Polysialylated neural cell adhesion molecule modulates photic signaling in the mouse suprachiasmatic nucleus

Neuroscience Letters

Volumn 280, Issue 3, 2000, Pages 207-210

  Glass, J David ^a   Shen, Huaming ^a   Fedorkova, Lenka ^a   Chen, Lei ^a   Tomasiewicz, Henry ^b   Watanabe, Michiko ^c  

^a KENT STATE UNIVERSITY   (United States)

^b EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c Pediatric Cardiology   (United States)

Author keywords

Aging; Neural cell adhesion molecule; Polysialic acid; Suprachiasmatic nucleus

Indexed keywords

NERVE CELL ADHESION MOLECULE; POLYSIALIC ACID; PROTEIN C FOS;

AGING; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL INTERACTION; CIRCADIAN RHYTHM; CONTROLLED STUDY; MALE; MOUSE; NERVE CELL PLASTICITY; NONHUMAN; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; SUPRACHIASMATIC NUCLEUS;

ANIMALS; CIRCADIAN RHYTHM; LIGHT; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MOTOR ACTIVITY; NEURAL CELL ADHESION MOLECULE L1; NEURAL CELL ADHESION MOLECULES; PROTO-ONCOGENE PROTEINS C-FOS; RECOMBINATION, GENETIC; SEQUENCE DELETION; SIALIC ACIDS; SIGNAL TRANSDUCTION; SUPRACHIASMATIC NUCLEUS;

EID: 0033954395     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-3940(00)00786-2     Document Type: Article

References (20)

1. Acheson A., Sunshine J., Rutishauser U. NCAM polysialic acid can regulate both cell-cell and cell-substrate interactions. J. Cell Biol. 114:1991;143-153.
2. Card J.P., Moore R.Y. Organization of lateral geniculate-hypothalamic connections in the rat. J. Comp. Neurol. 284:1989;135-147.
3. Cremer H., Lange K., Christoph A., Plomann M., Vopper G., Roes J., Brown R., Baldwin S., Kraemer P., Scheff S. Inactivation of the N-CAM gene in mice results in size reduction of the olfactory bulb and deficits in spacial learning. Nature. 367:1994;455-457.
4. 1A receptor agonists. Brain Res. 638:1994;235-242.
5. Hallenbeck P.C., Vimr E.R., Yu F., Bassler B., Troy F.A. Purification and properties of a bacteriophage-induced endo-N-acetylneuraminidase specific for poly-alpha-2-8-sialosyl carbohydrate units. J. Biol. Chem. 262:1987;3553-3561.
6. Liang F.-Q., Walline R., Earnest D.J. Circadian rhythm of brain-derived neurotrophic factor in the rat suprachiasmatic nucleus. Neurosci. Lett. 242:1998;89-92.
7. Moore R.Y. Organization and function of a central nervous system oscillator: The suprachiasmatic nucleus. Fed. Proc. 42:1983;2783-2789.
8. Moore R.Y., Lenn N.J. A retinohypothalamic projection in the rat. J. Comp. Neurol. 146:1971;1-14.
9. Müller D., Wang C., Skibo G., Toni N., Cremer H., Calaora V., Rougon G., Kiss J.Z. PSA-NCAM is required for activity-induced synaptic plasticity. Neuron. 17:1996;413-422.
10. Nishikawa Y., Shibata S., Watanabe S. Circadian changes in long-term potentiation of rat suprachiasmatic field potentials elicited by optic nerve stimulation in vitro. Brain Res. 695:1995;158-162.
11. Nothias F., Vernier P., von Boxberg Y., Mirman S., Vincent J.-D. Modulation of NCAM polysialylation is associated with morpho-functional modifications in the hypothalamoneurohypophysial system during lactation. Eur. J. Neurosci. 9:1997;1553-1565.
12. Obrietan K., van den Pol A.N. Neuropeptide Y depresses GABA-mediated calcium transients in developing suprachiasmatic nucleus neurons: a novel form of calcium long-term depression. J. Neurosci. 16:1996;3521-3533.
13. Pollerberg G., Burridge K., Krebs K., Goodman S., Schachner M. The 180-kDa component of the neural cell adhesion molecule NCAM is involved in cell-cell contacts and cytoskeleton-membrane interactions. Cell Tiss. Res. 250:1987;227-236.
14. Regan C.M., Fox G.B. Polysialylation as a regulator of neural plasticity in rodent learning and aging. Neurochem. Res. 20:1995;593-598.
15. Shen H., Glass J.D., Seki T., Watanabe M. Ultrastructural analysis of polysialylated neural cell adhesion molecule in the suprachiasmatic nuclei of the adult mouse. Anat. Rec. 256:1999;448-457.
16. Shen H., Watanabe M., Tomasiewicz H., Rutishauser U., Magnuson T., Glass J.D. Role of neural cell adhesion molecule and polysialic acid in mouse circadian clock function. J. Neurosci. 17:1997;5221-5229.
17. Theodosis D.T. El Majdoubi. M., Pierre, K. and Poulain, D.A., Factors governing activity-dependent structural plasticity of the hypothalamoneurohypophysial system. Cell. Mol. Neurobiol. 18:1998;285-298.
18. Tomasiewicz H., Ono K., Yee D., Thompson C., Gordis C., Rutishauser U., Magnuson T. Genetic deletion of a neural cell adhesion molecule variant (N-CAM 180) produces distinct deficits in the central nervous system. Neuron. 11:1993;1163-1174.
19. Vutskits L., Paccaud J.-P., Muller D., Djebbara-Hannas Z., Durbec P., Rougon G., Kiss J.Z. PSA-NCAM modulates the responsiveness of cortical neurons to BDNF, Proc. Polysialic acid: Biochemistry, Cell biology and Diseases. 1998;53 ile des Embiez, France.
20. Zhang Y., Kornhauser J.M., Zee P.C., Mayo K.E., Takahashi J.S., Turek F.W. Effects of aging on light-induced phase-shifting of circadian behavioral rhythms, fos expression and CREB phosphorylation in the hamster suprachiasmatic nucleus. Neuroscience. 70:1996;951-961.