Combined optical tweezers and laser dissector for controlled ablation of functional connections in neural networks.

Regeneration of functional connectivity within a neural network after different degrees of lesion is of utmost clinical importance. To test pharmacological approaches aimed at recovering from a total or partial damage of neuronal connections within a circuit, it is necessary to develop a precise method for controlled ablation of neuronal processes. We combined a UV laser microdissector to ablate neural processes in vitro at single neuron and neural network level with infrared holographic optical tweezers to carry out force spectroscopy measurements. Simultaneous force spectroscopy, down to the sub-pico-Newton range, was performed during laser dissection to quantify the tension release in a partially ablated neurite. Therefore, we could control and measure the damage inflicted to an individual neuronal process. To characterize the effect of the inflicted injury on network level, changes in activity of neural subpopulations were monitored with subcellular resolution and overall network activity with high temporal resolution by concurrent calcium imaging and microelectrode array recording. Neuronal connections have been sequentially ablated and the correlated changes in network activity traced and mapped. With this unique combination of electrophysiological and optical tools, neural activity can be studied and quantified in response to controlled injury at the subcellular, cellular, and network level.

[1]  Shelly R. Peyton,et al.  The emergence of ECM mechanics and cytoskeletal tension as important regulators of cell function , 2007, Cell Biochemistry and Biophysics.

[2]  Cecile O. Mejean,et al.  Cell stimulation with optically manipulated microsources , 2009, Nature Methods.

[3]  Luca Berdondini,et al.  Active pixel sensor array for high spatio-temporal resolution electrophysiological recordings from single cell to large scale neuronal networks. , 2009, Lab on a chip.

[4]  G J Brewer,et al.  Microcontact printing for precise control of nerve cell growth in culture. , 1999, Journal of biomechanical engineering.

[5]  Alessandro Laio,et al.  Force generation in lamellipodia is a probabilistic process with fast growth and retraction events. , 2010, Biophysical journal.

[6]  D. Ingber Tensegrity II. How structural networks influence cellular information processing networks , 2003, Journal of Cell Science.

[7]  Woodrow L. Shew,et al.  Simultaneous multi-electrode array recording and two-photon calcium imaging of neural activity , 2010, Journal of Neuroscience Methods.

[8]  Eric R Dufresne,et al.  Multiplexed force measurements on live cells with holographic optical tweezers. , 2009, Optics express.

[9]  Ernst H. K. Stelzer,et al.  Filopodia act as phagocytic tentacles and pull with discrete steps and a load-dependent velocity , 2007, Proceedings of the National Academy of Sciences.

[10]  Michael P. Sheetz,et al.  Talin1 is critical for force-dependent reinforcement of initial integrin–cytoskeleton bonds but not tyrosine kinase activation , 2003, The Journal of cell biology.

[11]  Mina J Bissell,et al.  Dissecting regional variations in stress fiber mechanics in living cells with laser nanosurgery. , 2010, Biophysical journal.

[12]  Fabio Benfenati,et al.  Simultaneous two-photon imaging and photo-stimulation with structured light illumination. , 2010, Optics express.

[13]  V. Torre,et al.  Optical tweezers microscopy: piconewton forces in cell and molecular biology , 2010 .

[14]  Frank Bradke,et al.  Axon Extension Occurs Independently of Centrosomal Microtubule Nucleation , 2010, Science.

[15]  Donald E Ingber,et al.  Tensegrity and mechanotransduction. , 2008, Journal of bodywork and movement therapies.

[16]  John V. Small,et al.  Mechanosensing in actin stress fibers revealed by a close correlation between force and protein localization , 2009, Journal of Cell Science.

[17]  Marc Tramier,et al.  Supplmentary Material Spatio-Temporal Analysis of Cell Response to a Rigidity Gradient : A Quantitative Study by Multiple Optical Tweezers , 2008 .

[18]  D. V. van Essen,et al.  A tension-based theory of morphogenesis and compact wiring in the central nervous system. , 1997, Nature.

[19]  Jagannathan Rajagopalan,et al.  Drosophila neurons actively regulate axonal tension in vivo. , 2010, Biophysical journal.

[20]  G. Banker,et al.  Culturing nerve cells , 1998 .

[21]  Mnh Culturing Nerve Cell , 1999 .

[22]  Marc Tramier,et al.  Spatiotemporal analysis of cell response to a rigidity gradient: a quantitative study using multiple optical tweezers. , 2009, Biophysical journal.

[23]  Akira Chiba,et al.  Mechanical tension contributes to clustering of neurotransmitter vesicles at presynaptic terminals , 2009, Proceedings of the National Academy of Sciences.

[24]  Digant P. Dave,et al.  Neuro-optical microfluidic platform to study injury and regeneration of single axons. , 2009, Lab on a chip.

[25]  V. Torre,et al.  Properties of the Force Exerted by Filopodia and Lamellipodia and the Involvement of Cytoskeletal Components , 2007, PloS one.

[26]  Julien Colombelli,et al.  Investigating relaxation processes in cells and developing organisms: from cell ablation to cytoskeleton nanosurgery. , 2007, Methods in cell biology.

[27]  A. Chisholm,et al.  Caenorhabditis elegans: A new model organism for studies of axon regeneration , 2010, Developmental dynamics : an official publication of the American Association of Anatomists.

[28]  Alexander Rohrbach,et al.  Switching and measuring a force of 25 femtoNewtons with an optical trap. , 2005, Optics express.