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Molecular interrogation of hypothalamic organization reveals distinct dopamine neuronal subtypes.

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  1. Du Vigneaud V., Harvey Lect., 50, 1 (1954-1955)
  2. Clarke I.J., Compr. Physiol., 5, 217 (2015)
  3. Lantos TiborÁgoston, Görcs Tamás Jen‖o, Palkovits Miklós, Immunohistochemical mapping of neuropeptides in the premamillary region of the hypothalamus in rats, 10.1016/0165-0173(94)00013-f
  4. Swanson L. W., Kuypers H. G. J. M., The paraventricular nucleus of the hypothalamus: Cytoarchitectonic subdivisions and organization of projections to the pituitary, dorsal vagal complex, and spinal cord as demonstrated by retrograde fluorescence double-labeling methods, 10.1002/cne.901940306
  5. Dahlström A., Acta Physiol. Scand. Suppl., 62, 1 (1964)
  6. Björklund Anders, Moore Robert Y., Nobin Anders, Stenevi Ulf, The organization of tubero-hypophyseal and reticulo-infundibular catecholamine neuron systems in the rat brain, 10.1016/0006-8993(73)90371-5
  7. Horvath Tamas L., Suprachiasmatic Efferents Avoid Phenestrated Capillaries but Innervate Neuroendocrine Cells, Including Those Producing Dopamine1, 10.1210/endo.138.3.4976
  8. Abizaid Alfonso, Horvath Balazs, Keefe David L., Leranth Csaba, Horvath Tamas L., Direct visual and circadian pathways target neuroendocrine cells in primates, 10.1111/j.1460-9568.2004.03737.x
  9. Zeisel A., Munoz-Manchado A. B., Codeluppi S., Lonnerberg P., La Manno G., Jureus A., Marques S., Munguba H., He L., Betsholtz C., Rolny C., Castelo-Branco G., Hjerling-Leffler J., Linnarsson S., Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq, 10.1126/science.aaa1934
  10. Scott Niv, Prigge Matthias, Yizhar Ofer, Kimchi Tali, A sexually dimorphic hypothalamic circuit controls maternal care and oxytocin secretion, 10.1038/nature15378
  11. Yang Cindy F., Chiang Michael C., Gray Daniel C., Prabhakaran Mahalakshmi, Alvarado Maricruz, Juntti Scott A., Unger Elizabeth K., Wells James A., Shah Nirao M., Sexually Dimorphic Neurons in the Ventromedial Hypothalamus Govern Mating in Both Sexes and Aggression in Males, 10.1016/j.cell.2013.04.017
  12. Xu Xiaohong, Coats Jennifer K., Yang Cindy F., Wang Amy, Ahmed Osama M., Alvarado Maricruz, Izumi Tetsuro, Shah Nirao M., Modular Genetic Control of Sexually Dimorphic Behaviors, 10.1016/j.cell.2011.12.018
  13. Yang X., Tissue-specific expression and regulation of sexually dimorphic genes in mice, 10.1101/gr.5217506
  14. Dulcis D., Jamshidi P., Leutgeb S., Spitzer N. C., Neurotransmitter Switching in the Adult Brain Regulates Behavior, 10.1126/science.1234152
  15. Meister B., Cort�s R., Villar M. J., Schalling M., H�kfelt T., Peptides and transmitter enzymes in hypothalamic magnocellular neurons after administration of hyperosmotic stimuli: comparison between messenger RNA and peptide/protein levels, 10.1007/bf00318631
  16. Pinto S., Rapid Rewiring of Arcuate Nucleus Feeding Circuits by Leptin, 10.1126/science.1089459
  17. Cristino L., Busetto G., Imperatore R., Ferrandino I., Palomba L., Silvestri C., Petrosino S., Orlando P., Bentivoglio M., Mackie K., Di Marzo V., Obesity-driven synaptic remodeling affects endocannabinoid control of orexinergic neurons, 10.1073/pnas.1219485110
  18. Romanov R. A., Alpar A., Zhang M.-D., Zeisel A., Calas A., Landry M., Fuszard M., Shirran S. L., Schnell R., Dobolyi A., Olah M., Spence L., Mulder J., Martens H., Palkovits M., Uhlen M., Sitte H. H., Botting C. H., Wagner L., Linnarsson S., Hokfelt T., Harkany T., A secretagogin locus of the mammalian hypothalamus controls stress hormone release, 10.15252/embj.201488977
  19. Henry Fredrick E, Sugino Ken, Tozer Adam, Branco Tiago, Sternson Scott M, Cell type-specific transcriptomics of hypothalamic energy-sensing neuron responses to weight-loss, 10.7554/elife.09800
  20. Krashes Michael J., Shah Bhavik P., Madara Joseph C., Olson David P., Strochlic David E., Garfield Alastair S., Vong Linh, Pei Hongjuan, Watabe-Uchida Mitsuko, Uchida Naoshige, Liberles Stephen D., Lowell Bradford B., An excitatory paraventricular nucleus to AgRP neuron circuit that drives hunger, 10.1038/nature12956
  21. Everitt Barry J., Hökfelt Tomas, Wu Jan-Yen, Goldstein Menek, Coexistence of Tyrosine Hydroxylase-Like and Gamma-Aminobutyric Acid-Like Immunoreactivities in Neurons of the Arcuate Nucleus, 10.1159/000123977
  22. Macosko Evan Z., Basu Anindita, Satija Rahul, Nemesh James, Shekhar Karthik, Goldman Melissa, Tirosh Itay, Bialas Allison R., Kamitaki Nolan, Martersteck Emily M., Trombetta John J., Weitz David A., Sanes Joshua R., Shalek Alex K., Regev Aviv, McCarroll Steven A., Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets, 10.1016/j.cell.2015.05.002
  23. Lee S. Y., Foldy C., Szabadics J., Soltesz I., Cell-Type-Specific CCK2 Receptor Signaling Underlies the Cholecystokinin-Mediated Selective Excitation of Hippocampal Parvalbumin-Positive Fast-Spiking Basket Cells, 10.1523/jneurosci.1970-11.2011
  24. Moriya Ryuichi, Sano Hideki, Umeda Tatsuya, Ito Makoto, Takahashi Yuki, Matsuda Masao, Ishihara Akane, Kanatani Akio, Iwaasa Hisashi, RFamide Peptide QRFP43 Causes Obesity with Hyperphagia and Reduced Thermogenesis in Mice, 10.1210/en.2005-1580
  25. Zagorácz Olga, Kovács Anita, László Kristóf, Ollmann Tamás, Péczely László, Lénárd László, Effects of direct QRFP-26 administration into the medial hypothalamic area on food intake in rats, 10.1016/j.brainresbull.2015.09.004
  26. Tekin Izel, Roskoski Robert, Carkaci-Salli Nurgul, Vrana Kent E., Complex molecular regulation of tyrosine hydroxylase, 10.1007/s00702-014-1238-7
  27. Meister Björn, Elde Robert, Dopamine Transporter mRNA in Neurons of the Rat Hypothalamus, 10.1159/000126568
  28. Ben-Jonathan N., Dopamine as a Prolactin (PRL) Inhibitor, 10.1210/er.22.6.724
  29. Stagkourakis Stefanos, Kim Hoseok, Lyons David J., Broberger Christian, Dopamine Autoreceptor Regulation of a Hypothalamic Dopaminergic Network, 10.1016/j.celrep.2016.03.062
  30. Goudreau John L., Lindley Steven E., Lookingland Keith J., Moore Kenneth E., Evidence That Hypothalamic Periventricular Dopamine Neurons Innervate the Intermediate Lobe of the Rat Pituitary, 10.1159/000126214
  31. Mori Kenji, Miyazato Mikiya, Ida Takanori, Murakami Noboru, Serino Ryota, Ueta Yoichi, Kojima Masayasu, Kangawa Kenji, Identification of neuromedin S and its possible role in the mammalian circadian oscillator system, 10.1038/sj.emboj.7600526
  32. Zhang Luoying, Hirano Arisa, Hsu Pei-Ken, Jones Christopher R., Sakai Noriaki, Okuro Masashi, McMahon Thomas, Yamazaki Maya, Xu Ying, Saigoh Noriko, Saigoh Kazumasa, Lin Shu-Ting, Kaasik Krista, Nishino Seiji, Ptáček Louis J., Fu Ying-Hui, APERIOD3variant causes a circadian phenotype and is associated with a seasonal mood trait, 10.1073/pnas.1600039113
  33. Vitaterna M. H., Selby C. P., Todo T., Niwa H., Thompson C., Fruechte E. M., Hitomi K., Thresher R. J., Ishikawa T., Miyazaki J., Takahashi J. S., Sancar A., Differential regulation of mammalian Period genes and circadian rhythmicity by cryptochromes 1 and 2, 10.1073/pnas.96.21.12114
  34. Hölttä Mikko, Minthon Lennart, Hansson Oskar, Holmén-Larsson Jessica, Pike Ian, Ward Malcolm, Kuhn Karsten, Rüetschi Ulla, Zetterberg Henrik, Blennow Kaj, Gobom Johan, An Integrated Workflow for Multiplex CSF Proteomics and Peptidomics—Identification of Candidate Cerebrospinal Fluid Biomarkers of Alzheimer’s Disease, 10.1021/pr501076j
  35. Bro Susan, Haycock John W., Visual cortex (translation of S. Ramón y Cajal) Translated from L'Écorce Cérébrale Suivant les Régions L'Écorce Visuelle, Chapter 25 in “Histologie du Système Nerveux de l'Homme et des Vertébrés,” 1911, 10.1016/s0091-6773(77)92165-4
  36. Ascoli Giorgio A., Alonso-Nanclares Lidia, Anderson Stewart A., Barrionuevo German, Benavides-Piccione Ruth, Burkhalter Andreas, Buzsáki György, Cauli Bruno, DeFelipe Javier, Fairén Alfonso, Feldmeyer Dirk, Fishell Gord, Fregnac Yves, Freund Tamas F., Gardner Daniel, Gardner Esther P., Goldberg Jesse H., Helmstaedter Moritz, Hestrin Shaul, Karube Fuyuki, Kisvárday Zoltán F., Lambolez Bertrand, Lewis David A., Marin Oscar, Markram Henry, Muñoz Alberto, Packer Adam, Petersen Carl C. H., Rockland Kathleen S., Rossier Jean, Rudy Bernardo, Somogyi Peter, Staiger Jochen F., Tamas Gabor, Thomson Alex M., Toledo-Rodriguez Maria, Wang Yun, West David C., Yuste Rafael, Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex, 10.1038/nrn2402
  37. Zivraj K. H., Tung Y. C. L., Piper M., Gumy L., Fawcett J. W., Yeo G. S. H., Holt C. E., Subcellular Profiling Reveals Distinct and Developmentally Regulated Repertoire of Growth Cone mRNAs, 10.1523/jneurosci.1800-10.2010
  38. Yulyaningsih Ernie, Loh Kim, Lin Shu, Lau Jackie, Zhang Lei, Shi Yanchuan, Berning Britt A., Enriquez Ronaldo, Driessler Frank, Macia Laurence, Khor Ee Cheng, Qi Yue, Baldock Paul, Sainsbury Amanda, Herzog Herbert, Pancreatic Polypeptide Controls Energy Homeostasis via Npy6r Signaling in the Suprachiasmatic Nucleus in Mice, 10.1016/j.cmet.2013.11.019
  39. Friedman Jeffrey M., Halaas Jeffrey L., 10.1038/27376
  40. Scott Michael M., Lachey Jennifer L., Sternson Scott M., Lee Charlotte E., Elias Carol F., Friedman Jeffrey M., Elmquist Joel K., Leptin targets in the mouse brain, 10.1002/cne.22025
  41. Boulland Jean-Luc, Jenstad Monica, Boekel Amber J., Wouterlood Floris G., Edwards Robert H., Storm-Mathisen Jon, Chaudhry Farrukh A., Vesicular Glutamate and GABA Transporters Sort to Distinct Sets of Vesicles in a Population of Presynaptic Terminals, 10.1093/cercor/bhn077
  42. Dawson T.M., J. Neurosci., 14, 5147 (1994)
  43. Jonas P., Corelease of Two Fast Neurotransmitters at a Central Synapse, 10.1126/science.281.5375.419
  44. Ajika Katsuya, Hökfelt Tomas, Ultrastructural identification of catecholamine neurones in the hypothalamic periventricular-arcuate nucleus-median eminence complex with special reference to quantitative aspects, 10.1016/0006-8993(73)90571-4
  45. Horvath T.L., J. Neurosci., 18, 1546 (1998)
  46. DeMaria Jamie E., Lerant Anna A., Freeman Marc E., Prolactin activates all three populations of hypothalamic neuroendocrine dopaminergic neurons in ovariectomized rats, 10.1016/s0006-8993(99)01667-4
  47. Lee Ivan T., Chang Alexander S., Manandhar Manabu, Shan Yongli, Fan Junmei, Izumo Mariko, Ikeda Yuichi, Motoike Toshiyuki, Dixon Shelley, Seinfeld Jeffrey E., Takahashi Joseph S., Yanagisawa Masashi, Neuromedin S-Producing Neurons Act as Essential Pacemakers in the Suprachiasmatic Nucleus to Couple Clock Neurons and Dictate Circadian Rhythms, 10.1016/j.neuron.2015.02.006
  48. Sellix M. T., Anatomical and functional characterization of clock gene expression in neuroendocrine dopaminergic neurons, 10.1152/ajpregu.00555.2005
  49. Tamamaki Nobuaki, Yanagawa Yuchio, Tomioka Ryohei, Miyazaki Jun-Ichi, Obata Kunihiko, Kaneko Takeshi, Green fluorescent protein expression and colocalization with calretinin, parvalbumin, and somatostatin in the GAD67-GFP knock-in mouse, 10.1002/cne.10905
  50. Máté Zoltán, Poles Marietta Zita, Szabó Gábor, Bagyánszki Mária, Talapka Petra, Fekete Éva, Bódi Nikolett, Spatiotemporal expression pattern of DsRedT3/CCK gene construct during postnatal development of myenteric plexus in transgenic mice, 10.1007/s00441-013-1552-7
  51. Pierreux Christophe E., Vanhorenbeeck Vinciane, Jacquemin Patrick, Lemaigre Frédéric P., Rousseau Guy G., The Transcription Factor Hepatocyte Nuclear Factor-6/Onecut-1 Controls the Expression of Its Paralog Onecut-3 in Developing Mouse Endoderm, 10.1074/jbc.m409038200
  52. WONG H.C., STERNINI C., LLOYD K., De GIORGIO R, WALSH J.H., Monoclonal Antibody to VIP: Production, Characterization, Immunoneutralizing Activity, and Usefulness in Cytochemical Staining, 10.1089/hyb.1996.15.133
  53. Miyazaki Taisuke, Fukaya Masahiro, Shimizu Hidemi, Watanabe Masahiko, Subtype switching of vesicular glutamate transporters at parallel fibre-Purkinje cell synapses in developing mouse cerebellum : Developmental switching of VGluT in parallel fibre, 10.1046/j.1460-9568.2003.02698.x
  54. Mulder Jan, Spence Lauren, Tortoriello Giuseppe, DiNieri Jennifer A., Uhlén Mathias, Shui Bo, Kotlikoff Michael I., Yanagawa Yuchio, Aujard Fabienne, Hökfelt Tomas, Hurd Yasmin L., Harkany Tibor, Secretagogin is a Ca2+-binding protein identifying prospective extended amygdala neurons in the developing mammalian telencephalon : Secretagogin in developing mammalian forebrain, 10.1111/j.1460-9568.2010.07275.x
  55. Weiss M.L., Cobbett P., Intravenous injection of evans blue labels magnocellular neuroendocrine cells of the rat supraoptic nucleusin situ and after dissociation, 10.1016/0306-4522(92)90498-q
  56. Murray Andrew J, Sauer Jonas-Frederic, Riedel Gernot, McClure Christina, Ansel Laura, Cheyne Lesley, Bartos Marlene, Wisden William, Wulff Peer, Parvalbumin-positive CA1 interneurons are required for spatial working but not for reference memory, 10.1038/nn.2751
  57. Pollak Dorocic Iskra, Fürth Daniel, Xuan Yang, Johansson Yvonne, Pozzi Laura, Silberberg Gilad, Carlén Marie, Meletis Konstantinos, A Whole-Brain Atlas of Inputs to Serotonergic Neurons of the Dorsal and Median Raphe Nuclei, 10.1016/j.neuron.2014.07.002
  58. Susaki Etsuo A., Tainaka Kazuki, Perrin Dimitri, Kishino Fumiaki, Tawara Takehiro, Watanabe Tomonobu M., Yokoyama Chihiro, Onoe Hirotaka, Eguchi Megumi, Yamaguchi Shun, Abe Takaya, Kiyonari Hiroshi, Shimizu Yoshihiro, Miyawaki Atsushi, Yokota Hideo, Ueda Hiroki R., Whole-Brain Imaging with Single-Cell Resolution Using Chemical Cocktails and Computational Analysis, 10.1016/j.cell.2014.03.042
  59. Tomer Raju, Ye Li, Hsueh Brian, Deisseroth Karl, Advanced CLARITY for rapid and high-resolution imaging of intact tissues, 10.1038/nprot.2014.123
  60. Schwanhäusser Björn, Busse Dorothea, Li Na, Dittmar Gunnar, Schuchhardt Johannes, Wolf Jana, Chen Wei, Selbach Matthias, Global quantification of mammalian gene expression control, 10.1038/nature10098
  61. Islam Saiful, Zeisel Amit, Joost Simon, La Manno Gioele, Zajac Pawel, Kasper Maria, Lönnerberg Peter, Linnarsson Sten, Quantitative single-cell RNA-seq with unique molecular identifiers, 10.1038/nmeth.2772
  62. Tsafrir D., Tsafrir I., Ein-Dor L., Zuk O., Notterman D.A., Domany E., Sorting points into neighborhoods (SPIN): data analysis and visualization by ordering distance matrices, 10.1093/bioinformatics/bti329
  63. Marques S., Zeisel A., Codeluppi S., van Bruggen D., Mendanha Falcao A., Xiao L., Li H., Haring M., Hochgerner H., Romanov R. A., Gyllborg D., Munoz-Manchado A. B., La Manno G., Lonnerberg P., Floriddia E. M., Rezayee F., Ernfors P., Arenas E., Hjerling-Leffler J., Harkany T., Richardson W. D., Linnarsson S., Castelo-Branco G., Oligodendrocyte heterogeneity in the mouse juvenile and adult central nervous system, 10.1126/science.aaf6463
  64. Fan Jean, Salathia Neeraj, Liu Rui, Kaeser Gwendolyn E, Yung Yun C, Herman Joseph L, Kaper Fiona, Fan Jian-Bing, Zhang Kun, Chun Jerold, Kharchenko Peter V, Characterizing transcriptional heterogeneity through pathway and gene set overdispersion analysis, 10.1038/nmeth.3734
  65. Tasic Bosiljka, Menon Vilas, Nguyen Thuc Nghi, Kim Tae Kyung, Jarsky Tim, Yao Zizhen, Levi Boaz, Gray Lucas T, Sorensen Staci A, Dolbeare Tim, Bertagnolli Darren, Goldy Jeff, Shapovalova Nadiya, Parry Sheana, Lee Changkyu, Smith Kimberly, Bernard Amy, Madisen Linda, Sunkin Susan M, Hawrylycz Michael, Koch Christof, Zeng Hongkui, Adult mouse cortical cell taxonomy revealed by single cell transcriptomics, 10.1038/nn.4216
  66. Fuzik János, Zeisel Amit, Máté Zoltán, Calvigioni Daniela, Yanagawa Yuchio, Szabó Gábor, Linnarsson Sten, Harkany Tibor, Integration of electrophysiological recordings with single-cell RNA-seq data identifies neuronal subtypes, 10.1038/nbt.3443
  67. Sprong Hein, Kruithof Boudewijn, Leijendekker Richtje, Slot Jan Willem, van Meer Gerrit, van der Sluijs Peter, UDP-Galactose:Ceramide Galactosyltransferase Is a Class I Integral Membrane Protein of the Endoplasmic Reticulum, 10.1074/jbc.273.40.25880
  68. Jahn Olaf, Tenzer Stefan, Werner Hauke B., Myelin Proteomics: Molecular Anatomy of an Insulating Sheath, 10.1007/s12035-009-8071-2
  69. Ebrahimi Majid, Yamamoto Yui, Sharifi Kazem, Kida Hiroyuki, Kagawa Yoshiteru, Yasumoto Yuki, Islam Ariful, Miyazaki Hirofumi, Shimamoto Chie, Maekawa Motoko, Mitsushima Dai, Yoshikawa Takeo, Owada Yuji, Astrocyte-expressed FABP7 regulates dendritic morphology and excitatory synaptic function of cortical neurons : Astrocyte FABP7 as a Regulator of Neuronal Morphology, 10.1002/glia.22902
  70. Roy Sudipto, The motile cilium in development and disease: emerging new insights, 10.1002/bies.200900031
  71. Liu Guangwei, Ma Haixia, Jiang Lingling, Zhao Yong, Allograft inflammatory factor-1 and its immune regulation, 10.1080/08916930601083946
  72. Ose A., Kusuhara H., Endo C., Tohyama K., Miyajima M., Kitamura S., Sugiyama Y., Functional Characterization of Mouse Organic Anion Transporting Peptide 1a4 in the Uptake and Efflux of Drugs Across the Blood-Brain Barrier, 10.1124/dmd.109.029454
  73. Li L., Miano J. M., Cserjesi P., Olson E. N., SM22 , a Marker of Adult Smooth Muscle, Is Expressed in Multiple Myogenic Lineages During Embryogenesis, 10.1161/01.res.78.2.188
  74. Tortoriello G., Morris C. V., Alpar A., Fuzik J., Shirran S. L., Calvigioni D., Keimpema E., Botting C. H., Reinecke K., Herdegen T., Courtney M., Hurd Y. L., Harkany T., Miswiring the brain:  9-tetrahydrocannabinol disrupts cortical development by inducing an SCG10/stathmin-2 degradation pathway, 10.1002/embj.201386035
  75. Benjamini Y., J. R. Stat. Soc. Series B Stat. Methodol., 57, 289 (1995)
  76. van der Maaten L., J. Mach. Learn. Res., 9, 2579 (2008)
  77. Dobin Alexander, Davis Carrie A., Schlesinger Felix, Drenkow Jorg, Zaleski Chris, Jha Sonali, Batut Philippe, Chaisson Mark, Gingeras Thomas R., STAR: ultrafast universal RNA-seq aligner, 10.1093/bioinformatics/bts635
  78. Schnell Stephen A., Staines William A., Wessendorf Martin W., Reduction of Lipofuscin-like Autofluorescence in Fluorescently Labeled Tissue, 10.1177/002215549904700601
Bibliographic reference Romanov, Roman A ; Zeisel, Amit ; Bakker, Joanne ; Girach, Fatima ; Hellysaz, Arash ; et. al. Molecular interrogation of hypothalamic organization reveals distinct dopamine neuronal subtypes.. In: Nature Neuroscience, Vol. 20, no. 2, p. 176-188 (Feb 2017)
Permanent URL http://hdl.handle.net/2078.1/179914