Developmental roles of brain histamine

Trends in Neurosciences

Volumn 37, Issue 3, 2014, Pages 159-168

  Panula, Pertti ^a,b   Sundvik, Maria ^a,b   Karlstedt, Kaj ^b  

^a UNIVERSITY OF HELSINKI   (Finland)

^b UNIVERSITY OF HELSINKI   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMALS; BRAIN; CELL DIFFERENTIATION; HISTAMINE; HUMANS; NEURAL STEM CELLS; NEUROGENESIS;

HISTAMINE; HISTAMINE RECEPTOR;

BRAIN DEVELOPMENT; BRAIN STEM; HUMAN; MEDICAL RESEARCH; NERVE CELL DIFFERENTIATION; NERVE CELL PLASTICITY; NONHUMAN; PROTEIN EXPRESSION; REVIEW; STEM CELL; ZEBRA FISH;

EID: 84894440343     PISSN: 01662236     EISSN: 1878108X     Source Type: Journal    
DOI: 10.1016/j.tins.2014.01.001     Document Type: Review

References (94)

1. Vassilatis D.K., et al. The G protein-coupled receptor repertoires of human and mouse. Proc. Natl. Acad. Sci. U.S.A. 2003, 100:4903-4908.
2. Fredriksson R., et al. The G-protein-coupled receptors in the human genome form five main families. Phylogenetic analysis, paralogon groups, and fingerprints. Mol. Pharmacol. 2003, 63:1256-1272.
3. Shimamura T., et al. Structure of the human histamine H1 receptor complex with doxepin. Nature 2011, 475:65-70.
4. Haas H., Panula P. The role of histamine and the tuberomamillary nucleus in the nervous system. Nat. Rev. Neurosci. 2003, 4:121-130.
5. Panula P., Nuutinen S. The histaminergic network in the brain: basic organization and role in disease. Nat. Rev. Neurosci. 2013, 14:472-487.
6. Ohtani N., et al. Dopamine modulates cell cycle in the lateral ganglionic eminence. J. Neurosci. 2003, 23:2840-2850.
7. Hoglinger G.U., et al. Dopamine depletion impairs precursor cell proliferation in Parkinson disease. Nat. Neurosci. 2004, 7:726-735.
8. Cases O., et al. Lack of barrels in the somatosensory cortex of monoamine oxidase A-deficient mice: role of a serotonin excess during the critical period. Neuron 1996, 16:297-307.
9. Salichon N., et al. Excessive activation of serotonin (5-HT) 1B receptors disrupts the formation of sensory maps in monoamine oxidase a and 5-ht transporter knock-out mice. J. Neurosci. 2001, 21:884-896.
10. Panula P., et al. Histamine-containing neurons in the rat hypothalamus. Proc. Natl. Acad. Sci. U.S.A. 1984, 81:2572-2576.
11. Watanabe T., et al. Distribution of the histaminergic neuron system in the central nervous system of rats; a fluorescent immunohistochemical analysis with histidine decarboxylase as a marker. Brain Res. 1984, 295:13-25.
12. Molina-Hernandez A., et al. Histamine in brain development. J. Neurochem. 2012, 122:872-882.
13. Auvinen S., Panula P. Development of histamine-immunoreactive neurons in the rat brain. J. Comp. Neurol. 1988, 276:289-303.
14. Kahlson G., et al. The site of increased formation of histamine in the pregnant rat. J. Physiol. 1958, 144:337-348.
15. Nissinen M.J., et al. Expression of histidine decarboxylase and cellular histamine-like immunoreactivity in rat embryogenesis. J. Histochem. Cytochem. 1995, 43:1241-1252.
16. Nissinen M.J., Panula P. Developmental patterns of histamine-like immunoreactivity in the mouse. J. Histochem. Cytochem. 1995, 43:211-227.
17. Kinnunen A., Panula P. Histamine and tyrosine hydroxylase in developing rat brain. Agents Actions 1991, 33:108-111.
18. Jutel M., et al. Histamine regulates T-cell and antibody responses by differential expression of H1 and H2 receptors. Nature 2001, 413:420-425.
19. Ohtsu H., et al. Mice lacking histidine decarboxylase exhibit abnormal mast cells. FEBS Lett. 2001, 502:53-56.
20. Nakamura E., et al. Lack of histamine alters gastric mucosal morphology: comparison of histidine decarboxylase-deficient and mast cell-deficient mice. Am. J. Physiol. Gastrointest. Liver Physiol. 2004, 287:G1053-G1061.
21. Fitzpatrick L.A., et al. Targeted deletion of histidine decarboxylase gene in mice increases bone formation and protects against ovariectomy-induced bone loss. Proc. Natl. Acad. Sci. U.S.A 2003, 100:6027-6032.
22. Yang X.D., et al. Histamine deficiency promotes inflammation-associated carcinogenesis through reduced myeloid maturation and accumulation of CD11b+Ly6G+ immature myeloid cells. Nat. Med. 2011, 17:87-95.
23. Vanhala A., et al. Distribution of histamine-, 5-hydroxytryptamine-, and tyrosine hydroxylase-immunoreactive neurons and nerve fibers in developing rat brain. J. Comp. Neurol. 1994, 347:101-114.
24. Reiner P.B., et al. Ontogeny of histidine-decarboxylase-immunoreactive neurons in the tuberomammillary nucleus of the rat hypothalamus: time of origin and development of transmitter phenotype. J. Comp. Neurol. 1988, 276:304-311.
25. Tuomisto L., Panula P. Development of histaminergic neurons. Histaminergic Neurons: Morphology and Function 1991, 177-192. CRC Press. T. Watanabe, H. Wada (Eds.).
26. Kinnunen A., et al. In situ detection of H1-receptor mRNA and absence of apoptosis in the transient histamine system of the embryonic rat brain. J. Comp. Neurol. 1998, 394:127-137.
27. Dulcis D., et al. Neurotransmitter switching in the adult brain regulates behavior. Science 2013, 340:449-453.
28. Eriksson K.S., et al. Development of the histaminergic neurons and expression of histidine decarboxylase mRNA in the zebrafish brain in the absence of all peripheral histaminergic systems. Eur. J. Neurosci. 1998, 10:3799-3812.
29. Karlstedt K., et al. Regional expression of the histamine H-2 receptor in adult and developing rat brain. Neuroscience 2001, 102:201-208.
30. Heron A., et al. Expression analysis of the histamine H-3 receptor in developing rat tissues. Mech. Dev. 2001, 105:167-173.
31. Karlstedt K., et al. Expression of the H-3 receptor in the developing CNS and brown fat suggests novel roles for histamine. Mol. Cell. Neurosci. 2003, 24:614-622.
32. Molina-Hernandez A., Velasco I. Histamine induces neural stem cell proliferation and neuronal differentiation by activation of distinct histamine receptors. J. Neurochem. 2008, 106:706-717.
33. Bernardino L., et al. Histamine stimulates neurogenesis in the rodent subventricular zone. Stem Cells 2012, 30:773-784.
34. Rodriguez-Martinez G., et al. Histamine is required during neural stem cell proliferation to increase neuron differentiation. Neuroscience 2012, 216:10-17.
35. Molina-Hernandez A., et al. Histamine up-regulates fibroblast growth factor receptor 1 and increases FOXP2 neurons in cultured neural precursors by histamine type 1 receptor activation: conceivable role of histamine in neurogenesis during cortical development in vivo. Neural Dev. 2013, 8:4.
36. Gaspard N., et al. An intrinsic mechanism of corticogenesis from embryonic stem cells. Nature 2008, 455:351-357.
37. Schuurmans C., et al. Sequential phases of cortical specification involve Neurogenin-dependent and -independent pathways. EMBO J. 2004, 23:2892-2902.
38. Panula P., et al. Histamine-immunoreactive nerve fibers in the rat brain. Neuroscience 1989, 28:585-610.
39. Kukko-Lukjanov T.K., Panula P. Subcellular distribution of histamine, GABA and galanin in tuberomamillary neurons in vitro. J. Chem. Neuroanat. 2003, 25:279-292.
40. Sundvik M., Panula P. The organization of the histaminergic system in adult zebrafish (Danio rerio) brain: neuron number, location and co-transmitters. J. Comp. Neurol. 2012, 520:3827-3845.
41. Kaslin J., Panula P. Comparative anatomy of the histaminergic and other aminergic systems in zebrafish (Danio rerio). J. Comp. Neurol. 2001, 440:342-377.
42. de Oliveira-Carlos V., et al. Notch receptor expression in neurogenic regions of the adult zebrafish brain. PLoS ONE 2013, 8:e73384.
43. Sherrington R., et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature 1995, 375:754-760.
44. Capell A., et al. Presenilin-1 differentially facilitates endoproteolysis of the beta-amyloid precursor protein and Notch. Nat. Cell Biol. 2000, 2:205-211.
45. Imayoshi I., et al. Essential roles of Notch signaling in maintenance of neural stem cells in developing and adult brains. J. Neurosci. 2010, 30:3489-3498.
46. Sundvik M., et al. Presenilin1 regulates histamine neuron development and behavior in zebrafish, danio rerio. J. Neurosci. 2013, 33:1589-1597.
47. Sundvik M., et al. The histaminergic system regulates wakefulness and orexin/hypocretin neuron development via histamine receptor H1 in zebrafish. FASEB J. 2011, 25:4338-4347.
48. Peitsaro N., et al. Identification of zebrafish histamine H1, H2 and H3 receptors and effects of histaminergic ligands on behavior. Biochem. Pharmacol. 2007, 73:1205-1214.
49. Eriksson K.S., et al. Orexin/hypocretin excites the histaminergic neurons of the tuberomammillary nucleus. J. Neurosci. 2001, 21:9273-9279.
50. Kaslin J., et al. The orexin/hypocretin system in zebrafish is connected to the aminergic and cholinergic systems. J. Neurosci. 2004, 24:2678-2689.
51. John J., et al. Greatly increased numbers of histamine cells in human narcolepsy with cataplexy. Ann. Neurol. 2013, 10.1002/ana.23968.
52. Nishino S., et al. Decreased CSF histamine in narcolepsy with and without low CSF hypocretin-1 in comparison to healthy controls. Sleep 2009, 32:175-180.
53. Bassetti C.L., et al. Cerebrospinal fluid histamine levels are decreased in patients with narcolepsy and excessive daytime sleepiness of other origin. J. Sleep Res. 2010, 19:620-623.
54. Thebault S., et al. Narcolepsy and H1N1 vaccination: a link?. Curr. Opin. Pulm. Med. 2013, 19:587-593.
55. Karlstedt K., et al. Multiple sites of L-histidine decarboxylase expression in mouse suggest novel developmental functions for histamine. Dev. Dyn. 2001, 221:81-91.
56. Budick S.A., O'Malley D.M. Locomotor repertoire of the larval zebrafish: swimming, turning and prey capture. J. Exp. Biol. 2000, 203:2565-2579.
57. Burgess H.A., Granato M. Sensorimotor gating in larval zebrafish. J. Neurosci. 2007, 27:4984-4994.
58. Zhdanova I.V., et al. Melatonin promotes sleep-like state in zebrafish. Brain Res. 2001, 903:263-268.
59. Rink E., Wullimann M.F. Connections of the ventral telencephalon (subpallium) in the zebrafish (Danio rerio). Brain Res. 2004, 1011:206-220.
60. Sallinen V., et al. MPTP and MPP+ target specific aminergic cell populations in larval zebrafish. J. Neurochem. 2009, 108:719-731.
61. Tay T.L., et al. Comprehensive catecholaminergic projectome analysis reveals single-neuron integration of zebrafish ascending and descending dopaminergic systems. Nat. Commun. 2011, 2:171.
62. Striedter G.F. The diencephalon of the channel catfish, Ictalurus punctatus. II. Retinal, tectal, cerebellar and telencephalic connections. Brain Behav. Evol. 1990, 36:355-377.
63. Scholpp S., Lumsden A. Building a bridal chamber: development of the thalamus. Trends Neurosci. 2010, 33:373-380.
64. Knopf F., et al. Bone regenerates via dedifferentiation of osteoblasts in the zebrafish fin. Dev. Cell 2011, 20:713-724.
65. Kizil C., et al. Regenerative neurogenesis from neural progenitor cells requires injury-induced expression of Gata3. Dev. Cell 2012, 23:1230-1237.
66. Zupanc G.K., et al. Proliferation, migration, neuronal differentiation, and long-term survival of new cells in the adult zebrafish brain. J. Comp. Neurol. 2005, 488:290-319.
67. Adolf B., et al. Conserved and acquired features of adult neurogenesis in the zebrafish telencephalon. Dev. Biol. 2006, 295:278-293.
68. Kaslin J., et al. Proliferation, neurogenesis and regeneration in the non-mammalian vertebrate brain. Philos. Trans. R. Soc. Lond. B: Biol. Sci. 2008, 363:101-122.
69. Bedard A., Parent A. Evidence of newly generated neurons in the human olfactory bulb. Brain Res. Dev. Brain Res. 2004, 151:159-168.
70. Altman J. Autoradiographic and histological studies of postnatal neurogenesis. IV. Cell proliferation and migration in the anterior forebrain, with special reference to persisting neurogenesis in the olfactory bulb. J. Comp. Neurol. 1969, 137:433-457.
71. Altman J., Das G.D. Post-natal origin of microneurones in the rat brain. Nature 1965, 207:953-956.
72. Altman J., Das G.D. Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats. J. Comp. Neurol. 1965, 124:319-335.
73. Migaud M., et al. Emerging new sites for adult neurogenesis in the mammalian brain: a comparative study between the hypothalamus and the classical neurogenic zones. Eur. J. Neurosci. 2010, 32:2042-2052.
74. Li J., et al. IKKbeta/NF-kappaB disrupts adult hypothalamic neural stem cells to mediate a neurodegenerative mechanism of dietary obesity and pre-diabetes. Nat. Cell Biol. 2012, 14:999-1012.
75. Matsuzaki K., et al. Proliferation of neuronal progenitor cells and neuronal differentiation in the hypothalamus are enhanced in heat-acclimated rats. Pflugers Arch. 2009, 458:661-673.
76. Batailler M., et al. DCX expressing cells in the vicinity of the hypothalamic neurogenic niche: a comparative study between mouse, sheep and human tissues. J. Comp. Neurol. 2013, 10.1002/cne.23514.
77. Kokoeva M.V., et al. Neurogenesis in the hypothalamus of adult mice: potential role in energy balance. Science 2005, 310:679-683.
78. Ryu S., et al. Orthopedia homeodomain protein is essential for diencephalic dopaminergic neuron development. Curr. Biol. 2007, 17:873-880.
79. Smidt M.P., Burbach J.P. How to make a mesodiencephalic dopaminergic neuron. Nat. Rev. Neurosci. 2007, 8:21-32.
80. Veenvliet J.V., et al. Specification of dopaminergic subsets involves interplay of En1 and Pitx3. Development 2013, 140:4116.
81. Sallinen V., et al. Hyperserotonergic phenotype after monoamine oxidase inhibition in larval zebrafish. J. Neurochem. 2009, 109:403-415.
82. Mahler J., et al. DeltaA/DeltaD regulate multiple and temporally distinct phases of notch signaling during dopaminergic neurogenesis in zebrafish. J. Neurosci. 2010, 30:16621-16635.
83. Del Giacco L., et al. Differential regulation of the zebrafish orthopedia 1 gene during fate determination of diencephalic neurons. BMC Dev. Biol. 2006, 6:50.
84. Eaton J.L., Glasgow E. The zebrafish bHLH PAS transcriptional regulator, single-minded 1 (sim1), is required for isotocin cell development. Dev. Dyn. 2006, 235:2071-2082.
85. Reifers F., et al. Fgf8 is mutated in zebrafish acerebellar (ace) mutants and is required for maintenance of midbrain-hindbrain boundary development and somitogenesis. Development 1998, 125:2381-2395.
86. Rhinn M., et al. Cloning, expression and relationship of zebrafish gbx1 and gbx2 genes to Fgf signaling. Mech. Dev. 2003, 120:919-936.
87. Thisse B., et al. Spatial and temporal expression of the zebrafish genome by large-scale in situ hybridization screening. Methods Cell Biol. 2004, 77:505-519.
88. Thisse B., Thisse C. Functions and regulations of fibroblast growth factor signaling during embryonic development. Dev. Biol. 2005, 287:390-402.
89. Zeng L., Childs S.J. The smooth muscle microRNA miR-145 regulates gut epithelial development via a paracrine mechanism. Dev. Biol. 2012, 367:178-186.
90. Kastenhuber E., et al. Genetic dissection of dopaminergic and noradrenergic contributions to catecholaminergic tracts in early larval zebrafish. J. Comp. Neurol. 2010, 518:439-458.
91. Filippi A., et al. Expression of the paralogous tyrosine hydroxylase encoding genes th1 and th2 reveals the full complement of dopaminergic and noradrenergic neurons in zebrafish larval and juvenile brain. J. Comp. Neurol. 2010, 518:423-438.
92. Pattyn A., et al. Ascl1/Mash1 is required for the development of central serotonergic neurons. Nat. Neurosci. 2004, 7:589-595.
93. Ercan-Sencicek A.G., et al. L-histidine decarboxylase and Tourette's syndrome. N. Engl. J. Med. 2010, 362:1901-1908.
94. Valko P.O., et al. Increase of histaminergic tuberomammillary neurons in narcolepsy. Ann. Neurol. 2013, 10.1002/ana.24019.