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Monkey adrenal chromaffin cells express α6ß4* nicotinic acetylcholine receptors.
Hernández-Vivanco, Alicia; Hone, Arik J; Scadden, Mick L; Carmona-Hidalgo, Beatriz; McIntosh, J Michael; Albillos, Almudena.
  • Hernández-Vivanco A; Departamento de Farmacología y Terapéutica, Facultad de Medicina, Universidad Autónoma de Madrid, Madrid, Spain.
  • Hone AJ; Departamento de Farmacología y Terapéutica, Facultad de Medicina, Universidad Autónoma de Madrid, Madrid, Spain.
  • Scadden ML; Department of Biology, University of Utah, Salt Lake City, Utah, United States of America.
  • Carmona-Hidalgo B; Departamento de Farmacología y Terapéutica, Facultad de Medicina, Universidad Autónoma de Madrid, Madrid, Spain.
  • McIntosh JM; George E. Whalen Veterans Affairs Medical Center, Salt Lake City, Utah, United States of America; Department of Biology, University of Utah, Salt Lake City, Utah, United States of America; Department of Psychiatry, University of Utah, Salt Lake City, Utah, United States of America.
  • Albillos A; Departamento de Farmacología y Terapéutica, Facultad de Medicina, Universidad Autónoma de Madrid, Madrid, Spain.
PLoS One ; 9(4): e94142, 2014.
Article en En | MEDLINE | ID: mdl-24727685
ABSTRACT
Nicotinic acetylcholine receptors (nAChRs) that contain α6 and ß4 subunits have been demonstrated functionally in human adrenal chromaffin cells, rat dorsal root ganglion neurons, and on noradrenergic terminals in the hippocampus of adolescent mice. In human adrenal chromaffin cells, α6ß4* nAChRs (the asterisk denotes the possible presence of additional subunits) are the predominant subtype whereas in rodents, the predominant nAChR is the α3ß4* subtype. Here we present molecular and pharmacological evidence that chromaffin cells from monkey (Macaca mulatta) also express α6ß4* receptors. PCR was used to show the presence of transcripts for α6 and ß4 subunits and pharmacological characterization was performed using patch-clamp electrophysiology in combination with α-conotoxins that target the α6ß4* subtype. Acetylcholine-evoked currents were sensitive to inhibition by BuIA[T5A,P6O] and MII[H9A,L15A]; α-conotoxins that inhibit α6-containing nAChRs. Two additional agonists were used to probe for the expression of α7 and ß2-containing nAChRs. Cells with currents evoked by acetylcholine were relatively unresponsive to the α7-selctive agonist choline but responded to the agonist 5-I-A-85380. These studies provide further insights into the properties of natively expressed α6ß4* nAChRs.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Receptores Nicotínicos / Células Cromafines Límite: Animals Idioma: En Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Receptores Nicotínicos / Células Cromafines Límite: Animals Idioma: En Año: 2014 Tipo del documento: Article