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Primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology
Primary cilia are non-motile, solitary (one per cell) microtubule-based organelles that emerge from the mother centriole after cells have exited the mitotic cycle. Identified as a mechanosensing organelle that responds to both mechanical and chemical stimuli, the primary cilium provides a fertile gr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552149/ https://www.ncbi.nlm.nih.gov/pubmed/33757184 http://dx.doi.org/10.3934/mbe.2021066 |
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author | Peng, Zhangli Resnick, Andrew Young, Y.-N. |
author_facet | Peng, Zhangli Resnick, Andrew Young, Y.-N. |
author_sort | Peng, Zhangli |
collection | PubMed |
description | Primary cilia are non-motile, solitary (one per cell) microtubule-based organelles that emerge from the mother centriole after cells have exited the mitotic cycle. Identified as a mechanosensing organelle that responds to both mechanical and chemical stimuli, the primary cilium provides a fertile ground for integrative investigations of mathematical modeling, numerical simulations, and experiments. Recent experimental findings revealed considerable complexity to the underlying mechanosensory mechanisms that transmit extracellular stimuli to intracellular signaling many of which include primary cilia. In this invited review, we provide a brief survey of experimental findings on primary cilia and how these results lead to various mathematical models of the mechanics of the primary cilium bent under an external forcing such as a fluid flow or a trap. Mathematical modeling of the primary cilium as a fluid-structure interaction problem highlights the importance of basal anchorage and the anisotropic moduli of the microtubules. As theoretical modeling and numerical simulations progress, along with improved state-of-the-art experiments on primary cilia, we hope that details of ciliary regulated mechano-chemical signaling dynamics in cellular physiology will be understood in the near future. |
format | Online Article Text |
id | pubmed-8552149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-85521492021-10-28 Primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology Peng, Zhangli Resnick, Andrew Young, Y.-N. Math Biosci Eng Article Primary cilia are non-motile, solitary (one per cell) microtubule-based organelles that emerge from the mother centriole after cells have exited the mitotic cycle. Identified as a mechanosensing organelle that responds to both mechanical and chemical stimuli, the primary cilium provides a fertile ground for integrative investigations of mathematical modeling, numerical simulations, and experiments. Recent experimental findings revealed considerable complexity to the underlying mechanosensory mechanisms that transmit extracellular stimuli to intracellular signaling many of which include primary cilia. In this invited review, we provide a brief survey of experimental findings on primary cilia and how these results lead to various mathematical models of the mechanics of the primary cilium bent under an external forcing such as a fluid flow or a trap. Mathematical modeling of the primary cilium as a fluid-structure interaction problem highlights the importance of basal anchorage and the anisotropic moduli of the microtubules. As theoretical modeling and numerical simulations progress, along with improved state-of-the-art experiments on primary cilia, we hope that details of ciliary regulated mechano-chemical signaling dynamics in cellular physiology will be understood in the near future. 2021-01-15 /pmc/articles/PMC8552149/ /pubmed/33757184 http://dx.doi.org/10.3934/mbe.2021066 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ) |
spellingShingle | Article Peng, Zhangli Resnick, Andrew Young, Y.-N. Primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology |
title | Primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology |
title_full | Primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology |
title_fullStr | Primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology |
title_full_unstemmed | Primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology |
title_short | Primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology |
title_sort | primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552149/ https://www.ncbi.nlm.nih.gov/pubmed/33757184 http://dx.doi.org/10.3934/mbe.2021066 |
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