Engineering a high throughput axon injury system

Several key biological mechanisms of traumatic injury to axons are being elucidated using in vitro stretch injury models. However, these models are based on the experimentation of single cultures keeping productivity slow. Indeed, low yield has hindered important and well-founded investigations requiring high throughput methods such as proteomic analyses. To meet this need, we engineered a multi-well high throughput injury device to accelerate and accommodate the next generation of traumatic brain injury research. This modular system stretch-injures neuronal cultures in either a 24-well culture plate format or 6 individual wells simultaneously. Custom software control allows the user to set the input pressure and valve timing to achieve the desired substrate deformation and injury parameters. Characterization plots were created to aid the user in choosing the programmed parameters. Precise control of the pressure pulse was achieved. Peak pressure was linearly related to input pressure and valve open times. Analysis of the pressure waveforms in the 6 and 24-well modules displayed rise times, peak pressures, and decays with extremely small standard deviations. Data also confirmed that the pressure pulse was distributed evenly throughout the pressure chambers and therefore to each injury well. Importantly, the relationship between substrate deformation and applied pressure was consistent among the multiple wells and displayed a predictable linear behavior in each module.

[1]  Ivan Soltesz,et al.  Long‐term hyperexcitability in the hippocampus after experimental head trauma , 2001, Annals of neurology.

[2]  J. Povlishock,et al.  Traumatically Induced Axonal Injury: Pathogenesis and Pathobiological Implications , 1991, Brain pathology.

[3]  H. Levin,et al.  Cognitive function outcomes after traumatic brain injury. , 1998, Current opinion in neurology.

[4]  R. Neumar,et al.  Calpain Mediates Proteolysis of the Voltage-Gated Sodium Channel α-Subunit , 2009, The Journal of Neuroscience.

[5]  J. Adams,et al.  Brain damage in fatal non-missile head injury. , 1980, Journal of clinical pathology.

[6]  J E Sniezek,et al.  Incidence of mild and moderate brain injury in the United States, 1991. , 1996, Brain injury.

[7]  David F. Meaney,et al.  Mechanical Characterization of an In Vitro Device Designed to Quantitatively Injure Living Brain Tissue , 1998, Annals of Biomedical Engineering.

[8]  John A. Wolf,et al.  High Tolerance and Delayed Elastic Response of Cultured Axons to Dynamic Stretch Injury , 1999, The Journal of Neuroscience.

[9]  David F Meaney,et al.  Traumatic Axonal Injury Induces Proteolytic Cleavage of the Voltage-Gated Sodium Channels Modulated by Tetrodotoxin and Protease Inhibitors , 2004, The Journal of Neuroscience.

[10]  L. Thibault,et al.  Mechanical and electrical responses of the squid giant axon to simple elongation. , 1993, Journal of biomechanical engineering.

[11]  M. Putt,et al.  Effect of acute calcium influx after mechanical stretch injury in vitro on the viability of hippocampal neurons. , 2004, Journal of neurotrauma.

[12]  P. London Epidemiology of head injury in England and wales , 1977 .

[13]  Michelle C LaPlaca,et al.  Mechanical trauma induces immediate changes in neuronal network activity , 2005, Journal of neural engineering.

[14]  T A Gennarelli,et al.  Biomechanical analysis of experimental diffuse axonal injury. , 1995, Journal of neurotrauma.

[15]  Timothy P. Weihs,et al.  An In Vitro Uniaxial Stretch Model for Axonal Injury , 2003, Annals of Biomedical Engineering.

[16]  M. LaPlaca,et al.  Susceptibility of hippocampal neurons to mechanically induced injury , 2003, Experimental Neurology.

[17]  Grace Scott,et al.  Diffuse axonal injury due to nonmissile head injury in humans: An analysis of 45 cases , 1982, Annals of neurology.

[18]  S. Margulies,et al.  A proposed tolerance criterion for diffuse axonal injury in man. , 1992, Journal of biomechanics.

[19]  Michelle C LaPlaca,et al.  High rate shear strain of three-dimensional neural cell cultures: a new in vitro traumatic brain injury model. , 2005, Journal of biomechanics.

[20]  M. L. Smith,et al.  Regional hippocampal alteration associated with cognitive deficit following experimental brain injury: A systems, network and cellular evaluation , 2005, Neuroscience.

[21]  L. Sundstrom,et al.  An in vitro model of traumatic brain injury utilising two-dimensional stretch of organotypic hippocampal slice cultures , 2006, Journal of Neuroscience Methods.

[22]  H. Levin,et al.  Cognitive impairment following closed head injury. , 1992, Neurologic clinics.

[23]  D. Meaney,et al.  Calcium-permeable AMPA receptors appear in cortical neurons after traumatic mechanical injury and contribute to neuronal fate. , 2008, Journal of neurotrauma.

[24]  S. Strich,et al.  SHEARING OF NERVE FIBRES AS A CAUSE OF BRAIN DAMAGE DUE TO HEAD INJURY: A Pathological Study of Twenty Cases , 1961 .

[25]  G. Xiong,et al.  Mechanisms underlying the inability to induce area CA1 LTP in the mouse after traumatic brain injury , 2006, Hippocampus.

[26]  J. Wolf,et al.  The separate roles of calcium and mechanical forces in mediating cell death in mechanically injured neurons. , 2003, Biorheology.

[27]  B. Stoica,et al.  Modulation of stretch-induced enhancement of neuronal NMDA receptor current by mGluR1 depends upon presence of glia. , 2003, Journal of neurotrauma.

[28]  J. Adams,et al.  Mechanisms of non-penetrating head injury. , 1988, Progress in clinical and biological research.

[29]  J. Adams,et al.  Diffuse axonal injury in head injury: Definition, diagnosis and grading , 1989, Histopathology.

[30]  T. Novack,et al.  Current concepts: diffuse axonal injury-associated traumatic brain injury. , 2001, Archives of physical medicine and rehabilitation.

[31]  David F. Meaney,et al.  A Device to Study the Initiation and Propagation of Calcium Transients in Cultured Neurons After Mechanical Stretch , 2004, Annals of Biomedical Engineering.

[32]  J. H. Lucas In vitro models of mechanical injury. , 1992, Journal of neurotrauma.

[33]  Michelle C LaPlaca,et al.  Mechanical stretch to neurons results in a strain rate and magnitude-dependent increase in plasma membrane permeability. , 2003, Journal of neurotrauma.

[34]  J. Weber,et al.  Intracellular Free Calcium Dynamics in Stretch‐Injured Astrocytes , 1998, Journal of neurochemistry.

[35]  L. Satin,et al.  Potentiation of GABA(A) currents after mechanical injury of cortical neurons. , 2004, Journal of neurotrauma.

[36]  L. Thibault,et al.  Anin vitro traumatic injury model to examine the response of neurons to a hydrodynamically-induced deformation , 1997, Annals of Biomedical Engineering.

[37]  T A Gennarelli,et al.  Physical model simulations of brain injury in the primate. , 1990, Journal of biomechanics.

[38]  D. Meaney,et al.  Axonal Damage in Traumatic Brain Injury , 2000 .

[39]  S. Usami,et al.  Erratum: “A Strain Device Imposing Dynamic and Uniform Equi-Biaxial Strain to Cultured Cells” [Ann. Biomed. Eng. 26, 181–189 (1998) , 1998, Annals of Biomedical Engineering.

[40]  S. J. Tavalin,et al.  Mechanical perturbation of cultured cortical neurons reveals a stretch-induced delayed depolarization. , 1995, Journal of neurophysiology.

[41]  J. Galbraith,et al.  Axonal structure and function after axolemmal leakage in the squid giant axon. , 1997, Journal of neurotrauma.

[42]  D. Meaney,et al.  Diffuse Axonal Injury in Head Trauma , 2003, The Journal of head trauma rehabilitation.

[43]  Douglas H. Smith,et al.  Sodium channelopathy induced by mild axonal trauma worsens outcome after a repeat injury , 2009, Journal of neuroscience research.

[44]  L. Thibault,et al.  Acute alterations in [Ca2+]i in NG108-15 cells subjected to high strain rate deformation and chemical hypoxia: an in vitro model for neural trauma. , 1996, Journal of neurotrauma.

[45]  David F Meaney,et al.  In-vitro approaches for studying blast-induced traumatic brain injury. , 2009, Journal of neurotrauma.

[46]  R. Cargill,et al.  An in vitro model of neural trauma: device characterization and calcium response to mechanical stretch. , 2001, Journal of biomechanical engineering.

[47]  Mechanically induced reactive gliosis causes ATP-mediated alterations in astrocyte stiffness. , 2009 .

[48]  J. Wolf,et al.  Traumatic Axonal Injury Induces Calcium Influx Modulated by Tetrodotoxin-Sensitive Sodium Channels , 2001, The Journal of Neuroscience.

[49]  J. W. Lighthall,et al.  Experimental models of brain injury. , 1989, Journal of neurotrauma.

[50]  L. Satin,et al.  Mechanical injury modulates AMPA receptor kinetics via an NMDA receptor-dependent pathway. , 2004, Journal of neurotrauma.

[51]  J. Povlishock,et al.  A new model for rapid stretch-induced injury of cells in culture: characterization of the model using astrocytes. , 1995, Journal of neurotrauma.

[52]  D F Meaney,et al.  In vitro central nervous system models of mechanically induced trauma: a review. , 1998, Journal of neurotrauma.

[53]  S. J. Tavalin,et al.  Inhibition of the electrogenic Na pump underlies delayed depolarization of cortical neurons after mechanical injury or glutamate. , 1997, Journal of neurophysiology.

[54]  A. Holbourn,et al.  The mechanics of brain injuries , 1945 .

[55]  M. Grady,et al.  Injury-induced alterations in CNS electrophysiology. , 2007, Progress in brain research.