Department of Neurology, Mayo Clinic, Rochester, United States.
Department of Neuroscience, Mayo Clinic, Jacksonville, United States.
Elife. 2020 Jul 27;9:e56502. doi: 10.7554/eLife.56502.
Microglial calcium signaling underlies a number of key physiological and pathological processes in situ, but has not been studied in vivo in awake mice. Using multiple GCaMP6 variants targeted to microglia, we assessed how microglial calcium signaling responds to alterations in neuronal activity across a wide range. We find that only a small subset of microglial somata and processes exhibited spontaneous calcium transients in a chronic window preparation. However, hyperactive shifts in neuronal activity (kainate status epilepticus and CaMKIIa Gq DREADD activation) triggered increased microglial process calcium signaling, often concomitant with process extension. Additionally, hypoactive shifts in neuronal activity (isoflurane anesthesia and CaMKIIa Gi DREADD activation) also increased microglial process calcium signaling. Under hypoactive neuronal conditions, microglia also exhibited process extension and outgrowth with greater calcium signaling. Our work reveals that microglia have highly distinct microdomain signaling, and that processes specifically respond to bi-directional shifts in neuronal activity through increased calcium signaling.
小胶质细胞钙信号在体内许多关键的生理和病理过程中都起着重要作用,但在清醒的小鼠中尚未进行体内研究。使用靶向小胶质细胞的多种 GCaMP6 变体,我们评估了小胶质细胞钙信号如何响应广泛范围内神经元活动的变化。我们发现,在慢性窗制剂中,只有一小部分小胶质细胞体和突起表现出自发的钙瞬变。然而,神经元活动的过度活跃变化(海人酸癫痫发作和 CaMKIIa Gq DREADD 激活)触发了小胶质细胞突起钙信号的增加,通常伴随着突起的延伸。此外,神经元活动的不活跃变化(异氟烷麻醉和 CaMKIIa Gi DREADD 激活)也增加了小胶质细胞突起钙信号。在神经元活动不活跃的情况下,小胶质细胞也表现出突起延伸和生长,伴随着更强的钙信号。我们的工作揭示了小胶质细胞具有高度独特的微域信号,并且突起通过增加钙信号特异性地响应神经元活动的双向变化。