 |
The Journal of Neuroscience, November 9, 2005, 25(45):10479-10493; doi:10.1523/JNEUROSCI.2103-05.2005
Previous Article | Next Article 
Cellular/Molecular
Src-Family Kinases Stabilize the Neuromuscular Synapse In Vivo via Protein Interactions, Phosphorylation, and Cytoskeletal Linkage of Acetylcholine Receptors
Gayathri Sadasivam,1
Raffaella Willmann,1
Shuo Lin,2
Susanne Erb-Vögtli,1
Xian Chu Kong,2
Markus A. Rüegg,2 and
Christian Fuhrer1
1Department of Neurochemistry, Brain Research Institute, University of Zürich, CH-8057 Zürich, Switzerland, and 2Biozentrum, University of Basel, CH-4056 Basel, Switzerland
Postnatal stabilization and maturation of the postsynaptic membrane are important for development and function of the neuromuscular junction (NMJ), but the underlying mechanisms remain poorly characterized. We examined the role of Src-family kinases (SFKs) in vivo. Electroporation of kinase-inactive Src constructs into soleus muscles of adult mice caused NMJ disassembly: acetylcholine receptor (AChR)-rich areas became fragmented; the topology of nerve terminal, AChRs, and synaptic nuclei was disturbed; and occasionally nerves started to sprout. Electroporation of kinase-overactive Src produced similar but milder effects. We studied the mechanism of SFK action using cultured src-/-;fyn-/- myotubes, focusing on clustering of postsynaptic proteins, their interaction with AChRs, and AChR phosphorylation. Rapsyn and the utrophin-glycoprotein complex were recruited normally into AChR-containing clusters by agrin in src-/-;fyn-/- myotubes. But after agrin withdrawal, clusters of these proteins disappeared rapidly in parallel with AChRs, revealing that SFKs are of general importance in postsynaptic stability. At the same time, AChR interaction with rapsyn and dystrobrevin and AChR phosphorylation decreased after agrin withdrawal from mutant myotubes. Unexpectedly, levels of rapsyn protein were increased in src-/-;fyn-/- myotubes, whereas rapsyn-cytoskeleton interactions were unaffected. The overall cytoskeletal link of AChRs was weak but still strengthened by agrin in mutant cells, consistent with the normal formation but decreased stability of AChR clusters. These data show that correctly balanced activity of SFKs is critical in maintaining adult NMJs in vivo. SFKs hold the postsynaptic apparatus together through stabilization of AChR-rapsyn interaction and AChR phosphorylation. In addition, SFKs control rapsyn levels and AChR-cytoskeletal linkage.
Key words: Src; acetylcholine receptor; neuromuscular synapse; agrin; tyrosine phosphorylation; postsynaptic membrane
Received May 25, 2005;
revised September 28, 2005;
accepted September 29, 2005.
This article has been cited by other articles:

|
 |

|
 |
 
S. Kumari, V. Borroni, A. Chaudhry, B. Chanda, R. Massol, S. Mayor, and F. J. Barrantes
Nicotinic acetylcholine receptor is internalized via a Rac-dependent, dynamin-independent endocytic pathway
J. Cell Biol.,
July 10, 2008;
181(7):
1179 - 1193.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. Zhu, Z. Yang, Z. Luo, S. Luo, W. C. Xiong, and L. Mei
Muscle-Specific Receptor Tyrosine Kinase Endocytosis in Acetylcholine Receptor Clustering in Response to Agrin
J. Neurosci.,
February 13, 2008;
28(7):
1688 - 1696.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Bruneau and M. Akaaboune
The Dynamics of the Rapsyn Scaffolding Protein at Individual Acetylcholine Receptor Clusters
J. Biol. Chem.,
March 30, 2007;
282(13):
9932 - 9940.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T. Cheusova, M. A. Khan, S. W. Schubert, A.-C. Gavin, T. Buchou, G. Jacob, H. Sticht, J. Allende, B. Boldyreff, H. R. Brenner, et al.
Casein kinase 2-dependent serine phosphorylation of MuSK regulates acetylcholine receptor aggregation at the neuromuscular junction.
Genes & Dev.,
July 1, 2006;
20(13):
1800 - 1816.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|