Integrated computational and experimental pipeline for quantifying local cell–matrix interactions
Abstract Cellular interactions with the extracellular matrix (ECM) play a key role in modulating biological processes. While studies have identified key molecular factors of these interactions, the mechanical regulation associated with these interactions is not well characterized. To address this, w...
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Nature Portfolio
2021
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oai:doaj.org-article:2a1a073e5be449128718a57ccb25c7852021-12-02T19:06:38ZIntegrated computational and experimental pipeline for quantifying local cell–matrix interactions10.1038/s41598-021-95935-22045-2322https://doaj.org/article/2a1a073e5be449128718a57ccb25c7852021-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-95935-2https://doaj.org/toc/2045-2322Abstract Cellular interactions with the extracellular matrix (ECM) play a key role in modulating biological processes. While studies have identified key molecular factors of these interactions, the mechanical regulation associated with these interactions is not well characterized. To address this, we present an image analysis platform to analyze time-dependent dynamics observed in lung fibroblasts embedded in a 3D collagen matrix. Combining drug studies with quantitative analysis of cell–matrix interactions, our results are able to provide cellular level quantitative insights for mechanical and biophysical phenomena relevant to cell-ECM interactions. This system overall represents an initial pipeline for understanding cell mechanics in a 3D collagen gel and their implications in a physiologically relevant context.Hugh XiaoRyan Y. NguyenRyan LaRangerErica L. HerzogMichael MakNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-11 (2021) |
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Medicine R Science Q |
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Medicine R Science Q Hugh Xiao Ryan Y. Nguyen Ryan LaRanger Erica L. Herzog Michael Mak Integrated computational and experimental pipeline for quantifying local cell–matrix interactions |
description |
Abstract Cellular interactions with the extracellular matrix (ECM) play a key role in modulating biological processes. While studies have identified key molecular factors of these interactions, the mechanical regulation associated with these interactions is not well characterized. To address this, we present an image analysis platform to analyze time-dependent dynamics observed in lung fibroblasts embedded in a 3D collagen matrix. Combining drug studies with quantitative analysis of cell–matrix interactions, our results are able to provide cellular level quantitative insights for mechanical and biophysical phenomena relevant to cell-ECM interactions. This system overall represents an initial pipeline for understanding cell mechanics in a 3D collagen gel and their implications in a physiologically relevant context. |
format |
article |
author |
Hugh Xiao Ryan Y. Nguyen Ryan LaRanger Erica L. Herzog Michael Mak |
author_facet |
Hugh Xiao Ryan Y. Nguyen Ryan LaRanger Erica L. Herzog Michael Mak |
author_sort |
Hugh Xiao |
title |
Integrated computational and experimental pipeline for quantifying local cell–matrix interactions |
title_short |
Integrated computational and experimental pipeline for quantifying local cell–matrix interactions |
title_full |
Integrated computational and experimental pipeline for quantifying local cell–matrix interactions |
title_fullStr |
Integrated computational and experimental pipeline for quantifying local cell–matrix interactions |
title_full_unstemmed |
Integrated computational and experimental pipeline for quantifying local cell–matrix interactions |
title_sort |
integrated computational and experimental pipeline for quantifying local cell–matrix interactions |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/2a1a073e5be449128718a57ccb25c785 |
work_keys_str_mv |
AT hughxiao integratedcomputationalandexperimentalpipelineforquantifyinglocalcellmatrixinteractions AT ryanynguyen integratedcomputationalandexperimentalpipelineforquantifyinglocalcellmatrixinteractions AT ryanlaranger integratedcomputationalandexperimentalpipelineforquantifyinglocalcellmatrixinteractions AT ericalherzog integratedcomputationalandexperimentalpipelineforquantifyinglocalcellmatrixinteractions AT michaelmak integratedcomputationalandexperimentalpipelineforquantifyinglocalcellmatrixinteractions |
_version_ |
1718377137843470336 |