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<pubDate>Thu, 21 Aug 2008 15:34:36 BST</pubDate>


	<title>CiteULike: lechristophe Fölsch</title>
	<description>CiteULike: lechristophe Fölsch</description>


	<link>http://www.citeulike.org/user/lechristophe/author/Fölsch</link>
	<dc:publisher>CiteULike.org</dc:publisher>
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        <rdf:li rdf:resource="http://www.citeulike.org/user/lechristophe/article/768020"/>

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<item rdf:about="http://www.citeulike.org/user/lechristophe/article/2695751">
    <title>Pathway selection to the axon depends on multiple targeting signals in NgCAM.</title>
    <link>http://www.citeulike.org/user/lechristophe/article/2695751</link>
    <description>&lt;i&gt;Journal of cell science (14 April 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Similar to most differentiated cells, both neurons and epithelial cells elaborate distinct plasma membrane domains that contain different membrane proteins. We have previously shown that the axonal cell-adhesion molecule L1/NgCAM accumulates on the axonal surface by an indirect transcytotic pathway via somatodendritic endosomes. MDCK epithelial cells similarly traffic NgCAM to the apical surface by transcytosis. In this study, we map the signals in NgCAM required for routing via the multi-step transcytotic pathway. We identify both a previously mapped tyrosine-based signal as a sufficient somatodendritic targeting signal, as well as a novel axonal targeting signal in the cytoplasmic tail of NgCAM. The axonal signal is glycine and serine rich, but only the glycine residues are required for activity. The somatodendritic signal is cis-dominant and needs to be inactivated in order for the axonal signal to be executed. Additionally, we show that the axonal cytoplasmic signal promotes apical targeting in MDCK cells. Transcytosis of NgCAM to the axon thus requires the sequential regulated execution of multiple targeting signals.</description>
    <dc:title>Pathway selection to the axon depends on multiple targeting signals in NgCAM.</dc:title>

    <dc:creator>Chan Choo Yap</dc:creator>
    <dc:creator>Rita L Nokes</dc:creator>
    <dc:creator>Dolora Wisco</dc:creator>
    <dc:creator>Eric Anderson</dc:creator>
    <dc:creator>Heike Fölsch</dc:creator>
    <dc:creator>Bettina Winckler</dc:creator>
    <dc:identifier>doi:10.1242/jcs.022442</dc:identifier>
    <dc:source>Journal of cell science (14 April 2008)</dc:source>
    <dc:date>2008-04-21T11:44:23-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Journal of cell science</prism:publicationName>
    <prism:issn>0021-9533</prism:issn>
    <prism:category>axon</prism:category>
    <prism:category>epithelial</prism:category>
    <prism:category>motif</prism:category>
    <prism:category>ngcam</prism:category>
    <prism:category>targeting</prism:category>
    <prism:category>transcytosis</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/lechristophe/article/768020">
    <title>Uncovering multiple axonal targeting pathways in hippocampal neurons.</title>
    <link>http://www.citeulike.org/user/lechristophe/article/768020</link>
    <description>&lt;i&gt;J Cell Biol, Vol. 162, No. 7. (29 September 2003), pp. 1317-1328.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Neuronal polarity is, at least in part, mediated by the differential sorting of membrane proteins to distinct domains, such as axons and somata/dendrites. We investigated the pathways underlying the subcellular targeting of NgCAM, a cell adhesion molecule residing on the axonal plasma membrane. Following transport of NgCAM kinetically, surprisingly we observed a transient appearance of NgCAM on the somatodendritic plasma membrane. Down-regulation of endocytosis resulted in loss of axonal accumulation of NgCAM, indicating that the axonal localization of NgCAM was dependent on endocytosis. Our data suggest the existence of a dendrite-to-axon transcytotic pathway to achieve axonal accumulation. NgCAM mutants with a point mutation in a crucial cytoplasmic tail motif (YRSL) are unable to access the transcytotic route. Instead, they were found to travel to the axon on a direct route. Therefore, our results suggest that multiple distinct pathways operate in hippocampal neurons to achieve axonal accumulation of membrane proteins.</description>
    <dc:title>Uncovering multiple axonal targeting pathways in hippocampal neurons.</dc:title>

    <dc:creator>D Wisco</dc:creator>
    <dc:creator>ED Anderson</dc:creator>
    <dc:creator>MC Chang</dc:creator>
    <dc:creator>C Norden</dc:creator>
    <dc:creator>T Boiko</dc:creator>
    <dc:creator>H Fölsch</dc:creator>
    <dc:creator>B Winckler</dc:creator>
    <dc:identifier>doi:10.1083/jcb.200307069</dc:identifier>
    <dc:source>J Cell Biol, Vol. 162, No. 7. (29 September 2003), pp. 1317-1328.</dc:source>
    <dc:date>2006-07-21T09:12:36-00:00</dc:date>
    <prism:publicationYear>2003</prism:publicationYear>
    <prism:publicationName>J Cell Biol</prism:publicationName>
    <prism:issn>0021-9525</prism:issn>
    <prism:volume>162</prism:volume>
    <prism:number>7</prism:number>
    <prism:startingPage>1317</prism:startingPage>
    <prism:endingPage>1328</prism:endingPage>
    <prism:category>axon</prism:category>
    <prism:category>endocytosis</prism:category>
    <prism:category>endosomes</prism:category>
    <prism:category>motif</prism:category>
    <prism:category>ngcam</prism:category>
    <prism:category>somatodendritic</prism:category>
    <prism:category>targeting</prism:category>
    <prism:category>transcytosis</prism:category>
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