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Bi-directional cell-pericellular matrix interactions direct stem cell fate

Modifiable hydrogels have revealed tremendous insight into how physical characteristics of cells’ 3D environment drive stem cell lineage specification. However, in native tissues, cells do not passively receive signals from their niche. Instead they actively probe and modify their pericellular space...

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Autores principales: Ferreira, Silvia A., Motwani, Meghna S., Faull, Peter A., Seymour, Alexis J., Yu, Tracy T. L., Enayati, Marjan, Taheem, Dheraj K., Salzlechner, Christoph, Haghighi, Tabasom, Kania, Ewa M., Oommen, Oommen P., Ahmed, Tarek, Loaiza, Sandra, Parzych, Katarzyna, Dazzi, Francesco, Varghese, Oommen P., Festy, Frederic, Grigoriadis, Agamemnon E., Auner, Holger W., Snijders, Ambrosius P., Bozec, Laurent, Gentleman, Eileen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170409/
https://www.ncbi.nlm.nih.gov/pubmed/30282987
http://dx.doi.org/10.1038/s41467-018-06183-4
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author Ferreira, Silvia A.
Motwani, Meghna S.
Faull, Peter A.
Seymour, Alexis J.
Yu, Tracy T. L.
Enayati, Marjan
Taheem, Dheraj K.
Salzlechner, Christoph
Haghighi, Tabasom
Kania, Ewa M.
Oommen, Oommen P.
Ahmed, Tarek
Loaiza, Sandra
Parzych, Katarzyna
Dazzi, Francesco
Varghese, Oommen P.
Festy, Frederic
Grigoriadis, Agamemnon E.
Auner, Holger W.
Snijders, Ambrosius P.
Bozec, Laurent
Gentleman, Eileen
author_facet Ferreira, Silvia A.
Motwani, Meghna S.
Faull, Peter A.
Seymour, Alexis J.
Yu, Tracy T. L.
Enayati, Marjan
Taheem, Dheraj K.
Salzlechner, Christoph
Haghighi, Tabasom
Kania, Ewa M.
Oommen, Oommen P.
Ahmed, Tarek
Loaiza, Sandra
Parzych, Katarzyna
Dazzi, Francesco
Varghese, Oommen P.
Festy, Frederic
Grigoriadis, Agamemnon E.
Auner, Holger W.
Snijders, Ambrosius P.
Bozec, Laurent
Gentleman, Eileen
author_sort Ferreira, Silvia A.
collection PubMed
description Modifiable hydrogels have revealed tremendous insight into how physical characteristics of cells’ 3D environment drive stem cell lineage specification. However, in native tissues, cells do not passively receive signals from their niche. Instead they actively probe and modify their pericellular space to suit their needs, yet the dynamics of cells’ reciprocal interactions with their pericellular environment when encapsulated within hydrogels remains relatively unexplored. Here, we show that human bone marrow stromal cells (hMSC) encapsulated within hyaluronic acid-based hydrogels modify their surroundings by synthesizing, secreting and arranging proteins pericellularly or by degrading the hydrogel. hMSC’s interactions with this local environment have a role in regulating hMSC fate, with a secreted proteinaceous pericellular matrix associated with adipogenesis, and degradation with osteogenesis. Our observations suggest that hMSC participate in a bi-directional interplay between the properties of their 3D milieu and their own secreted pericellular matrix, and that this combination of interactions drives fate.
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spelling pubmed-61704092018-10-09 Bi-directional cell-pericellular matrix interactions direct stem cell fate Ferreira, Silvia A. Motwani, Meghna S. Faull, Peter A. Seymour, Alexis J. Yu, Tracy T. L. Enayati, Marjan Taheem, Dheraj K. Salzlechner, Christoph Haghighi, Tabasom Kania, Ewa M. Oommen, Oommen P. Ahmed, Tarek Loaiza, Sandra Parzych, Katarzyna Dazzi, Francesco Varghese, Oommen P. Festy, Frederic Grigoriadis, Agamemnon E. Auner, Holger W. Snijders, Ambrosius P. Bozec, Laurent Gentleman, Eileen Nat Commun Article Modifiable hydrogels have revealed tremendous insight into how physical characteristics of cells’ 3D environment drive stem cell lineage specification. However, in native tissues, cells do not passively receive signals from their niche. Instead they actively probe and modify their pericellular space to suit their needs, yet the dynamics of cells’ reciprocal interactions with their pericellular environment when encapsulated within hydrogels remains relatively unexplored. Here, we show that human bone marrow stromal cells (hMSC) encapsulated within hyaluronic acid-based hydrogels modify their surroundings by synthesizing, secreting and arranging proteins pericellularly or by degrading the hydrogel. hMSC’s interactions with this local environment have a role in regulating hMSC fate, with a secreted proteinaceous pericellular matrix associated with adipogenesis, and degradation with osteogenesis. Our observations suggest that hMSC participate in a bi-directional interplay between the properties of their 3D milieu and their own secreted pericellular matrix, and that this combination of interactions drives fate. Nature Publishing Group UK 2018-10-03 /pmc/articles/PMC6170409/ /pubmed/30282987 http://dx.doi.org/10.1038/s41467-018-06183-4 Text en © The Author(s) 2018 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
Ferreira, Silvia A.
Motwani, Meghna S.
Faull, Peter A.
Seymour, Alexis J.
Yu, Tracy T. L.
Enayati, Marjan
Taheem, Dheraj K.
Salzlechner, Christoph
Haghighi, Tabasom
Kania, Ewa M.
Oommen, Oommen P.
Ahmed, Tarek
Loaiza, Sandra
Parzych, Katarzyna
Dazzi, Francesco
Varghese, Oommen P.
Festy, Frederic
Grigoriadis, Agamemnon E.
Auner, Holger W.
Snijders, Ambrosius P.
Bozec, Laurent
Gentleman, Eileen
Bi-directional cell-pericellular matrix interactions direct stem cell fate
title Bi-directional cell-pericellular matrix interactions direct stem cell fate
title_full Bi-directional cell-pericellular matrix interactions direct stem cell fate
title_fullStr Bi-directional cell-pericellular matrix interactions direct stem cell fate
title_full_unstemmed Bi-directional cell-pericellular matrix interactions direct stem cell fate
title_short Bi-directional cell-pericellular matrix interactions direct stem cell fate
title_sort bi-directional cell-pericellular matrix interactions direct stem cell fate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170409/
https://www.ncbi.nlm.nih.gov/pubmed/30282987
http://dx.doi.org/10.1038/s41467-018-06183-4
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