Single-cell analysis of dorsal root ganglia reveals metalloproteinase signaling in satellite glial cells and pain

Satellite glial cells (SGCs) are among the most abundant non-neuronal cells in dorsal root ganglia (DRGs) and closely envelop sensory neurons that detect painful stimuli. However, little is still known about their homeostatic activities and their contribution to pain. Using single-cell RNA sequencing (scRNA-seq), we were able to obtain a unique transcriptional profile for SGCs. We found enriched expression of the tissue inhibitor metalloproteinase 3 (TIMP3) and other metalloproteinases in SGCs. Small interfering RNA and neutralizing antibody experiments revealed that TIMP3 modulates somatosensory stimuli. TIMP3 expression decreased after paclitaxel treatment, and its rescue by delivery of a recombinant TIMP3 protein reversed and prevented paclitaxel-induced pain. We also established that paclitaxel directly impacts metalloproteinase signaling in cultured SGCs, which may be used to identify potential new treatments for pain. Therefore, our results reveal a metalloproteinase signaling pathway in SGCs for proper processing of somatosensory stimuli and potential discovery of novel pain treatments.

Automated summary

Using single-cell RNA sequencing, this study identified a transcriptional profile for satellite glial cells (SGCs) and found enriched expression of TIMP3 and other metalloproteinases in SGCs. Experiments showed that TIMP3 modulates somatosensory stimuli and that paclitaxel directly impacts metalloproteinase signaling in cultured SGCs, suggesting potential new treatments for pain.