Source:http://linkedlifedata.com/resource/pubmed/id/15483121
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
41
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pubmed:dateCreated |
2004-10-14
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pubmed:abstractText |
N-cadherin is a prominent component of developing and mature synapses, yet very little is known about its trafficking within neurons. To investigate N-cadherin dynamics in developing axons, we used in vivo two-photon time-lapse microscopy of N-cadherin--green fluorescent protein (Ncad-GFP), which was expressed in Rohon-Beard neurons of the embryonic zebrafish spinal cord. Ncad-GFP was present as either stable accumulations or highly mobile transport packets. The mobile transport packets were of two types: tubulovesicular structures that moved preferentially in the anterograde direction and discrete-punctate structures that exhibited bidirectional movement. Stable puncta of Ncad-GFP accumulated in the wake of the growth cone with a time course. Colocalization of Ncad-GFP puncta with synaptic markers suggests that N-cadherin is a very early component of nascent synapses. Expression of deletion mutants revealed a potential role of the extracellular domain in appropriate N-cadherin trafficking and targeting. These results are the first to characterize the trafficking of a synaptic cell-adhesion molecule in developing axons in vivo. In addition, we have begun to investigate the cell biology of N-cadherin trafficking and targeting in the context of an intact vertebrate embryo.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cadherins,
http://linkedlifedata.com/resource/pubmed/chemical/Green Fluorescent Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/R-SNARE Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1529-2401
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
13
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
9027-34
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15483121-Animals,
pubmed-meshheading:15483121-Cadherins,
pubmed-meshheading:15483121-Cells, Cultured,
pubmed-meshheading:15483121-Embryo, Nonmammalian,
pubmed-meshheading:15483121-Green Fluorescent Proteins,
pubmed-meshheading:15483121-Membrane Proteins,
pubmed-meshheading:15483121-Microscopy,
pubmed-meshheading:15483121-Mutagenesis, Site-Directed,
pubmed-meshheading:15483121-Neurons,
pubmed-meshheading:15483121-Presynaptic Terminals,
pubmed-meshheading:15483121-Protein Transport,
pubmed-meshheading:15483121-R-SNARE Proteins,
pubmed-meshheading:15483121-Rats,
pubmed-meshheading:15483121-Recombinant Fusion Proteins,
pubmed-meshheading:15483121-Sequence Deletion,
pubmed-meshheading:15483121-Spinal Cord,
pubmed-meshheading:15483121-Zebrafish
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pubmed:year |
2004
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pubmed:articleTitle |
In vivo trafficking and targeting of N-cadherin to nascent presynaptic terminals.
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pubmed:affiliation |
Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, California 94305-5345, USA. jontes@stanford.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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