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A role for the redox site in the modulation of the NMDA receptor by light
Author(s) -
Leszkiewicz Daniel,
Aizenman Elias
Publication year - 2002
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2002.032755
Subject(s) - nmda receptor , chemistry , redox , biophysics , receptor , biochemistry , biology , organic chemistry
Light has been shown to modulate NMDA receptor function. In this study, we have performed experiments aimed at elucidating the putative site of action of light within the receptor structure. Whole‐cell recordings were performed in Chinese hamster ovary cells expressing various combinations of NMDA receptor subunits. Although there was no apparent difference in the actions of light between wild‐type NR1‐NR2A and NR1‐NR2B subunit configurations, the light enhancement of NMDA‐induced currents was either completely abolished or substantially diminished in the redox site mutants NR1a (C744A, C798A)‐NR2B and NR1a (C744A, C798A)‐NR2A. Further studies demonstrated that chemical reduction of NR1a‐NR2B NMDA receptors decreased its sensitivity to light. In addition, sodium (2‐sulfonatoethyl) methanethiosulfonate (MTSES), used to irreversibly bind free sulfhydryl groups and inactivate the redox site, abolished the effects of light on wild‐type receptors. In contrast, no free sulfhydryls were available for MTSES following light stimulation, suggesting that light itself could not reduce the redox modulatory site. Our results suggest that a functionally intact, oxidized redox site is necessary for light‐induced potentiation. Hence, light and redox modulation of the NMDA receptor may share a common intramolecular pathway for altering the function of this ion channel.

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