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Engineered barriers regulate osteoblast cell migration in vertical direction
Considering cell migration is essential for understanding physiological processes and diseases. The vertical migration of cells in three dimensions is vital, but most previous studies on cell migration have only focused on two-dimensional horizontal migration. In this paper, cell migration in the ve...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924172/ https://www.ncbi.nlm.nih.gov/pubmed/35292702 http://dx.doi.org/10.1038/s41598-022-08262-5 |
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author | Chen, X. Xu, Y. Cheng, Y. Pang, S. W. |
author_facet | Chen, X. Xu, Y. Cheng, Y. Pang, S. W. |
author_sort | Chen, X. |
collection | PubMed |
description | Considering cell migration is essential for understanding physiological processes and diseases. The vertical migration of cells in three dimensions is vital, but most previous studies on cell migration have only focused on two-dimensional horizontal migration. In this paper, cell migration in the vertical direction was studied. Barriers with a height of 1, 5, 10, and 25 µm with grating and arrows in channels as guiding patterns were fabricated. The effects of barrier height and guiding patterns on the vertical migration of MC3T3 cells were explored. The study revealed that taller barriers hinder vertical migration of MC3T3 cells, whereas grating and arrows in channels promote it. The time-lapse and micrograph images showed that as the barrier height increased, the cell climbing angle along the barrier sidewall decreased, and the time taken to climb over the barrier increased. These results indicate that taller barriers increase the difficulty of vertical migration by MC3T3 cells. To promote the vertical migration of MC3T3 cells, 10 µm tall barriers with 18° and 40° sloped sidewalls were fabricated. For barriers with 18° sloped sidewalls, the probability for MC3T3 cells to climb up and down the 10 µm tall barriers was 40.6% and 20.3%, respectively; this is much higher than the migration probability over vertical barriers. This study shows topographic guidance on the vertical migration of MC3T3 cells and broadens the understanding of cell migration in the vertical direction. |
format | Online Article Text |
id | pubmed-8924172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89241722022-03-16 Engineered barriers regulate osteoblast cell migration in vertical direction Chen, X. Xu, Y. Cheng, Y. Pang, S. W. Sci Rep Article Considering cell migration is essential for understanding physiological processes and diseases. The vertical migration of cells in three dimensions is vital, but most previous studies on cell migration have only focused on two-dimensional horizontal migration. In this paper, cell migration in the vertical direction was studied. Barriers with a height of 1, 5, 10, and 25 µm with grating and arrows in channels as guiding patterns were fabricated. The effects of barrier height and guiding patterns on the vertical migration of MC3T3 cells were explored. The study revealed that taller barriers hinder vertical migration of MC3T3 cells, whereas grating and arrows in channels promote it. The time-lapse and micrograph images showed that as the barrier height increased, the cell climbing angle along the barrier sidewall decreased, and the time taken to climb over the barrier increased. These results indicate that taller barriers increase the difficulty of vertical migration by MC3T3 cells. To promote the vertical migration of MC3T3 cells, 10 µm tall barriers with 18° and 40° sloped sidewalls were fabricated. For barriers with 18° sloped sidewalls, the probability for MC3T3 cells to climb up and down the 10 µm tall barriers was 40.6% and 20.3%, respectively; this is much higher than the migration probability over vertical barriers. This study shows topographic guidance on the vertical migration of MC3T3 cells and broadens the understanding of cell migration in the vertical direction. Nature Publishing Group UK 2022-03-15 /pmc/articles/PMC8924172/ /pubmed/35292702 http://dx.doi.org/10.1038/s41598-022-08262-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 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 | Article Chen, X. Xu, Y. Cheng, Y. Pang, S. W. Engineered barriers regulate osteoblast cell migration in vertical direction |
title | Engineered barriers regulate osteoblast cell migration in vertical direction |
title_full | Engineered barriers regulate osteoblast cell migration in vertical direction |
title_fullStr | Engineered barriers regulate osteoblast cell migration in vertical direction |
title_full_unstemmed | Engineered barriers regulate osteoblast cell migration in vertical direction |
title_short | Engineered barriers regulate osteoblast cell migration in vertical direction |
title_sort | engineered barriers regulate osteoblast cell migration in vertical direction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924172/ https://www.ncbi.nlm.nih.gov/pubmed/35292702 http://dx.doi.org/10.1038/s41598-022-08262-5 |
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