Potentiating interactions between morphogenetic protein and neurotrophic factors in developing neurons

mRNA for bone morphogenetic protein receptor type II (BMPR‐II) was mapped to different neurons in peripheral ganglia and spinal cord of the chicken embryo. The expression of this serine/threonine kinase receptor partially overlaps with that of tyrosine kinase receptors Trk and Ret. Biological activi...

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Veröffentlicht in:Journal of neuroscience research 1998-09, Vol.53 (5), p.559-568
Hauptverfasser: Bengtsson, Henrik, Söderström, Stine, Kylberg, Annika, Charette, Marc F., Ebendal, Ted
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container_end_page 568
container_issue 5
container_start_page 559
container_title Journal of neuroscience research
container_volume 53
creator Bengtsson, Henrik
Söderström, Stine
Kylberg, Annika
Charette, Marc F.
Ebendal, Ted
description mRNA for bone morphogenetic protein receptor type II (BMPR‐II) was mapped to different neurons in peripheral ganglia and spinal cord of the chicken embryo. The expression of this serine/threonine kinase receptor partially overlaps with that of tyrosine kinase receptors Trk and Ret. Biological activities of osteogenic protein‐1 (OP‐1), a documented ligand for BMPR‐II, were tested in explanted embryonic chicken ganglia and dissociated ganglionic neurons. OP‐1 had only a limited stimulatory effect on neuronal survival. However, OP‐1 combined with either neurotrophin‐3 (NT‐3, a relative of nerve growth factor) or glial cell line–derived neurotrophic factor (GDNF) potentiated neuronal survival three‐ to fourfold. We also show that OP‐1 strongly potentiates nerve fiber outgrowth from ganglia stimulated with NT‐3 or GDNF. Signaling by BMPR‐II in neurons may potentiate the tyrosine kinase pathway activated by NT‐3 and GDNF. The data suggest that morphogenetic proteins may modulate neurotrophic activities during neuronal development and plasticity. J. Neurosci. Res. 53:559–568, 1998. © 1998 Wiley‐Liss, Inc.
doi_str_mv 10.1002/(SICI)1097-4547(19980901)53:5<559::AID-JNR6>3.0.CO;2-8
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The expression of this serine/threonine kinase receptor partially overlaps with that of tyrosine kinase receptors Trk and Ret. Biological activities of osteogenic protein‐1 (OP‐1), a documented ligand for BMPR‐II, were tested in explanted embryonic chicken ganglia and dissociated ganglionic neurons. OP‐1 had only a limited stimulatory effect on neuronal survival. However, OP‐1 combined with either neurotrophin‐3 (NT‐3, a relative of nerve growth factor) or glial cell line–derived neurotrophic factor (GDNF) potentiated neuronal survival three‐ to fourfold. We also show that OP‐1 strongly potentiates nerve fiber outgrowth from ganglia stimulated with NT‐3 or GDNF. Signaling by BMPR‐II in neurons may potentiate the tyrosine kinase pathway activated by NT‐3 and GDNF. The data suggest that morphogenetic proteins may modulate neurotrophic activities during neuronal development and plasticity. J. Neurosci. 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Neurosci. Res</addtitle><description>mRNA for bone morphogenetic protein receptor type II (BMPR‐II) was mapped to different neurons in peripheral ganglia and spinal cord of the chicken embryo. The expression of this serine/threonine kinase receptor partially overlaps with that of tyrosine kinase receptors Trk and Ret. Biological activities of osteogenic protein‐1 (OP‐1), a documented ligand for BMPR‐II, were tested in explanted embryonic chicken ganglia and dissociated ganglionic neurons. OP‐1 had only a limited stimulatory effect on neuronal survival. However, OP‐1 combined with either neurotrophin‐3 (NT‐3, a relative of nerve growth factor) or glial cell line–derived neurotrophic factor (GDNF) potentiated neuronal survival three‐ to fourfold. We also show that OP‐1 strongly potentiates nerve fiber outgrowth from ganglia stimulated with NT‐3 or GDNF. Signaling by BMPR‐II in neurons may potentiate the tyrosine kinase pathway activated by NT‐3 and GDNF. The data suggest that morphogenetic proteins may modulate neurotrophic activities during neuronal development and plasticity. J. Neurosci. Res. 53:559–568, 1998. © 1998 Wiley‐Liss, Inc.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>BMPR-II</subject><subject>Bone Morphogenetic Protein 7</subject><subject>bone morphogenetic protein receptor type II</subject><subject>Bone Morphogenetic Protein Receptors, Type II</subject><subject>Bone Morphogenetic Proteins - pharmacology</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>Chick Embryo</subject><subject>Drosophila Proteins</subject><subject>Drug Synergism</subject><subject>Ganglia, Autonomic</subject><subject>Ganglia, Sensory</subject><subject>GDNF</subject><subject>Gene Expression Regulation</subject><subject>glial cell line-derived neurotrophic factor</subject><subject>Glial Cell Line-Derived Neurotrophic Factor Receptors</subject><subject>In Situ Hybridization</subject><subject>Molecular Sequence Data</subject><subject>Nerve Growth Factors - genetics</subject><subject>Nerve Tissue Proteins - pharmacology</subject><subject>Neurites - drug effects</subject><subject>Neurons - cytology</subject><subject>Neurons - drug effects</subject><subject>neurotrophin-3</subject><subject>NT-3</subject><subject>Oncogene Proteins - genetics</subject><subject>OP-1</subject><subject>osteogenic protein-1</subject><subject>Protein-Serine-Threonine Kinases - genetics</subject><subject>Proto-Oncogene Proteins - genetics</subject><subject>Proto-Oncogene Proteins c-ret</subject><subject>Receptor Protein-Tyrosine Kinases - genetics</subject><subject>Receptors, Cell Surface - genetics</subject><subject>serine/threonine kinase receptors</subject><subject>Transforming Growth Factor beta</subject><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v00AQxVcIVELhIyD5hNqDw3j_2N6AKlUGSlDaIAJU4jJa2-PW4KyN16H027NuQjiAxGk12je_N3qPsZMIphEAf360mmfz4wh0Ekolk6NI6xQ0RMdKzNRLpfRsdjp_Fb67-BCfiClMs-ULHqb32GS_cp9NQMQQSoj4Q_bIua8AoLUSB-xAJzyWPJmw6n07kB1qM9T2KqjtQL0phrq1LshpuCGywbrtu-v2iiwNdRF0vV-obWBsGVja-Klvu2v_Ufm9tneeEZT0g5q2G4l3EusesweVaRw92b2H7NOb1x-zt-FieTbPThdhIbWOQy0SRbkpIuK85JSUZJQWFOdxmuclCFOBSKuygLQocpMLKdNSauIVcahMAuKQPdty_ZnfN-QGXNeuoKYxltqNwyiWmoOMvfDzVlj0rXM9Vdj19dr0txgBjgUgjgXgmCaOaeLvAlAJVOgLQPQF4FgACgTMlsgx9eCnuws2-ZrKPXaX-B_jm7qh279c_2v6D8-72YPDLbh2A_3cg03_DePE54qXF2eYLC5Xq_Nzjl_EL6gttBc</recordid><startdate>19980901</startdate><enddate>19980901</enddate><creator>Bengtsson, Henrik</creator><creator>Söderström, Stine</creator><creator>Kylberg, Annika</creator><creator>Charette, Marc F.</creator><creator>Ebendal, Ted</creator><general>John Wiley &amp; 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Neurosci. Res</addtitle><date>1998-09-01</date><risdate>1998</risdate><volume>53</volume><issue>5</issue><spage>559</spage><epage>568</epage><pages>559-568</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>mRNA for bone morphogenetic protein receptor type II (BMPR‐II) was mapped to different neurons in peripheral ganglia and spinal cord of the chicken embryo. The expression of this serine/threonine kinase receptor partially overlaps with that of tyrosine kinase receptors Trk and Ret. Biological activities of osteogenic protein‐1 (OP‐1), a documented ligand for BMPR‐II, were tested in explanted embryonic chicken ganglia and dissociated ganglionic neurons. OP‐1 had only a limited stimulatory effect on neuronal survival. However, OP‐1 combined with either neurotrophin‐3 (NT‐3, a relative of nerve growth factor) or glial cell line–derived neurotrophic factor (GDNF) potentiated neuronal survival three‐ to fourfold. We also show that OP‐1 strongly potentiates nerve fiber outgrowth from ganglia stimulated with NT‐3 or GDNF. Signaling by BMPR‐II in neurons may potentiate the tyrosine kinase pathway activated by NT‐3 and GDNF. The data suggest that morphogenetic proteins may modulate neurotrophic activities during neuronal development and plasticity. J. Neurosci. Res. 53:559–568, 1998. © 1998 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>9726427</pmid><doi>10.1002/(SICI)1097-4547(19980901)53:5&lt;559::AID-JNR6&gt;3.0.CO;2-8</doi><tpages>10</tpages></addata></record>
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subjects Amino Acid Sequence
Animals
BMPR-II
Bone Morphogenetic Protein 7
bone morphogenetic protein receptor type II
Bone Morphogenetic Protein Receptors, Type II
Bone Morphogenetic Proteins - pharmacology
Cell Survival - drug effects
Cells, Cultured
Chick Embryo
Drosophila Proteins
Drug Synergism
Ganglia, Autonomic
Ganglia, Sensory
GDNF
Gene Expression Regulation
glial cell line-derived neurotrophic factor
Glial Cell Line-Derived Neurotrophic Factor Receptors
In Situ Hybridization
Molecular Sequence Data
Nerve Growth Factors - genetics
Nerve Tissue Proteins - pharmacology
Neurites - drug effects
Neurons - cytology
Neurons - drug effects
neurotrophin-3
NT-3
Oncogene Proteins - genetics
OP-1
osteogenic protein-1
Protein-Serine-Threonine Kinases - genetics
Proto-Oncogene Proteins - genetics
Proto-Oncogene Proteins c-ret
Receptor Protein-Tyrosine Kinases - genetics
Receptors, Cell Surface - genetics
serine/threonine kinase receptors
Transforming Growth Factor beta
title Potentiating interactions between morphogenetic protein and neurotrophic factors in developing neurons
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