Investigating the effects of microtubules in the neuronal cell response to the blast load using fluid-structure interactions method

Authors

1 Master Student, Aerospace Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran.

2 Associate Professor, Biomedical Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran.

3 Assistant Professor, Aerospace Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran.

Abstract

Traumatic brain injury states to the brain damage causing from sudden trauma. Undrestanding the mechanism and effects of such damages to the brain is of importance toward the treatment. In this research, a computational framework for considering the response of a neuronal cell is presented. The neuronal cell consists of three components including nucleus, cytoplasm, and membrane, and also the network of microtubules with the different arrays including crossing, stellate as well as random. In the simulation of blast loads, the pressure load driven by laser-induced and finite elements setup with fluid-structure interactions are considered. Cell components are assumed to follow viscoelastic and elastic mechanical behavior. The obtained results as compared to those of the experimental works showed different levels of cell damage. The presence of the microtubles network in cytoplasm, regardless of the types of array, reduces the total displacement of the cell and the von Mises stress in the other cell components. Furthermore, the network of microtubules plays a significant role in the total strength of the cell under the external imposed pressure. The membrane von Mises stress decrease 50 percent from 30 to 165 Pascals in presence of the network of microtubules.

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Main Subjects


[1]  Bernick KB (2011) Cell biomechanics of the central nervous system. Thesis, Massachusetts Institute of Technology.
[2]  Felgner H, Frank R, Biernat J, Mandelkow EM, Mandelkow E, Ludin B, Matus A, Schliwa M (1997) Domains of neuronal microtubule-associated proteins and flexural rigidity of microtubules. J Cell Biol 138(5): 1067-1075.
[3]  Jérusalem A, Dao M (2012) Continuum modeling of a neuronal cell under blast loading. Acta Biomater 8(9): 3360-3371.
[4]  Brown KA (2016) Blast loading of cells. in: Blast Injury Science and Engineering, Eds., Springer.
[5]  Edwards DS, Clasper J (2016) Blast injury mechanism. in: Blast Injury Science and Engineering, Eds., Springer.
[6]  Chen Y, Constantini S (2013) Caveats for using shock tube in blast-induced traumatic brain injury research. Front Neurol 4: 117.
[7]  Willinger R, Baumgartner D (2003) Numerical and physical modelling of the human head under impact-towards new injury criteria. Int J Vehicle Des 32(1-2): 94-115.
[8]  Salvador‐Silva M, Aoi S, Parker A, Yang P, Pecen P, Hernandez MR (2004) Responses and signaling pathways in human optic nerve head astrocytes exposed to hydrostatic pressure in vitro. Glia 45(4): 364-377.
[9]  Murphy EJ, Horrocks LA (1993) A model for compression trauma: pressure-induced injury in cell cultures. J Neurotraum 10(4): 431-444.
[10] Alford PW, Dabiri BE, Goss JA, Hemphill MA, Brigham MD, Parker KK (2011) Blast-induced phenotypic switching in cerebral vasospasm. P Natl A Sci India 108(31): 12705-12710.
[11] Bernick KB, Prevost TP, Suresh S, Socrate S (2011) Biomechanics of single cortical neurons. Acta Biomater 7(3): 1210-1219.
[12] Mofrad MR, Kamm RD (2006) Cytoskeletal mechanics: Models and measurements in cell mechanics. Cambridge University Press.
[13] Jean RP, Chen CS, Spector AA (2005) Finite-element analysis of the adhesion-cytoskeleton-nucleus mechanotransduction pathway during endothelial cell rounding: axisymmetric model. J Biomech Eng-T ASME 127(4): 594-600.
[14] Gladilin E, Micoulet A, Hosseini B, Rohr K,   Spatz J, Eils R (2007) 3D finite element analysis of uniaxial cell stretching: from image to insight. Phys Biol 4(2): 104.
[15] O'Connor CM, Adams JU, Fairman J (2010) Essentials of cell biology. Cambridge, MA: NPG Education, Vol. 1.
[16] Zander NE, Piehler T, Boggs ME, Banton R, Benjamin R (2015) In vitro studies of primary explosive blast loading on neurons. J Neurosci Res 93(9): 1353-1363.
[17] Sondén A, Svensson B, Roman N, Östmark H, Brismar B, Palmblad J, Kjellström BT (2000) Laser‐induced shock wave endothelial cell injury, Lasers in surgery and medicine. 26(4): 364-375.
[18] Drumheller DS (1998) Introduction to wave propagation in nonlinear fluids and solids. Cambridge University Press.
[19] Prado GR, Ross JD, DeWeerth SP, LaPlaca MC (2005) Mechanical trauma induces immediate changes in neuronal network activity. J Neural Eng 2(4): 148.
[20] Mathieu PS, Loboa EG (2012) Cytoskeletal       and focal adhesion influences on mesenchymal stem cell shape, mechanical properties, and differentiation down osteogenic, adipogenic, and chondrogenic pathways. Tissue Eng Pt B-Rev 18(6): 436-444.
[21] Barreto S, Clausen CH, Perrault CM, Fletcher DA, Lacroix D (2013) A multi-structural single cell model of force-induced interactions of cytoskeletal components. Biomaterials 34(26): 6119-6126.
[22] Barreto S, Perrault CM, Lacroix D (2014) Structural finite element analysis to explain cell mechanics variability. J Mech Behav Biomed 38: 219-231.