First published online 21 September 2005
doi: 10.1242/dev.02029
Development 132, 4545-4552 (2005)
Published by The Company of Biologists 2005
Adaptation is not required to explain the long-term response of axons to molecular gradients
Jun Xu1,
William J. Rosoff1,
Jeffrey S. Urbach2 and
Geoffrey J. Goodhill3,*
1 Department of Neuroscience, Georgetown University Medical Center, 3900
Reservoir Road NW, Washington, DC 20007, USA
2 Department of Physics, Georgetown University, 37th and O Streets NW,
Washington, DC 20057, USA
3 Queensland Brain Institute, Department of Mathematics and Institute for
Molecular Bioscience, University of Queensland, St Lucia, QLD 4072,
Australia

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Fig. 1. Typical dorsal root ganglia (DRG) explants generated experimentally by
Rosoff et al. (Rosoff et al.,
2004 ) (A,B), and by the computational model (C,D). In A,C, there
is no nerve growth factor (NGF) gradient; in B,D, an exponential NGF gradient
is present increasing upwards in the figure with a fractional change of 0.2%
over 10 µm. All images are 480x480 pixels and presented at the same
scale. The diameter of the explants in the simulated cases is 700 µm.
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Fig. 2. Sensitivity of the model (as measured by the guidance ratio) to its
parameters. (A) Proportion of neurites competent to respond to the gradient.
Response increases roughly linearly with this proportion. (B) Width of spatial
averaging, i.e. effective spatial spread of signaling effects downstream from
receptor binding. Note the peak at 5%. (C) Duration of temporal averaging,
i.e. the time over which signaling effects decay.
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Fig. 4. The complete two-dimensional sensitivity surface for the model. Note that
the peak along the concentration axis becomes higher and broader at the higher
values of gradient steepness.
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© The Company of Biologists Ltd 2005