Developmental origins of central norepinephrine neuron diversity

Nature Neuroscience

Volumn 16, Issue 8, 2013, Pages 1016-1023

  Robertson, Sabrina D ^a   Plummer, Nicholas W ^a   De Marchena, Jacqueline ^a   Jensen, Patricia ^a  

^a NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

NORADRENALIN;

ANATOMIC LANDMARK; ANIMAL CELL; ANIMAL TISSUE; APPETITE; AROUSAL; ARTICLE; ATTENTION; BASOLATERAL AMYGDALA; CELL POPULATION; CELL STRUCTURE; HOMEOSTASIS; INSULA; LOCUS CERULEUS; MEMORY; MOOD; MOUSE; NERVE CELL; NERVE FIBER; NONHUMAN; PHYSIOLOGICAL PROCESS; PONTINE NUCLEUS; PREFRONTAL CORTEX; PRIORITY JOURNAL; RHOMBENCEPHALON; STRIA TERMINALIS;

ADRENERGIC FIBERS; ADRENERGIC NEURONS; AFFERENT PATHWAYS; ANIMALS; AXONS; CELL COUNT; CELL LINEAGE; DOPAMINE BETA-HYDROXYLASE; FEMALE; GENES, REPORTER; GREEN FLUORESCENT PROTEINS; LOCUS COERULEUS; MALE; MICE; NERVE TISSUE PROTEINS; NEURAL STEM CELLS; NEUROGENESIS; NOREPINEPHRINE; ORGAN SPECIFICITY; PREFRONTAL CORTEX; RECOMBINANT FUSION PROTEINS; RHOMBENCEPHALON;

EID: 84880924300     PISSN: 10976256     EISSN: 15461726     Source Type: Journal    
DOI: 10.1038/nn.3458     Document Type: Article

References (58)

1. Berridge, C.W. & Waterhouse, B.D. The locus coeruleus-noradrenergic system: modulation of behavioral state and state-dependent cognitive processes. Brain Res. Brain Res. Rev. 42, 33-84 (2003). (Pubitemid 36369264)
2. Rinaman, L. Hindbrain noradrenergic A2 neurons: diverse roles in autonomic, endocrine, cognitive, and behavioral functions. Am. J. Physiol. Regul. Integr. Comp. Physiol. 300, R222-R235 (2011).
3. Sara, S.J. & Bouret, S. Orienting and reorienting: the locus coeruleus mediates cognition through arousal. Neuron 76, 130-141 (2012).
4. Dahlström, A. & Fuxe, K. Evidence for the existence of monoamine containing neurons in the central nervous system, I. Demonstration of monoamines in the cell bodies of brain stem neurons. Acta Physiol. Scand. 62 (suppl. 232): 1-55 (1964).
5. Grzanna, R. & Fritschy, J.M. Efferent projections of different subpopulations of central noradrenaline neurons. Prog. Brain Res. 88, 89-101 (1991).
6. German, D.C. et al. Disease-specific patterns of locus coeruleus cell loss. Ann. Neurol. 32, 667-676 (1992).
7. Brunnström, H., Friberg, N., Lindberg, E. & Englund, E. Differential degeneration of the locus coeruleus in dementia subtypes. Clin. Neuropathol. 30, 104-110 (2011).
8. Benarroch, E.E., Schmeichel, A.M., Low, P.A., Sandroni, P. & Parisi, J.E. Loss of A5 noradrenergic neurons in multiple system atrophy. Acta Neuropathol. 115, 629-634 (2008).
9. Bertrand, E., Lechowicz, W., Szpak, G.M. & Dymecki, J. Qualitative and quantitative analysis of locus coeruleus neurons in Parkinson's disease. Folia Neuropathol. 35, 80-86 (1997). (Pubitemid 127535387)
10. Miller, M.A., Kolb, P.E., Leverenz, J.B., Peskind, E.R. & Raskind, M.A. Preservation of noradrenergic neurons in the locus ceruleus that coexpress galanin mRNA in Alzheimer's disease. J. Neurochem. 73, 2028-2036 (1999). (Pubitemid 29491817)
11. Busch, C., Bohl, J. & Ohm, T.G. Spatial, temporal and numeric analysis of Alzheimer changes in the nucleus coeruleus. Neurobiol. Aging 18, 401-406 (1997). (Pubitemid 27435082)
12. Mohideen, S.S., Ichihara, G., Ichihara, S. & Nakamura, S. Exposure to 1-bromopropane causes degeneration of noradrenergic axons in the rat brain. Toxicology 285, 67-71 (2011).
13. Soulage, C. et al. Central and peripheral changes in catecholamine biosynthesis and turnover in rats after a short period of ozone exposure. Neurochem. Int. 45, 979-986 (2004). (Pubitemid 39164922)
14. Del Pino, J. et al. Effects of prenatal and postnatal exposure to amitraz on norepinephrine, serotonin and dopamine levels in brain regions of male and female rats. Toxicology 287, 145-152 (2011).
15. Slotkin, T.A. & Seidler, F.J. Mimicking maternal smoking and pharmacotherapy of preterm labor: fetal nicotine exposure enhances the effect of late gestational dexamethasone treatment on noradrenergic circuits. Brain Res. Bull. 86, 435-440 (2011).
16. Swanson, L.W. The locus coeruleus: a cytoarchitectonic, Golgi and immunohistochemical study in the albino rat. Brain Res. 110, 39-56 (1976).
17. Dymecki, S.M. & Kim, J.C. Molecular neuroanatomy's "three Gs": a primer. Neuron 54, 17-34 (2007).
18. Champagnat, J., Morin-Surun, M.P., Fortin, G. & Thoby-Brisson, M. Developmental basis of the rostro-caudal organization of the brainstem respiratory rhythm generator. Phil. Trans. R. Soc. Lond. B 364, 2469-2476 (2009).
19. Gray, P.A. et al. Developmental origin of preBotzinger complex respiratory neurons. J. Neurosci. 30, 14883-14895 (2010).
20. Grossmann, K.S., Giraudin, A., Britz, O., Zhang, J. & Goulding, M. Genetic dissection of rhythmic motor networks in mice. Prog. Brain Res. 187, 19-37 (2010).
21. Dasen, J.S. & Jessell, T.M. Hox networks and the origins of motor neuron diversity. Curr. Top. Dev. Biol. 88, 169-200 (2009).
22. Lumsden, A. & Krumlauf, R. Patterning the vertebrate neuraxis. Science 274, 1109-1115 (1996). (Pubitemid 26389266)
23. Krumlauf, R. et al. Hox homeobox genes and regionalisation of the nervous system. J. Neurobiol. 24, 1328-1340 (1993). (Pubitemid 23307850)
24. Chambers, D. et al. Rhombomere-specific analysis reveals the repertoire of genetic cues expressed across the developing hindbrain. Neural Dev. 4, 6 (2009).
25. Aroca, P., Lorente-Canovas, B., Mateos, F.R. & Puelles, L. Locus coeruleus neurons originate in alar rhombomere 1 and migrate into the basal plate: Studies in chick and mouse embryos. J. Comp. Neurol. 496, 802-818 (2006).
26. Gaufo, G.O., Wu, S. & Capecchi, M.R. Contribution of Hox genes to the diversity of the hindbrain sensory system. Development 131, 1259-1266 (2004). (Pubitemid 38443880)
27. Simon, H.H., Scholz, C. & O'Leary, D.D. Engrailed genes control developmental fate of serotonergic and noradrenergic neurons in mid- and hindbrain in a gene dose-dependent manner. Mol. Cell Neurosci. 28, 96-105 (2005). (Pubitemid 39656015)
28. Awatramani, R., Soriano, P., Rodriguez, C., Mai, J.J. & Dymecki, S.M. Cryptic boundaries in roof plate and choroid plexus identified by intersectional gene activation. Nat. Genet. 35, 70-75 (2003). (Pubitemid 37048598)
29. Farago, A.F., Awatramani, R.B. & Dymecki, S.M. Assembly of the brainstem cochlear nuclear complex is revealed by intersectional and subtractive genetic fate maps. Neuron 50, 205-218 (2006).
30. Jensen, P. et al. Redefining the serotonergic system by genetic lineage. Nat. Neurosci. 11, 417-419 (2008). (Pubitemid 351441875)
31. Bang, S.J., Jensen, P., Dymecki, S.M. & Commons, K.G. Projections and interconnections of genetically defined serotonin neurons in mice. Eur. J. Neurosci. 35, 85-96 (2012).
32. Engleka, K.A. et al. Islet1 derivatives in the heart are of both neural crest and second heart field origin. Circ. Res. 110, 922-926 (2012).
33. Li, J.Y., Lao, Z. & Joyner, A.L. Changing requirements for Gbx2 in development of the cerebellum and maintenance of the mid/hindbrain organizer. Neuron 36, 31-43 (2002).
34. Voiculescu, O., Charnay, P. & Schneider-Maunoury, S. Expression pattern of a Krox-20/Cre knock-in allele in the developing hindbrain, bones, and peripheral nervous system. Genesis 26, 123-126 (2000). (Pubitemid 30158095)
35. O'Gorman, S. Second branchial arch lineages of the middle ear of wild-type and Hoxa2 mutant mice. Dev. Dyn. 234, 124-131 (2005). (Pubitemid 41192756)
36. Goridis, C. & Rohrer, H. Specification of catecholaminergic and serotonergic neurons. Nat. Rev. Neurosci. 3, 531-541 (2002). (Pubitemid 135706663)
37. Paxinos, G. & Franklin, K.B.J. The Mouse Brain in Stereotaxic Coordinates (Elsevier Academic, 2004).
38. Hökfelt, T., Fuxe, K., Goldstein, M. & Johansson, O. Evidence for adrenaline neurons in the rat brain. Acta Physiol. Scand. 89, 286-288 (1973).
39. Garel, S., Garcia-Dominguez, M. & Charnay, P. Control of the migratory pathway of facial branchiomotor neurones. Development 127, 5297-5307 (2000). (Pubitemid 32049186)
40. Fritschy, J.M. & Grzanna, R. Distribution of locus coeruleus axons within the rat brainstem demonstrated by Phaseolus vulgaris leucoagglutinin anterograde tracing in combination with dopamine-beta-hydroxylase immunofluorescence. J. Comp. Neurol. 293, 616-631 (1990). (Pubitemid 20111769)
41. Aston-Jones, G. & Cohen, J.D. An integrative theory of locus coeruleus-norepinephrine function: adaptive gain and optimal performance. Annu. Rev. Neurosci. 28, 403-450 (2005). (Pubitemid 41098911)
42. Lorang, D., Amara, S.G. & Simerly, R.B. Cell-type-specific expression of catecholamine transporters in the rat brain. J. Neurosci. 14, 4903-4914 (1994). (Pubitemid 24237912)
43. Sawchenko, P.E. & Swanson, L.W. Central noradrenergic pathways for the integration of hypothalamic neuroendocrine and autonomic responses. Science 214, 685-687 (1981). (Pubitemid 12208596)
44. Mejías-Aponte, C.A., Drouin, C. & Aston-Jones, G. Adrenergic and noradrenergic innervation of the midbrain ventral tegmental area and retrorubral field: prominent inputs from medullary homeostatic centers. J. Neurosci. 29, 3613-3626 (2009).
45. Chandler, D. & Waterhouse, B.D. Evidence for broad versus segregated projections from cholinergic and noradrenergic nuclei to functionally and anatomically discrete subregions of prefrontal cortex. Front. Behav. Neurosci. 6, 20 (2012).
46. Forray, M.I., Gysling, K., Andres, M.E., Bustos, G. & Araneda, S. Medullary noradrenergic neurons projecting to the bed nucleus of the stria terminalis express mRNA for the NMDA-NR1 receptor. Brain Res. Bull. 52, 163-169 (2000). (Pubitemid 30261505)
47. Myers, E.A., Banihashemi, L. & Rinaman, L. The anxiogenic drug yohimbine activates central viscerosensory circuits in rats. J. Comp. Neurol. 492, 426-441 (2005). (Pubitemid 41572460)
48. Davenport, P.W. & Vovk, A. Cortical and subcortical central neural pathways in respiratory sensations. Respir. Physiol. Neurobiol. 167, 72-86 (2009).
49. Adams, D.J. et al. A genome-wide, end-sequenced 129Sv BAC library resource for targeting vector construction. Genomics 86, 753-758 (2005). (Pubitemid 41752956)
50. Warming, S., Costantino, N., Court, D.L., Jenkins, N.A. & Copeland, N.G. Simple and highly efficient BAC recombineering using galK selection. Nucleic Acids Res. 33, e36 (2005).
51. Raymond, C.S. & Soriano, P. High-efficiency FLP and PhiC31 site-specific recombination in mammalian cells. PLoS ONE 2, e162 (2007).
52. Liu, P., Jenkins, N.A. & Copeland, N.G. A highly efficient recombineering-based method for generating conditional knockout mutations. Genome Res. 13, 476-484 (2003). (Pubitemid 36395405)
53. Thomas, S.A., Marck, B.T., Palmiter, R.D. & Matsumoto, A.M. Restoration of norepinephrine and reversal of phenotypes in mice lacking dopamine beta-hydroxylase. J. Neurochem. 70, 2468-2476 (1998). (Pubitemid 28252372)
54. Thomas, S.A., Matsumoto, A.M. & Palmiter, R.D. Noradrenaline is essential for mouse fetal development. Nature 374, 643-646 (1995).
55. Lewandoski, M., Meyers, E.N. & Martin, G.R. Analysis of Fgf8 gene function in vertebrate development. Cold Spring Harb. Symp. Quant. Biol. 62, 159-168 (1997). (Pubitemid 28198533)
56. Kimmel, R.A. et al. Two lineage boundaries coordinate vertebrate apical ectodermal ridge formation. Genes Dev. 14, 1377-1389 (2000). (Pubitemid 30397081)
57. Jin, S.H., Kim, H.J., Harris, D.C. & Thomas, S.A. Postnatal development of the cerebellum and the CNS adrenergic system is independent of norepinephrine and epinephrine. J. Comp. Neurol. 477, 300-309 (2004). (Pubitemid 39129613)
58. Schofield, B.R. Retrograde axonal tracing with fluorescent markers. Curr. Protoc. Neurosci. Ch. 1, Unit 1 17 (2008).