OB protein binds specifically to the choroid plexus of mice and rats

Binding studies were conducted to identify the anatomical location of brain target sites for OB protein, the ob gene product. 125I-labeled recombinant mouse OB protein or alkaline phosphatase-OB fusion proteins were used for in vitro and in vivo binding studies. Coronal brain sections or fresh tissu...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 93; no. 11; pp. 5668 - 5673
Main Authors Devos, R. (Roche Research Gent, Gent, Belgium.), Richards, J.G, Campfield, L.A, Tartaglia, L.A, Guisez, Y, Heyden, J. van der, Travernier, J, Plaetinck, G, Burn, P
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences of the United States of America 28.05.1996
National Acad Sciences
National Academy of Sciences
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Abstract Binding studies were conducted to identify the anatomical location of brain target sites for OB protein, the ob gene product. 125I-labeled recombinant mouse OB protein or alkaline phosphatase-OB fusion proteins were used for in vitro and in vivo binding studies. Coronal brain sections or fresh tissue from lean, obese ob/ob, and obese db/db mice as well as lean and obese Zucker rats were probed to identify potential central OB protein-binding sites. We report here that recombinant OB protein binds specifically to the choroid plexus. The binding of OB protein (either radiolabeled or the alkaline phosphatase-OB fusion protein) and its displacement by unlabeled OB protein was similar in lean, obese ob/ob, and obese db/db mice as well as lean and obese Zucker rats. These findings suggest that OB protein binds with high affinity to a specific receptor in the choroid plexus. After binding to the choroid plexus receptor, OB protein may then be transported across the blood-brain barrier into the cerebrospinal fluid. Alternatively, binding of OB protein to a specific receptor in the choroid plexus may activate afferent neural inputs to the neural network that regulates feeding behavior and energy balance or may result in the clearance or degradation of OB protein. The identification of the choroid plexus as a brain binding site for OB protein will provide the basis for the construction of expression libraries and facilitate the rapid cloning of the choroid plexus OB receptor.
AbstractList Binding studies were conducted to identify the anatomical location of brain target sites for OB protein, the ob gene product. 125I-labeled recombinant mouse OB protein or alkaline phosphatase-OB fusion proteins were used for in vitro and in vivo binding studies. Coronal brain sections or fresh tissue from lean, obese ob/ob, and obese db/db mice as well as lean and obese Zucker rats were probed to identify potential central OB protein-binding sites. We report here that recombinant OB protein binds specifically to the choroid plexus. The binding of OB protein (either radiolabeled or the alkaline phosphatase-OB fusion protein) and its displacement by unlabeled OB protein was similar in lean, obese ob/ob, and obese db/db mice as well as lean and obese Zucker rats. These findings suggest that OB protein binds with high affinity to a specific receptor in the choroid plexus. After binding to the choroid plexus receptor, OB protein may then be transported across the blood-brain barrier into the cerebrospinal fluid. Alternatively, binding of OB protein to a specific receptor in the choroid plexus may activate afferent neural inputs to the neural network that regulates feeding behavior and energy balance or may result in the clearance or degradation of OB protein. The identification of the choroid plexus as a brain binding site for OB protein will provide the basis for the construction of expression libraries and facilitate the rapid cloning of the choroid plexus OB receptor
Binding studies were conducted to identify the anatomical location of brain target sites for OB protein, the ob gene product. 125I-labeled recombinant mouse OB protein or alkaline phosphatase-OB fusion proteins were used for in vitro and in vivo binding studies. Coronal brain sections or fresh tissue from lean, obese ob/ob, and obese db/db mice as well as lean and obese Zucker rats were probed to identify potential central OB protein-binding sites. We report here that recombinant OB protein binds specifically to the choroid plexus. The binding of OB protein (either radiolabeled or the alkaline phosphatase-OB fusion protein) and its displacement by unlabeled OB protein was similar in lean, obese ob/ob, and obese db/db mice as well as lean and obese Zucker rats. These findings suggest that OB protein binds with high affinity to a specific receptor in the choroid plexus. After binding to the choroid plexus receptor, OB protein may then be transported across the blood-brain barrier into the cerebrospinal fluid. Alternatively, binding of OB protein to a specific receptor in the choroid plexus may activate afferent neural inputs to the neural network that regulates feeding behavior and energy balance or may result in the clearance or degradation of OB protein. The identification of the choroid plexus as a brain binding site for OB protein will provide the basis for the construction of expression libraries and facilitate the rapid cloning of the choroid plexus OB receptor.
Binding studies were conducted to identify the anatomical location of brain target sites for OB protein, the ob gene product. super(125)I-labeled recombinant mouse OB protein or alkaline phosphatase-OB fusion proteins were used for in vitro and in vivo binding studies. Coronal brain sections or fresh tissue from lean, obese ob/ob, and obese db/db mice as well as lean and obese Zucker rats were probed to identify potential central OB protein-binding sites. We report here that recombinant OB protein binds specifically to the choroid plexus. The binding of OB protein (either radiolabeled or the alkaline phosphatase-OB fusion protein) and its displacement by unlabeled OB protein was similar in lean, obese ob/ob, and obese db/db mice as well as lean and obese Zucker rats. These findings suggest that OB protein binds with high affinity to a specific receptor in the choroid plexus. After binding to the choroid plexus receptor, OB protein may then be transported across the blood-brain barrier into the cerebrospinal fluid. Alternatively, binding of OB protein to a specific receptor in the choroid plexus may activate afferent neural inputs to the neural network that regulates feeding behavior and energy balance or may result in the clearance or degradation of OB protein. The identification of the choroid plexus as a brain binding site for OB protein will provide the basis for the construction of expression libraries and facilitate the rapid cloning of the choroid plexus OB receptor.
Devos et al recently conducted binding studies to identify the anatomical location of brain targets sites for OB protein, the ob gene product, in mice and rats. Results suggest that OB protein binds with high affinity to a specific receptor in the choroid plexus.
Author Plaetinck, G
Travernier, J
Heyden, J. van der
Burn, P
Devos, R. (Roche Research Gent, Gent, Belgium.)
Richards, J.G
Campfield, L.A
Tartaglia, L.A
Guisez, Y
AuthorAffiliation Roche Research Gent, Belgium
AuthorAffiliation_xml – name: Roche Research Gent, Belgium
Author_xml – sequence: 1
  fullname: Devos, R. (Roche Research Gent, Gent, Belgium.)
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  fullname: Richards, J.G
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  fullname: Campfield, L.A
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  fullname: Tartaglia, L.A
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  fullname: Travernier, J
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Snippet Binding studies were conducted to identify the anatomical location of brain target sites for OB protein, the ob gene product. 125I-labeled recombinant mouse OB...
Devos et al recently conducted binding studies to identify the anatomical location of brain targets sites for OB protein, the ob gene product, in mice and...
Binding studies were conducted to identify the anatomical location of brain target sites for OB protein, the ob gene product. super(125)I-labeled recombinant...
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StartPage 5668
SubjectTerms Adipose tissues
Alkaline Phosphatase - metabolism
Animals
Autoradiography
Binding Sites
Biochemistry
Body weight
Brain - metabolism
CHIMIE
Choroid plexus
Choroid Plexus - metabolism
Food intake
Genes
Genetic mutation
HORMONAS
HORMONE
Iodine Radioisotopes
Leptin
MENINGE
MENINGES
Mice
Mice, Inbred C57BL
Mice, Obese
Obesity
Obesity - metabolism
Organ Specificity
PEPTIDE
PEPTIDOS
Proteins
Proteins - metabolism
QUIMICA
RADIOGRAFIA
RADIOGRAPHIE
RAT
RATA
RATON
Rats
Rats, Zucker
RECEPTEUR D'HORMONE
RECEPTORES DE HORMONAS
Receptors
Recombinant Fusion Proteins - metabolism
Recombinant Proteins - metabolism
Rodents
SOBREPESO
SOURIS
SURPOIDS
TECHNIQUE DES TRACEURS
TECNICAS DE TRAZADORES
Tritium
Title OB protein binds specifically to the choroid plexus of mice and rats
URI https://www.jstor.org/stable/39492
http://www.pnas.org/content/93/11/5668.abstract
https://www.ncbi.nlm.nih.gov/pubmed/8643634
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Volume 93
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