Anatomical Distribution of Prolactin-Releasing Peptide and Its Receptor Suggests Additional Functions in the Central Nervous System and Periphery
A recently identified neuropeptide with PRL-releasing capabilities binds to and activates a previously known orphan G protein-coupled receptor, GPR10. We initiated a study to define the pharmacology of the peptide/receptor interaction and to identify the distribution of the peptide and its receptor...
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Veröffentlicht in: | Endocrinology (Philadelphia) 1999-12, Vol.140 (12), p.5736-5745 |
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creator | Roland, Barbara L Sutton, Steven W Wilson, Sandy J Luo, Lin Pyati, Jayashree Huvar, Rene Erlander, Mark G Lovenberg, Timothy W |
description | A recently identified neuropeptide with PRL-releasing capabilities
binds to and activates a previously known orphan G protein-coupled
receptor, GPR10. We initiated a study to define the pharmacology of the
peptide/receptor interaction and to identify the distribution of the
peptide and its receptor in the central nervous system to elucidate
sites of action of the peptide. The PRL-releasing peptide (PrRP) is a
C-terminally amidated, 31-amino acid peptide derived from a 98-amino
acid precursor. Radioiodinated PrRP-(1–31) binds to its receptor with
high affinity (1 nm) and stimulates calcium mobilization in
CHOK1 cells stably transfected with the receptor. A series of
N-terminal deletions reveals that the PrRP-(12–31) amino acid is
equipotent to PrRP-(1–31). Further N-terminal deletions reduce the
affinity of the ligand considerably, although PrRP-(25–31) is still
able to compete for binding and behaves as an agonist. The arginine
residues at position 26 and 30 are critical for binding, as
substitution with either lysine or citrulline reduces the affinity
substantially. In situ hybridization reveals a distinct
tissue distribution for both the peptide and receptor messenger RNAs.
The receptor is expressed abundantly in the reticular thalamic nucleus,
periventricular hypothalamus, dorsomedial hypothalamus, nucleus of the
solitary tract, area postrema, anterior pituitary, and adrenal medulla.
The peptide messenger RNA is expressed in the dorsomedial hypothalamus,
nucleus of the solitary tract, ventrolateral reticular nucleus, and
intestine. This tissue distribution suggests an alternative function of
PrRP than its purported hypophysiotropic function, such as a potential
role for PrRP in the central feedback control of neuroendocrine and
autonomic homeostasis. Further work using selective agonists and
antagonists should help define additional physiological roles of this
novel mammalian neuropeptide. |
doi_str_mv | 10.1210/endo.140.12.7211 |
format | Article |
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binds to and activates a previously known orphan G protein-coupled
receptor, GPR10. We initiated a study to define the pharmacology of the
peptide/receptor interaction and to identify the distribution of the
peptide and its receptor in the central nervous system to elucidate
sites of action of the peptide. The PRL-releasing peptide (PrRP) is a
C-terminally amidated, 31-amino acid peptide derived from a 98-amino
acid precursor. Radioiodinated PrRP-(1–31) binds to its receptor with
high affinity (1 nm) and stimulates calcium mobilization in
CHOK1 cells stably transfected with the receptor. A series of
N-terminal deletions reveals that the PrRP-(12–31) amino acid is
equipotent to PrRP-(1–31). Further N-terminal deletions reduce the
affinity of the ligand considerably, although PrRP-(25–31) is still
able to compete for binding and behaves as an agonist. The arginine
residues at position 26 and 30 are critical for binding, as
substitution with either lysine or citrulline reduces the affinity
substantially. In situ hybridization reveals a distinct
tissue distribution for both the peptide and receptor messenger RNAs.
The receptor is expressed abundantly in the reticular thalamic nucleus,
periventricular hypothalamus, dorsomedial hypothalamus, nucleus of the
solitary tract, area postrema, anterior pituitary, and adrenal medulla.
The peptide messenger RNA is expressed in the dorsomedial hypothalamus,
nucleus of the solitary tract, ventrolateral reticular nucleus, and
intestine. This tissue distribution suggests an alternative function of
PrRP than its purported hypophysiotropic function, such as a potential
role for PrRP in the central feedback control of neuroendocrine and
autonomic homeostasis. Further work using selective agonists and
antagonists should help define additional physiological roles of this
novel mammalian neuropeptide.</description><identifier>ISSN: 0013-7227</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/endo.140.12.7211</identifier><language>eng</language><publisher>Washington: Endocrine Society</publisher><subject>Adrenal medulla ; Affinity ; Agonists ; Amino acid substitution ; Amino acids ; Antagonists ; Area postrema ; Autonomic nervous system ; Binding ; Calcium mobilization ; Central nervous system ; Citrulline ; Feedback control ; Homeostasis ; Hybridization ; Hypothalamus ; Hypothalamus (anterior) ; Hypothalamus (dorsomedial) ; Intestine ; Lysine ; mRNA ; Nervous system ; Neuropeptides ; Nuclei (cytology) ; Peptides ; Pharmacology ; Pituitary (anterior) ; Prolactin ; Prolactin-releasing peptide ; Receptors ; Releasing ; Solitary tract nucleus ; Thalamic reticular nucleus ; Thalamus</subject><ispartof>Endocrinology (Philadelphia), 1999-12, Vol.140 (12), p.5736-5745</ispartof><rights>Copyright © 1999 by The Endocrine Society 1999</rights><rights>Copyright © 1999 by The Endocrine Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3761-e1aeb5ba914f29ca10a64a13acb63ad67061e6fa259e9119d2c94febb41aae2c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Roland, Barbara L</creatorcontrib><creatorcontrib>Sutton, Steven W</creatorcontrib><creatorcontrib>Wilson, Sandy J</creatorcontrib><creatorcontrib>Luo, Lin</creatorcontrib><creatorcontrib>Pyati, Jayashree</creatorcontrib><creatorcontrib>Huvar, Rene</creatorcontrib><creatorcontrib>Erlander, Mark G</creatorcontrib><creatorcontrib>Lovenberg, Timothy W</creatorcontrib><title>Anatomical Distribution of Prolactin-Releasing Peptide and Its Receptor Suggests Additional Functions in the Central Nervous System and Periphery</title><title>Endocrinology (Philadelphia)</title><description>A recently identified neuropeptide with PRL-releasing capabilities
binds to and activates a previously known orphan G protein-coupled
receptor, GPR10. We initiated a study to define the pharmacology of the
peptide/receptor interaction and to identify the distribution of the
peptide and its receptor in the central nervous system to elucidate
sites of action of the peptide. The PRL-releasing peptide (PrRP) is a
C-terminally amidated, 31-amino acid peptide derived from a 98-amino
acid precursor. Radioiodinated PrRP-(1–31) binds to its receptor with
high affinity (1 nm) and stimulates calcium mobilization in
CHOK1 cells stably transfected with the receptor. A series of
N-terminal deletions reveals that the PrRP-(12–31) amino acid is
equipotent to PrRP-(1–31). Further N-terminal deletions reduce the
affinity of the ligand considerably, although PrRP-(25–31) is still
able to compete for binding and behaves as an agonist. The arginine
residues at position 26 and 30 are critical for binding, as
substitution with either lysine or citrulline reduces the affinity
substantially. In situ hybridization reveals a distinct
tissue distribution for both the peptide and receptor messenger RNAs.
The receptor is expressed abundantly in the reticular thalamic nucleus,
periventricular hypothalamus, dorsomedial hypothalamus, nucleus of the
solitary tract, area postrema, anterior pituitary, and adrenal medulla.
The peptide messenger RNA is expressed in the dorsomedial hypothalamus,
nucleus of the solitary tract, ventrolateral reticular nucleus, and
intestine. This tissue distribution suggests an alternative function of
PrRP than its purported hypophysiotropic function, such as a potential
role for PrRP in the central feedback control of neuroendocrine and
autonomic homeostasis. Further work using selective agonists and
antagonists should help define additional physiological roles of this
novel mammalian neuropeptide.</description><subject>Adrenal medulla</subject><subject>Affinity</subject><subject>Agonists</subject><subject>Amino acid substitution</subject><subject>Amino acids</subject><subject>Antagonists</subject><subject>Area postrema</subject><subject>Autonomic nervous system</subject><subject>Binding</subject><subject>Calcium mobilization</subject><subject>Central nervous system</subject><subject>Citrulline</subject><subject>Feedback control</subject><subject>Homeostasis</subject><subject>Hybridization</subject><subject>Hypothalamus</subject><subject>Hypothalamus (anterior)</subject><subject>Hypothalamus (dorsomedial)</subject><subject>Intestine</subject><subject>Lysine</subject><subject>mRNA</subject><subject>Nervous system</subject><subject>Neuropeptides</subject><subject>Nuclei (cytology)</subject><subject>Peptides</subject><subject>Pharmacology</subject><subject>Pituitary (anterior)</subject><subject>Prolactin</subject><subject>Prolactin-releasing peptide</subject><subject>Receptors</subject><subject>Releasing</subject><subject>Solitary tract nucleus</subject><subject>Thalamic reticular nucleus</subject><subject>Thalamus</subject><issn>0013-7227</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqNUMFO3DAQtapWYku5c7TEEWXxxN64Oa62pSAhWEE5RxNnshjt2qntIO1n9I_rsEg9IXGaeTPvPT09xk5BzKEEcUGu83NQE5rrEuATm0GtFoUGLT6zmRAgC12W-oh9jfE5Q6WUnLG_S4fJ76zBLf9hYwq2HZP1jvuer4PfoknWFfe0JYzWbfiahmQ74ug6fp0ivyeTLz7wh3GzoZgvy66zk0M2vBydmdbIrePpifiKXAr5cUvhxY-RP-xjot2r2ZqCHZ4o7L-xLz1uI528zWP2ePnz9-qquLn7db1a3hRG6goKAqR20WINqi9rgyCwUggSTVtJ7CotKqCqx3JRUw1Qd6WpVU9tqwCRSiOP2dnBdwj-z5ijN89-DDl2bCRIsRDyu9SZJQ4sE3yMgfpmCHaHYd-AaKbim6n4JhefUTMVnyXnB4kfh4-w9YE9fUywjoZAMf4P867yHyAImmM</recordid><startdate>19991201</startdate><enddate>19991201</enddate><creator>Roland, Barbara L</creator><creator>Sutton, Steven W</creator><creator>Wilson, Sandy J</creator><creator>Luo, Lin</creator><creator>Pyati, Jayashree</creator><creator>Huvar, Rene</creator><creator>Erlander, Mark G</creator><creator>Lovenberg, Timothy W</creator><general>Endocrine Society</general><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope></search><sort><creationdate>19991201</creationdate><title>Anatomical Distribution of Prolactin-Releasing Peptide and Its Receptor Suggests Additional Functions in the Central Nervous System and Periphery</title><author>Roland, Barbara L ; Sutton, Steven W ; Wilson, Sandy J ; Luo, Lin ; Pyati, Jayashree ; Huvar, Rene ; Erlander, Mark G ; Lovenberg, Timothy W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3761-e1aeb5ba914f29ca10a64a13acb63ad67061e6fa259e9119d2c94febb41aae2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adrenal medulla</topic><topic>Affinity</topic><topic>Agonists</topic><topic>Amino acid substitution</topic><topic>Amino acids</topic><topic>Antagonists</topic><topic>Area postrema</topic><topic>Autonomic nervous system</topic><topic>Binding</topic><topic>Calcium mobilization</topic><topic>Central nervous system</topic><topic>Citrulline</topic><topic>Feedback control</topic><topic>Homeostasis</topic><topic>Hybridization</topic><topic>Hypothalamus</topic><topic>Hypothalamus (anterior)</topic><topic>Hypothalamus (dorsomedial)</topic><topic>Intestine</topic><topic>Lysine</topic><topic>mRNA</topic><topic>Nervous system</topic><topic>Neuropeptides</topic><topic>Nuclei (cytology)</topic><topic>Peptides</topic><topic>Pharmacology</topic><topic>Pituitary (anterior)</topic><topic>Prolactin</topic><topic>Prolactin-releasing peptide</topic><topic>Receptors</topic><topic>Releasing</topic><topic>Solitary tract nucleus</topic><topic>Thalamic reticular nucleus</topic><topic>Thalamus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roland, Barbara L</creatorcontrib><creatorcontrib>Sutton, Steven W</creatorcontrib><creatorcontrib>Wilson, Sandy J</creatorcontrib><creatorcontrib>Luo, Lin</creatorcontrib><creatorcontrib>Pyati, Jayashree</creatorcontrib><creatorcontrib>Huvar, Rene</creatorcontrib><creatorcontrib>Erlander, Mark G</creatorcontrib><creatorcontrib>Lovenberg, Timothy W</creatorcontrib><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roland, Barbara L</au><au>Sutton, Steven W</au><au>Wilson, Sandy J</au><au>Luo, Lin</au><au>Pyati, Jayashree</au><au>Huvar, Rene</au><au>Erlander, Mark G</au><au>Lovenberg, Timothy W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anatomical Distribution of Prolactin-Releasing Peptide and Its Receptor Suggests Additional Functions in the Central Nervous System and Periphery</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><date>1999-12-01</date><risdate>1999</risdate><volume>140</volume><issue>12</issue><spage>5736</spage><epage>5745</epage><pages>5736-5745</pages><issn>0013-7227</issn><eissn>1945-7170</eissn><abstract>A recently identified neuropeptide with PRL-releasing capabilities
binds to and activates a previously known orphan G protein-coupled
receptor, GPR10. We initiated a study to define the pharmacology of the
peptide/receptor interaction and to identify the distribution of the
peptide and its receptor in the central nervous system to elucidate
sites of action of the peptide. The PRL-releasing peptide (PrRP) is a
C-terminally amidated, 31-amino acid peptide derived from a 98-amino
acid precursor. Radioiodinated PrRP-(1–31) binds to its receptor with
high affinity (1 nm) and stimulates calcium mobilization in
CHOK1 cells stably transfected with the receptor. A series of
N-terminal deletions reveals that the PrRP-(12–31) amino acid is
equipotent to PrRP-(1–31). Further N-terminal deletions reduce the
affinity of the ligand considerably, although PrRP-(25–31) is still
able to compete for binding and behaves as an agonist. The arginine
residues at position 26 and 30 are critical for binding, as
substitution with either lysine or citrulline reduces the affinity
substantially. In situ hybridization reveals a distinct
tissue distribution for both the peptide and receptor messenger RNAs.
The receptor is expressed abundantly in the reticular thalamic nucleus,
periventricular hypothalamus, dorsomedial hypothalamus, nucleus of the
solitary tract, area postrema, anterior pituitary, and adrenal medulla.
The peptide messenger RNA is expressed in the dorsomedial hypothalamus,
nucleus of the solitary tract, ventrolateral reticular nucleus, and
intestine. This tissue distribution suggests an alternative function of
PrRP than its purported hypophysiotropic function, such as a potential
role for PrRP in the central feedback control of neuroendocrine and
autonomic homeostasis. Further work using selective agonists and
antagonists should help define additional physiological roles of this
novel mammalian neuropeptide.</abstract><cop>Washington</cop><pub>Endocrine Society</pub><doi>10.1210/endo.140.12.7211</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current) |
subjects | Adrenal medulla Affinity Agonists Amino acid substitution Amino acids Antagonists Area postrema Autonomic nervous system Binding Calcium mobilization Central nervous system Citrulline Feedback control Homeostasis Hybridization Hypothalamus Hypothalamus (anterior) Hypothalamus (dorsomedial) Intestine Lysine mRNA Nervous system Neuropeptides Nuclei (cytology) Peptides Pharmacology Pituitary (anterior) Prolactin Prolactin-releasing peptide Receptors Releasing Solitary tract nucleus Thalamic reticular nucleus Thalamus |
title | Anatomical Distribution of Prolactin-Releasing Peptide and Its Receptor Suggests Additional Functions in the Central Nervous System and Periphery |
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