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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on July 16, 2008; DOI: 10.1124/jpet.108.140459


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Received for publication April 28, 2008.
Revised July 13, 2008.
Accepted for publication July 16, 2008.

The Pore Region of N-Methyl-D-Aspartate Receptors Differentially Influences Stimulation and Block by Spermine

Lihua Jin 1, Maki Miyazaki 1, Satomi Mizuno 1, Miki Takigawa 1, Tadao Hirose 1, Kazuhiro Nishimura 1, Toshihiko Toida 1, Keith Williams 2, Keiko Kashiwagi 3, Kazuei Igarashi 1*

1 Graduate School of Pharmaceutical Sciences, Chiba University 2 SUNY Health Science Center at Brooklyn 3 Faculty of Pharmacy, Chiba Institute of Science

* Address correspondence to: E-mail: iga16077{at}p.chiba-u.ac.jp

Abstract

The transmembrane and pore-forming regions of N-methyl-D-aspartate (NMDA) receptors containing the NR1 and NR2B subunits were studied by measuring the effects of various NR1 and NR2B mutants on stimulation and block by spermine. Block by spermine was predominantly affected by mutations in the M3 segment of NR1 and especially in the M1 and M3 segments of NR2B. These regions are in the outer vestibule of the channel pore and may contribute to a spermine binding site. Mutations in different regions - predominantly the M3 segment and M2 loop of NR1 and the M3 segment of NR2B - influenced spermine stimulation, a surprising finding since spermine stimulation is thought to involve a spermine binding site in the distal, exracellular regulatory (R) domain. However, some of these mutations also influence sensitivity to ifenprodil and protons, and changes in spermine sensitivity may be secondary to changes in proton sensitivity. The results are consistent with the proposal that the relative positions of the M1 and M3 transmembrane segments and M2 loops are staggered or asymmetric in NR1 and NR2 subunits, and with the idea that stimulation and block by spermine involve separate binding sites and distinct mechanisms, although some residues in the receptor subunits can affect both stimulation and block.


Key words: Channel pore, NMDA receptor, Polyamine, R domain, Site-directed mutagenesis, Spermine





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