The Notch effector gene Hes1 regulates migration of hypothalamic neurons, neuropeptide content and axon targeting to the pituitary

Developmental Biology

Volumn 353, Issue 1, 2011, Pages 61-71

  Aujla, Paven K ^a   Bora, Adriana ^a   Monahan, Pamela ^a   Sweedler, Jonathan V ^a   Raetzman, Lori T ^a  

^a UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

Author keywords

AVP; Development; Hes1; Hypothalamus; Notch; PVN; SON; SS

Indexed keywords

ARGIPRESSIN; GLUTAMATE DECARBOXYLASE 67; NEUROPEPTIDE; SOMATOSTATIN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; BRAIN NERVE CELL; CELL MIGRATION; CELL PROLIFERATION; CONTROLLED STUDY; DIENCEPHALON; EMBRYO; EMBRYO DEVELOPMENT; FEMALE; GENE; HES1 GENE; HYPOPHYSIS; HYPOTHALAMIC PARAVENTRICULAR NUCLEUS; HYPOTHALAMUS; MALE; MOUSE; NERVE CELL NECROSIS; NERVE FIBER; NERVE PROJECTION; NERVE TRACT; NONHUMAN; PERIKARYON; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; SUPRAOPTIC NUCLEUS;

MUS;

EID: 79953761076     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2011.02.018     Document Type: Article

References (52)

1. Akimoto M., Nishimaki T., Arai Y., Uchinuma E., Yamauchi H., Kameda Y. Hes1 regulates formations of the hypophyseal pars tuberalis and the hypothalamus. Cell Tissue Res. 2010, 340:509-521.
2. Alcantara S., Ruiz M., D'Arcangelo G., Ezan F., de Lecea L., Curran T., Sotelo C., Soriano E. Regional and cellular patterns of Reelin mRNA expression in the forebrain of the developing and adult mouse. J. Neurosci. 1998, 18:7779-7799.
3. Altman J., Bayer S.A. Development of the diencephalon in the rat. I. Autoradiographic study of the time of origin and settling patterns of neurons of the hypothalamus. J. Comp. Neurol. 1978, 182:945-971.
4. Altman J., Bayer S.A. Development of the diencephalon in the rat. IV. Quantitative study of the time of origin of neurons and the internuclear chronological gradients in the thalamus. J. Comp. Neurol. 1979, 188:455-471.
5. Bayer S.A., Altman J. Development of the preoptic area: time and site of origin, migratory routes, and settling patterns of its neurons. J. Comp. Neurol. 1987, 265:65-95.
6. Brooks L.R., Chung W.C., Tsai P.S. Abnormal hypothalamic oxytocin system in fibroblast growth factor 8-deficient mice. Endocrine 2010, 38:174-180.
7. Couly G.F., Le Douarin N.M. Mapping of the early neural primordium in quail-chick chimeras. II. The prosencephalic neural plate and neural folds: implications for the genesis of cephalic human congenital abnormalities. Dev. Biol. 1987, 120:198-214.
8. Couly G., Le Douarin N.M. The fate map of the cephalic neural primordium at the presomitic to the 3-somite stage in the avian embryo. Development 1988, 103:101-113. Suppl.
9. Davis A.M., Henion T.R., Tobet S.A. Gamma-aminobutyric acidB receptors and the development of the ventromedial nucleus of the hypothalamus. J. Comp. Neurol. 2002, 449:270-280.
10. Deiner M.S., Sretavan D.W. Altered midline axon pathways and ectopic neurons in the developing hypothalamus of netrin-1- and DCC-deficient mice. J. Neurosci. 1999, 19:9900-9912.
11. Dellovade T.L., Davis A.M., Ferguson C., Sieghart W., Homanics G.E., Tobet S.A. GABA influences the development of the ventromedial nucleus of the hypothalamus. J. Neurobiol. 2001, 49:264-276.
12. Givalois L., Arancibia S., Alonso G., Tapia-Arancibia L. Expression of brain-derived neurotrophic factor and its receptors in the median eminence cells with sensitivity to stress. Endocrinology 2004, 145:4737-4747.
13. Goshu E., Jin H., Lovejoy J., Marion J.F., Michaud J.L., Fan C.M. Sim2 contributes to neuroendocrine hormone gene expression in the anterior hypothalamus. Mol. Endocrinol. 2004, 18:1251-1262.
14. Hashimoto-Torii K., Torii M., Sarkisian M.R., Bartley C.M., Shen J., Radtke F., Gridley T., Sestan N., Rakic P. Interaction between Reelin and notch signaling regulates neuronal migration in the cerebral cortex. Neuron 2008, 60:273-284.
15. Hatakeyama J., Bessho Y., Katoh K., Ookawara S., Fujioka M., Guillemot F., Kageyama R. Hes genes regulate size, shape and histogenesis of the nervous system by control of the timing of neural stem cell differentiation. Development 2004, 131:5539-5550.
16. Heinrichs M., von Dawans B., Domes G. Oxytocin, vasopressin, and human social behavior. Front. Neuroendocrinol. 2009, 30:548-557.
17. Himes A.D., Raetzman L.T. Premature differentiation and aberrant movement of pituitary cells lacking both Hes1 and Prop1. Dev. Biol. 2009, 325:151-161.
18. Hirata H., Tomita K., Bessho Y., Kageyama R. Hes1 and Hes3 regulate maintenance of the isthmic organizer and development of the mid/hindbrain. EMBO J. 2001, 20:4454-4466.
19. Hosoya T., Oda Y., Takahashi S., Morita M., Kawauchi S., Ema M., Yamamoto M., Fujii-Kuriyama Y. Defective development of secretory neurones in the hypothalamus of Arnt2-knockout mice. Genes Cells 2001, 6:361-374.
20. Ishibashi M., Moriyoshi K., Sasai Y., Shiota K., Nakanishi S., Kageyama R. Persistent expression of helix-loop-helix factor Hes-1 prevents mammalian neural differentiation in the central nervous system. EMBO J. 1994, 13:1799-1805.
21. Jensen J., Pedersen E.E., Galante P., Hald J., Heller R.S., Ishibashi M., Kageyama R., Guillemot F., Serup P., Madsen O.D. Control of endodermal endocrine development by Hes-1. Nat. Genet. 2000, 24:36-44.
22. Kabos P., Kabosova A., Neuman T. Blocking HES1 expression initiates GABAergic differentiation and induces the expression of p21(CIP1/WAF1) in human neural stem cells. J. Biol. Chem. 2002, 277:8763-8766.
23. Karim M.A., Sloper J.C. Histogenesis of the supraoptic and paraventricular neurosecretory cells of the mouse hypothalamus. J. Anat. 1980, 130:341-347.
24. Kawamura K., Kikuyama S. Induction from posterior hypothalamus is essential for the development of the pituitary proopiomelacortin (POMC) cells of the toad (Bufo japonicus). Cell Tissue Res. 1995, 279:233-239.
25. Kita A., Imayoshi I., Hojo M., Kitagawa M., Kokubu H., Ohsawa R., Ohtsuka T., Kageyama R., Hashimoto N. Hes1 and Hes5 control the progenitor pool, intermediate lobe specification, and posterior lobe formation in the pituitary development. Mol. Endocrinol. 2007, 21:1458-1466.
26. Kouki T., Imai H., Aoto K., Eto K., Shioda S., Kawamura K., Kikuyama S. Developmental origin of the rat adenohypophysis prior to the formation of Rathke's pouch. Development 2001, 128:959-963.
27. Kramer K.M., Yamamoto Y., Hoffman G.E., Cushing B.S. Estrogen receptor alpha and vasopressin in the paraventricular nucleus of the hypothalamus in peromyscus. Brain Res. 2005, 1032:154-161.
28. Li L., Sweedler J.V. Peptides in our brain: mass spectrometric-based measurement approaches and challenges. Annu. Rev. Anal. Chem. 2008, 1:451-483.
29. Lim M.M., Young L.J. Neuropeptidergic regulation of affiliative behavior and social bonding in animals. Horm. Behav. 2006, 50:506-517.
30. Lim M.M., Bielsky I.F., Young L.J. Neuropeptides and the social brain: potential rodent models of autism. Int. J. Dev. Neurosci. 2005, 23:235-243.
31. Lutolf S., Radtke F., Aguet M., Suter U., Taylor V. Notch1 is required for neuronal and glial differentiation in the cerebellum. Development 2002, 129:373-385.
32. McClellan K.M., Calver A.R., Tobet S.A. GABAB receptors role in cell migration and positioning within the ventromedial nucleus of the hypothalamus. Neuroscience 2008, 151:1119-1131.
33. McClellan K.M., Stratton M.S., Tobet S.A. Roles for gamma-aminobutyric acid in the development of the paraventricular nucleus of the hypothalamus. J. Comp. Neurol. 2010, 518:2710-2728.
34. Metin C., Vallee R.B., Rakic P., Bhide P.G. Modes and mishaps of neuronal migration in the mammalian brain. J. Neurosci. 2008, 28:11746-11752.
35. Michaud J.L., Rosenquist T., May N.R., Fan C.M. Development of neuroendocrine lineages requires the bHLH-PAS transcription factor SIM1. Genes Dev. 1998, 12:3264-3275.
36. Michaud J.L., DeRossi C., May N.R., Holdener B.C., Fan C.M. ARNT2 acts as the dimerization partner of SIM1 for the development of the hypothalamus. Mech. Dev. 2000, 90:253-261.
37. Monahan P., Rybak S., Raetzman L.T. The Notch target gene HES1 regulates cell cycle inhibitor expression in the developing pituitary. Endocrinology 2009, 150:4386-4394.
38. Ohtsuka T., Sakamoto M., Guillemot F., Kageyama R. Roles of the basic helix-loop-helix genes Hes1 and Hes5 in expansion of neural stem cells of the developing brain. J. Biol. Chem. 2001, 276:30467-30474.
39. Prevot V., Dehouck B., Poulain P., Beauvillain J.C., Buee-Scherrer V., Bouret S. Neuronal-glial-endothelial interactions and cell plasticity in the postnatal hypothalamus: implications for the neuroendocrine control of reproduction. Psychoneuroendocrinology 2007, 32(Suppl 1):S46-S51.
40. Prevot V., Bellefontaine N., Baroncini M., Sharif A., Hanchate N.K., Parkash J., Campagne C., de Seranno S. Gonadotrophin-releasing hormone nerve terminals, tanycytes and neurohaemal junction remodelling in the adult median eminence: functional consequences for reproduction and dynamic role of vascular endothelial cells. J. Neuroendocrinol. 2010, 22:639-649.
41. Raetzman L.T., Wheeler B.S., Ross S.A., Thomas P.Q., Camper S.A. Persistent expression of Notch2 delays gonadotrope differentiation. Mol. Endocrinol. 2006, 20:2898-2908.
42. Raetzman L.T., Cai J.X., Camper S.A. Hes1 is required for pituitary growth and melanotrope specification. Dev. Biol. 2007, 304:455-466.
43. Rogers M.C., Silverman A.J., Gibson M.J. Gonadotropin-releasing hormone axons target the median eminence: in vitro evidence for diffusible chemoattractive signals from the mediobasal hypothalamus. Endocrinology 1997, 138:3956-3966.
44. Schuurmans C., Guillemot F. Molecular mechanisms underlying cell fate specification in the developing telencephalon. Curr. Opin. Neurobiol. 2002, 12:26-34.
45. Shimada M., Nakamura T. Time of neuron origin in mouse hypothalamic nuclei. Exp. Neurol. 1973, 41:163-173.
46. Sibbe M., Forster E., Basak O., Taylor V., Frotscher M. Reelin and Notch1 cooperate in the development of the dentate gyrus. J. Neurosci. 2009, 29:8578-8585.
47. Solecki D.J., Liu X.L., Tomoda T., Fang Y., Hatten M.E. Activated Notch2 signaling inhibits differentiation of cerebellar granule neuron precursors by maintaining proliferation. Neuron 2001, 31:557-568.
48. Wetsel W.C., Hill D.F., Ojeda S.R. Basic fibroblast growth factor regulates the conversion of pro-luteinizing hormone-releasing hormone (Pro-LHRH) to LHRH in immortalized hypothalamic neurons. Endocrinology 1996, 137:2606-2616.
49. Xu C., Fan C.M. Allocation of paraventricular and supraoptic neurons requires Sim1 function: a role for a Sim1 downstream gene PlexinC1. Mol. Endocrinol. 2007, 21:1234-1245.
50. Xu C., Fan C.M. Expression of robo/slit and semaphorin/plexin/neuropilin family members in the developing hypothalamic paraventricular and supraoptic nuclei. Gene Expr. Patterns 2008, 8:502-507.
51. Yang X., Tomita T., Wines-Samuelson M., Beglopoulos V., Tansey M.G., Kopan R., Shen J. Notch1 signaling influences v2 interneuron and motor neuron development in the spinal cord. Dev. Neurosci. 2006, 28:102-117.
52. Zhu X., Zhang J., Tollkuhn J., Ohsawa R., Bresnick E.H., Guillemot F., Kageyama R., Rosenfeld M.G. Sustained Notch signaling in progenitors is required for sequential emergence of distinct cell lineages during organogenesis. Genes Dev. 2006, 20:2739-2753.