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MARCKS Is Necessary for Netrin-DCC Signaling and Corpus Callosum Formation
- Source :
- Molecular Neurobiology. 55:8388-8402
- Publication Year :
- 2018
- Publisher :
- Springer Science and Business Media LLC, 2018.
-
Abstract
- Axons of the corpus callosum (CC), the white matter tract that connects the left and right hemispheres of the brain, receive instruction from a number of chemoattractant and chemorepulsant cues during their initial navigation towards and across the midline. While it has long been known that the CC is malformed in the absence of Myristoylated alanine-rich C-kinase substrate (MARCKS), evidence for a direct role of MARCKS in axon navigation has been lacking. Here, we show that MARCKS is necessary for netrin-1 (NTN1) signaling through the DCC receptor, which is critical for axon guidance decisions. Marcks null (Marcks(−/−)) neurons fail to respond to exogenous NTN1 and are deficient in markers of DCC activation. Without MARCKS, the subcellular distributions of two critical mediators of NTN1-DCC signaling, the tyrosine kinases PTK2 and SRC, are disrupted. Together, this work establishes a novel role for MARCKS in axon dynamics and highlights the necessity of MARCKS as an organizer of DCC signaling at the membrane.
- Subjects :
- 0301 basic medicine
Neuroscience (miscellaneous)
Biology
Corpus callosum
Models, Biological
Article
Corpus Callosum
White matter
03 medical and health sciences
Cellular and Molecular Neuroscience
0302 clinical medicine
Netrin
medicine
Animals
Phosphorylation
Axon
MARCKS
Myristoylated Alanine-Rich C Kinase Substrate
Cell Membrane
fungi
DCC Receptor
Embryo, Mammalian
Axons
Mice, Inbred C57BL
src-Family Kinases
030104 developmental biology
medicine.anatomical_structure
nervous system
Neurology
Focal Adhesion Kinase 1
Netrins
Axon guidance
Tyrosine kinase
Neuroscience
030217 neurology & neurosurgery
Protein Binding
Signal Transduction
Proto-oncogene tyrosine-protein kinase Src
Subjects
Details
- ISSN :
- 15591182 and 08937648
- Volume :
- 55
- Database :
- OpenAIRE
- Journal :
- Molecular Neurobiology
- Accession number :
- edsair.doi.dedup.....3c8f7ef079a3f3fee236aeaf1273991e
- Full Text :
- https://doi.org/10.1007/s12035-018-0990-3