4.8 Article

Muskelin Regulates Actin Filament- and Microtubule-Based GABAA Receptor Transport in Neurons

Journal

NEURON
Volume 70, Issue 1, Pages 66-81

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2011.03.008

Keywords

-

Categories

Funding

  1. National Institutes of Health [NINDS NS060698]
  2. University of Hamburg Medical School, DFG [KN556/1-1, KN556/1-2, KN556/1-3, FG885-KN556/4-1, FG885-KN556/4-2]
  3. Chica and Heinz Schaller Foundation
  4. Hamburg State Excellence Initiative: Neurodapt
  5. [DFG-FG885]

Ask authors/readers for more resources

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 alpha 1 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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available