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.
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29 September 2003
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September 29 2003
Uncovering multiple axonal targeting pathways in hippocampal neurons
Dolora Wisco,
Dolora Wisco
1Brookdale Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029
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Eric D. Anderson,
Eric D. Anderson
2Department of Cell Biology, Yale Medical School, New Haven, CT 06520
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Michael C. Chang,
Michael C. Chang
1Brookdale Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029
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Caren Norden,
Caren Norden
1Brookdale Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029
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Tatiana Boiko,
Tatiana Boiko
1Brookdale Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029
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Heike Fölsch,
Heike Fölsch
2Department of Cell Biology, Yale Medical School, New Haven, CT 06520
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Bettina Winckler
Bettina Winckler
1Brookdale Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029
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Dolora Wisco
1Brookdale Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029
Eric D. Anderson
2Department of Cell Biology, Yale Medical School, New Haven, CT 06520
Michael C. Chang
1Brookdale Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029
Caren Norden
1Brookdale Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029
Tatiana Boiko
1Brookdale Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029
Heike Fölsch
2Department of Cell Biology, Yale Medical School, New Haven, CT 06520
Bettina Winckler
1Brookdale Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029
Address correspondence to Bettina Winckler, Department of Molecular, Cell, and Developmental Biology, Mount Sinai School of Medicine, One Gustave Levy Place, Box 1007, New York, NY 10029. Tel.: (212) 241-8619. Fax: (212) 860-1174. email: [email protected]
D. Wisco and E.D. Anderson contributed equally to this work.
H. Fölsch's present address is Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, 2205 Tech Drive, Evanston, IL 60208.
Abbreviations used in this paper: BFA, brefeldin A; DIV, days in vitro; MDCK, Madin-Darby canine kidney; PI, polarity index.
Received:
July 11 2003
Accepted:
August 13 2003
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2003
J Cell Biol (2003) 162 (7): 1317–1328.
Article history
Received:
July 11 2003
Accepted:
August 13 2003
Citation
Dolora Wisco, Eric D. Anderson, Michael C. Chang, Caren Norden, Tatiana Boiko, Heike Fölsch, Bettina Winckler; Uncovering multiple axonal targeting pathways in hippocampal neurons . J Cell Biol 29 September 2003; 162 (7): 1317–1328. doi: https://doi.org/10.1083/jcb.200307069
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