Signaling mechanisms of daidzein-induced axonal outgrowth in hippocampal neurons

Biochemical and Biophysical Research Communications

Volumn 366, Issue 2, 2008, Pages 393-400

  Wang, Pei ^a   Jeng, Chung Jiuan ^b   Chien, Chung Liang ^a   Wang, Seu Mei ^a  

^a NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^b NATIONAL YANG MING UNIVERSITY   (Taiwan)

Author keywords

Axonal outgrowth; Daidzein; Estrogen receptor; Growth associated protein 43; Hippocampal neuron; Protein kinase C

Indexed keywords

12 (2 CYANOETHYL) 6,7,12,13 TETRAHYDRO 13 METHYL 5 OXOINDOLO[2,3 A]PYRROLO[3,4 C]CARBAZOLE; CARRIER PROTEIN; DAIDZEIN; ESTROGEN RECEPTOR; ESTROGEN RECEPTOR BETA; FULVESTRANT; NEUROMODULIN; PROTEIN KINASE C ALPHA;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL CULTURE; CELL ELONGATION; CELL MEMBRANE; EFFECTOR CELL; EMBRYO; ENZYME ACTIVATION; FEMALE; GROWTH CONE; HIPPOCAMPUS; IMMUNOHISTOCHEMISTRY; IMMUNOREACTIVITY; NERVE CELL; NERVE FIBER GROWTH; NONHUMAN; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; RAT; SIGNAL TRANSDUCTION;

ANIMALS; AXONS; CELL ENLARGEMENT; CELLS, CULTURED; DOSE-RESPONSE RELATIONSHIP, DRUG; HIPPOCAMPUS; ISOFLAVONES; NERVE TISSUE PROTEINS; NEURONS; PHYTOESTROGENS; RATS; RATS, WISTAR; SIGNAL TRANSDUCTION;

EID: 37449014452     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.11.147     Document Type: Article

References (29)

1. Cos P., De Bruyne T., Apers S., Vanden Berghe D., Pieters L., and Vlietinck A.J. Phytoestrogens: recent developments. Planta Med. 69 (2003) 589-599
2. Zhao L., Chen Q., and Diaz Brinton R. Neuroprotective and neurotrophic efficacy of phytoestrogens in cultured hippocampal neurons. Exp. Biol. Med. (Maywood) 227 (2002) 509-519
3. Lee Y.B., Lee H.J., and Sohn H.S. Soy isoflavones and cognitive function. J. Nutr. Biochem. 16 (2005) 641-649
4. Woolley C.S. Acute effects of estrogen on neuronal physiology. Annu. Rev. Pharmacol. Toxicol. 47 (2007) 657-680
5. Kelly M.J., and Levin E.R. Rapid actions of plasma membrane estrogen receptors. Trends Endocrinol. Metab. 12 (2001) 152-156
6. Kalita K., Szymczak S., and Kaczmarek L. Non-nuclear estrogen receptor beta and alpha in the hippocampus of male and female rats. Hippocampus 15 (2005) 404-412
7. Bjornstrom L., and Sjoberg M. Mechanisms of estrogen receptor signaling: convergence of genomic and nongenomic actions on target genes. Mol. Endocrinol. 19 (2005) 833-842
8. de Wilde A., Heberden C., Chaumaz G., Bordat C., and Lieberherr M. Signaling networks from Gbeta1 subunit to transcription factors and actin remodeling via a membrane-located ERbeta-related protein in the rapid action of daidzein in osteoblasts. J. Cell. Physiol. 209 (2006) 786-801
9. Fukata Y., Kimura T., and Kaibuchi K. Axon specification in hippocampal neurons. Neurosci. Res. 43 (2002) 305-315
10. Oestreicher A.B., De Graan P.N., Gispen W.H., Verhaagen J., and Schrama L.H. B-50, the growth associated protein-43: modulation of cell morphology and communication in the nervous system. Prog. Neurobiol. 53 (1997) 627-686
11. Dotti C.G., Sullivan C.A., and Banker G.A. The establishment of polarity by hippocampal neurons in culture. J. Neurosci. 8 (1988) 1454-1468
12. Goslin K., and Banker G. Rapid changes in the distribution of GAP-43 correlate with the expression of neuronal polarity during normal development and under experimental conditions. J. Cell. Biol. 110 (1990) 1319-1331
13. Dent E.W., and Meiri K.F. Distribution of phosphorylated GAP-43 (neuromodulin) in growth cones directly reflects growth cone behavior. J. Neurobiol. 35 (1998) 287-299
14. von Schassen C., Fester L., Prange-Kiel J., Lohse C., Huber C., Bottner M., and Rune G.M. Oestrogen synthesis in the hippocampus: role in axon outgrowth. J. Neuroendocrinol. 18 (2006) 847-856
15. Yeh J.H., Jeng C.J., Chen Y.W., Lin H.M., Wu Y.S., and Tang C.Y. Selective enhancement of tonic inhibition by increasing ambient GABA is insufficient to suppress excitotoxicity in hippocampal neurons. Biochem. Biophys. Res. Commun. 338 (2005) 1417-1425
16. Chen C.H., Chen Y.J., Jeng C.J., Yang S.H., Tung P.Y., and Wang S.M. Role of PKA in the anti-Thy-1 antibody-induced neurite outgrowth of dorsal root ganglionic neurons. J. Cell. Biochem. 101 (2007) 566-575
17. Honig M.G., and Kueter J. The expression of cell adhesion molecules on the growth cones of chick cutaneous and muscle sensory neurons. Dev. Biol. 167 (1995) 563-583
18. Jin Y., Wu H., Cohen E.M., Wei J., Jin H., Prentice H., and Wu J.Y. Genistein and daidzein induce neurotoxicity at high concentrations in primary rat neuronal cultures. J. Biomed. Sci. 14 (2007) 275-284
19. Korshunova I., Novitskaya V., Kiryushko D., Pedersen N., Kolkova K., Kropotova E., Mosevitsky M., Rayko M., Morrow J.S., Ginzburg I., Berezin V., and Bock E. GAP-43 regulates NCAM-180-mediated neurite outgrowth. J. Neurochem. 100 (2007) 1599-1612
20. Tejero-Diez P., Rodriguez-Sanchez P., Martin-Cofreces N.B., and Diez-Guerra F.J. bFGF stimulates GAP-43 phosphorylation at ser41 and modifies its intracellular localization in cultured hippocampal neurons. Mol. Cell. Neurosci. 16 (2000) 766-780
21. Kuiper G.G., Lemmen J.G., Carlsson B., Corton J.C., Safe S.H., van der Saag P.T., van der Burg B., and Gustafsson J.A. Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor beta. Endocrinology 139 (1998) 4252-4263
22. Halabalaki M., Alexi X., Aligiannis N., Lambrinidis G., Pratsinis H., Florentin I., Mitakou S., Mikros E., Skaltsounis A.L., and Alexis M.N. Estrogenic activity of isoflavonoids from Onobrychis ebenoides. Planta Med. 72 (2006) 488-493
23. Gerecke K.M., Wyss J.M., and Carroll S.L. Neuregulin-1beta induces neurite extension and arborization in cultured hippocampal neurons. Mol. Cell. Neurosci. 27 (2004) 379-393
24. Zeidman R., Troller U., Raghunath A., Pahlman S., and Larsson C. Protein kinase Cepsilon actin-binding site is important for neurite outgrowth during neuronal differentiation. Mol. Biol. Cell. 13 (2002) 12-24
25. + channels in hippocampal neurons by protein kinase C epsilon. J. Neurosci. 25 (2005) 507-513
26. Davies S.P., Reddy H., Caivano M., and Cohen P. Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem. J. 351 (2000) 95-105
27. Hawkins M.B., and Thomas P. The unusual binding properties of the third distinct teleost estrogen receptor subtype ERbeta are accompanied by highly conserved amino acid changes in the ligand binding domain. Endocrinology 145 (2004) 2968-2977
28. Young E., Cesena T., Meiri K.F., and Perrone-Bizzozero N.I. Changes in protein kinase C (PKC) activity, isozyme translocation, and GAP-43 phosphorylation in the rat hippocampal formation after a single-trial contextual fear conditioning paradigm. Hippocampus 12 (2002) 457-464
29. Spencer S.A., Schuh S.M., Liu W.S., and Willard M.B. GAP-43, a protein associated with axon growth, is phosphorylated at three sites in cultured neurons and rat brain. J. Biol. Chem. 267 (1992) 9059-9064