Skip to main content
. 2010 Oct 27;30(43):14513–14521. doi: 10.1523/JNEUROSCI.4025-10.2010

Figure 1.

Figure 1.

Maintenance of DRG position requires sodium current. A, B, Whereas DRG neurons (arrows) (A) are regularly arranged along the ventral boundary of the spinal cord in 4 dpf Tg(-3.4neurog1:GFP) dH2O-injected embryos, DRG cells (B) are absent from this location in several segments and GFP-expressing cells are instead located in ectopic ventral positions (arrowheads) in sibling embryos injected with 250 μm TTX. Insets correspond to the boxed regions in A and B. C, The median number of ectopic DRG neurons per embryo at 4 dpf increases in a dose-dependent manner with TTX concentration (*p < 0.05 vs 100; **p < 0.001 vs 250, and 500 μm TTX, nonparametric Kruskal–Wallis test; sample sizes ranged between 15 and 22 embryos). The graph presents the inner quartiles as a box with an internal line indicating the median; whiskers extend to the 5th and 95th percentiles; filled circles indicate outliers. D, E, In 4 dpf Tg(-3.4neurog1:GFP) embryos, both normally positioned as well as ectopic GFP-expressing DRG cells (arrows and arrowheads, respectively) express HuA (red), a marker of neuronal differentiation. Scale bars; A, B, 200 μm; D, E, 50 μm.