möllmann, Charlotte
Solbach, Christine
Louwen, Frank
Yuan, Juping
author_facet Ritter, Andreas
Friemel, Alexandra
Roth, Susanne
Kreis, Nina-Naomi
Hoock, Samira Catharina
Safdar, Babek Khan
Fischer, Kyra
Möllmann, Charlotte
Solbach, Christine
Louwen, Frank
Yuan, Juping
author_sort Ritter, Andreas
collection PubMed
description Adipose-derived mesenchymal stem cells (ASCs) are considered to be a useful tool for regenerative medicine, owing to their capabilities in differentiation, self-renewal, and immunomodulation. These cells have become a focus in the clinical setting due to their abundance and easy isolation. However, ASCs from different depots are not well characterized. Here, we analyzed the functional similarities and differences of subcutaneous and visceral ASCs. Subcutaneous ASCs have an extraordinarily directed mode of motility and a highly dynamic focal adhesion turnover, even though they share similar surface markers, whereas visceral ASCs move in an undirected random pattern with more stable focal adhesions. Visceral ASCs have a higher potential to differentiate into adipogenic and osteogenic cells when compared to subcutaneous ASCs. In line with these observations, visceral ASCs demonstrate a more active sonic hedgehog pathway that is linked to a high expression of cilia/differentiation related genes. Moreover, visceral ASCs secrete higher levels of inflammatory cytokines interleukin-6, interleukin-8, and tumor necrosis factor α relative to subcutaneous ASCs. These findings highlight, that both ASC subpopulations share multiple cellular features, but significantly differ in their functions. The functional diversity of ASCs depends on their origin, cellular context and surrounding microenvironment within adipose tissues. The data provide important insight into the biology of ASCs, which might be useful in choosing the adequate ASC subpopulation for regenerative therapies.
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spelling pubmed-68300912019-11-18 Subcutaneous and Visceral Adipose-Derived Mesenchymal Stem Cells: Commonality and Diversity Ritter, Andreas Friemel, Alexandra Roth, Susanne Kreis, Nina-Naomi Hoock, Samira Catharina Safdar, Babek Khan Fischer, Kyra Möllmann, Charlotte Solbach, Christine Louwen, Frank Yuan, Juping Cells Article Adipose-derived mesenchymal stem cells (ASCs) are considered to be a useful tool for regenerative medicine, owing to their capabilities in differentiation, self-renewal, and immunomodulation. These cells have become a focus in the clinical setting due to their abundance and easy isolation. However, ASCs from different depots are not well characterized. Here, we analyzed the functional similarities and differences of subcutaneous and visceral ASCs. Subcutaneous ASCs have an extraordinarily directed mode of motility and a highly dynamic focal adhesion turnover, even though they share similar surface markers, whereas visceral ASCs move in an undirected random pattern with more stable focal adhesions. Visceral ASCs have a higher potential to differentiate into adipogenic and osteogenic cells when compared to subcutaneous ASCs. In line with these observations, visceral ASCs demonstrate a more active sonic hedgehog pathway that is linked to a high expression of cilia/differentiation related genes. Moreover, visceral ASCs secrete higher levels of inflammatory cytokines interleukin-6, interleukin-8, and tumor necrosis factor α relative to subcutaneous ASCs. These findings highlight, that both ASC subpopulations share multiple cellular features, but significantly differ in their functions. The functional diversity of ASCs depends on their origin, cellular context and surrounding microenvironment within adipose tissues. The data provide important insight into the biology of ASCs, which might be useful in choosing the adequate ASC subpopulation for regenerative therapies. MDPI 2019-10-21 /pmc/articles/PMC6830091/ /pubmed/31640218 http://dx.doi.org/10.3390/cells8101288 Text en © 2019 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
Ritter, Andreas
Friemel, Alexandra
Roth, Susanne
Kreis, Nina-Naomi
Hoock, Samira Catharina
Safdar, Babek Khan
Fischer, Kyra
Möllmann, Charlotte
Solbach, Christine
Louwen, Frank
Yuan, Juping
Subcutaneous and Visceral Adipose-Derived Mesenchymal Stem Cells: Commonality and Diversity
title Subcutaneous and Visceral Adipose-Derived Mesenchymal Stem Cells: Commonality and Diversity
title_full Subcutaneous and Visceral Adipose-Derived Mesenchymal Stem Cells: Commonality and Diversity
title_fullStr Subcutaneous and Visceral Adipose-Derived Mesenchymal Stem Cells: Commonality and Diversity
title_full_unstemmed Subcutaneous and Visceral Adipose-Derived Mesenchymal Stem Cells: Commonality and Diversity
title_short Subcutaneous and Visceral Adipose-Derived Mesenchymal Stem Cells: Commonality and Diversity
title_sort subcutaneous and visceral adipose-derived mesenchymal stem cells: commonality and diversity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830091/
https://www.ncbi.nlm.nih.gov/pubmed/31640218
http://dx.doi.org/10.3390/cells8101288
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