Extended Data Figure 2: RTX treatment diminishes noxious heat sensation and decreases the expression of nociceptor markers on dorsal root ganglia.
From: Nociceptive sensory neurons drive interleukin-23-mediated psoriasiform skin inflammation

a, Schematic protocol of nociceptor ablation and induction of psoriasiform skin inflammation. RTX was injected subcutaneously into the back in three escalating doses (30 μg kg−1, 70 μg kg−1 and 100 μg kg−1) on consecutive days and mice were allowed to rest for at least 4 weeks before IMQ treatment. b, Denervation was confirmed by immersing the tail of mice into a temperature-controlled water bath maintained at 52 °C and the latency to the first tail movement to avoid water was measured (n = 6). c, Total RNA was isolated from dorsal root ganglia (level C1–C7) of vehicle (DMSO)- and RTX-treated mice and the levels of Trpv1, Scn10a (Nav1.8), Tac1 (substance P), Mrgprd, Trpm8 and Trpa1 mRNA relative to Gapdh were determined (n = 3).