Method: Indirect dual immunofluorescence to analyze co-expression of receptor components for NGF (TrkA), TNFα (p55) and IL-6 (gp130), and thermo-transducers TRPV1 and TRPM8 within neurochemically defined sub-populations. Immunocytochemistry to examine activation status of STAT3 in TG neuronal cells following exposure to IL-6, quantified using Western blot. CGRP-release EIA and electrophysiological analysis to explore mechanisms by which activation of gp130 by IL-6 might lead to sensitization of TRPV1.
Result: Our data show significant differences in proportions of neurochemical populations, cell size distributions and patterns of co-expression of receptor components and transducers between TG and DRG. Moreover, we have described novel populations of TG neurons displaying unusual phenotype. In addition, we show that the action of IL-6 on TG neuronal cells results in atypical response mechanisms.
Conclusion: Our findings support the emerging picture of a complex combinatorial pattern of co-expression of sensory neurochemicals, transducers and receptor components that help to define TG neuronal modality and function.