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...
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doaj-729c9112777d4f65b451ca382a92305c2021-04-12T01:08:48ZengAIMS PressMathematical Biosciences and Engineering1551-00182021-04-011821214123710.3934/mbe.2021066Primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiologyZhangli Peng0Andrew Resnick1Y.-N. Young21. Department of Bioengineering, University of Illinois at Chicago, 851 S. Morgan St., Chicago, IL 60607, USA2. Department of Physics, Center for Gene Regulation in Health and Disease, Cleveland State University, Cleveland, OH 44115, USA3. Department of Mathematical Sciences, New Jersey Institute of Technology, University Heights, Newark, NJ 07102, USAPrimary 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.http://www.aimspress.com/article/doi/10.3934/mbe.2021066?viewType=HTMLciliumfluid-structure interactionselastohydrodynamicsmechanosensingslender-body |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zhangli Peng Andrew Resnick Y.-N. Young |
spellingShingle |
Zhangli Peng Andrew Resnick Y.-N. Young Primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology Mathematical Biosciences and Engineering cilium fluid-structure interactions elastohydrodynamics mechanosensing slender-body |
author_facet |
Zhangli Peng Andrew Resnick Y.-N. Young |
author_sort |
Zhangli Peng |
title |
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_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_sort |
primary cilium: a paradigm for integrating mathematical modeling with experiments and numerical simulations in mechanobiology |
publisher |
AIMS Press |
series |
Mathematical Biosciences and Engineering |
issn |
1551-0018 |
publishDate |
2021-04-01 |
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. |
topic |
cilium fluid-structure interactions elastohydrodynamics mechanosensing slender-body |
url |
http://www.aimspress.com/article/doi/10.3934/mbe.2021066?viewType=HTML |
work_keys_str_mv |
AT zhanglipeng primaryciliumaparadigmforintegratingmathematicalmodelingwithexperimentsandnumericalsimulationsinmechanobiology AT andrewresnick primaryciliumaparadigmforintegratingmathematicalmodelingwithexperimentsandnumericalsimulationsinmechanobiology AT ynyoung primaryciliumaparadigmforintegratingmathematicalmodelingwithexperimentsandnumericalsimulationsinmechanobiology |
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1721530476871548928 |