Seto Chiaki, Toyoda Kenta, Inada Kousuke, Oka Kotaro, Ito Etsuro
Department of Biology, Waseda University, Shinjuku, Tokyo 162-8480, Japan.
Department of Biosciences and Informatics, Faculty of Science and Technology, Keio University, Yokohama, Kanagawa 223-8522, Japan.
Biophys Physicobiol. 2022 Sep 22;19:e190041. doi: 10.2142/biophysico.bppb-v19.0041. eCollection 2022.
Epidermal cells, such as keratinocytes, are regarded as the first sensory cells to transmit nociception and mechanoreception to free nerve endings extended from the dorsal root ganglion (DRG). Previous studies suggested that this transmission occurs as Ca propagation via ATP receptors. Conversely, the influence of gap junctions on this Ca propagation is largely unknown. Thus, we examined the localization and the role of connexin 43 among keratinocytes and DRG neurons. We co-cultured keratinocytes and DRG neurons and investigated the effect of pharmacological blockade of gap junctions on Ca propagation upon stimulation of a single keratinocyte. Immunocytochemical experiments showed that connexin 43 is localized between keratinocytes and between keratinocytes and DRG neurons. Octanol, a gap junction inhibitor, significantly suppressed the concentrical Ca propagation. Therefore, we conclude that the Ca propagation mechanism via gap junctions from stimulated keratinocytes to free nerve endings should be taken into account.
表皮细胞,如角质形成细胞,被认为是将伤害感受和机械感受传递到从背根神经节(DRG)延伸出的游离神经末梢的首批感觉细胞。先前的研究表明,这种传递是通过ATP受体以钙传播的形式发生的。相反,缝隙连接对这种钙传播的影响在很大程度上尚不清楚。因此,我们研究了角质形成细胞和DRG神经元中连接蛋白43的定位和作用。我们将角质形成细胞和DRG神经元共同培养,并研究了缝隙连接的药理学阻断对单个角质形成细胞刺激后钙传播的影响。免疫细胞化学实验表明,连接蛋白43定位于角质形成细胞之间以及角质形成细胞与DRG神经元之间。缝隙连接抑制剂辛醇显著抑制了同心钙传播。因此,我们得出结论,应考虑从受刺激的角质形成细胞通过缝隙连接到游离神经末梢的钙传播机制。