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Soft substrate maintains proliferative and adipogenic differentiation potential of human mesenchymal stem cells on long-term expansion by delaying senescence

Human mesenchymal stem cells (hMSCs), during in vitro expansion, gradually lose their distinct spindle morphology, self-renewal ability, multi-lineage differentiation potential and enter replicative senescence. This loss of cellular function is a major roadblock for clinical applications which deman...

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Autores principales: Kureel, Sanjay Kumar, Mogha, Pankaj, Khadpekar, Akshada, Kumar, Vardhman, Joshi, Rohit, Das, Siddhartha, Bellare, Jayesh, Majumder, Abhijit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503999/
https://www.ncbi.nlm.nih.gov/pubmed/31023646
http://dx.doi.org/10.1242/bio.039453
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author Kureel, Sanjay Kumar
Mogha, Pankaj
Khadpekar, Akshada
Kumar, Vardhman
Joshi, Rohit
Das, Siddhartha
Bellare, Jayesh
Majumder, Abhijit
author_facet Kureel, Sanjay Kumar
Mogha, Pankaj
Khadpekar, Akshada
Kumar, Vardhman
Joshi, Rohit
Das, Siddhartha
Bellare, Jayesh
Majumder, Abhijit
author_sort Kureel, Sanjay Kumar
collection PubMed
description Human mesenchymal stem cells (hMSCs), during in vitro expansion, gradually lose their distinct spindle morphology, self-renewal ability, multi-lineage differentiation potential and enter replicative senescence. This loss of cellular function is a major roadblock for clinical applications which demand cells in large numbers. Here, we demonstrate a novel role of substrate stiffness in the maintenance of hMSCs over long-term expansion. When serially passaged for 45 days from passage 3 to passage 18 on polyacrylamide gel of Young's modulus E=5 kPa, hMSCs maintained their proliferation rate and showed nine times higher population doubling in comparison to their counterparts cultured on plastic Petri-plates. They did not express markers of senescence, maintained their morphology and other mechanical properties such as cell stiffness and cellular traction, and were significantly superior in adipogenic differentiation potential. These results were demonstrated in hMSCs from two different sources, umbilical cord and bone marrow. In summary, our result shows that a soft gel is a suitable substrate to maintain the stemness of mesenchymal stem cells. As preparation of polyacrylamide gel is a well-established, and well-standardized protocol, we propose that this novel system of cell expansion will be useful in therapeutic and research applications of hMSCs.
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spelling pubmed-65039992019-05-08 Soft substrate maintains proliferative and adipogenic differentiation potential of human mesenchymal stem cells on long-term expansion by delaying senescence Kureel, Sanjay Kumar Mogha, Pankaj Khadpekar, Akshada Kumar, Vardhman Joshi, Rohit Das, Siddhartha Bellare, Jayesh Majumder, Abhijit Biol Open Research Article Human mesenchymal stem cells (hMSCs), during in vitro expansion, gradually lose their distinct spindle morphology, self-renewal ability, multi-lineage differentiation potential and enter replicative senescence. This loss of cellular function is a major roadblock for clinical applications which demand cells in large numbers. Here, we demonstrate a novel role of substrate stiffness in the maintenance of hMSCs over long-term expansion. When serially passaged for 45 days from passage 3 to passage 18 on polyacrylamide gel of Young's modulus E=5 kPa, hMSCs maintained their proliferation rate and showed nine times higher population doubling in comparison to their counterparts cultured on plastic Petri-plates. They did not express markers of senescence, maintained their morphology and other mechanical properties such as cell stiffness and cellular traction, and were significantly superior in adipogenic differentiation potential. These results were demonstrated in hMSCs from two different sources, umbilical cord and bone marrow. In summary, our result shows that a soft gel is a suitable substrate to maintain the stemness of mesenchymal stem cells. As preparation of polyacrylamide gel is a well-established, and well-standardized protocol, we propose that this novel system of cell expansion will be useful in therapeutic and research applications of hMSCs. The Company of Biologists Ltd 2019-04-25 /pmc/articles/PMC6503999/ /pubmed/31023646 http://dx.doi.org/10.1242/bio.039453 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Kureel, Sanjay Kumar
Mogha, Pankaj
Khadpekar, Akshada
Kumar, Vardhman
Joshi, Rohit
Das, Siddhartha
Bellare, Jayesh
Majumder, Abhijit
Soft substrate maintains proliferative and adipogenic differentiation potential of human mesenchymal stem cells on long-term expansion by delaying senescence
title Soft substrate maintains proliferative and adipogenic differentiation potential of human mesenchymal stem cells on long-term expansion by delaying senescence
title_full Soft substrate maintains proliferative and adipogenic differentiation potential of human mesenchymal stem cells on long-term expansion by delaying senescence
title_fullStr Soft substrate maintains proliferative and adipogenic differentiation potential of human mesenchymal stem cells on long-term expansion by delaying senescence
title_full_unstemmed Soft substrate maintains proliferative and adipogenic differentiation potential of human mesenchymal stem cells on long-term expansion by delaying senescence
title_short Soft substrate maintains proliferative and adipogenic differentiation potential of human mesenchymal stem cells on long-term expansion by delaying senescence
title_sort soft substrate maintains proliferative and adipogenic differentiation potential of human mesenchymal stem cells on long-term expansion by delaying senescence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503999/
https://www.ncbi.nlm.nih.gov/pubmed/31023646
http://dx.doi.org/10.1242/bio.039453
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