Cited by 87Nicotinic Acetylcholine Receptors StudyNeuroscience and Neuropharmacology ResearchSmoking Behavior and Cessation

Nicotinic acetylcholine receptor subunit mRNA expression and channel function in medial habenula neurons

Sheffield, Elise B, Quick, Michael W, Lester, Robin A.J·2000·Neuropharmacology

Abstract

Relationships between nicotinic acetylcholine receptor (nAChR) channel function and nAChR subunit mRNA expression were explored in acutely isolated rat medial habenula (MHb) neurons using a combination of whole-cell recording and single cell RT-PCR techniques. Following amplification using subunit-specific primers, subunits could be categorized in one of three ways: (i) present in 95-100% cells: alpha3, alpha4, alpha5, beta2 and beta4; (ii) never present: alpha2; and (iii) sometimes present ( approximately 40% cells): alpha6, alpha7 and beta3. These data imply that alpha2 subunits do not participate in nAChRs on MHb cells, that alpha6, alpha7 and beta3 subunits are not necessary for functional channels but may contribute in some cells, and that nAChRs may require combinations of all or subsets of alpha3, alpha4, alpha5, beta2 and beta4 subunits. Little difference in the patterns of subunit expression between nicotine-sensitive and insensitive cells were revealed based on this qualitative analysis, implying that gene transcription per se may be an insufficient determinant of nAChR channel function. Normalization of nAChR subunit levels to the amount of actin mRNA, however, revealed that cells with functional channels were associated with high levels (>0.78 relative to actin; 11/12 cells) of all of the category (i) subunits: alpha3, alpha4, alpha5, beta2 and beta4. Conversely, one or more of these subunits was always low (<0.40 relative to actin) in all cells with no detectable…

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Crossref · 10.1016/s0028-3908(00)00138-6

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  • Approximately 90%-100% of MHb neurons express α3, α4, α5, β2, and β4 nAChR subunits.

    “Indeed, approximately 90%-100% of MHb neurons express α3, α4, α5, β2, and β4 nAChR subunits (Sheffield et al. 2000)”

    From Mechanisms of Nicotine Addiction (2021) · cites this paper as Sheffield et al. 2000

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Authors
Sheffield, E. B., Quick, M. W., & Lester, R. A. J.
Affiliations
University of Alabama at Birmingham (US)
Corresponding author
Lester, Robin A.J
Venue
Neuropharmacology
Publisher
Elsevier BV
Published
2000-12
Volume
39
Issue
13
Pages
2591-2603
ISSN
0028-3908 (ISSN-L)
OpenAlex
W1998125901
Cited by
87
References
0
Citations by year
2025: 5 · 2024: 3 · 2023: 2 · 2022: 2 · 2021: 2 · 2020: 5 · 2019: 5 · 2018: 4 · 2017: 5 · 2016: 5 · 2015: 3 · 2014: 11 · 2013: 2 · 2012: 5
FWCI
1.08
Type
journal article
Language
en
Open access
closed
Locations
  • Neuropharmacology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • U.S. Public Health Service
  • National Institute of Neurological Disorders and Stroke (NS 31669)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Health Sciences › Medicine › Physiology › Smoking Behavior and Cessation
Keywords
nicotinic acetylcholine receptors, subunit stoichiometry, alpha3 subunit, alpha4 subunit, alpha5 subunit, beta2 subunit, beta4 subunit, alpha2 subunit, nicotine sensitivity
MeSH terms
Animals, Animals, Newborn, Cell Line, Cell Separation, Electrophysiology, Kidney, Neurons, Nicotine, Oocytes, Receptors, Nicotinic, RNA, Messenger, Xenopus, Patch-Clamp Techniques, Nicotinic Agonists, Habenula, Reverse Transcriptase Polymerase Chain Reaction, Rats

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