Neural cells without functional N-Methyl-D-Aspartate (NMDA) receptors contribute extensively to normal postnatal brain development in efficiently generated chimaeric NMDA R1 -/- ↔ +/+ mice

Developmental Biology

Volumn 262, Issue 1, 2003, Pages 119-136

  Maskos, U ^a,b   McKay, R D G ^a  

^a NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^b INSTITUT PASTEUR   (France)

Author keywords

Chimaeras; Differentiation; Embryonic stem cells; Migration; Neurodevelopment; NMDA receptor

Indexed keywords

BETA GALACTOSIDASE; GLUTAMIC ACID; IONOTROPIC RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BLASTOCYTE; BRAIN DEVELOPMENT; BRAIN NERVE CELL; CELL SURVIVAL; CHIMERA; CONTROLLED STUDY; EMBRYO; EMBRYO DEVELOPMENT; FEMALE; GENE; HETEROZYGOSITY; HOMOZYGOSITY; KNOCKOUT MOUSE; LACZ GENE; MALE; MATING; NONHUMAN; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; WILD TYPE;

ANIMALIA; CHIMAERIFORMES;

EID: 0141794066     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0012-1606(03)00354-3     Document Type: Article

References (51)

1. Altman, J., Bayer, S.A., 1997. The Cerebellar System CRC Press, Boca Raton.
2. Blanton M.G., Lo Turco J.J., Kriegstein A.R. Endogenous neurotransmitter activates N-methyl-D-aspartate receptors on differentiating neurons in embryonic cortex. Proc. Natl. Acad. Sci. USA. 87:1990;8027-8030.
3. Bliss T.V., Collingridge G.L. A synaptic model of memory long-term potentiation in the hippocampus . Nature. 361:1993;31-39.
4. Brüstle O., Maskos U., McKay R.D.G. Host-guided migration allows targeted introduction of neurons into the embryonic brain. Neuron. 15:1995;1275-1285.
5. Capecchi M.R. Altering the genome by homologous recombination. Science. 244:1989;1288-1292.
6. Cepeda C., Li Z., Levine M.S. Aging reduces neostriatal responsiveness to N-methyl-D-aspartate and dopamine an in vitro electrophysiological study . Neuroscience. 73:1996;733-750.
7. Chalfie M., Tu Y., Euskichen G., Ward W.W., Prasher D.C. Green fluorescent protein as a marker for gene expression. Science. 263:1994;802-805.
8. Chernevskaya N.I., Obukhov A.G., Krishtal O.A. NMDA receptor agonists selectively block N-type calcium channels in hippocampal neurons. Nature. 349:1991;418-420.
9. Constantine-Paton M., Cline H.T., Debski E. Patterned activity, synaptic convergence, and the NMDA receptor in developing visual pathways. Annu. Rev. Neurosci. 13:1990;129-154.
10. Durand G.M., Kovalchuk Y., Konnerth A. Long-term potentiation and functional synapse induction in developing hippocampus. Nature. 381:1996;71-75.
11. Forrest D., Yuzaki M., Soares H.D., Ng L., Luk D.C., Sheng M., Stewart C.L., Morgan J.I., Connor J.A., Curran T. Targeted disruption of NMDA receptor 1 gene abolishes NMDA response and results in neonatal death. Neuron. 13:1994;325-338.
12. Friedrich G., Soriano P. Promoter traps in embryonic stem cells a genetic screen to identify and mutate developmental genes in mice . Genes Dev. 5:1991;1513-1523.
13. Gould E., Cameron H.A., McEwen B.S. Blockade of NMDA receptors increases cell death and birth in the developing rat dentate gyrus. J. Comp. Neurol. 340:1994;551-565.
14. Hogan B., Beddington R., Constantini F., Lacy E. Manipulating the Mouse Embryo. 1994;Cold Spring Harbor Laboratory Press, Cold Spring Harbon ny.
15. Ikonomidou C., Bosch F., Miksa M., Bittigau P., Vöckler J., Dikranian K., Tenkova T.I., Stefovska V., Turski L., Olney J.W. Blockade of NMDA receptors and apoptotic neurodegeneration in the developing brain. Science. 283:1999;70-74.
16. Inagaki N., Kuromi H., Gonoi T., Okamoto Y., Ishida H., Seine Y., Kaneko T., Iwanaga T., Seino S. Expression and role of ionotropic glutamate receptors in pancreatic islet cells. FASEB J. 9:1995;686-691.
17. Iwasato T., Erzurumlu R.S., Huerta P.T., Chen D.F., Sasaoka T., Ulupinar E., Tonegawa S. NMDA receptor-dependent refinement of somatotopic maps. Neuron. 19:1997;1201-1210.
18. Jerecic J., Schulze C.H., Jonas P., Sprengel R., Seeburg P.H., Bischofberger J. Impaired NMDA receptor function in mouse olfactory bulb neurons by tetracycline-sensitive NR1 (N598R) expression. Mol. Brain Res. 94:2001;96-104.
19. Komuro H., Rakic P. Modulation of neuronal migration by NMDA receptors. Science. 260:1993;95-97.
20. Laird P.W., Zijderveld A., Linders K., Rudnicki M.A., Jaenisch R., Berns A. Simplified mammalian DNA isolation procedure. Nucleic Acids Res. 19:1991;4293.
21. Li Y., Erzurumlu R.S., Chen C., Jhaveri S., Tonegawa S. Whisker-related neuronal patterns fail to develop in the trigeminal brainstem nuclei of NMDAR1 knockout mice. Cell. 76:1994;427-437.
22. Luque J.M., Richards J.G. Expression of NMDA 2B receptor subunit mRNA in Bergmann glia. Glia. 13:1995;228-232.
23. Margeta-Mitrovic M., Mitrovic I., Riley R.C., Jan Y.L., Basbaum A. Immunohistochemical localization of GABA-B receptors in the rat central nervous system. J. Comp. Neurol. 405:1999;231-299.
24. Marret S., Gressens P., Evrard P. Arrest of neuronal migration by excitatory amino acids in hamster developing brain. Proc. Natl. Acad. Sci. USA. 93:1996;15463-15468.
25. Maskos U., Brüstle O., McKay R.D.G. Long-term survival, migration, and differentiation of neural cells without functional NMDA receptors in vivo. Dev. Biol. 231:2001;103-112.
26. Maskos U., Kissa K., St Cloment C., Brület P. Retrograde trans- synaptic transfer of green fluorescent protein allows the genetic mapping of neuronal circuits in transgenic mice. Proc. Natl. Acad. Sci. USA. 99:2002;10120-10125.
27. Messersmith E.K., Feller M.B., Zhang H., Shatz C.J. Migration of neocortical neurons in the absence of functional NMDA receptors. Mol. Cell Neurosci. 9:1997;347-357.
28. Mohn A.R., Gainetdinov R.R., Caron M.G., Koller B.H. Mice with reduced NMDA receptor expression display behaviors related to schizophrenia. Cell. 98:1999;427-436.
29. Monyer H., Burnashev N., Laurie D.J., Sakmann B., Seeburg P.H. Development and regional expression in the rat brain and functional properties of four NMDA receptors. Neuron. 12:1994;529-540.
30. Nakazawa K., Quirk M.C., Chitwood R.A., Watanabe M., Yeckel M.F., Sun L.D., Kato A., Carr C.A., Johnston D., Wilson M.A., Tonegawa S. Requirement for hippocampal CA3 NMDA receptors in associative memory recall. Science. 297:2002;211-218.
31. Nagy A., Rossant J., Nagy R., Abramow-Newerly W., Roder J.C. Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc. Natl. Acad. Sci. USA. 90:1993;8424-8428.
32. Nichols J., Evans E.P., Smith A.G. Establishment of germ-line- competent embryonic stem (ES) cells using differentiation inhibiting activity. Development. 110:1990;1341-1348.
33. Okabe S., Vicario-Abejon C., Segal M., McKay R.D.G. Survival and synaptogenesis of hippocampal neurons without NMDA receptor function in culture. Eur. J. Neurosci. 10:1998;2192-2198.
34. Petralia R.S., Yokotani N., Wenthold R.J. Light and electron microscope distribution of the NMDA receptor subunit NMDAR1 in the rat nervous system using a selective anti-peptide antibody. J. Neurosci. 14:1994;667-696.
35. Rossi D.J., Slater N.T. The developmental onset of NMDA receptor channel activity during neuronal migration. Neuropharmacology. 32:1993;1239-1248.
36. Said S.I., Berisha H.I., Pakbaz H. Excitotoxicity in the lung N-Methyl-D-aspartate-induced, nitric-oxide dependent, pulmonary edema is attenuated by vasoactive intestinal peptide and by inhibitors of poly(ADP-ribose) polymerase . Proc. Natl. Acad. Sci. USA. 93:1996;4688-4692.
37. Seeburg P.H., Single F., Kuner T., Higochi M., Sprengel R. Genetic manipulation of key determinants of ion flow in glutamate receptor channels in the mouse. Brain Res. 907:2001;233-243.
38. Shannon H.E., Sawyer B.D. Glutamate receptors of the N-methyl-D-aspartate subtype in the myenteric plexus of the guinea pig ileum. J. Pharmacol. Exp. Ther. 251:1989;518-523.
39. Shigemoto R., Ohishi H., Nakanishi S., Mizuno N. Expression of the mRNA for the rat NMDA receptor (NMDAR1) in the sensory and autonomic ganglion neurons. Neurosci. Lett. 144:1992;229-232.
40. Sibilia M., Wagner E.F. Strain-dependent epithelial defects in mice lacking the EGF receptor. Science. 269:1995;234-238.
41. Single F.N., Rozov A., Burnashev N., Zimmermann F., Hanley D.F., Forrest D., Curran T., Jensen V., Hvalby O., Sprengel R., Seeburg P.H. Dysfunctions in mice by NMDA receptor point mutations NR1 (N598Q) and NR1 (N598R). J. Neurosci. 20:2000;2558-2566.
42. Thomson J., Itskovitz-Eldor J., Shapiro S., Waknitz M., Swiergiel J., Marshall V., Jones J. Embryonic stem cell lines derived from human blastocysts. Science. 282:1998;1145-1147.
43. Threadgill D.W., Dlugosz A.A., Hansen L.A., Tennenbaum T., Lichti U., Yee D., LaMantia C., Mourton T., Herrup K., Harris R.C., et al. Targeted disruption of mouse EGF receptor effect of genetic background on mutant phenotype . Science. 269:1995;230-234.
44. Tokita Y., Bessho Y., Masu M., Nakamura K., Nakao K., Katsuki M., Nakanishi S. Characterization of excitatory amino acid neurotoxicity in N-methyl-D-aspartate receptor-deficient mouse cortical neuronal cells. Eur. J. Neurosci. 8:1996;69-78.
45. Tsien J.Z., Chen D.F., Gerber D., Tom C., Metcer E.H., Anderson D.J., Mayford M., Kandel E.R., Tonegawa S. Subregion- and cell type-restricted gene knockout in mouse brain. Cell. 87:1996;1317-1326.
46. Tsien J.Z., Huerta P.T., Tonegawa S. The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory. Cell. 87:1996;1327-1338.
47. Wang C., Pralong W.F., Schulz M.F., Rougon G., Aubry J.M., Pagliusi S., Robert A., Kiss J.Z. Functional N-methyl-D-aspartate receptors in O-2A glial precursor cells a critical role in regulating polysialic acid-neural cell adhesion molecule expression and cell migration . J. Cell Biol. 135:1996;1565-1581.
48. Weiser M., Bueno E., Sekirnjak C., Martone M.E., Baker H., Hillman D., Chen S., Thornhill W., Ellisman M., Rudy B. The potassium channel subunit Kv3. 1b is localized to somatic and axonal membranes of specific populations of CNS neurons. J. Neurosci. 15:1995;4298-4314.
49. Yoneda Y., Ogita K. Localization of [3H]glutamate binding sites in rat adrenal medulla. Brain Res. 383:1986;387-391.
50. Yuzaki M., Forrest D., Curran T., Connor J.A. Selective activation of calcium permeability by aspartate in Purkinje cells. Science. 273:1996;1112-1114.
51. Yuzaki M., Forrest D., Verselis L.M., Sun S.C., Curran T., Connor J.A. Functional NMDA receptors are transiently active and support the survival of Purkinje cells in culture. J. Neurosci. 16:1996;4651-4661.