Molecular Neurobiology. 2022 Oct 17
Jian-Ya Peng, Kang-Li Shen, Xiu-Juan Fan, Zeng-Xin Qi, Hui-Wei Huang, Jian-Lan Jiang, Jian-Hua Lu, Xiao-Qin Wang, Xiao-Xia Fang, Wang-Rui Yuan, Qiao-Xuan Deng, Shu Chen, Liang Chen & Qian-Xing Zhuang
Products used in the paper Details Operation
AAV vector packaging The injection volume of AAV9-CMV-Ncx3 sgRNA-EGFP targeting 5’- GAG CAG AGG CTG GTG ACT CGGGG-3’, 5’- CCT TGG GGA CAA GAT TGC CAGGG-3’, and 5’- TCG GGG GAT GTG CCC AGT GCAGG-3’ (viral titers were 1.0 × 10^13 viral genomes per milliliter, PackGene, Guangzhou, China) or AAV9- CMV-neg-EGFP (control virus, viral titers were 1.32 × 10^13 viral genomes per milliliter, PackGene) was 0.2 μL/site. Request Quote

Research Field: CNS

Keywords: Histamine · Dorsolateral Striatum · H1R · H2R · H3R · Ionic Mechanisms

AAV Serotype: AAV9

Dose: For adeno-associated virus (AAV) injection, the viral solution was injected at three sites of the DLS according to the mouse
brain atlas. The injection volume of AAV9-hSyn-DIO-EGFP (viral titers were 3.12 × 10^13 viral genomes per milliliter, Obio Technology Company, Shanghai, China) was 0.15 μL/site. The injection volume of AAV9-CMV-Ncx3 sgRNA-EGFP (viral titers were 1.0 × 10^13 viral genomes per milliliter, PackGene, Guangzhou, China) or AAV9- CMV-neg-EGFP (control virus, viral titers were 1.32 × 10^13 viral genomes per milliliter, PackGene) was 0.2 μL/site. The injection volume of AAV9-CMV-Hcn2 sgRNA-EGFP (viral titers were 4.2 × 10^12 viral genomes per milliliter, Genechem, Shanghai, China) or AAV9-CMV-neg-EGFP (control virus, viral titers were 6.5 × 10^12 viral genomes per milliliter, Genechem) was 0.3 μL/site.

Routes of Administration: Stereotactic Surgeries and Injections

Targeted organ: brain

Animal or cell line strain: Six to 8-week-old B6/JGpt-Drd1em1Cin(P2A−iCre)/Gpt (D1-Cre), B6/JGpt-Drd2em1Cin(P2A−iCre)/Gpt (D2-Cre), and B6/JGpt-Rosa26tm1Cin(CAG−LSL−Cas9−tdTomato)/Gpt mice (LSLCas9-tdTomato)

Abstract

The dorsolateral striatum (DLS) is the critical neural substrate that plays a role in motor control and motor learning. Our past study revealed a direct histaminergic projection from the tuberomammillary nucleus (TMN) of the hypothalamus to the rat striatum. However, the afferent of histaminergic fibers in the mouse DLS, the effect of histamine on DLS neurons, and the underlying receptor and ionic mechanisms remain unclear. Here, we demonstrated a direct histaminergic innervation from the TMN in the mouse DLS, and histamine excited both the direct-pathway spiny projection neurons (d-SPNs) and the indirect-pathway spiny projection neurons (i-SPNs) of DLS via activation of postsynaptic H1R and H2R, albeit activation of presynaptic H3R suppressed neuronal activity by inhibiting glutamatergic synaptic transmission on d-SPNs and i-SPNs in DLS. Moreover, sodium-calcium exchanger 3 (NCX3), potassium-leak channels linked to H1R, and hyperpolarization-activated cyclic nucleotide-gated channel 2 (HCN2) coupled to H2R co-mediated the excitatory effect induced by histamine on d-SPNs and i-SPNs in DLS. These results demonstrated the pre- and postsynaptic receptors and their downstream multiple ionic mechanisms underlying the inhibitory and excitatory effects of histamine on d-SPNs and i-SPNs in DLS, suggesting a potential modulatory effect of the central histaminergic system on the DLS as well as its related motor control and motor learning.

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