AUTHOR=Ma Longfei , Huang Yangyuxin , Zhang Fengjiang , Gao Dave Schwinn , Sun Na , Ren Jinxuan , Xia Suyun , Li Jia , Peng Xinyi , Yu Lina , Jiang Bao-Chun , Yan Min 

TITLE=MMP24 Contributes to Neuropathic Pain in an FTO-Dependent Manner in the Spinal Cord Neurons

JOURNAL=Frontiers in Pharmacology

VOLUME=Volume 12 - 2021

YEAR=2021

URL=https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2021.673831

DOI=10.3389/fphar.2021.673831

ISSN=1663-9812

ABSTRACT=<p>Nerve injury-induced gene expression change in the spinal cord is critical for neuropathic pain genesis. RNA N<sup>6</sup>-methyladenosine (m<sup>6</sup>A) modification represents an additional layer of gene regulation. We showed that spinal nerve ligation (SNL) upregulated the expression of matrix metallopeptidase 24 (MMP24) protein, but not <italic>Mmp24</italic> mRNA, in the spinal cord neurons. Blocking the SNL-induced upregulation of spinal MMP24 attenuated local neuron sensitization, neuropathic pain development and maintenance. Conversely, mimicking MMP24 increase promoted the spinal ERK activation and produced evoked nociceptive hypersensitivity. Methylated RNA Immunoprecipitation Sequencing (MeRIP-seq) and RNA Immunoprecipitation (RIP) assay indicated the decreased m<sup>6</sup>A enrichment in the <italic>Mmp24</italic> mRNA under neuropathic pain condition. Moreover, fat-mass and obesity-associated protein (FTO) was colocalized with MMP24 in spinal neurons and shown increased binding to the <italic>Mmp24</italic> mRNA in the spinal cord after SNL. Overexpression or suppression of FTO correlates with promotion or inhibition of MMP24 expression in cultured spinal cord neurons. In conclusion, SNL promoted the m<sup>6</sup>A eraser FTO binding to the <italic>Mmp24</italic> mRNA, which subsequently facilitated the translation of MMP24 in the spinal cord, and ultimately contributed to neuropathic pain genesis.</p>