Glial IL-33 signaling through an ST2-to-CXCL12 pathway in the spinal cord contributes to morphine-induced hyperalgesia and tolerance
Glial IL-33 signaling through an ST2-to-CXCL12 pathway in the spinal cord contributes to morphine-induced hyperalgesia and tolerance
复制标题
脊髓中通过 ST2 至 CXCL12 通路的胶质细胞 IL-33 信号传导有助于吗啡诱导的痛觉过敏和耐受
DOI:
10.1126/scisignal.abe3773
复制
发表时间:
2021-09-07
影响因子:
7.3
通讯作者:
Mi, Wen-Li
中科院分区:
文献类型:
--
作者:
Hu, Xue-Ming;Yang, Wei;Mi, Wen-Li
Description Blocking opioid-induced chemokine release from astrocytes may improve long-term pain management. Astrocytes attenuate opioids Morphine and other opioids are highly effective for treating pain. However, their chronic use can lead to tolerance and even a paradoxical increase in pain in patients. Hu et al. found that this phenomenon of morphine-induced tolerance and hyperalgesia was mediated, in part, by autocrine IL-33 signaling by astrocytes and paracrine IL-33 signaling by oligodendrocytes in the spine. Treating mice with morphine increased the abundance of IL-33 and its receptor ST2, which consequently activated the production and release of the chemokine CXCL12 from astrocytes. Suppressing this pathway specifically in astrocytes or pharmacologically blocking the chemokine receptor CXCR4 dampened morphine-induced hyperalgesia in mice. The findings suggest that targeting this pathway may improve the long-term efficacy of opioids in pain management. Morphine and other opiates are highly effective for treating moderate to severe pain. However, morphine-induced hyperalgesia and analgesic tolerance prevent durable efficacy in patients. Here, we investigated the underlying molecular mechanisms of this phenomenon. We found that repeated subcutaneous injections of morphine in mice increased the abundance of the cytokine interleukin-33 (IL-33) primarily in oligodendrocytes and astrocytes and that of its receptor ST2 mainly in astrocytes. Pharmacological inhibition or knockdown of IL-33 or ST2 in the spinal cord attenuated morphine-induced hyperalgesia and analgesic tolerance in mice, as did global knockout of either Il33 or St2, which also reduced morphine-enhanced astroglial activation and excitatory synaptic transmission. Furthermore, a pathway mediated by tumor necrosis factor receptor–associated factor 6 (TRAF6) and the kinase JNK in astrocytes was required for IL-33–mediated hyperalgesia and tolerance through promoting the production of the chemokine CXCL12 in the spinal cord. The findings suggest that targeting IL-33–ST2 signaling could enable opioids to produce sustained analgesic effects in chronic pain management.