Afferent and Efferent Connections of the Postinspiratory Complex (PiCo) Revealed by AAV and Monosynaptic Rabies Viral Tracing

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Luiz M. Oliveira, Alyssa Huff, Aguan Wei, Nicole C. Miranda, Ginny Wu, Xiangmin Xu, Jan-Marino Ramirez
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引用次数: 0

Abstract

The control of the respiratory rhythm and airway motor activity is essential for life. Accumulating evidence indicates that the postinspiratory complex (PiCo) is crucial for generating behaviors that occur during the postinspiratory phase, including expiratory laryngeal activity and swallowing. Located in the ventromedial medulla, PiCo is defined by neurons co-expressing two neurotransmitter markers (ChAT and Vglut2/Slc17a6). Here, we mapped the input–output connections of these neurons using viral tracers and intersectional viral-genetic tools. PiCo neurons were specifically targeted by focal injection of a doubly conditional Cre- and FlpO-dependent AAV8 viral marker (AAV8-Con/Fon-TVA-mCherry) into the left PiCo of adult ChatCre/wt: Vglut2FlpO/wt mice, for anterograde axonal tracing. These experiments revealed projections to various brain regions, including the Cu, nucleus of the solitary tract (NTS), Amb, X, XII, Sp5, RMg, intermediate reticular nucleus (IRt), lateral reticular nucleus (LRt), pre-Bötzinger complex (preBötC), contralateral PiCo, laterodorsal tegmental nucleus (LDTg), pedunculopontine tegmental nucleus (PPTg), periaqueductal gray matter (PAG), Kölliker–Fuse (KF), PB, and external cortex of the inferior colliculus (ECIC). A rabies virus (RV) retrograde transsynaptic approach was taken with EnvA-pseudotyped G-deleted (RV-SAD-G-GFP) to similarly target PiCo neurons in ChatCre/wt: Vglut2FlpO/wt mice, following prior injections of helper AAVs (a mixture of AAV-Ef1a-Con/Fon oG and viral vector AAV8-Con/Fon-TVA-mCherry). This combined approach revealed prominent synaptic inputs to PiCo neurons from NTS, IRt, and A1/C1. Although PiCo neurons project axons to the contralateral PiCo area, this approach did not detect direct contralateral connections. We suggest that PiCo serves as a critical integration site, projecting and receiving neuronal connections implicated in breathing, arousal, swallowing, and autonomic regulation.

通过 AAV 和单突触狂犬病病毒追踪揭示吸气后复合体 (PiCo) 的传入和传出联系
呼吸节奏和气道运动活动的控制对生命至关重要。越来越多的证据表明,吸气后复合体(PiCo)对产生吸气后阶段的行为(包括呼气性喉活动和吞咽)至关重要。PiCo 位于腹侧髓质,由共同表达两种神经递质标记(ChAT 和 Vglut2/Slc17a6)的神经元定义。在这里,我们利用病毒示踪剂和交叉病毒基因工具绘制了这些神经元的输入-输出连接图。通过向成年 ChatCre/wt 的左侧 PiCo 局灶注射双条件 Cre 和 FlpO 依赖性 AAV8 病毒标记物(AAV8-Con/Fon-TVA-mCherry),特异性地靶向 PiCo 神经元:Vglut2FlpO/wt 小鼠,进行轴突顺行追踪。这些实验揭示了向不同脑区的投射,包括Cu、孤束核(NTS)、Amb、X、XII、Sp5、RMg、中间网状核(IRt)、外侧网状核(LRt)、前伯丁格复合体(preBötC)、对侧 PiCo、背侧被盖核(LDTg)、脐周被盖核(PPTg)、脐周灰质(PAG)、Kölliker-Fuse(KF)、PB 和下丘外侧皮质(ECIC)。采用狂犬病病毒(RV)逆行突触传递方法,用 EnvA 伪型 G 缺失(RV-SAD-G-GFP)同样靶向 ChatCre/wt 中的 PiCo 神经元:Vglut2FlpO/wt 小鼠中的 PiCo 神经元为靶点,事先注射辅助 AAV(AAV-Ef1a-Con/Fon oG 和病毒载体 AAV8-Con/FonTVA-mCherry 的混合物)。这种综合方法揭示了来自 NTS、IRt 和 A1/C1 对 PiCo 神经元的突出突触输入。虽然 PiCo 神经元向对侧 PiCo 区域投射轴突,但这种方法并未检测到直接的对侧连接。我们认为,PiCo 是一个关键的整合部位,投射和接收与呼吸、唤醒、吞咽和自主神经调节有关的神经元连接。
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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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