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. 2020 Jan 3;28:105092. doi: 10.1016/j.dib.2019.105092

Fig. 2.

Fig. 2

A–G: Confocal photomicrographs of transverse sections of the spinal cord showing glycine-ir neurons in control animals (A) and in the rostral (B–D) and caudal (E–G) stumps of the cord of 1 hpl (B, E), 2 wpl (C, F) and 10 wpl (D, G) larvae. H–M: Graphs showing changes in the number of glycine-ir dorsal interneurons (H and K), lateral interneurons (I and L) and CSFc cells (J and M) rostral (H–J) and caudal (K–M) to the site of injury. Arrows indicate glycine-ir dorsal cells; arrowheads indicate glycine-ir lateral cells; barbed arrowheads indicate glycine-ir CSF-c cells; the star indicates the central canal. Dorsal is to the top and the midline to the right. In the graphs, each dot represents one animal and bars represent mean and 95% confidence interval. Abbreviations: R, rostral; C, caudal; D: dorsal interneurons; LAT: lateral interneurons. Scale bars: 40 μm. *0.01–0.05; **0.001–0.01; ***0.0001–0.001.