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Development of Local Circuit Connections to Hilar Mossy Cells in the Mouse Dentate Gyrus

机译:小鼠齿状回中肺门生苔细胞的局部电路连接的发展。

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摘要

Hilar mossy cells in the dentate gyrus (DG) shape the firing and function of the hippocampal circuit. However, the neural circuitry providing afferent input to mossy cells is incompletely understood, and little is known about the development of these inputs. Thus, we used whole-cell recording and laser scanning photostimulation (LSPS) to characterize the developmental trajectory of local excitatory and inhibitory synaptic inputs to mossy cells in the mouse hippocampus. Hilar mossy cells were targeted by visualizing non-red fluorescent cells in the dentate hilus of GAD2-Cre; Ai9 mice that expressed tdTomato in GAD+ neurons, and were confirmed by post hoc morphological characterization. Our results show that at postnatal day (P)6–P7, mossy cells received more excitatory input from neurons in the proximal CA3 versus those in the DG. In contrast, at P13–P14 and P21–P28, the largest source of excitatory input originated in DG cells, while the strength of CA3 and hilar inputs declined. A developmental trend was also evident for inhibitory inputs. Overall inhibitory input at P6–P7 was weak, while inhibitory inputs from the DG cell layer and the hilus predominated at P13–P14 and P21–P28. The strength of local DG excitation and inhibition to mossy cells peaked at P13–P14 and decreased slightly in older P21–P28 mice. Together, these data provide new detailed information on the development of local synaptic connectivity of mossy cells, and suggests mechanisms through which developmental changes in local circuit inputs to hilar mossy cells shape their physiology and vulnerability to injury during postnatal periods.
机译:齿状回(DG)中的肺门苔藓细胞决定着海马回路的放电和功能。然而,对苔藓细胞提供传入输入的神经电路还不完全了解,对这些输入的发展知之甚少。因此,我们使用全细胞记录和激光扫描光刺激(LSPS)来表征小鼠海马体中苔藓细胞的局部兴奋性和抑制性突触输入的发展轨迹。通过可视化GAD2-Cre齿状齿节中的非红色荧光细胞来靶向肝苔藓细胞。在GAD +神经元中表达tdTomato的Ai9小鼠,并通过事后形态学特征证实。我们的结果表明,在出生后第(P)6-P7天,与DG中的苔藓细胞相比,近端CA3中的神经元接受了更多的苔藓细胞兴奋性输入。相反,在P13–P14和P21–P28,最大的兴奋性输入来源是DG细胞,而CA3和肺门输入的强度却下降了。抑制性输入的发展趋势也很明显。 P6-P7的总体抑制性输入较弱,而DG细胞层和的抑制性输入主要在P13-P14和P21-P28中。局部DG激发和抑制苔藓细胞的强度在P13–P14达到峰值,而在老年P21–P28小鼠中则略有下降。总之,这些数据提供了关于苔藓细胞局部突触连通性发展的新的详细信息,并提出了机制,通过这些机制,局部回路输入到肺门苔藓细胞的发育变化会影响其在出生后的生理状态和易受伤害性。

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