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

Authors
Tonello, RaquelPrudente, Arthur SilveiraLee, Sang HoonCohen, Cinder FaithXie, WenruiParanjpe, AditiRoh, JueunPark, Chul-KyuChung, GehoonStrong, Judith A.Zhang, Jun-MingBerta, Temugin
Issue Date
Oct-2023
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Satellite glial cells; Neuropathic pain; Metalloproteinases; Single-cell RNA sequencing
Citation
BRAIN BEHAVIOR AND IMMUNITY, v.113, pp.401 - 414
Journal Title
BRAIN BEHAVIOR AND IMMUNITY
Volume
113
Start Page
401
End Page
414
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/89131
DOI
10.1016/j.bbi.2023.08.005
ISSN
0889-1591
Abstract
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.
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