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J Neurophysiol 99: 3136-3143, 2008. First published March 12, 2008; doi:10.1152/jn.91327.2007
0022-3077/08 $8.00
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INNOVATIVE METHODOLOGY

Artificial Dirt: Microfluidic Substrates for Nematode Neurobiology and Behavior

S. R. Lockery1, K. J. Lawton1, J. C. Doll2, S. Faumont1, S. M. Coulthard2, T. R. Thiele1, N. Chronis4, K. E. McCormick1, M. B. Goodman3 and B. L. Pruitt2

1Department of Biology, University of Oregon, Eugene, Oregon; 2Department of Mechanical Engineering and 3Department of Molecular and Cellular Physiology, Stanford University, Stanford, California; and 4Department of Mechanical Engineering, University of Michigan, Ann Arbor, Michigan

Submitted 9 December 2007; accepted in final form 11 January 2008

With a nervous system of only 302 neurons, the free-living nematode Caenorhabditis elegans is a powerful experimental organism for neurobiology. However, the laboratory substrate commonly used in C. elegans research, a planar agarose surface, fails to reflect the complexity of this organism's natural environment, complicates stimulus delivery, and is incompatible with high-resolution optophysiology experiments. Here we present a new class of microfluidic devices for C. elegans neurobiology and behavior: agarose-free, micron-scale chambers and channels that allow the animals to crawl as they would on agarose. One such device mimics a moist soil matrix and facilitates rapid delivery of fluid-borne stimuli. A second device consists of sinusoidal channels that can be used to regulate the waveform and trajectory of crawling worms. Both devices are thin and transparent, rendering them compatible with high-resolution microscope objectives for neuronal imaging and optical recording. Together, the new devices are likely to accelerate studies of the neuronal basis of behavior in C. elegans.


Address for reprint requests and other correspondence: S. Lockery, 305 Huestis Hall, 1210 University of Oregon, Eugene, OR 97403-1210 (E-mail: shawn{at}uoregon.edu)







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