| Literature DB >> 21482357 |
Frank F Heisler1, Sven Loebrich, Yvonne Pechmann, Nikolaus Maier, Aleksandar R Zivkovic, Mariko Tokito, Torben J Hausrat, Michaela Schweizer, Robert Bähring, Erika L F Holzbaur, Dietmar Schmitz, Matthias Kneussel.
Abstract
Intracellular transport regulates protein turnover including endocytosis. Because of the spatial segregation of F-actin and microtubules, internalized cargo vesicles need to employ myosin and dynein motors to traverse both cytoskeletal compartments. Factors specifying cargo delivery across both tracks remain unknown. We identified muskelin to interconnect retrograde F-actin- and microtubule-dependent GABA(A) receptor (GABA(A)R) trafficking. GABA(A)Rs regulate synaptic transmission, plasticity, and network oscillations. GABA(A)R α1 and muskelin interact directly, undergo neuronal cotransport, and associate with myosin VI or dynein motor complexes in subsequent steps of GABA(A)R endocytosis. Inhibition of either transport route selectively interferes with receptor internalization or degradation. Newly generated muskelin KO mice display depletion of both transport steps and a high-frequency ripple oscillation phenotype. A diluted coat color of muskelin KOs further suggests muskelin transport functions beyond neurons. Our data suggest the concept that specific trafficking factors help cargoes to traverse both F-actin and microtubule compartments, thereby regulating their fate.Entities:
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Year: 2011 PMID： 21482357 PMCID： PMC3101366 DOI： 10.1016/j.neuron.2011.03.008
Source DB: PubMed Journal: Neuron ISSN： 0896-6273 Impact factor: 17.173