Skip to main content
. 2010 Jun 15;8(6):e1000395. doi: 10.1371/journal.pbio.1000395

Figure 8. Axons of inhibitory interneurons located in the non-deprived rows following whisker plucking.

Figure 8

(A) Top, the whisker barrel map. Rectangular box depicts the region of axonal reconstructions shown on the right. Middle, axons located within non-deprived rows before whisker plucking. Right, same area after 2 d of plucking. In the reconstruction, the axons that persisted over both sessions are shown in blue, axons retracted from the first to second imaging session in red, and new axons in yellow. Scale bar  = 50 µm. (B–D) Changes in axonal length for 2 (B), 14 (C), and 30 (D) d of whisker plucking. Left, the distribution of axonal length that was lost between each baseline and post-plucking time point. Right, the distribution of axonal length that was gained between the baseline and post-plucking time points. The data for each pair of time points were obtained by averaging over several mice. Here, the magnitude of the axonal changes for each data pair is normalized with respect to the maximum length of axon that was retracted within any bin. The maximum length of retracted axon in each data pair is therefore 1.0 (in arbitrary units of length), and the length of added axon is measured with respect to that value. The dimensions of the bins are 50 µm×50 µm. The average locations of barrel columns for animals in each condition are marked on each map, with deprived barrel columns indicated in white and non-deprived barrel columns indicated in green.