2015 Fiscal Year Final Research Report
Molecular mechanisms of the formation and maintenance of NMJs
Project/Area Number |
25460357
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
General medical chemistry
|
Research Institution | The University of Tokyo |
Principal Investigator |
TEZUKA Tohru 東京大学, 医科学研究所, 助教 (50312319)
|
Co-Investigator(Renkei-kenkyūsha) |
Yamanashi Yuji 東京大学, 医科学研究所, 教授 (40202387)
|
Project Period (FY) |
2013-04-01 – 2016-03-31
|
Keywords | 神経科学 / 神経筋接合部 |
Outline of Final Research Achievements |
The formation and maintenance of neuromuscular junctions (NMJs), a synapse essential for motoneural control of skeletal muscle contraction, is governed by the muscle-specific receptor-tyrosine kinase MuSK. Activation of MuSK involves Agrin, Lrp4, and Dok-7. Dok-7 is an essential muscle-intrinsic activator of MuSK. On the other hand, motor neuron-derived MuSK activator Agrin binds to MuSK’s co-receptor Lrp4 and indirectly activates MuSK. In the current study, by analysis of muscle-specific Dok-7 transgenic mice lacking Lrp4, we demonstrated that Lrp4 is required for efficient activation of MuSK by Dok-7 in vivo. In addition, using recombinant adeno-associated virus vectors carrying short hairpin RNAs targeting the mouse dok-7 gene, we showed that the correct, physiological level of dok-7 gene expression is critical for the postnatal maintenance of NMJs.
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Free Research Field |
分子生物学
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