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Modified cantilever arrays improve sensitivity and reproducibility of nanomechanical sensing in living cells

Mechanical signaling involved in molecular interactions lies at the heart of materials science and biological systems, but the mechanisms involved are poorly understood. Here we use nanomechanical sensors and intact human cells to provide unique insights into the signaling pathways of connectivity n...

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Autores principales: Patil, Samadhan B., Al-Jehani, Rajai M., Etayash, Hashem, Turbe, Valerian, Jiang, Keren, Bailey, Joe, Al-Akkad, Walid, Soudy, Rania, Kaur, Kamaljit, McKendry, Rachel A., Thundat, Thomas, Ndieyira, Joseph W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200835/
https://www.ncbi.nlm.nih.gov/pubmed/30374465
http://dx.doi.org/10.1038/s42003-018-0179-3
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author Patil, Samadhan B.
Al-Jehani, Rajai M.
Etayash, Hashem
Turbe, Valerian
Jiang, Keren
Bailey, Joe
Al-Akkad, Walid
Soudy, Rania
Kaur, Kamaljit
McKendry, Rachel A.
Thundat, Thomas
Ndieyira, Joseph W.
author_facet Patil, Samadhan B.
Al-Jehani, Rajai M.
Etayash, Hashem
Turbe, Valerian
Jiang, Keren
Bailey, Joe
Al-Akkad, Walid
Soudy, Rania
Kaur, Kamaljit
McKendry, Rachel A.
Thundat, Thomas
Ndieyira, Joseph W.
author_sort Patil, Samadhan B.
collection PubMed
description Mechanical signaling involved in molecular interactions lies at the heart of materials science and biological systems, but the mechanisms involved are poorly understood. Here we use nanomechanical sensors and intact human cells to provide unique insights into the signaling pathways of connectivity networks, which deliver the ability to probe cells to produce biologically relevant, quantifiable and reproducible signals. We quantify the mechanical signals from malignant cancer cells, with 10 cells per ml in 1000-fold excess of non-neoplastic human epithelial cells. Moreover, we demonstrate that a direct link between cells and molecules creates a continuous connectivity which acts like a percolating network to propagate mechanical forces over both short and long length-scales. The findings provide mechanistic insights into how cancer cells interact with one another and with their microenvironments, enabling them to invade the surrounding tissues. Further, with this system it is possible to understand how cancer clusters are able to co-ordinate their migration through narrow blood capillaries.
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spelling pubmed-62008352018-10-29 Modified cantilever arrays improve sensitivity and reproducibility of nanomechanical sensing in living cells Patil, Samadhan B. Al-Jehani, Rajai M. Etayash, Hashem Turbe, Valerian Jiang, Keren Bailey, Joe Al-Akkad, Walid Soudy, Rania Kaur, Kamaljit McKendry, Rachel A. Thundat, Thomas Ndieyira, Joseph W. Commun Biol Article Mechanical signaling involved in molecular interactions lies at the heart of materials science and biological systems, but the mechanisms involved are poorly understood. Here we use nanomechanical sensors and intact human cells to provide unique insights into the signaling pathways of connectivity networks, which deliver the ability to probe cells to produce biologically relevant, quantifiable and reproducible signals. We quantify the mechanical signals from malignant cancer cells, with 10 cells per ml in 1000-fold excess of non-neoplastic human epithelial cells. Moreover, we demonstrate that a direct link between cells and molecules creates a continuous connectivity which acts like a percolating network to propagate mechanical forces over both short and long length-scales. The findings provide mechanistic insights into how cancer cells interact with one another and with their microenvironments, enabling them to invade the surrounding tissues. Further, with this system it is possible to understand how cancer clusters are able to co-ordinate their migration through narrow blood capillaries. Nature Publishing Group UK 2018-10-24 /pmc/articles/PMC6200835/ /pubmed/30374465 http://dx.doi.org/10.1038/s42003-018-0179-3 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Patil, Samadhan B.
Al-Jehani, Rajai M.
Etayash, Hashem
Turbe, Valerian
Jiang, Keren
Bailey, Joe
Al-Akkad, Walid
Soudy, Rania
Kaur, Kamaljit
McKendry, Rachel A.
Thundat, Thomas
Ndieyira, Joseph W.
Modified cantilever arrays improve sensitivity and reproducibility of nanomechanical sensing in living cells
title Modified cantilever arrays improve sensitivity and reproducibility of nanomechanical sensing in living cells
title_full Modified cantilever arrays improve sensitivity and reproducibility of nanomechanical sensing in living cells
title_fullStr Modified cantilever arrays improve sensitivity and reproducibility of nanomechanical sensing in living cells
title_full_unstemmed Modified cantilever arrays improve sensitivity and reproducibility of nanomechanical sensing in living cells
title_short Modified cantilever arrays improve sensitivity and reproducibility of nanomechanical sensing in living cells
title_sort modified cantilever arrays improve sensitivity and reproducibility of nanomechanical sensing in living cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200835/
https://www.ncbi.nlm.nih.gov/pubmed/30374465
http://dx.doi.org/10.1038/s42003-018-0179-3
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