| Summary: | <p>Abstract</p> <p>Background</p> <p>Itch is one of the major somatosensory modalities. Some recent findings have proposed that gastrin releasing peptide (Grp) is expressed in a subset of dorsal root ganglion (DRG) neurons and functions as a selective neurotransmitter for transferring itch information to spinal cord interneurons. However, expression data from public databases and earlier literatures indicate that <it>Grp</it> mRNA is only detected in dorsal spinal cord (dSC) whereas its family member neuromedin B (<it>Nmb</it>) is highly expressed in DRG neurons. These contradictory results argue that a thorough characterization of the expression of <it>Grp</it> and <it>Nmb</it> is warranted.</p> <p>Findings</p> <p><it>Grp</it> mRNA is highly expressed in dSC but is barely detectable in DRGs of juvenile and adult mice. Anti-bombesin serum specifically recognizes Grp but not Nmb. Grp is present in a small number of small-diameter DRG neurons and in abundance in layers I and II of the spinal cord. The reduction of dSC Grp after dorsal root rhizotomy is significantly different from those of DRG derived markers but similar to that of a spinal cord neuronal marker. Double fluorescent <it>in situ</it> of <it>Nmb</it> and other molecular markers indicate that <it>Nmb</it> is highly and selectively expressed in nociceptive and itch-sensitive DRG neurons.</p> <p>Conclusion</p> <p>The majority of dSC Grp is synthesized locally in dorsal spinal cord neurons. On the other hand, <it>Nmb</it> is highly expressed in pain- and itch-sensing DRG neurons. Our findings provide direct anatomic evidence that Grp could function locally in the dorsal spinal cord in addition to its roles in DRG neurons and that Nmb has potential roles in nociceptive and itch-sensitive neurons. These results will improve our understanding about roles of Grp and Nmb in mediating itch sensation.</p>
|
|---|