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Somatodendritic targeting of M5 muscarinic receptor in the rat ventral tegmental area: Implications for mesolimbic dopamine transmission

ABSTRACT Muscarinic modulation of mesolimbic dopaminergic neurons in the ventral tegmental area (VTA) plays an important role in reward, potentially mediated through the M5 muscarinic acetylcholine receptor (M5R). However, the key sites for M5R‐mediated control of dopamine neurons within this region...

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Published in:Journal of comparative neurology (1911) 2013-09, Vol.521 (13), p.2927-2946
Main Authors: Garzón, Miguel, Pickel, Virginia M.
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description ABSTRACT Muscarinic modulation of mesolimbic dopaminergic neurons in the ventral tegmental area (VTA) plays an important role in reward, potentially mediated through the M5 muscarinic acetylcholine receptor (M5R). However, the key sites for M5R‐mediated control of dopamine neurons within this region are still unknown. To address this question we examined the electron microscopic immunocytochemical localization of antipeptide antisera against M5R and the plasmalemmal dopamine transporter (DAT) in single sections through the rat VTA. M5R was located mainly to VTA somatodendritic profiles (71%; n = 627), at least one‐third (33.2%; n = 208) of which also contained DAT. The M5R immunoreactivity was distributed along cytoplasmic tubulovesicular endomembrane systems in somata and large dendrites, but was more often located at plasmalemmal sites in small dendrites, the majority of which did not express DAT. The M5R‐immunoreactive dendrites received a balanced input from unlabeled terminals forming either asymmetric or symmetric synapses. Compared with dendrites, M5R was less often seen in axon terminals, comprising only 10.8% (n = 102) of the total M5R‐labeled profiles. These terminals were usually presynaptic to unlabeled dendrites, suggesting that M5R activation can indirectly modulate non–DAT‐containing dendrites through presynaptic mechanisms. Our results provide the first ultrastructural evidence that in the VTA, M5R has a subcellular location conducive to major involvement in postsynaptic signaling in many dendrites, only some of which express DAT. These findings suggest that cognitive and rewarding effects ascribed to muscarinic activation in the VTA can primarily be credited to M5R activation at postsynaptic plasma membranes distinct from dopamine transport. J. Comp. Neurol. 521: 2927–2946, 2013. © 2013 Wiley Periodicals, Inc. We have shown that the muscarinic M5 receptor subtype is located primarily in somatodendritic compartments of midbrain ventral tegmental area neurons, but also in some of their afferent axon terminals. These potential activation sites confer on the M5R subtype a critical position for fine adjustment of dopamine (DA)‐related mesocorticolimbic‐guided behaviors. DAT, dopamine transporter.
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However, the key sites for M5R‐mediated control of dopamine neurons within this region are still unknown. To address this question we examined the electron microscopic immunocytochemical localization of antipeptide antisera against M5R and the plasmalemmal dopamine transporter (DAT) in single sections through the rat VTA. M5R was located mainly to VTA somatodendritic profiles (71%; n = 627), at least one‐third (33.2%; n = 208) of which also contained DAT. The M5R immunoreactivity was distributed along cytoplasmic tubulovesicular endomembrane systems in somata and large dendrites, but was more often located at plasmalemmal sites in small dendrites, the majority of which did not express DAT. The M5R‐immunoreactive dendrites received a balanced input from unlabeled terminals forming either asymmetric or symmetric synapses. Compared with dendrites, M5R was less often seen in axon terminals, comprising only 10.8% (n = 102) of the total M5R‐labeled profiles. These terminals were usually presynaptic to unlabeled dendrites, suggesting that M5R activation can indirectly modulate non–DAT‐containing dendrites through presynaptic mechanisms. Our results provide the first ultrastructural evidence that in the VTA, M5R has a subcellular location conducive to major involvement in postsynaptic signaling in many dendrites, only some of which express DAT. These findings suggest that cognitive and rewarding effects ascribed to muscarinic activation in the VTA can primarily be credited to M5R activation at postsynaptic plasma membranes distinct from dopamine transport. J. Comp. Neurol. 521: 2927–2946, 2013. © 2013 Wiley Periodicals, Inc. We have shown that the muscarinic M5 receptor subtype is located primarily in somatodendritic compartments of midbrain ventral tegmental area neurons, but also in some of their afferent axon terminals. These potential activation sites confer on the M5R subtype a critical position for fine adjustment of dopamine (DA)‐related mesocorticolimbic‐guided behaviors. 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Comp. Neurol</addtitle><description>ABSTRACT Muscarinic modulation of mesolimbic dopaminergic neurons in the ventral tegmental area (VTA) plays an important role in reward, potentially mediated through the M5 muscarinic acetylcholine receptor (M5R). However, the key sites for M5R‐mediated control of dopamine neurons within this region are still unknown. To address this question we examined the electron microscopic immunocytochemical localization of antipeptide antisera against M5R and the plasmalemmal dopamine transporter (DAT) in single sections through the rat VTA. M5R was located mainly to VTA somatodendritic profiles (71%; n = 627), at least one‐third (33.2%; n = 208) of which also contained DAT. The M5R immunoreactivity was distributed along cytoplasmic tubulovesicular endomembrane systems in somata and large dendrites, but was more often located at plasmalemmal sites in small dendrites, the majority of which did not express DAT. The M5R‐immunoreactive dendrites received a balanced input from unlabeled terminals forming either asymmetric or symmetric synapses. Compared with dendrites, M5R was less often seen in axon terminals, comprising only 10.8% (n = 102) of the total M5R‐labeled profiles. These terminals were usually presynaptic to unlabeled dendrites, suggesting that M5R activation can indirectly modulate non–DAT‐containing dendrites through presynaptic mechanisms. Our results provide the first ultrastructural evidence that in the VTA, M5R has a subcellular location conducive to major involvement in postsynaptic signaling in many dendrites, only some of which express DAT. These findings suggest that cognitive and rewarding effects ascribed to muscarinic activation in the VTA can primarily be credited to M5R activation at postsynaptic plasma membranes distinct from dopamine transport. J. Comp. Neurol. 521: 2927–2946, 2013. © 2013 Wiley Periodicals, Inc. We have shown that the muscarinic M5 receptor subtype is located primarily in somatodendritic compartments of midbrain ventral tegmental area neurons, but also in some of their afferent axon terminals. These potential activation sites confer on the M5R subtype a critical position for fine adjustment of dopamine (DA)‐related mesocorticolimbic‐guided behaviors. 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Pickel, Virginia M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5143-d3613f7b67cfedc1ec0f841ece02c9affdd0b955f4dc3d810da1a891ee730e6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>acetylcholine</topic><topic>Acetylcholine receptors (muscarinic)</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Dendrites - metabolism</topic><topic>Dendrites - ultrastructure</topic><topic>Dopamine - metabolism</topic><topic>Dopamine Plasma Membrane Transport Proteins - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microscopy, Electron</topic><topic>Microscopy, Immunoelectron</topic><topic>motivation</topic><topic>Neuroglia - metabolism</topic><topic>Neuroglia - ultrastructure</topic><topic>Neurons - metabolism</topic><topic>Neurons - ultrastructure</topic><topic>Presynaptic Terminals - metabolism</topic><topic>Presynaptic Terminals - ultrastructure</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor, Muscarinic M5 - metabolism</topic><topic>Receptor, Muscarinic M5 - ultrastructure</topic><topic>reinforcement</topic><topic>reward</topic><topic>Synapses - metabolism</topic><topic>Synapses - ultrastructure</topic><topic>ultrastructure</topic><topic>Ventral Tegmental Area - cytology</topic><topic>Ventral Tegmental Area - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garzón, Miguel</creatorcontrib><creatorcontrib>Pickel, Virginia M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; 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Comp. Neurol</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>521</volume><issue>13</issue><spage>2927</spage><epage>2946</epage><pages>2927-2946</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>ABSTRACT Muscarinic modulation of mesolimbic dopaminergic neurons in the ventral tegmental area (VTA) plays an important role in reward, potentially mediated through the M5 muscarinic acetylcholine receptor (M5R). However, the key sites for M5R‐mediated control of dopamine neurons within this region are still unknown. To address this question we examined the electron microscopic immunocytochemical localization of antipeptide antisera against M5R and the plasmalemmal dopamine transporter (DAT) in single sections through the rat VTA. M5R was located mainly to VTA somatodendritic profiles (71%; n = 627), at least one‐third (33.2%; n = 208) of which also contained DAT. The M5R immunoreactivity was distributed along cytoplasmic tubulovesicular endomembrane systems in somata and large dendrites, but was more often located at plasmalemmal sites in small dendrites, the majority of which did not express DAT. The M5R‐immunoreactive dendrites received a balanced input from unlabeled terminals forming either asymmetric or symmetric synapses. Compared with dendrites, M5R was less often seen in axon terminals, comprising only 10.8% (n = 102) of the total M5R‐labeled profiles. These terminals were usually presynaptic to unlabeled dendrites, suggesting that M5R activation can indirectly modulate non–DAT‐containing dendrites through presynaptic mechanisms. Our results provide the first ultrastructural evidence that in the VTA, M5R has a subcellular location conducive to major involvement in postsynaptic signaling in many dendrites, only some of which express DAT. These findings suggest that cognitive and rewarding effects ascribed to muscarinic activation in the VTA can primarily be credited to M5R activation at postsynaptic plasma membranes distinct from dopamine transport. J. Comp. Neurol. 521: 2927–2946, 2013. © 2013 Wiley Periodicals, Inc. We have shown that the muscarinic M5 receptor subtype is located primarily in somatodendritic compartments of midbrain ventral tegmental area neurons, but also in some of their afferent axon terminals. These potential activation sites confer on the M5R subtype a critical position for fine adjustment of dopamine (DA)‐related mesocorticolimbic‐guided behaviors. DAT, dopamine transporter.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>23504804</pmid><doi>10.1002/cne.23323</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record>
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ispartof Journal of comparative neurology (1911), 2013-09, Vol.521 (13), p.2927-2946
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source Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list)
subjects acetylcholine
Acetylcholine receptors (muscarinic)
Analysis of Variance
Animals
Dendrites - metabolism
Dendrites - ultrastructure
Dopamine - metabolism
Dopamine Plasma Membrane Transport Proteins - metabolism
Male
Mice
Mice, Inbred C57BL
Microscopy, Electron
Microscopy, Immunoelectron
motivation
Neuroglia - metabolism
Neuroglia - ultrastructure
Neurons - metabolism
Neurons - ultrastructure
Presynaptic Terminals - metabolism
Presynaptic Terminals - ultrastructure
Rats
Rats, Sprague-Dawley
Receptor, Muscarinic M5 - metabolism
Receptor, Muscarinic M5 - ultrastructure
reinforcement
reward
Synapses - metabolism
Synapses - ultrastructure
ultrastructure
Ventral Tegmental Area - cytology
Ventral Tegmental Area - metabolism
title Somatodendritic targeting of M5 muscarinic receptor in the rat ventral tegmental area: Implications for mesolimbic dopamine transmission
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