Xu Qian, Ford Neil C, He Shaoqiu, Huang Qian, Anderson Michael, Chen Zhiyong, Yang Fei, Crawford LaTasha K, Caterina Michael J, Guan Yun, Dong Xinzhong
The Solomon H. Snyder Department of Neuroscience, Center for Sensory Biology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sci Adv. 2021 Nov 5;7(45):eabi6287. doi: 10.1126/sciadv.abi6287. Epub 2021 Nov 3.
Various pain therapies have been developed on the basis of the gate control theory of pain, which postulates that nonpainful sensory inputs mediated by large-diameter afferent fibers (Aβ-fibers) can attenuate noxious signals relayed to the brain. To date, this theory has focused only on neuronal mechanisms. Here, we identified an unprecedented function of astrocytes in the gating of nociceptive signals transmitted by neurokinin 1 receptor–positive (NK1R) projection neurons in the spinal cord. Electrical stimulation of peripheral Aβ-fibers in naïve mice activated spinal astrocytes, which in turn induced long-term depression (LTD) in NK1R neurons and antinociception through activation of endogenous adenosinergic mechanisms. Suppression of astrocyte activation by pharmacologic, chemogenetic, and optogenetic manipulations blocked the induction of LTD in NK1R neurons and pain inhibition by Aβ-fiber stimulation. Collectively, our study introduces astrocytes as an important component of pain gating by activation of Aβ-fibers, which thus exert nonneuronal control of pain.
基于疼痛的闸门控制理论,已经开发出了各种疼痛疗法。该理论假定,由大直径传入纤维(Aβ纤维)介导的非疼痛性感觉输入可以减弱传递到大脑的有害信号。迄今为止,该理论仅关注神经元机制。在这里,我们发现了星形胶质细胞在脊髓中由神经激肽1受体阳性(NK1R)投射神经元传递的伤害性信号的门控中具有前所未有的功能。对未处理小鼠的外周Aβ纤维进行电刺激会激活脊髓星形胶质细胞,进而通过激活内源性腺苷能机制在NK1R神经元中诱导长时程抑制(LTD)并产生抗痛觉作用。通过药理学、化学遗传学和光遗传学操作抑制星形胶质细胞激活,会阻断NK1R神经元中LTD的诱导以及Aβ纤维刺激对疼痛的抑制作用。总的来说,我们的研究表明,星形胶质细胞是通过激活Aβ纤维进行疼痛门控的重要组成部分,从而对疼痛发挥非神经元控制作用。