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Clay microparticles for the enhancement of bone regeneration: in vitro studies
Humans develop osteoporosis as they age, a disease characterized by the slow and consistent reduction in bone mass and the subsequent risk of fractures. Due to aging, the mesenchymal stem cells within the bone marrow niche, show a shift in differentiation from osteogenesis to adipogenesis. The chall...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082439/ https://www.ncbi.nlm.nih.gov/pubmed/37029830 http://dx.doi.org/10.1007/s00418-023-02189-2 |
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author | Abduljauwad, Sahel N. Habib, Taimur ur-Rehman, Habib |
author_facet | Abduljauwad, Sahel N. Habib, Taimur ur-Rehman, Habib |
author_sort | Abduljauwad, Sahel N. |
collection | PubMed |
description | Humans develop osteoporosis as they age, a disease characterized by the slow and consistent reduction in bone mass and the subsequent risk of fractures. Due to aging, the mesenchymal stem cells within the bone marrow niche, show a shift in differentiation from osteogenesis to adipogenesis. The challenge of osteoporosis treatment is being met with advances in nanotechnology and tissue engineering. In this study , we evaluated the potential of palygorskite clay mineral microparticles for the promotion of the osteogenic differentiation in human mesenchymal stem cells (hMSCs) in vitro. Alkaline phosphatase (ALP) activity and Alizarin red staining showed that osteogenic differentiation of hMSCs is enhanced in the presence of palygorskite clay. Although, gene expression analysis did not reveal upregulation of several osteogenic markers in the presence of the clay microparticles, another interaction mechanism resulted in the enhanced osteogenic differentiation of hMSCs. The charged surfaces of the palygorskite clay particles interact with the stem cells using their high adhesion characteristics, leading to complete bridging, adherence, and enveloping of the stem cells’ cadherins and integrins with their environment. This restoration of the adhesion among the stem cells and their environment most probably promotes/restores the osteogenic differentiation of hMSCs. Therefore, palygorskite clay microparticles are a promising candidate for further in vivo studies on bone regeneration. |
format | Online Article Text |
id | pubmed-10082439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-100824392023-04-11 Clay microparticles for the enhancement of bone regeneration: in vitro studies Abduljauwad, Sahel N. Habib, Taimur ur-Rehman, Habib Histochem Cell Biol Original Paper Humans develop osteoporosis as they age, a disease characterized by the slow and consistent reduction in bone mass and the subsequent risk of fractures. Due to aging, the mesenchymal stem cells within the bone marrow niche, show a shift in differentiation from osteogenesis to adipogenesis. The challenge of osteoporosis treatment is being met with advances in nanotechnology and tissue engineering. In this study , we evaluated the potential of palygorskite clay mineral microparticles for the promotion of the osteogenic differentiation in human mesenchymal stem cells (hMSCs) in vitro. Alkaline phosphatase (ALP) activity and Alizarin red staining showed that osteogenic differentiation of hMSCs is enhanced in the presence of palygorskite clay. Although, gene expression analysis did not reveal upregulation of several osteogenic markers in the presence of the clay microparticles, another interaction mechanism resulted in the enhanced osteogenic differentiation of hMSCs. The charged surfaces of the palygorskite clay particles interact with the stem cells using their high adhesion characteristics, leading to complete bridging, adherence, and enveloping of the stem cells’ cadherins and integrins with their environment. This restoration of the adhesion among the stem cells and their environment most probably promotes/restores the osteogenic differentiation of hMSCs. Therefore, palygorskite clay microparticles are a promising candidate for further in vivo studies on bone regeneration. Springer Berlin Heidelberg 2023-04-08 /pmc/articles/PMC10082439/ /pubmed/37029830 http://dx.doi.org/10.1007/s00418-023-02189-2 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Paper Abduljauwad, Sahel N. Habib, Taimur ur-Rehman, Habib Clay microparticles for the enhancement of bone regeneration: in vitro studies |
title | Clay microparticles for the enhancement of bone regeneration: in vitro studies |
title_full | Clay microparticles for the enhancement of bone regeneration: in vitro studies |
title_fullStr | Clay microparticles for the enhancement of bone regeneration: in vitro studies |
title_full_unstemmed | Clay microparticles for the enhancement of bone regeneration: in vitro studies |
title_short | Clay microparticles for the enhancement of bone regeneration: in vitro studies |
title_sort | clay microparticles for the enhancement of bone regeneration: in vitro studies |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082439/ https://www.ncbi.nlm.nih.gov/pubmed/37029830 http://dx.doi.org/10.1007/s00418-023-02189-2 |
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