Department of Life Science and Medical Bioscience, School of Advanced Science and Engineering, Waseda University, Tokyo 1628480, Japan.
Department of Anatomy and Cell Biology, Interdisciplinary School of Medicine & Engineering, University of Yamanashi, Yamanashi 4093898, Japan.
J Biol Chem. 2019 Nov 1;294(44):16034-16048. doi: 10.1074/jbc.RA119.007883. Epub 2019 Sep 10.
Sonic hedgehog (SHH) is important for organogenesis during development. Recent studies have indicated that SHH is also involved in the proliferation and transformation of astrocytes to the reactive phenotype. However, the mechanisms underlying these are unknown. Involvement of SHH signaling in calcium (Ca) signaling has not been extensively studied. Here, we report that SHH and Smoothened agonist (SAG), an activator of the signaling receptor Smoothened (SMO) in the SHH pathway, activate Ca oscillations in cultured murine hippocampal astrocytes. The response was rapid, on a minute time scale, indicating a noncanonical pathway activity. Pertussis toxin blocked the SAG effect, indicating an involvement of a G coupled to SMO. Depletion of extracellular ATP by apyrase, an ATP-degrading enzyme, inhibited the SAG-mediated activation of Ca oscillations. These results indicate that SAG increases extracellular ATP levels by activating ATP release from astrocytes, resulting in Ca oscillation activation. We hypothesize that SHH activates SMO-coupled Gi in astrocytes, causing ATP release and activation of G-coupled P2 receptors on the same cell or surrounding astrocytes. Transcription factor activities are often modulated by Ca patterns; therefore, SHH signaling may trigger changes in astrocytes by activating Ca oscillations. This enhancement of Ca oscillations by SHH signaling may occur in astrocytes in the brain because we also observed it in hippocampal brain slices. In summary, SHH and SAG enhance Ca oscillations in hippocampal astrocytes, G mediates SAG-induced Ca oscillations downstream of SMO, and ATP-permeable channels may promote the ATP release that activates Ca oscillations in astrocytes.
声波刺猬(SHH)在发育过程中的器官发生中很重要。最近的研究表明,SHH 还参与了星形胶质细胞向反应性表型的增殖和转化。然而,这些机制尚不清楚。SHH 信号转导在钙(Ca)信号转导中的参与尚未得到广泛研究。在这里,我们报告 SHH 和 Smoothened 激动剂(SAG),SHH 途径中信号受体 Smoothened(SMO)的激活剂,可激活培养的小鼠海马星形胶质细胞中的 Ca 振荡。该反应迅速,在分钟时间尺度上,表明存在非经典途径活性。百日咳毒素阻断了 SAG 的作用,表明涉及与 SMO 偶联的 G。用三磷酸腺苷酶(一种降解三磷酸腺苷的酶)耗尽细胞外 ATP 抑制了 SAG 介导的 Ca 振荡的激活。这些结果表明,SAG 通过激活星形胶质细胞中三磷酸腺苷的释放来增加细胞外 ATP 水平,从而导致 Ca 振荡的激活。我们假设 SAG 通过激活星形胶质细胞中三磷酸腺苷的释放来激活 SMO 偶联的 Gi,导致细胞内或周围星形胶质细胞上的 ATP 释放和 G 偶联 P2 受体的激活。转录因子活性通常受 Ca 模式的调节;因此,SHH 信号可能通过激活 Ca 振荡来触发星形胶质细胞的变化。SHH 信号增强 Ca 振荡可能发生在大脑中的星形胶质细胞中,因为我们也在海马脑片中观察到了这种情况。总之,SHH 和 SAG 增强了海马星形胶质细胞中的 Ca 振荡,G 介导了 SMO 下游的 SAG 诱导的 Ca 振荡,并且 ATP 通透通道可能促进激活星形胶质细胞中 Ca 振荡的 ATP 释放。