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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 |
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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. |
doi_str_mv | 10.1002/cne.23323 |
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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.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.23323</identifier><identifier>PMID: 23504804</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>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</subject><ispartof>Journal of comparative neurology (1911), 2013-09, Vol.521 (13), p.2927-2946</ispartof><rights>Copyright © 2013 Wiley Periodicals, Inc.</rights><rights>2013 Wiley Periodicals, Inc. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5143-d3613f7b67cfedc1ec0f841ece02c9affdd0b955f4dc3d810da1a891ee730e6f3</citedby><cites>FETCH-LOGICAL-c5143-d3613f7b67cfedc1ec0f841ece02c9affdd0b955f4dc3d810da1a891ee730e6f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23504804$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garzón, Miguel</creatorcontrib><creatorcontrib>Pickel, Virginia M.</creatorcontrib><title>Somatodendritic targeting of M5 muscarinic receptor in the rat ventral tegmental area: Implications for mesolimbic dopamine transmission</title><title>Journal of comparative neurology (1911)</title><addtitle>J. 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. DAT, dopamine transporter.</description><subject>acetylcholine</subject><subject>Acetylcholine receptors (muscarinic)</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Dendrites - metabolism</subject><subject>Dendrites - ultrastructure</subject><subject>Dopamine - metabolism</subject><subject>Dopamine Plasma Membrane Transport Proteins - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microscopy, Electron</subject><subject>Microscopy, Immunoelectron</subject><subject>motivation</subject><subject>Neuroglia - metabolism</subject><subject>Neuroglia - ultrastructure</subject><subject>Neurons - metabolism</subject><subject>Neurons - ultrastructure</subject><subject>Presynaptic Terminals - metabolism</subject><subject>Presynaptic Terminals - ultrastructure</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor, Muscarinic M5 - metabolism</subject><subject>Receptor, Muscarinic M5 - ultrastructure</subject><subject>reinforcement</subject><subject>reward</subject><subject>Synapses - metabolism</subject><subject>Synapses - ultrastructure</subject><subject>ultrastructure</subject><subject>Ventral Tegmental Area - cytology</subject><subject>Ventral Tegmental Area - metabolism</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNks9uEzEQxlcIREPhwAsgS1zgsO043n_mgAShlKJQDhT1aDneceqyawfbKfQNeGwmpI0ACYmTR5rf9-mb8RTFYw4HHGB6aDweTIWYijvFhINsStk1_G4xoR4vpWzaveJBSpcAIKXo7hd7U1FD1UE1KX58CqPOoUffR5edYVnHJWbnlyxY9qFm4zoZHZ2nVkSDqxwic57lC2RRZ3aFPkc9sIzLkUqqdET9gp2Mq8EZnV3wiVnSjJjC4MYF-fRhpUfnkZHSp9GlRNTD4p7VQ8JHN-9-8fnt0dnsXTn_eHwyezUvTc0rUfai4cK2i6Y1FnvD0YDtKnoQpkZqa_seFrKubdUb0Xcces11JzliKwAbK_aLl1vf1XoxksM2v1pFN-p4rYJ26s-OdxdqGa5UBYI2BmTw7MYghq9rTFnRBAaHQXsM66QoZQW8gbr6DxQ4ULhOEvr0L_QyrKOnTWwoEE0nmw31fEuZGFKKaHe5OajNKSg6BfXrFIh98vugO_L27wk43ALf3IDX_3ZSs9OjW8tyq3Ap4_edQscvqmlFW6vz02N1Jubn71-_kVT8BHVD0MA</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Garzón, Miguel</creator><creator>Pickel, Virginia M.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130901</creationdate><title>Somatodendritic targeting of M5 muscarinic receptor in the rat ventral tegmental area: Implications for mesolimbic dopamine transmission</title><author>Garzón, Miguel ; 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 & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garzón, Miguel</au><au>Pickel, Virginia M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Somatodendritic targeting of M5 muscarinic receptor in the rat ventral tegmental area: Implications for mesolimbic dopamine transmission</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. 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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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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