A finite element model of an osteoblast to quantify the transduction of exogenous forces to cellular components. (August 2021)
- Record Type:
- Journal Article
- Title:
- A finite element model of an osteoblast to quantify the transduction of exogenous forces to cellular components. (August 2021)
- Main Title:
- A finite element model of an osteoblast to quantify the transduction of exogenous forces to cellular components
- Authors:
- Papadakis, Labros
Kanakousaki, Dimitra
Bakopoulou, Athina
Tsouknidas, Alexander
Michalakis, Konstantinos - Abstract:
- Highlights: Consideration of all cellular components vital to its function, e.g. mitochondria. Force driven cell deformation depends on site-specific stiffness/elasticity. Only a small % of the cytoskeleton contributes to force-driven cellular events. Abstract: Encouraged by recent advances of biophysical and biochemical assays we introduce a 3D finite element model of an osteoblast, seeking an analogue between exogenous forces and intracellularly activated sensory mechanisms. The cell was reverse engineered and the dimensions of the internal cellular structures were based on literature data. The model was verified and validated against atomic force microscopy experiments and four loading scenarios were considered. The stress distributions developing on the main cellular components were calculated along with their corresponding strain values. The nucleus and mitochondria exhibited similar loading trends, with the mitochondria being stressed by an order of magnitude higher than the nucleus (e.g. 1.4 vs. 0.16 MPa). Equivalent stiffness was determined to increase by almost 50%, from the apex to the cell's periphery, as was the cell's elasticity, which was lowest when the load was exerted directly above the nucleus. The assessment of how extrinsic loads are propagated to a cell's internal structures is inherently a problem of high complexity. The findings presented in this study can provide important insight into biophysical and biochemical responses elicited in cells throughHighlights: Consideration of all cellular components vital to its function, e.g. mitochondria. Force driven cell deformation depends on site-specific stiffness/elasticity. Only a small % of the cytoskeleton contributes to force-driven cellular events. Abstract: Encouraged by recent advances of biophysical and biochemical assays we introduce a 3D finite element model of an osteoblast, seeking an analogue between exogenous forces and intracellularly activated sensory mechanisms. The cell was reverse engineered and the dimensions of the internal cellular structures were based on literature data. The model was verified and validated against atomic force microscopy experiments and four loading scenarios were considered. The stress distributions developing on the main cellular components were calculated along with their corresponding strain values. The nucleus and mitochondria exhibited similar loading trends, with the mitochondria being stressed by an order of magnitude higher than the nucleus (e.g. 1.4 vs. 0.16 MPa). Equivalent stiffness was determined to increase by almost 50%, from the apex to the cell's periphery, as was the cell's elasticity, which was lowest when the load was exerted directly above the nucleus. The assessment of how extrinsic loads are propagated to a cell's internal structures is inherently a problem of high complexity. The findings presented in this study can provide important insight into biophysical and biochemical responses elicited in cells through mechanical stimulus. This was evident in both the nuclear and mitochondrial loading and would stipulate the important contribution of even more accurate models in the interpretation of cellular events. One Sentence Summary: The results of this numerical biomechanical study demonstrated that even minor extrinsic loads irrespective of the application site, are transduced by a fraction of the cytoskeleton to its internal structure (primarily to its mitochondria and secondary to the cell's nucleus), indicating mechanical stimulus as the dominant pathway to cell expression. … (more)
- Is Part Of:
- Medical engineering & physics. Volume 94(2021)
- Journal:
- Medical engineering & physics
- Issue:
- Volume 94(2021)
- Issue Display:
- Volume 94, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 94
- Issue:
- 2021
- Issue Sort Value:
- 2021-0094-2021-0000
- Page Start:
- 61
- Page End:
- 69
- Publication Date:
- 2021-08
- Subjects:
- Mechanotransduction -- Cell stiffness -- Cell elasticity -- Structural contribution
Biomedical engineering -- Periodicals
Biomedical Engineering -- Periodicals
Physics -- Periodicals
Génie biomédical -- Périodiques
Biomedical engineering
Electronic journals
Periodicals
610.28 - Journal URLs:
- http://www.medengphys.com ↗
http://www.sciencedirect.com/science/journal/13504533 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/13504533 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/13504533 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.medengphy.2021.06.010 ↗
- Languages:
- English
- ISSNs:
- 1350-4533
- Deposit Type:
- Legaldeposit
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- British Library DSC - 5527.323000
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