Methods: VNUT mRNA expression in mouse trigeminal ganglion was examined by semi-quantitatively RT-PCR and in situ hybridization. Total RNA was isolated from the mouse TG cells, and RT-PCR was performed with the specific primers for the VNUT gene. In situ hybridization was performed on tissue fixed in 4% paraformaldehyde with digoxigenin-labeled VNUT gene-specific probes. Sense probes were generated as negative control.
Results: RT-PCR data showed that VNUT mRNA was expressed in TG cells. The expression of VNUT mRNA was found in both neurons and SGCs in TG by in situ hybridization.
Conclusions: Our results suggest that ATP is released by VNUT in neurons and SGCs, which may contribute to the communication between neurons and SGCs in TG.