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Long-term osteogenic differentiation of human bone marrow stromal cells in simulated microgravity: novel proteins sighted
Microgravity-induced bone loss is a major concern for space travelers. Ground-based microgravity simulators are crucial to study the effect of microgravity exposure on biological systems and to address the limitations posed by restricted access to real space. In this work, for the first time, we ado...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526692/ https://www.ncbi.nlm.nih.gov/pubmed/36181557 http://dx.doi.org/10.1007/s00018-022-04553-2 |
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author | Montagna, Giulia Pani, Giuseppe Flinkman, Dani Cristofaro, Francesco Pascucci, Barbara Massimino, Luca Lamparelli, Luigi Antonio Fassina, Lorenzo James, Peter Coffey, Eleanor Rea, Giuseppina Visai, Livia Rizzo, Angela Maria |
author_facet | Montagna, Giulia Pani, Giuseppe Flinkman, Dani Cristofaro, Francesco Pascucci, Barbara Massimino, Luca Lamparelli, Luigi Antonio Fassina, Lorenzo James, Peter Coffey, Eleanor Rea, Giuseppina Visai, Livia Rizzo, Angela Maria |
author_sort | Montagna, Giulia |
collection | PubMed |
description | Microgravity-induced bone loss is a major concern for space travelers. Ground-based microgravity simulators are crucial to study the effect of microgravity exposure on biological systems and to address the limitations posed by restricted access to real space. In this work, for the first time, we adopt a multidisciplinary approach to characterize the morphological, biochemical, and molecular changes underlying the response of human bone marrow stromal cells to long-term simulated microgravity exposure during osteogenic differentiation. Our results show that osteogenic differentiation is reduced while energy metabolism is promoted. We found novel proteins were dysregulated under simulated microgravity, including CSC1-like protein, involved in the mechanotransduction of pressure signals, and PTPN11, SLC44A1 and MME which are involved in osteoblast differentiation pathways and which may become the focus of future translational projects. The investigation of cell proteome highlighted how simulated microgravity affects a relatively low number of proteins compared to time and/or osteogenic factors and has allowed us to reconstruct a hypothetical pipeline for cell response to simulated microgravity. Further investigation focused on the application of nanomaterials may help to increase understanding of how to treat or minimize the effects of microgravity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04553-2. |
format | Online Article Text |
id | pubmed-9526692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-95266922022-10-03 Long-term osteogenic differentiation of human bone marrow stromal cells in simulated microgravity: novel proteins sighted Montagna, Giulia Pani, Giuseppe Flinkman, Dani Cristofaro, Francesco Pascucci, Barbara Massimino, Luca Lamparelli, Luigi Antonio Fassina, Lorenzo James, Peter Coffey, Eleanor Rea, Giuseppina Visai, Livia Rizzo, Angela Maria Cell Mol Life Sci Original Article Microgravity-induced bone loss is a major concern for space travelers. Ground-based microgravity simulators are crucial to study the effect of microgravity exposure on biological systems and to address the limitations posed by restricted access to real space. In this work, for the first time, we adopt a multidisciplinary approach to characterize the morphological, biochemical, and molecular changes underlying the response of human bone marrow stromal cells to long-term simulated microgravity exposure during osteogenic differentiation. Our results show that osteogenic differentiation is reduced while energy metabolism is promoted. We found novel proteins were dysregulated under simulated microgravity, including CSC1-like protein, involved in the mechanotransduction of pressure signals, and PTPN11, SLC44A1 and MME which are involved in osteoblast differentiation pathways and which may become the focus of future translational projects. The investigation of cell proteome highlighted how simulated microgravity affects a relatively low number of proteins compared to time and/or osteogenic factors and has allowed us to reconstruct a hypothetical pipeline for cell response to simulated microgravity. Further investigation focused on the application of nanomaterials may help to increase understanding of how to treat or minimize the effects of microgravity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04553-2. Springer International Publishing 2022-10-01 2022 /pmc/articles/PMC9526692/ /pubmed/36181557 http://dx.doi.org/10.1007/s00018-022-04553-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Montagna, Giulia Pani, Giuseppe Flinkman, Dani Cristofaro, Francesco Pascucci, Barbara Massimino, Luca Lamparelli, Luigi Antonio Fassina, Lorenzo James, Peter Coffey, Eleanor Rea, Giuseppina Visai, Livia Rizzo, Angela Maria Long-term osteogenic differentiation of human bone marrow stromal cells in simulated microgravity: novel proteins sighted |
title | Long-term osteogenic differentiation of human bone marrow stromal cells in simulated microgravity: novel proteins sighted |
title_full | Long-term osteogenic differentiation of human bone marrow stromal cells in simulated microgravity: novel proteins sighted |
title_fullStr | Long-term osteogenic differentiation of human bone marrow stromal cells in simulated microgravity: novel proteins sighted |
title_full_unstemmed | Long-term osteogenic differentiation of human bone marrow stromal cells in simulated microgravity: novel proteins sighted |
title_short | Long-term osteogenic differentiation of human bone marrow stromal cells in simulated microgravity: novel proteins sighted |
title_sort | long-term osteogenic differentiation of human bone marrow stromal cells in simulated microgravity: novel proteins sighted |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526692/ https://www.ncbi.nlm.nih.gov/pubmed/36181557 http://dx.doi.org/10.1007/s00018-022-04553-2 |
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