Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2001-6-1
pubmed:abstractText
The membrane receptors DCC and UNC5H have been shown to be crucial for axon guidance and neuronal migration by acting as receptors for netrin-1. DCC has also been proposed as a dependence receptor inducing apoptosis in cells that are beyond netrin-1 availability. Here we show that the netrin-1 receptors UNC5H (UNC5H1, UNC5H2, UNC5H3) also act as dependence receptors. UNC5H receptors induce apoptosis, but this effect is blocked in the presence of netrin-1. Moreover, we demonstrate that UNC5H receptors are cleaved in vitro by caspase in their intracellular domains. This cleavage may lead to the exposure of a fragment encompassing a death domain required for cell death induction in vivo. Finally, we present evidence that during development of the nervous system, the presence of netrin-1 is crucial to maintain survival of UNC5H- and DCC-expressing neurons, especially in the ventricular zone of the brainstem. Altogether, these results argue for a role of netrin-1 during the development of the nervous system, not only as a guidance cue but as a survival factor via its receptors DCC and UNC5H.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-10200485, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-10341242, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-10348349, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-10399920, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-10548102, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-10595513, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-10921886, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-10971635, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-11038171, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-11048721, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-11248093, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-7556620, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-7604039, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-7749329, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-7758116, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-8062385, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-8332899, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-8861902, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-8895455, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-8978605, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-9126742, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-9126743, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-9143507, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-9218414, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-9427246, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-9568393, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-9721089, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-9796814, http://linkedlifedata.com/resource/pubmed/commentcorrection/11387206-9886069
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0261-4189
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
20
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2715-22
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:11387206-Animals, pubmed-meshheading:11387206-Apoptosis, pubmed-meshheading:11387206-Base Sequence, pubmed-meshheading:11387206-Brain Stem, pubmed-meshheading:11387206-Caspases, pubmed-meshheading:11387206-Cell Adhesion Molecules, pubmed-meshheading:11387206-Cell Death, pubmed-meshheading:11387206-Cell Line, pubmed-meshheading:11387206-Cell Survival, pubmed-meshheading:11387206-DNA Primers, pubmed-meshheading:11387206-Humans, pubmed-meshheading:11387206-Mice, pubmed-meshheading:11387206-Mice, Knockout, pubmed-meshheading:11387206-Molecular Sequence Data, pubmed-meshheading:11387206-Mutagenesis, Site-Directed, pubmed-meshheading:11387206-Nerve Growth Factors, pubmed-meshheading:11387206-Neurons, pubmed-meshheading:11387206-Receptors, Cell Surface, pubmed-meshheading:11387206-Transfection, pubmed-meshheading:11387206-Tumor Suppressor Proteins
pubmed:year
2001
pubmed:articleTitle
Netrin-1 acts as a survival factor via its receptors UNC5H and DCC.
pubmed:affiliation
Apoptosis/Differentiation Laboratory-label La Ligue, Molecular and Cellular Genetic Center, CNRS UMR 5534, University of Lyon, 69622 Villeurbanne, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't