Raudales Ricardo, Kim Gukhan, Kelly Sean M, Hatfield Joshua, Guan Wuqiang, Zhao Shengli, Paul Anirban, Qian Yongjun, Li Bo, Huang Z Josh
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Program in Neurobiology, Stony Brook University, NY, 11794, USA.
bioRxiv. 2024 Mar 25:2023.11.07.566059. doi: 10.1101/2023.11.07.566059.
Axo-axonic cells (AACs), also called chandelier cells (ChCs) in the cerebral cortex, are the most distinctive type of GABAergic interneurons described in the neocortex, hippocampus, and basolateral amygdala (BLA). AACs selectively innervate glutamatergic projection neurons (PNs) at their axon initial segment (AIS), thus may exert decisive control over PN spiking and regulate PN functional ensembles. However, the brain-wide distribution, synaptic connectivity, and circuit function of AACs remains poorly understood, largely due to the lack of specific and reliable experimental tools. Here, we have established an intersectional genetic strategy that achieves specific and comprehensive targeting of AACs throughout the mouse brain based on their lineage () and molecular () markers. We discovered that AACs are deployed across essentially all the pallium-derived brain structures, including not only the dorsal pallium-derived neocortex and medial pallium-derived hippocampal formation, but also the lateral pallium-derived claustrum-insular complex, and the ventral pallium-derived extended amygdaloid complex and olfactory centers. AACs are also abundant in anterior olfactory nucleus, taenia tecta and lateral septum. AACs show characteristic variations in density across neocortical areas and layers and across subregions of the hippocampal formation. Neocortical AACs comprise multiple laminar subtypes with distinct dendritic and axonal arborization patterns. Retrograde monosynaptic tracing from AACs across neocortical, hippocampal and BLA regions reveal shared as well as distinct patterns of synaptic input. Specific and comprehensive targeting of AACs facilitates the study of their developmental genetic program and circuit function across brain structures, providing a ground truth platform for understanding the conservation and variation of a bona fide cell type across brain regions and species.
轴突 - 轴突细胞(AACs),在大脑皮层中也被称为吊灯细胞(ChCs),是新皮层、海马体和基底外侧杏仁核(BLA)中描述的最具特色的γ-氨基丁酸能中间神经元类型。AACs在其轴突起始段(AIS)选择性地支配谷氨酸能投射神经元(PNs),因此可能对PNs的放电发挥决定性控制并调节PN功能集合。然而,AACs在全脑的分布、突触连接和回路功能仍知之甚少,这主要是由于缺乏特异性和可靠的实验工具。在这里,我们建立了一种交叉遗传策略,基于其谱系()和分子()标记,在整个小鼠大脑中实现对AACs的特异性和全面靶向。我们发现,AACs分布在基本上所有源自大脑皮质的脑结构中,不仅包括源自背侧大脑皮质的新皮层和源自内侧大脑皮质的海马结构,还包括源自外侧大脑皮质的屏状核 - 岛叶复合体,以及源自腹侧大脑皮质的扩展杏仁核复合体和嗅觉中枢。AACs在前嗅核、带状终板和外侧隔中也很丰富。AACs在新皮层区域和层以及海马结构的子区域中显示出密度的特征性变化。新皮层AACs包括具有不同树突和轴突分支模式的多个层状亚型。从新皮层、海马体和BLA区域的AACs进行逆行单突触追踪揭示了共享以及不同的突触输入模式。对AACs的特异性和全面靶向有助于研究它们在整个脑结构中的发育遗传程序和回路功能,为理解真正细胞类型在脑区和物种间的保守性和变异性提供了一个基本事实平台。