Whole-brain mapping of inputs to projection neurons and cholinergic interneurons in the dorsal striatum

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Abstract

The dorsal striatum integrates inputs from multiple brain areas to coordinate voluntary movements, associative plasticity, and reinforcement learning. Its projection neurons consist of the GABAergic medium spiny neurons (MSNs) that express dopamine receptor type 1 (D1) or dopamine receptor type 2 (D2). Cholinergic interneurons account for a small portion of striatal neuron populations, but they play important roles in striatal functions by synapsing onto the MSNs and other local interneurons. By combining the modified rabies virus with specific Cre-mouse lines, a recent study mapped the monosynaptic input patterns to MSNs. Because only a small number of extrastriatal neurons were labeled in the prior study, it is important to reexamine the input patterns of MSNs with higher labeling efficiency. Additionally, the whole-brain innervation pattern of cholinergic interneurons remains unknown. Using the rabies virus-based transsynaptic tracing method in this study, we comprehensively charted the brain areas that provide direct inputs to D1-MSNs, D2-MSNs, and cholinergic interneurons in the dorsal striatum. We found that both types of projection neurons and the cholinergic interneurons receive extensive inputs from discrete brain areas in the cortex, thalamus, amygdala, and other subcortical areas, several of which were not reported in the previous study. The MSNs and cholinergic interneurons share largely common inputs from areas outside the striatum. However, innervations within the dorsal striatum represent a significantly larger proportion of total inputs for cholinergic interneurons than for the MSNs. The comprehensive maps of direct inputs to striatal MSNs and cholinergic interneurons shall assist future functional dissection of the striatal circuits.

Figures

  • Fig 1. Validation of Chat-Cre, D1-Cre, and D2-Cre mouse lines. (A) Experimental design for axonal tracing. AAV-DIO-EmGFP virus was injected into the dorsal striatum of ChAT-Cre, D1-Cre, or D2-Cre mice. Histology was performed two weeks later. (B) Following the injection of AAV-DIO-EmGFP virus into the dorsal striatum of a D1-Cre mouse, we observed strong terminal fluorescent signals in the GPi/EP and the SNr. For clarity, EmGFP signals are shown in white. (C) AAV-DIO-EmGFP virus injection into the dorsal striatum of a D2-Cre mouse produced EmGFP+ terminal signals mainly in the GPe. (D) Infusion of AAV-DIO-EmGFP viral vectors in the dorsal striatum of a ChAT-Cre mouse resulted in EmGFP expression (green) exclusively in ChAT-immunopositive (red) neurons. Abbreviations: GPe, external globus pallidus; GPi/EP, internal globus pallidus/entopeduncular nucleus; SNr, substantia nigra, reticular part.
  • Fig 2. Themethod of rabies-based retrograde tracing. (A) AAV virus and rabies virus for transsynaptic retrograde tracing. Double-floxed EGFP-TVA and rabies glycoprotein (RG) under control of CAG were respectively packaged into AAV viral vectors. The rabies virus without glycoprotein (SADΔG) was equipped with the mCherry fluorescent protein. (B) Experimental design. On Day 1, AAV-DIO-EGFP-TVA and AAV-DIO-RG viral vectors were injected into the dorsal striatum of ChAT-Cre, D1-Cre, or D2-Cre mice. Two weeks later, SADΔG-mCherry was injected into the same site of the dorsal striatum. Histology was performed after one more week. The starter cells are labeled both in green and red, whereas the input neurons are labeled only in red. (C) Confirmation of effective transsynaptic labeling using rabies virus. Sequential injections of AAV-DIO-EGFP-TVA, AAV-DIO-RG and SADΔG-mCherry viruses into the dorsal striatum of a D1-Cre mouse labeled starter cells (green) and input neurons (red; left panel). Same virus injections did not label any neurons in a wildtype C57BL/6J mouse (right panel). (D) Zoom-in view of starter cells and transsynaptically labeled cells in the dorsal striatum of the D1-Cre mouse shown in (C). (E) Transsynaptic retrograde labeling neurons in the cingulate cortex (cg).
  • Fig 3. Monosynaptic inputs onto D1, D2, and ChAT neurons in the dorsal striatum. (A) Coronal representation of retrograde monosynaptic labeling of input neurons onto D1 MSNs, D2 MSNs, and cholinergic interneurons. (B) Sagittal brain sections of an infected ChAT-Cre mouse, showing innervations to
  • Fig 5. Strong retrograde labeling in representative brain areas following rabies virus infection of striatal D1 MSNs, D2 MSNs, and cholinergic interneurons. (A) The cingulate cortex and secondary motor cortex (Cg/M2). (B) The secondary visual cortex (V2). (C) The centrolateral/paracentral thalamic nucleus (CL/PL). (D) The external globus pallidus (GPe). (E) The substantia nigra compacta (SNc). (F) The dorsal raphe nucleus (DRN).
  • Fig 6. Themajority of the intrastriatal input neurons targeting the ChAT neurons are non-cholinergic. Following the injection of rabies virus and its helper virus, retrograde labeled neurons (red) and cholinergic neurons (green) did not overlap. Additionally, the intrastriatal input neurons and ChAT neurons exhibited distinct morphology and soma sizes.
  • Fig 7. Summary of the inputs to the dorsal striatum cholinergic interneurons and D1/D2 projection neurons. Blue, green, and red lines indicate monosynaptic inputs to striatal ChAT, D1, and D2 neurons, respectively. Thickness of the lines represents proportional input strength (cell numbers) from given brain areas. Abbreviations: CPu, caudate putamen; GPe, external globus pallidus; GPi/EP, internal globus pallidus/entopeduncular nucleus; SNc, substantia nigra, compact part; SNr, substantia nigra, reticular part; STN, subthalamic nucleus;.

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Guo, Q., Wang, D., He, X., Feng, Q., Lin, R., Xu, F., … Luo, M. (2015). Whole-brain mapping of inputs to projection neurons and cholinergic interneurons in the dorsal striatum. PLoS ONE, 10(4). https://doi.org/10.1371/journal.pone.0123381

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