Li W E, Nagy J I
Department of Physiology, Faculty of Medicine, University of Manitoba, 730 William Avenue, Winnipeg, Canada.
Neuroscience. 2000;97(1):113-23. doi: 10.1016/s0306-4522(00)00032-4.
Intercellular communication via gap junction channels composed of connexin-43 is known to be regulated by phosphorylation of this protein. We investigated whether connexin-43 at astrocytic gap junctions is similarly regulated in response to neural activation. The effect of peripheral nerve stimulation on connexin-43 phosphorylation state in the spinal cord of rats was examined with a monoclonal antibody (designated 13-8300) shown previously to recognize selectively a dephosphorylated form of connexin-43. Immunolabelling with 13-8300 was absent in the lumbar spinal cord in control animals, but was induced in the dorsal horn ipsilateral to sciatic nerve electrical stimulation for 15min or 1h at a frequency of 1 or 100Hz. Immunorecognition of connexin-43 by a polyclonal anti-connexin-43 antibody, shown previously to undergo epitope masking under various conditions, was reduced in the dorsal horn on the stimulated side. These responses were abolished by local anaesthetic or tetrodotoxin application proximal to the site of nerve stimulation. Selective electrical stimulation of A-fibres or activation of cutaneous C-fibres by capsaicin evoked labelling with 13-8300 in deep and superficial laminae of the dorsal horn, respectively. Nerve stimulation increased the number of 13-8300-positive astrocytic gap junctions, as well as the levels of dephosphorylated connexin-43 in the dorsal horn on the stimulated side. Sciatic nerve transection produced results similar to those seen after C-fibre activation with capsaicin.Thus, peripheral nerve stimulation evokes astrocytic connexin-43 dephosphorylation in the spinal cord dorsal horn, suggesting that gap junctional coupling between astrocytes in vivo is subject to regulation by neuronal-glial interactions following neural activation.
已知由连接蛋白-43组成的间隙连接通道介导的细胞间通讯受该蛋白磷酸化的调控。我们研究了星形胶质细胞间隙连接中的连接蛋白-43是否也会在神经激活时受到类似的调控。用一种单克隆抗体(命名为13 - 8300)检测外周神经刺激对大鼠脊髓中连接蛋白-43磷酸化状态的影响,该抗体先前已被证明能选择性识别连接蛋白-43的去磷酸化形式。在对照动物的腰段脊髓中,未观察到用13 - 8300进行的免疫标记,但在坐骨神经以1Hz或100Hz频率进行15分钟或1小时电刺激后,同侧背角诱导产生了免疫标记。先前已证明在各种条件下会发生表位掩盖的多克隆抗连接蛋白-43抗体对连接蛋白-43的免疫识别,在受刺激侧的背角中减少。这些反应在神经刺激部位近端应用局部麻醉剂或河豚毒素后被消除。分别选择性电刺激A纤维或用辣椒素激活皮肤C纤维,可在背角深层和浅层诱导产生13 - 8300标记。神经刺激增加了受刺激侧背角中13 - 8300阳性星形胶质细胞间隙连接的数量以及去磷酸化连接蛋白-43的水平。坐骨神经横断产生的结果与用辣椒素激活C纤维后相似。因此,外周神经刺激可诱发脊髓背角星形胶质细胞连接蛋白-43去磷酸化,这表明体内星形胶质细胞之间的间隙连接耦合在神经激活后受神经元-胶质细胞相互作用的调控。