Goenaga Julianna, Nanclares Carmen, Hall Megan, Kofuji Paulo, Mermelstein Paul G, Araque Alfonso
Department of Neuroscience, University of Minnesota, 6 - 145 Jackson Hall, 321 Church Street SE, Minneapolis, MN, 55455, USA.
Mol Neurobiol. 2025 Apr 10. doi: 10.1007/s12035-025-04905-6.
Accumulating evidence has revealed the existence of functional astrocyte-neuron communication based on the ability of astrocytes to respond to neurotransmitters and release gliotransmitters. However, little is known about how other signaling molecules, such as hormones, impact astrocyte function. Estradiol (E2) is an important hormone known to regulate neuronal activity, synaptic transmission, plasticity, and animal behavior. However, whether E2 specifically signals to astrocytes in situ and the functional consequences on astrocyte-neuron communication remain unknown. Therefore, we investigated the impact of estradiol on astrocyte activity and astrocyte-neuron communication in the mouse hippocampus. Using an RNAscope approach, we determined that estrogen receptors (ERα and ERβ) are expressed in astrocytes in both female and male mice. In both sexes, confocal imaging of hippocampal slices determined that astrocytes respond to locally applied E2 with calcium elevations. In pyramidal neurons, slow inward currents (SICs) are mediated by the activation of extrasynaptic NMDA receptors and indicate gliotransmission. Electrophysiological recordings of hippocampal neurons determined that E2 increases the frequency, but not the amplitude, of SICs. We also recorded excitatory synaptic transmission evoked by Schaffer collateral stimulation. Here, only in females, did E2 produce a reduction in excitatory synaptic transmission. The E2-induced effects on the astrocyte calcium signal and gliotransmission were prevented by the broad estrogen receptor antagonist ICI 182,780. Taken together, these results demonstrate the existence of estradiol-mediated astrocyte-neuron communication in both female and male mice. They reveal that E2 can signal to astrocytes and, through this signaling, E2 may regulate neuronal activity and synaptic transmission.
越来越多的证据表明,基于星形胶质细胞对神经递质作出反应并释放神经胶质递质的能力,功能性星形胶质细胞 - 神经元通讯是存在的。然而,关于其他信号分子,如激素,如何影响星形胶质细胞功能,我们却知之甚少。雌二醇(E2)是一种重要的激素,已知其可调节神经元活动、突触传递、可塑性和动物行为。然而,E2是否在原位特异性地向星形胶质细胞发出信号,以及对星形胶质细胞 - 神经元通讯的功能后果仍不清楚。因此,我们研究了雌二醇对小鼠海马体中星形胶质细胞活性和星形胶质细胞 - 神经元通讯的影响。使用RNAscope方法,我们确定雌激素受体(ERα和ERβ)在雌性和雄性小鼠的星形胶质细胞中均有表达。在两性中,海马切片的共聚焦成像确定星形胶质细胞对局部应用的E2有钙升高反应。在锥体神经元中,缓慢内向电流(SICs)由突触外NMDA受体的激活介导,并表明神经胶质传递。海马神经元的电生理记录确定E2增加了SICs的频率,但不增加其幅度。我们还记录了由Schaffer侧支刺激诱发的兴奋性突触传递。在这里,只有在雌性小鼠中,E2才会使兴奋性突触传递减少。广泛的雌激素受体拮抗剂ICI 182,780可阻止E2对星形胶质细胞钙信号和神经胶质传递的诱导作用。综上所述,这些结果证明了在雌性和雄性小鼠中均存在雌二醇介导的星形胶质细胞 - 神经元通讯。它们揭示了E2可以向星形胶质细胞发出信号,并且通过这种信号传导,E2可能调节神经元活动和突触传递。