Nicotinic acetylcholine receptors assembled from the α7 and β3 subunits

Eleonora Palma, Laura Maggi, Benedetta Barabino, Fabrizio Eusebi, Marco Ballivet

Research output: Contribution to journalArticle

Abstract

Intracellular recordings were performed in voltage-clamped Xenopus oocytes upon injection with a mixture of cDNAs encoding the β3 and mutant α7 ((L24VT)α7) neuronal nicotinic acetylcholine receptor (nAChR) subunits. The expressed receptors maintained sensitivity to methyllycaconitine and to α-bungarotoxin but exhibited a functional profile strikingly different from that of the homomeric (L24VT)α7 receptor. The heteromeric (L24VT)α7β3 nAChR had a lower apparent affinity and a faster rate of desensitization than (L247T)α7 nAChR, exhibited nonlinearity in the I-V relationship, and was inhibited by 5-hydroxytryptamine, much like wild type α7 ((WT)α7) nAChR. Single channel recordings in cell-attached mode revealed unitary events with a slope conductance of 19 picosiemens and a lifetime of 5 ms, both values being much smaller than those of the homomeric receptor channel. Upon injection with a mixture of (WT)α7 and β3 cDNAs, clear evidence was obtained for the plasma membrane assembly of heteromeric nAChRs, although ACh could not activate these receptors. It is concluded that β3, long believed to be an orphan subunit, readily co-assembles with other subunits to form heteromeric receptors, some of which may be negative regulators of cholinergic function.

Original languageEnglish
Pages (from-to)18335-18340
Number of pages6
JournalJournal of Biological Chemistry
Volume274
Issue number26
DOIs
Publication statusPublished - Jun 25 1999

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ASJC Scopus subject areas

  • Biochemistry

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