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Neurofilament‐light increases the cell surface expression of the N ‐methyl‐ d ‐aspartate receptor and prevents its ubiquitination
Author(s) -
Ratnam Joseline,
Teichberg Vivian I.
Publication year - 2005
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2004.02936.x
Subject(s) - hek 293 cells , nmda receptor , microbiology and biotechnology , receptor , glutamate receptor , postsynaptic density , biology , cytoskeleton , postsynaptic potential , neurofilament , chemistry , cell , biochemistry , immunology , immunohistochemistry
NMDA ( N ‐methyl‐ d ‐aspartate) subtype of glutamate receptors are core components of dendritic spine postsynaptic densities (PSDs), in which they are anchored via their carboxy‐terminal tails to cytoskeletal proteins. In this study, we examined the role of the neuronal intermediate filament protein, neurofilament‐light (NF‐L), also a component of the PSD, in the regulation of NMDA receptor (NMDAR) expression and function in a heterologous system. Coexpression of NF‐L with NR1 or NR2B subunits of the NMDAR in HEK293 (human embryonic kidney 293) cells did not result in surface expression as measured by surface biotinylation and cell ELISAs, whereas the combined expression of the three elements resulted in a 20% increase in the surface abundance of NR1, along with a concomitant increase in NMDAR‐mediated cytotoxicity. Investigating the origin of this increase, we found that the NR1 subunits are ubiquitinated in HEK293 cells, and that the coexpression of NF‐L antagonizes this process. These results suggest a possible means of stabilization of NR1 via its association with NF‐L.