Abstract
Neuropilin-1 (NP-1) has been identified as a necessary component of a semaphorin D (SemD) receptor that repulses dorsal root ganglion (DRG) axons during development. SemA and SemE are related to SemD and bind to NP-1, but do not repulse DRG axons. By expressing NP-1 in retinal neurons and NP-2 in DRG neurons, we demonstrate that neuropilins are sufficient to determine the functional specificity of semaphorin responsiveness. SemA and SemE block SemD binding to NP-1 and abolish SemD repulsion in axons expressing NP-1. SemA and SemE seem to have a newly discovered protein antagonist capacity at NP-1 receptors, whereas they act as agonists at receptors containing NP-2.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Carrier Proteins / pharmacology
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Carrier Proteins / physiology*
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Cell Line
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Chick Embryo / cytology
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Ganglia, Spinal / drug effects
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Ganglia, Spinal / metabolism
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Glycoproteins / antagonists & inhibitors
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Glycoproteins / pharmacology
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Growth Cones / drug effects
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Humans
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Mice
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Nerve Growth Factors / pharmacology
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Nerve Growth Factors / physiology*
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Nerve Tissue Proteins / agonists*
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Nerve Tissue Proteins / antagonists & inhibitors*
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Nerve Tissue Proteins / pharmacology
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Nerve Tissue Proteins / physiology*
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Neuropilin-1
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Retinal Ganglion Cells / drug effects
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Semaphorin-3A
Substances
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Carrier Proteins
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Glycoproteins
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Nerve Growth Factors
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Nerve Tissue Proteins
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SEMA3A protein, human
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Sema3a protein, mouse
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Semaphorin-3A
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semaphorin A(V)
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Neuropilin-1