Accession Number:

ADA532355

Title:

Mechanical Loading of Neurons and Astrocytes with Application to Blast Traumatic Brain Injury

Descriptive Note:

Conference paper

Corporate Author:

MASSACHUSETTS INST OF TECH CAMBRIDGE

Report Date:

2010-01-01

Pagination or Media Count:

10.0

Abstract:

Investigations of the mechanical properties of cells are essential for linking mechanical deformation and loading to injury mechanisms at the cellular level. This is especially important when studying traumatic brain injury TBI. Neurons and astrocytes are susceptible to damage mechanisms arising from various loading scenarios ranging from motor vehicle accidents to sports injuries and pressure waves generated by explosions. Obtaining the mechanical properties of cells of the central nervous system CNS is a critical step for the development of hierarchical models and multi-scale simulation tools to elucidate how applied macroscopic loading conditions such as pressure waves, translate into cell deformation and damage. Here we present atomic force microscopy AFM indentation data and finite element simulation results on the mechanical response of single neurons and astrocytes to dynamic loading at large strains. Specific AFM testing protocols were developed to characterize the mechanical behavior of both cortical neurons and astrocytes over a range of indentation rates spanning three orders of magnitude - i.e. 10, 1, and 0.1 micrometerss. The response of both cell types showed similar qualitative nonlinear viscoelastic patterns although, quantitatively some differences were noted between the two CNS cell populations. The rheological data were complemented with geometrical measurements of cell body morphology obtained through bright-field and confocal microscopy images. A constitutive model was developed, enabling quantitative comparisons within and between populations of neurons and astrocytes. The proposed model, built upon previous constitutive model developments carried out at the cortical tissue level, was implemented into a three-dimensional finite element framework. The simulated cell responses were successfully calibrated to the experimental measurement under the selected test conditions.

Subject Categories:

  • Anatomy and Physiology
  • Medicine and Medical Research
  • Stress Physiology

Distribution Statement:

APPROVED FOR PUBLIC RELEASE