Ontogeny of neurotrophin receptor TrkC expression in the rat forebrain and anterior hypothalamus with emphasis on the suprachiasmatic nucleus

Neuroscience

Volumn 92, Issue 2, 1999, Pages 705-712

  Hassink, G C ^a   Van Esseveldt, K E ^a   Dijkhuizen, P A ^a   Verhaagen, J ^a   Boer, G J ^a  

^a NETHERLANDS INSTITUTE FOR NEUROSCIENCE   (Netherlands)

Author keywords

Forebrain; Hypothalamus; In situ hybridization; Ontogeny; Suprachiasmatic nucleus; TrkC

Indexed keywords

NEUROTROPHIN RECEPTOR; RECEPTOR PROTEIN;

ANIMAL TISSUE; ANTERIOR HYPOTHALAMUS; ARTICLE; BRAIN DEVELOPMENT; CELL SURVIVAL; FOREBRAIN; GENE OVEREXPRESSION; GESTATIONAL AGE; IN SITU HYBRIDIZATION; NERVE FIBER GROWTH; NONHUMAN; ONTOGENY; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; SUPRACHIASMATIC NUCLEUS; TISSUE DISTRIBUTION;

ANIMALS; ANIMALS, NEWBORN; FEMALE; HYPOTHALAMUS, ANTERIOR; PREGNANCY; PROSENCEPHALON; RATS; RATS, WISTAR; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, TRKC; RECEPTORS, NERVE GROWTH FACTOR; RNA, MESSENGER; SUPRACHIASMATIC NUCLEUS;

EID: 0033040156     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0306-4522(99)00007-X     Document Type: Article

References (44)

1. Aguilar-Roblero R., Drucker-Colin R., Moore R.Y. Behavioral and morphological studies of fetal neural transplants into SCN-lesioned rats. Chronobiol. Int. 9:1992;278-296.
2. Alcantara S., Frisen J., del Rio J.A., Soriano E., Barbacid M., Silos-Santiago I. TrkB signaling is required for postnatal survival of CNS neurons and protects hippocampal and motor neurons from axotomy-induced cell death. J. Neurosci. 17:1997;3623-3633.
3. Allendoerfer K.L., Cabelli R.J., Escandon E., Kaplan D.R., Nikolics K., Shatz C.J. Regulation of neurotrophin receptors during the maturation of the mammalian visual system. J. Neurosci. 14:1994;1795-1811.
4. Altar C.A., Siuciak J.A., Wright P., Ip N.Y., Lindsay R.M., Wiegand S.J. In situ hybridization of trkB and trkC receptor mRNA in rat forebrain and association with high-affinity binding of [125I]BDNF, [125I]NT-4/5 and [125I]NT-3. Eur. J. Neurosci. 6:1994;1389-1405.
5. Altman J., Bayer S.A. Development of the diencephalon. I: Autoradiographic study of time of origin and settling patterns of neurons of the hypothalamus. J. comp. Neurol. 182:1978;945-972.
6. Altman J., Bayer S.A. Development of the diencephalon. IV: Quantitative study of the time of origin of neurons and the internuclear chronological gradients in the thalamus. J. comp. Neurol. 188:1979;455-472.
7. Altman J. and Bayer S. A. (1995) Atlas of Prenatal Rat Brain Development. CRC, Boca Raton, Florida.
8. Anderson K.D., Alderson R.F., Altar C.A., DiStefano P.S., Corcoran T.L., Lindsay R.M., Wiegand S.J. Differential distribution of exogenous BDNF, NGF, and NT-3 in the brain corresponds to the relative abundance and distribution of high-affinity and low-affinity neurotrophin receptors. J. comp. Neurol. 357:1995;296-317.
9. Arenas E., Persson H. Neurotrophin-3 prevents the death of adult central noradrenergic neurons in vivo. Nature. 367:1994;368-375.
10. Barbacid M. The Trk family of neurotrophin receptors. J. Neurobiol. 25:1994;1386-1403.
11. Bayer S.A. Neurogenesis in the rat neostriatum. Int. J. dev. Neurosci. 2:1984;163-175.
12. Biffo S., Offenhauser N., Carter B.D., Barde Y.A. Selective binding and internalisation by truncated receptors restrict the availability of BDNF during development. Development. 121:1995;2461-2470.
13. Boer G. J. (1987) Development of vasopressin systems and their functions. In Vasopressin, Principles and Properties (eds Gash D. M. and Boer G. J.), pp. 117-174. Plenum, New York and London.
14. Boer G.J., Griffioen H.A. Light/dark-induced effects on behavioral rhythms in SCN lesioned rats irrespective of the presence of functional SCN implants. J. interdisc. Cycle Res. 24:1993;118-136.
15. Card J. P. and Moore R. Y. (1991) The organization of visual circuits influencing the circadian activity of the suprachiasmatic nucleus. In Suprachiasmatic Nucleus, the Minds Clock (eds Klein D. C., Moore R. Y. and Reppert S. M.), pp. 51-76. Oxford University Press, New York.
16. Dekker A.J., Winkler J., Ray J., Thal L.J., Gage F.H. Grafting of nerve growth factor-producing fibroblasts reduces behavioral deficits in rats with lesions of the nucleus basalis magnocellularis. Neuroscience. 60:1994;299-309.
17. Emerich D.F., Winn S.R., Harper J., Hammang J.P., Baetge E.E., Kordower J.H. Implants of polymer-encapsulated human NGF-secreting cells in the nonhuman primate: rescue and sprouting of degenerating cholinergic basal forebrain neurons. J. comp. Neurol. 349:1994;148-164.
18. Escandon E., Soppet D., Rosenthal A., Mendoza-Ramirez J.L., Szonyi E., Burton L.E., Henderson C.E., Parada L.F., Nikolics K. Regulation of neurotrophin receptor expression during embryonic and postnatal development. J. Neurosci. 14:1994;2054-2068.
19. Gibbs R.B., Pfaff D.W. In situ hybridization detection of trkA mRNA in the brain: distribution colocalization with p75NGFR and up-regulation by nerve growth factor. J. comp. Neurol. 341:1994;324-339.
20. Giger R.J., Wolfer D.P., De Wit G.M.J., Verhaagen J. Anatomy of rat semaphorin III/collapsin-1 mRNA expression and relationship to developing nerve tracts during neuroembryogenesis. J. comp. Neurol. 375:1996;378-392.
21. Griffioen H.A., Duindam H., van der Woude T.P., Rietveld W.J., Boer G.J. Functional development of fetal suprachiasmatic nucleus grafts in suprachiasmatic nucleus lesioned rats. Brain Res. Bull. 34:1993;145-160.
22. Hantzopoulos P.A., Suri C., Glass D.J., Goldfarb M.P., Yancopoulos G.D. The low affinity NGF receptor, p75, can collaborate with each of the Trks to potentiate functional responses to the neurotrophins. Neuron. 13:1994;187-201.
23. Harvey A.R. Expression of low affinity NGF (p75) receptors in rat superior colliculus: studies in vivo, in vitro, and in fetal tectal grafts. Expl Neurol. 130:1994;237-249.
24. Humpel C., Giacobini M.M., Wetmore C., Olson L. Brain-derived neurotrophic factor and trkB receptor mRNAs in grafts of cortex cerebri. Expl Neurol. 127:1994;171-177.
25. Jung A.B., Bennett J.P. Jr. Development of striatal dopaminergic function. III: Pre- and postnatal development of striatal and cortical mRNAs for the neurotrophin receptors trkBTK+ and trkC and their regulation by synaptic dopamine. Devl Brain Res. 94:1996;133-143.
26. Knüsel B., Rabin S.J., Hefti F., Kaplan D.R. Regulated neurotrophin responsiveness during neuronal migration and early differentiation. J. Neurosci. 14:1994;1542-1554.
27. Lachyankar M.B., Condon P.J., Quesenberry P.J., Litofsky N.S., Recht L.D., Ross A.H. Embryonic precursor cells that express Trk receptors: induction of different cell fates by NGF, BDNF, NT-3, and CNTF. Expl Neurol. 144:1997;350-360.
28. Lamballe F., Smeyne R.J., Barbacid M. Developmental expression of TrkC, the neurotrophin-3 receptor, in the mammalian nervous system. J. Neurosci. 14:1994;14-28.
29. Lehman M. N., Jansen H. T., Wortman M., Stevens P., Kim C., Norgren R. B. and Zeitler P. (1996) Neurotrophin and neurotrophin receptor expression in the suprachiasmatic nucleus of rats and hamsters, Abstract of Society for Neuroscience, p. 1141, Washington, DC.
30. McAllister A.K., Katz L.C., Lo D.C. Neurotrophins regulate dendritic growth in developing visual cortex. Neuron. 15:1995;791-803.
31. McAllister A.K., Katz L.C., Lo D.C. Opposing roles for endogenous BDNF and NT-3 in regulating cortical dendritic growth. Neuron. 18:1997;767-778.
32. McGregor L.M., Baylin S.B., Griffin C.A., Hawkins A.L., Nelkin B.D. Molecular cloning of the cDNA for human TrkC (NTRK3), chromosomal assignment, and evidence for a splice variant. Genomics. 22:1994;267-272.
33. Merlio J.P., Ernfors P., Jaber M., Persson H. Molecular cloning of rat trkC and distribution of cells expressing messenger RNAs for members of the trk family in the rat central nervous system. Neuroscience. 51:1992;513-532.
34. Okazawa H., Kamei M., Kanazawa I. Molecular cloning and expression of a novel truncated form of chicken trkC. Fedn Eur. biochem. Socs Lett. 329:1993;171-177.
35. Pappas I.S., Parnavelas J.G. Neurotrophins and basic fibroblast growth factor induce the differentiation of calbinding-containing neurons in the cerebral cortex. Expl Neurol. 144:1997;302-314.
36. Ringstedt T., Lagercrantz H., Persson H. Expression of members of the trk family in the developing postnatal rat brain. Devl Brain Res. 72:1993;119-131.
37. Saitoh Y., Matsui Y., Nihonmatsu I., Kawamura H. Cross-species transplantation of the suprachiasmatic nuclei from rats to Siberian chipmunks (Eutamias sibiricus) with suprachiasmatic lesions. Neurosci. Lett. 123:1991;77-81.
38. Saitoh Y., Nihonmatsu I., Kawamura H. Location of the suprachiasmatic nucleus grafts in rats which restored circadian rhythmicity after transplantation. Neurosci. Lett. 118:1990;45-48.
39. Sawaki Y., Nihonmatsu I., Kawamura H. Transplantation of the neonatal suprachiasmatic nuclei into rats with complete bilateral suprachiasmatic lesions. Neurosci. Res. 1:1984;67-72.
40. Snyder D.E., Li J., Salton S.R. Comparison of VGF and trk mRNA distributions in the developing and adult nervous systems. Molec. Brain Res. 49:1997;307-311.
41. Tessarollo L., Tsoulfas P., Martin-Zanca D., Gilbert D.J., Jenkins N.A., Copeland N.G., Parada L.F. TrkC, a receptor for neurotrophin-3, is widely expressed in the developing nervous system and in non-neuronal tissues. Development. 118:1993;463-475.
42. Valenzuela D.M., Maisonpierre P.C., Glass D.J., Rojas E., Nunez L., Kong Y., Gies D.R., Stitt T.N., Ip N.Y., Yancopoulos G.D. Alternative forms of rat TrkC with different functional capabilities. Neuron. 10:1993;963-974.
43. Yan Q., Johnson E.M. Jr. An immunohistochemical study of the nerve growth factor receptor in developing rats. J. Neurosci. 8:1988;3481-3498.
44. Yan Q., Matheson C., Sun J., Radeke M.J., Feinstein S.C., Miller J.A. Distribution of intracerebral ventricularly administered neurotrophins in rat brain and its correlation with Trk receptor expression. Expl Neurol. 127:1994;23-36.