NACHRS heterologously expressed in human cells after transient transfe
ction with alpha(3) beta(4) alpha(5) or alpha(3) beta(4) subunit cDNAs
exhibited similar sensitivities to antagonists and comparable functio
nal channel profiles. However, the sum of two Hill equations was requi
red for best fitting the ACh dose-current response curves after co-exp
ression of alpha(5), alpha(3) and beta(4) subunits. One component was
comparable to that obtained in alpha(3) beta(4)-transfected cells, whi
le the additional component, putatively attributed to an alpha(3) beta
(4) alpha(5) nAChR population, showed a Hill coefficient >2 and a nine
-fold greater half-maximal ACh concentration (EC50). These results sug
gest that the alpha(5) subunit participates in the assembly of alpha(3
) beta(4) alpha(5) nAChRs complexes in human cells, adding a new membe
r to the family of neuronal nicotinic receptors.