Properties of neuronal α7 mutant nicotinic acetylcholine receptors gated by bicuculline

Raffaella Tonini, E. Palma, R. Miledi, F. Eusebi

Research output: Contribution to journalArticle

Abstract

We have shown previously that mutating to threonine the leucine residue in the M2 domain of the α7 nicotinic acetylcholine receptor (human L248T, L248T; chick L247T, L247T) converts bicuculline (BIC) from an antagonist into an agonist. In this work we studied the functional properties of the BIC-activated channels and report that, in Xenopus oocytes injected with L248T subunit cDNA, BIC activates single-channel currents that have similar conductances, but shorter mean burst duration, than the channels activated by ACh. In contrast, both the conductance and kinetics of the channels activated by either ACh or BIC are substantially the same in oocytes expressing L247T receptors. We have also shown previously that if Cys 189 and 190, which are thought to be at or near the transmitter binding site, are additionally mutated to Ser, the new mutant receptor (L247T-C189S-C190S) has a reduced affinity for ACh. We now find that the EC50 in the BIC dose-current response relation, as well the characteristics of the channels activated by BIC, are similar in oocytes expressing either L247T or L247T-C189S-C190S receptors. On the other hand, ACh activation of L247T-C189S-C190S receptors gates channels whose mean open time and burst duration are much shorter than those of ACh-gated L247T-channels. Therefore, the gating kinetics of both L248T and L247R-C189S-C190S receptor-channels change when BIC is replaced by ACh; and we conclude that both ACh and BIC activate mutant α7 receptors with different patterns of activation.

Original languageEnglish
Pages (from-to)765-771
Number of pages7
JournalNeuropharmacology
Volume44
Issue number6
DOIs
Publication statusPublished - May 2003

    Fingerprint

Keywords

  • Chick L247Tα7 mutant
  • Chick L247T/C189-190Sα7 mutant
  • Human L248Tα7 mutant
  • Xenopus oocyte

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Drug Discovery
  • Pharmacology

Cite this