論文

国際誌
2022年

Conditioned Medium From the Stem Cells of Human Exfoliated Deciduous Teeth Ameliorates Neuropathic Pain in a Partial Sciatic Nerve Ligation Model.

Frontiers in pharmacology
  • Yao Liu
  • Fumiya Kano
  • Noboru Hashimoto
  • Linze Xia
  • Qiao Zhou
  • Xingmei Feng
  • Hideharu Hibi
  • Aya Miyazaki
  • Tsutomu Iwamoto
  • Yoshizo Matsuka
  • Zhijun Zhang
  • Eiji Tanaka
  • Akihito Yamamoto
  • 全て表示

13
開始ページ
745020
終了ページ
745020
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.3389/fphar.2022.745020

In neuropathic pain (NP), injury or diseases of the somatosensory system often result in highly debilitating chronic pain. Currently, there is no effective drug for the complete and definitive treatment of NP. We investigated the therapeutic potential of conditioned medium (CM) derived from stem cells from human exfoliated deciduous teeth (SHED-CM) against NP using a mouse partial sciatic nerve ligation (PSL) model. Abnormal pain sensation, such as tactile allodynia and hyperalgesia, can be caused by PSL. In the behavioral test, intravenous administration of SHED-CM greatly improved the PSL-induced hypersensitivity. We found that treatment with SHED-CM resulted in the recruitment of M2 macrophages in the injured sciatic nerve and ipsilateral L4/L5 dorsal root ganglion and suppressed microglial activation in the spinal cord. Notably, specific depletion of the anti-inflammatory M2 macrophages by mannosylated-Clodrosome markedly reduced the antinociceptive effect of SHED-CM. Intravenous administration of CM from M2 induced by SHED-CM (M2-CM) ameliorated the PSL-induced hypersensitivity. We found that M2-CM directly suppressed the expression of nociceptive receptors as well as proinflammatory mediators in Schwann cells. Taken together, our data suggest that SHED-CM ameliorates NP through the induction of the analgesic anti-inflammatory M2 macrophages. Thus, SHED-CM may be a novel therapeutic candidate for NP.

リンク情報
DOI
https://doi.org/10.3389/fphar.2022.745020
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/35431971
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9009354
ID情報
  • DOI : 10.3389/fphar.2022.745020
  • PubMed ID : 35431971
  • PubMed Central 記事ID : PMC9009354

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