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Localization of nAChR subunit mRNAs in the brain of Macaca mulatta
Open accessAbstract
We present here a systematic mapping of nAChR subunit mRNAs in Macaca mulatta brain. A fragment, from the transmembrane segments MIII to MIV of Macaca neuronal nAChR subunits was cloned, and shown to exhibit high identity (around 95%) to the corresponding human subunits. Then, specific oligodeoxynucleotides were synthesized for in situ hybridization experiments. Both alpha4 and beta2 mRNA signals were widely distributed in the brain, being stronger in the thalamus and in the dopaminergic cells of the mesencephalon. Most brain nuclei displayed both alpha4 and beta2 signals with the exception of some basal ganglia regions and the reticular thalamic nucleus which were devoid of alpha4 signal. alpha6 and beta3 mRNA signals were selectively concentrated in the substantia nigra and the medial habenula. The strongest signals for alpha3 or beta4 mRNAs were found in the epithalamus (medial habenula and pineal gland), whereas there were no specific alpha3 or beta4 signals in mesencephalic dopaminergic nuclei. alpha5 and alpha7 mRNA signals were found in several brain areas, including cerebral cortex, thalamus and substantia nigra, although at a lower level than alpha4 and beta2. The distribution of alpha3, alpha4, alpha5, alpha6, alpha7, beta2, beta3 and beta4 subunit mRNAs in the monkey is substantially similar to that observed in rodent brain. Surprisingly, alpha2 mRNA signal was largely distributed in the Macaca brain, at levels comparable with those of alpha4 and beta2. This observation represents the main difference between rodent and Macaca subunit mRNA distribution and suggests that, besides alpha4beta2*, alpha2beta2* nAChRs constitute a main nAChR isoform in primate brain.
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Séguéla, P., Wadiche, J. I., Dineley‐Miller, K., Dani, J., & Jw, P. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-02-00596.1993 · Cited by 1,471
Picciotto, M. R., Zoli, M., Rimondini, R., Léna, C., Marubio, L. M., Pich, E. M., Fuxe, K., & Changeux, J.-P. (1998) · Nature · doi:10.1038/34413 · Cited by 1,320
Self-citationLinkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus
Freedman, R., Coon, H., Myles-Worsley, M., Orr-Urtreger, A., Olincy, A., Davis, A., Polymeropoulos, M., Holik, J., Hopkins, J., Hoff, M., et al. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.2.587 · Cited by 1,141
Steinlein, O. K., Mulley, J. C., Propping, P., Wallace, R. H., Phillips, H. A., Sutherland, G. R., Scheffer, I. E., & Berkovic, S. F. (1995) · Nature Genetics · doi:10.1038/ng1095-201 · Cited by 1,134
The Diversity of Neuronal Nicotinic Acetylcholine Receptors
Sargent, P. B. (1993) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.16.030193.002155 · Cited by 1,052
Wada, E., Wada, K., Boulter, J., Deneris, E. S., Heinemann, S., Patrick, J., & Swanson, L. W. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902840212 · Cited by 1,044
Acetylcholine receptor channel imaged in the open state
Unwin, P. N. T. (1995) · Nature · doi:10.1038/373037a0 · Cited by 1,000
Neurobiology of the Caenorhabditis elegans Genome
Bargmann, C. I. (1998) · Science · doi:10.1126/science.282.5396.2028 · Cited by 929
Nicotine activates and desensitizes midbrain dopamine neurons
Pidoplichko, V. I., DeBiasi, M., Williams, J. T., & Dani, J. A. (1997) · Nature · doi:10.1038/37120 · Cited by 769
Nicotinic Receptors in the Development and Modulation of CNS Synapses
Role, L. W., & Berg, D. K. (1996) · Neuron · doi:10.1016/s0896-6273(00)80134-8 · Cited by 762
Research works printed but not linked: 5
- Changeux J.‐P., 1990, Functional architecture and dynamics of the nicotinic acetylcholine receptor: an allosteric ligand‐gated ion channel, Fidia Res. Found. Neurosci. Award, 4, 21
- Chavez‐Noriega L., 1997, Pharmacological characterization of recombinant human neuronal nicotinic acetylcholine receptors hα2β2, hα2β4, hα3β2, hα3β4, hα4β2, hα4β4 and hα7 expressed in Xenopus oocytes, J. Pharm. Exp. Ther., 280, 346
- Han Z.‐Y., 1999, Cloning of Macacus Rhesus Nachr Subunit Gene Fragments and Localisation of the Transcripts in the Brain. Neuronal Nicotinic Receptors: from Structure to Therapeutics
- Paxinos G., 2000, The Rhesus Monkey Brain
- Wisden W., 1994, Hybridization Protocols for the Brain
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Timmermann, D. B., Sandager‐Nielsen, K., Dyhring, T., Smith, M., Jacobsen, A., Nielsen, E., Grunnet, M., Christensen, J., Peters, D., Kohlhaas, K. L., et al. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.01989.x · Cited by 103
Chatterjee, S., Steensland, P., Simms, J. A., Holgate, J. Y., Coe, J. W., Hurst, R. S., Shaffer, C. L., Lowe, J. A., III, Rollema, H., & Bartlett, S. E. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.191 · Cited by 103
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Lotfipour, S., Byun, J. S., Leach, P., Fowler, C. D., Murphy, N. P., Kenny, P. J., Gould, T. J., & Boulter, J. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.4731-12.2013 · Cited by 68
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Major, A. J., Vijayraghavan, S., & Everling, S. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2454-15.2015 · Cited by 33
Ghasemi, M., & Niktarash, A. H. (2015) · Reviews in the Neurosciences · doi:10.1515/revneuro-2014-0044 · Cited by 33
Machaalani, R., Kashi, P. K., & Waters, K. A. (2010) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2010.05.009 · Cited by 32
Section I. The Cholinergic System
Smythies, J. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)64001-9 · Cited by 32
Nicotinic Receptors in Sleep-Related Hypermotor Epilepsy: Pathophysiology and Pharmacology
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Cholinergic Receptors and Addiction
Papke, R. L., Brunzell, D. H., & Biasi, M. D. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_139 · Cited by 30
Pleiotropic functional effects of the first epilepsy‐associated mutation in the human CHRNA2 gene
Hoda, J., Wanischeck, M., Bertrand, D., & Steinlein, O. K. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.04.024 · Cited by 30
Dehkordi, O., Haxhiu, M. A., Millis, R. M., Dennis, G. C., Kc, P., Jafri, A., Khajavi, M., Trouth, C. O., & Zaidi, S. I. A. (2004) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2004.03.006 · Cited by 30
Mello, N. K., Fivel, P. A., & Kohut, S. J. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.25 · Cited by 28
Whiteaker, P., Wilking, J. A., Brown, R. W. B., Brennan, R. J., Collins, A. C., Lindstrom, J. M., & Boulter, J. (2009) · Acta Pharmacologica Sinica · doi:10.1038/aps.2009.68 · Cited by 28
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Resta, C. D., Ambrosi, P., Curia, G., & Becchetti, A. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.05.063 · Cited by 28
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Martin-Ruiz, C. M., Lawrence, S., Piggott, M. A., Kuryatov, A., Lindstrom, J. M., Gotti, C., Cookson, M., Perry, R. H., Jaros, E., Perry, E. K., et al. (2002) · Neuroscience Letters · doi:10.1016/s0304-3940(02)01183-7 · Cited by 26
Disney, A. A., & Robert, J. S. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902280116 · Cited by 25
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Metadata
- Authors
- Han, Z., Le Novère, N., Zoli, M., Hill, J. A., Champtiaux, N., & Changeux, J.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- University of Iowa (US)
- Corresponding author
- Changeux, Jean‐Pierre
- Venue
- European Journal of Neuroscience
- Publisher
- Wiley
- Published
- 2000-10
- Volume
- 12
- Issue
- 10
- Pages
- 3664-3674
- ISSN
- 0953-816X (ISSN-L)
- 1460-9568
- OpenAlex
- W2047331648
- Cited by
- 156
- References
- 78
- Citations by year
- 2026: 2 · 2024: 6 · 2023: 5 · 2022: 3 · 2021: 6 · 2020: 7 · 2019: 4 · 2018: 7 · 2017: 3 · 2016: 4 · 2015: 18 · 2014: 6 · 2013: 9 · 2012: 9
- FWCI
- 2.17
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Locations
- European Journal of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- IRIS UNIMORE (University of Modena and Reggio Emilia) (submittedVersion, cc-by)
- Funders
- Fondation Simone et Cino Del Duca
- 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 › Public Health, Environmental and Occupational Health › Smoking Behavior and Cessation
- Keywords
- nicotinic acetylcholine receptors, rhesus monkeys, primate brain, alpha2 subunit, alpha4beta2 nAChR, thalamus, substantia nigra, medial habenula, dopaminergic neurons, alpha7 subunit, alpha3 subunit, alpha5 subunit, alpha6 subunit, beta3 subunit, beta4 subunit, mRNA localization
- MeSH terms
- Animals, Brain, Brain Chemistry, Cloning, Molecular, Cytoplasm, Macaca mulatta, Neurons, Receptors, Nicotinic, RNA, Messenger
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