P2 receptor expression in the dopaminergic system of the rat brain during development

Abstract Extracellular ATP facilitates the release of dopamine via P2 receptor activation in parts of the mesolimbic system. To characterize P2X/Y receptor subtypes in the developing dopaminergic system, their expression in organotypic slice co-cultures including the ventral tegmental area/substanti...

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Veröffentlicht in:Neuroscience 2007-10, Vol.149 (1), p.165-181
Hauptverfasser: Heine, C, Wegner, A, Grosche, J, Allgaier, C, Illes, P, Franke, H
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creator Heine, C
Wegner, A
Grosche, J
Allgaier, C
Illes, P
Franke, H
description Abstract Extracellular ATP facilitates the release of dopamine via P2 receptor activation in parts of the mesolimbic system. To characterize P2X/Y receptor subtypes in the developing dopaminergic system, their expression in organotypic slice co-cultures including the ventral tegmental area/substantia nigra (VTA/SN) complex and the prefrontal cortex (PFC) was studied in comparison to the receptor expression in 3–5 day-old and adult rats. Reverse transcriptase–polymerase chain reaction (RT-PCR) with specific primers for the P2X1,2,3,4,6,7 and P2Y1 receptors in the tissue extracts of organotypic co-cultures revealed the presence of the P2X and P2Y receptor mRNAs investigated. Multiple immunofluorescence labeling of the P2X/Y receptor protein indicated differences in the regional expression in the organotypic co-cultures after 10 days of cultivation (VTA/SN, P2X1,2,3,4,6,7 , P2Y1,6,12 ; PFC, P2X1,3,4,6,7 , P2Y1,2,4,6,12 ). At postnatal days 3–5, an immunofluorescence mostly comparable to that of adult rats was observed (VTA/SN and PFC: P2X1,2,3,4,6,7 , P2Y1,2,4,6,12 ). There was one important exception: the P2X7 receptor immunocytochemistry was not found in adult tissue, suggesting a potential role of this receptor in the development. Only few P2 receptors (e.g. P2X1 , P2Y1 ) were expressed at fibers interconnecting the dopaminergic VTA/SN with the PFC in the organotypic co-cultures. The treatment of the cultures with the ATP analogues 2-methylthio-ATP and α,β-methylene-ATP induced an increase in axonal outgrowth and fiber density, which could be inhibited by pre-treatment with the P2X/Y receptor antagonist pyridoxal-phosphate-6-azophenyl-2′,4′-disulphonic acid. The co-localization of the dopamine-(D1) receptor with the P2X1 receptor in organotypic slice cultures was evident. In the PFC of the co-cultures, and that of young but not adult rats, a number of tyrosine hydroxylase (TH)–positive cells also possessed P2Y1 -immunoreactivity (IR). Additionally, a strong P2Y1 -IR was observed on astrocytes. The present results show a time-, region- and cell type–dependent in vitro and in vivo expression pattern of different P2 receptor subtypes in the dopaminergic system indicating the involvement of ATP and its receptors in neuronal development and growth.
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To characterize P2X/Y receptor subtypes in the developing dopaminergic system, their expression in organotypic slice co-cultures including the ventral tegmental area/substantia nigra (VTA/SN) complex and the prefrontal cortex (PFC) was studied in comparison to the receptor expression in 3–5 day-old and adult rats. Reverse transcriptase–polymerase chain reaction (RT-PCR) with specific primers for the P2X1,2,3,4,6,7 and P2Y1 receptors in the tissue extracts of organotypic co-cultures revealed the presence of the P2X and P2Y receptor mRNAs investigated. Multiple immunofluorescence labeling of the P2X/Y receptor protein indicated differences in the regional expression in the organotypic co-cultures after 10 days of cultivation (VTA/SN, P2X1,2,3,4,6,7 , P2Y1,6,12 ; PFC, P2X1,3,4,6,7 , P2Y1,2,4,6,12 ). At postnatal days 3–5, an immunofluorescence mostly comparable to that of adult rats was observed (VTA/SN and PFC: P2X1,2,3,4,6,7 , P2Y1,2,4,6,12 ). There was one important exception: the P2X7 receptor immunocytochemistry was not found in adult tissue, suggesting a potential role of this receptor in the development. Only few P2 receptors (e.g. P2X1 , P2Y1 ) were expressed at fibers interconnecting the dopaminergic VTA/SN with the PFC in the organotypic co-cultures. The treatment of the cultures with the ATP analogues 2-methylthio-ATP and α,β-methylene-ATP induced an increase in axonal outgrowth and fiber density, which could be inhibited by pre-treatment with the P2X/Y receptor antagonist pyridoxal-phosphate-6-azophenyl-2′,4′-disulphonic acid. The co-localization of the dopamine-(D1) receptor with the P2X1 receptor in organotypic slice cultures was evident. In the PFC of the co-cultures, and that of young but not adult rats, a number of tyrosine hydroxylase (TH)–positive cells also possessed P2Y1 -immunoreactivity (IR). Additionally, a strong P2Y1 -IR was observed on astrocytes. 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To characterize P2X/Y receptor subtypes in the developing dopaminergic system, their expression in organotypic slice co-cultures including the ventral tegmental area/substantia nigra (VTA/SN) complex and the prefrontal cortex (PFC) was studied in comparison to the receptor expression in 3–5 day-old and adult rats. Reverse transcriptase–polymerase chain reaction (RT-PCR) with specific primers for the P2X1,2,3,4,6,7 and P2Y1 receptors in the tissue extracts of organotypic co-cultures revealed the presence of the P2X and P2Y receptor mRNAs investigated. Multiple immunofluorescence labeling of the P2X/Y receptor protein indicated differences in the regional expression in the organotypic co-cultures after 10 days of cultivation (VTA/SN, P2X1,2,3,4,6,7 , P2Y1,6,12 ; PFC, P2X1,3,4,6,7 , P2Y1,2,4,6,12 ). At postnatal days 3–5, an immunofluorescence mostly comparable to that of adult rats was observed (VTA/SN and PFC: P2X1,2,3,4,6,7 , P2Y1,2,4,6,12 ). There was one important exception: the P2X7 receptor immunocytochemistry was not found in adult tissue, suggesting a potential role of this receptor in the development. Only few P2 receptors (e.g. P2X1 , P2Y1 ) were expressed at fibers interconnecting the dopaminergic VTA/SN with the PFC in the organotypic co-cultures. The treatment of the cultures with the ATP analogues 2-methylthio-ATP and α,β-methylene-ATP induced an increase in axonal outgrowth and fiber density, which could be inhibited by pre-treatment with the P2X/Y receptor antagonist pyridoxal-phosphate-6-azophenyl-2′,4′-disulphonic acid. The co-localization of the dopamine-(D1) receptor with the P2X1 receptor in organotypic slice cultures was evident. In the PFC of the co-cultures, and that of young but not adult rats, a number of tyrosine hydroxylase (TH)–positive cells also possessed P2Y1 -immunoreactivity (IR). Additionally, a strong P2Y1 -IR was observed on astrocytes. 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Psychology</subject><subject>Gene Expression Regulation, Developmental - genetics</subject><subject>Gene Expression Regulation, Developmental - physiology</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>growth</subject><subject>immunocytochemistry</subject><subject>Lysine - analogs &amp; derivatives</subject><subject>Lysine - metabolism</subject><subject>Microtubule-Associated Proteins - metabolism</subject><subject>Neurology</subject><subject>Organ Culture Techniques</subject><subject>organotypic co-culture</subject><subject>Prefrontal Cortex - growth &amp; development</subject><subject>Prefrontal Cortex - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Purinergic P2 - genetics</subject><subject>Receptors, Purinergic P2 - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - methods</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Substantia Nigra - growth &amp; development</subject><subject>Substantia Nigra - metabolism</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><subject>Ventral Tegmental Area - growth &amp; development</subject><subject>Ventral Tegmental Area - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkl2L1TAQhoMo7nH1L0gR9K7HyUeT1gthWT9hQUH3OqTJdM2xTWrSLp5_b7unsOKVYSAXeTJveDKEvKCwp0Dl68M-4Jxith6DxT0DUPu1aPWA7GiteKkqIR6SHXCQpagYOyNPcj7AsirBH5MzqmrZAMgduf7KioQWxymmAn-PCXP2MRQ-FNMPLFwczeADphtvi3zMEw5F7O6OkpmKNpkFdHPy4aZweIt9HAcM01PyqDN9xmfbfk6uP7z_fvmpvPry8fPlxVVpheRTyVsHznRAjWMtM6A6gXXdSSUN564VrJY1a3hjWyURKtk63jFkFYiWA6cVPyevTn3HFH_NmCc9-Gyx703AOGcta15RLlbwzQm0i7ecsNNj8oNJR01Br1L1Qf8tVa9S9Vp3Kc-3lLkd0N1f3SwuwMsNMNmavksmWJ_vuYZKJUAs3LsTh4uTW49Jb3HOL38waRf9_73n7T9tbO-DX5J_4hHzIc4pLNY11Zlp0N_WMVinABRArVTD_wAEU7GU</recordid><startdate>20071012</startdate><enddate>20071012</enddate><creator>Heine, C</creator><creator>Wegner, A</creator><creator>Grosche, J</creator><creator>Allgaier, C</creator><creator>Illes, P</creator><creator>Franke, H</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>20071012</creationdate><title>P2 receptor expression in the dopaminergic system of the rat brain during development</title><author>Heine, C ; Wegner, A ; Grosche, J ; Allgaier, C ; Illes, P ; Franke, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-3bd0daf01ad2b2a07f4e88f676a33db428682939cb76e056bd3f2e2504b303153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Animals, Newborn</topic><topic>astrocytes</topic><topic>ATP and P2 receptors</topic><topic>Biological and medical sciences</topic><topic>Brain - growth &amp; development</topic><topic>Brain - metabolism</topic><topic>Coculture Techniques - methods</topic><topic>Dopamine - metabolism</topic><topic>dopaminergic system</topic><topic>Fundamental and applied biological sciences. 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To characterize P2X/Y receptor subtypes in the developing dopaminergic system, their expression in organotypic slice co-cultures including the ventral tegmental area/substantia nigra (VTA/SN) complex and the prefrontal cortex (PFC) was studied in comparison to the receptor expression in 3–5 day-old and adult rats. Reverse transcriptase–polymerase chain reaction (RT-PCR) with specific primers for the P2X1,2,3,4,6,7 and P2Y1 receptors in the tissue extracts of organotypic co-cultures revealed the presence of the P2X and P2Y receptor mRNAs investigated. Multiple immunofluorescence labeling of the P2X/Y receptor protein indicated differences in the regional expression in the organotypic co-cultures after 10 days of cultivation (VTA/SN, P2X1,2,3,4,6,7 , P2Y1,6,12 ; PFC, P2X1,3,4,6,7 , P2Y1,2,4,6,12 ). At postnatal days 3–5, an immunofluorescence mostly comparable to that of adult rats was observed (VTA/SN and PFC: P2X1,2,3,4,6,7 , P2Y1,2,4,6,12 ). There was one important exception: the P2X7 receptor immunocytochemistry was not found in adult tissue, suggesting a potential role of this receptor in the development. Only few P2 receptors (e.g. P2X1 , P2Y1 ) were expressed at fibers interconnecting the dopaminergic VTA/SN with the PFC in the organotypic co-cultures. The treatment of the cultures with the ATP analogues 2-methylthio-ATP and α,β-methylene-ATP induced an increase in axonal outgrowth and fiber density, which could be inhibited by pre-treatment with the P2X/Y receptor antagonist pyridoxal-phosphate-6-azophenyl-2′,4′-disulphonic acid. The co-localization of the dopamine-(D1) receptor with the P2X1 receptor in organotypic slice cultures was evident. In the PFC of the co-cultures, and that of young but not adult rats, a number of tyrosine hydroxylase (TH)–positive cells also possessed P2Y1 -immunoreactivity (IR). Additionally, a strong P2Y1 -IR was observed on astrocytes. The present results show a time-, region- and cell type–dependent in vitro and in vivo expression pattern of different P2 receptor subtypes in the dopaminergic system indicating the involvement of ATP and its receptors in neuronal development and growth.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>17869006</pmid><doi>10.1016/j.neuroscience.2007.07.015</doi><tpages>17</tpages></addata></record>
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subjects Animals
Animals, Newborn
astrocytes
ATP and P2 receptors
Biological and medical sciences
Brain - growth & development
Brain - metabolism
Coculture Techniques - methods
Dopamine - metabolism
dopaminergic system
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation, Developmental - genetics
Gene Expression Regulation, Developmental - physiology
Glial Fibrillary Acidic Protein - metabolism
growth
immunocytochemistry
Lysine - analogs & derivatives
Lysine - metabolism
Microtubule-Associated Proteins - metabolism
Neurology
Organ Culture Techniques
organotypic co-culture
Prefrontal Cortex - growth & development
Prefrontal Cortex - metabolism
Rats
Rats, Wistar
Receptors, Purinergic P2 - genetics
Receptors, Purinergic P2 - metabolism
Reverse Transcriptase Polymerase Chain Reaction - methods
RNA, Messenger - biosynthesis
Substantia Nigra - growth & development
Substantia Nigra - metabolism
Tyrosine 3-Monooxygenase - metabolism
Ventral Tegmental Area - growth & development
Ventral Tegmental Area - metabolism
Vertebrates: nervous system and sense organs
title P2 receptor expression in the dopaminergic system of the rat brain during development
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