Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA, USA.
Department of Physiology and Biophysics, University of Washington, Seattle, WA, USA.
Neurochem Res. 2023 Oct;48(10):3212-3227. doi: 10.1007/s11064-023-03979-9. Epub 2023 Jul 4.
Astrocytes release numerous factors known to contribute to the process of synaptogenesis, yet knowledge about the signals that control their release is limited. We hypothesized that neuron-derived signals stimulate astrocytes, which respond to neurons through the modulation of astrocyte-released synaptogenic factors. Here we investigate the effect of cholinergic stimulation of astrocytes on synaptogenesis in co-cultured neurons. Using a culture system where primary rat astrocytes and primary rat neurons are first grown separately allowed us to independently manipulate astrocyte cholinergic signaling. Subsequent co-culture of pre-stimulated astrocytes with naïve neurons enabled us to assess how prior stimulation of astrocyte acetylcholine receptors uniquely modulates neuronal synapse formation. Pre-treatment of astrocytes with the acetylcholine receptor agonist carbachol increased the expression of synaptic proteins, the number of pre- and postsynaptic puncta, and the number of functional synapses in hippocampal neurons after 24 h in co-culture. Astrocyte secretion of the synaptogenic protein thrombospondin-1 increased after cholinergic stimulation and inhibition of the receptor for thrombospondins prevented the increase in neuronal synaptic structures. Thus, we identified a novel mechanism of neuron-astrocyte-neuron communication, where neuronal release of acetylcholine stimulates astrocytes to release synaptogenic proteins leading to increased synaptogenesis in neurons. This study provides new insights into the role of neurotransmitter receptors in developing astrocytes and into our understanding of the modulation of astrocyte-induced synaptogenesis.
星形胶质细胞释放许多已知有助于突触发生的因子,但控制其释放的信号知之甚少。我们假设神经元衍生的信号刺激星形胶质细胞,星形胶质细胞通过调节星形胶质细胞释放的促突触发生因子来响应神经元。在这里,我们研究了星形胶质细胞胆碱能刺激对共培养神经元中突触发生的影响。使用一种培养系统,首先分别培养原代大鼠星形胶质细胞和原代大鼠神经元,使我们能够独立地操纵星形胶质细胞的胆碱能信号。随后将预先刺激的星形胶质细胞与未成熟神经元共培养,使我们能够评估星形胶质细胞乙酰胆碱受体的预先刺激如何独特地调节神经元突触形成。乙酰胆碱受体激动剂 carbachol 预处理星形胶质细胞可增加突触蛋白的表达、突触前和突触后斑点的数量以及共培养 24 小时后海马神经元的功能性突触数量。胆碱能刺激后星形胶质细胞分泌促突触形成蛋白血栓素原-1 增加,而血栓素原受体的抑制可阻止神经元突触结构的增加。因此,我们确定了一种新的神经元-星形胶质细胞-神经元通讯机制,其中神经元释放乙酰胆碱刺激星形胶质细胞释放促突触形成蛋白,从而导致神经元中突触发生增加。这项研究为神经递质受体在发育中的星形胶质细胞中的作用以及我们对星形胶质细胞诱导的突触发生的调节的理解提供了新的见解。