Fol. Biol. 2012, 58, 115-120
https://doi.org/10.14712/fb2012058030115
Expression of Wnt 3a, β-Catenin, Cyclin D1 and PCNA in Mouse Dentate Gyrus Subgranular Zone (SGZ): a Possible Role of Wnt Pathway in SGZ Neural Stem Cell Proliferation
References
1. 2003) Stem cells in the skin: waste not, Wnt not. Genes Dev. 17, 1189-1200.
< , L., Fuchs, E. (https://doi.org/10.1101/gad.1086903>
2. 1993) Cyclin D1 is a nuclear protein required for cell cycle progression in G1. Genes Dev. 7, 812-821.
< , V., Lukas, J., Marcote, M. J., Pagano, M., Draetta, G. (https://doi.org/10.1101/gad.7.5.812>
3. 2008) Mutations in Fbx4 inhibit dimerization of the SCF(Fbx4) ligase and contribute to cyclin D1 overexpression in human cancer. Cancer Cell 14, 68-78.
< , O., Zamfirova, P., Lin, D. I., Chen, X., Yang, K., Nakagawa, H., Lu, F., Rustgi, A. K., Diehl, J. A. (https://doi.org/10.1016/j.ccr.2008.05.017>
4. 2004) The Wnt connection to tumorigenesis. Int. J. Dev. Biol. 48, 477-487.
< , J., Lustig, B. (https://doi.org/10.1387/ijdb.041815jb>
5. 2005) WNTs in the vertebrate nervous system: from patterning to neuronal connectivity. Nat. Rev. Neurosci. 6, 351-362.
< , L., Salinas, P. C. (https://doi.org/10.1038/nrn1665>
6. 2006) Wnt/β-catenin signaling in development and disease. Cell 127, 469-480.
< , H. (https://doi.org/10.1016/j.cell.2006.10.018>
7. 2006) Molecular bases of the regulation of bone remodeling by the canonical Wnt signaling pathway. Curr. Top. Dev. Biol. 73, 43-84.
< , D. A., Karsenty, G. (https://doi.org/10.1016/S0070-2153(05)73002-7>
8. 2005) Phosphorylation of cyclin D1 at Thr 286 during S phase leads to its proteasomal degradation and allows efficient DNA synthesis. Oncogene 24, 2599-2612.
< , Y., Yang, K., Harwalkar, J., Nye, J. M., Mason, D. R., Garrett, M. D., Hitomi, M., Stacey, D. W. (https://doi.org/10.1038/sj.onc.1208326>
9. 1999) Cyclin D1 production in cycling cells depends on ras in a cell cycle specific manner. Curr. Biol. 9, 1075-1084.
< , M., Stacey, D. W. (https://doi.org/10.1016/S0960-9822(99)80476-X>
10. 2003) Adult born hippocampal neurons mature into activity dependent responsiveness. Eur. J. Neurosci. 18, 2707-2712.
< , S., Kempermann, G. (https://doi.org/10.1111/j.1460-9568.2003.02986.x>
11. 2001) Reconstitution of Cyclin D1-associated kinase activity drives terminally differentiated cells into the cell cycle. Mol. Cell. Biol. 21, 5631-5643.
< , L., Sacco, A., Pajalunga, D., Tiainen, M., Macera, D., D’Angelo, M., Felici, A., Sacchi, A., Crescenzi, M. (https://doi.org/10.1128/MCB.21.16.5631-5643.2001>
12. 2000) A local Wnt-3a signal is required for development of the mammalian hippocampus. Development 127, 457-467.
< , S. M., Tole, S., Grove, E., McMahon, A. P. (https://doi.org/10.1242/dev.127.3.457>
13. 2006) Phosphorylation dependent ubiquitination of cyclin D1 by the SCF(FBX4-αB crystallin) complex. Mol. Cell 24, 355-366.
< , D. I., Barbash, O., Kumar, K. G. S, Weber, J. D., Harper, J. W., Klein-Szanto, A. J. P., Rustgi, A., Fuchs, S. Y., Diehl, J. A. (https://doi.org/10.1016/j.molcel.2006.09.007>
14. 2004) The Wnt signaling pathway in development and disease. Annu. Rev. Cell. Dev. Biol. 20, 781-810.
< , C. Y., Nusse, R. (https://doi.org/10.1146/annurev.cellbio.20.010403.113126>
15. 1994) D-type cyclin dependent kinase activity in mammalian cells. Mol. Cell. Biol. 14, 2066-2076.
, H., Quelle, D. E., Shurtleff, S. A., Shibuya, M., Sherr, C. J., Kato, J. Y. (
16. 2003) Correlation of cytoplasmic β-catenin and cyclin D1 overexpression during thyroid carcinogenesis around Semipalatinsk nuclear test site. Thyroid 13, 537-545.
< , S., Nakashima, M., Kondo, H., Matsufuji, R., Takamura, N., Ishigaki, K., Ito, M., Prouglo, Y., Yamashita, S., Sekine, I. (https://doi.org/10.1089/105072503322238791>
17. 2004) Cyclin D1 overexpression in thyroid tumours from a radio-contaminated area and its correlation with Pin1 and aberrant β-catenin expression. J. Pathol. 202, 446-455.
< , M., Meirmanov, S., Naruke, Y., Kondo, H., Saenko, V., Rogounovitch, T., Shimizu-Yoshida, Y., Takamura, N., Namba, H., Ito, M., Abrosimov, A., Lushnikov, E., Roumiantsev, P., Tsyb, A., Yamashita, S., Sekine, I. (https://doi.org/10.1002/path.1534>
18. 2004) Convergence of Wnt, β-catenin, and cadherin pathways. Science 303, 1483-1487.
< , W. J., Nusse, R. (https://doi.org/10.1126/science.1094291>
19. 2003) Canonical Wnt signals are essential for homeostasis of the intestinal epithelium. Genes Dev. 17, 1709-1713.
< , D., Gregorieff, A., Begthel, H., Clevers, H. (https://doi.org/10.1101/gad.267103>
20. 2003) A role for Wnt signalling in self-renewal of haematopoietic stem cells. Nature 423, 409-414.
< , T., Duncan, A. W., Ailles, L., Domen, J., Scherer, D. C., Willert, K., Hintz, L., Nusse, R., Weissman, I. L. (https://doi.org/10.1038/nature01593>
21. 2004) Signaling pathways in intestinal development and cancer. Annu. Rev. Cell. Dev. Biol. 20, 695-723.
< , E., Batlle, E., Clevers, H. (https://doi.org/10.1146/annurev.cellbio.20.010403.092805>
22. 2004) A hypothesis about the role of adult neurogenesis in hippocampal function. Physiology (Bethesda) 19, 253-261.
, A. F., Gage, F. H. (
23. 1996) Cancer cell cycles. Science 274, 1672-1677.
< , C. J. (https://doi.org/10.1126/science.274.5293.1672>
24. 1999) CDK inhibitors: positive and negative regulators of Gl phase progression. Genes Dev. 13, 1501-1512.
< , C. J., Roberts, J. M. (https://doi.org/10.1101/gad.13.12.1501>
25. 1999) The cyclin D1 gene is a target of the β-catenin/LEF-1 pathway. Proc. Natl. Acad. Sci. USA 96, 5522-5527.
< , M., Zhurinsky, J., Simcha, I., Albanese, C., D’Amico, M., Pestell, R., Ben-Ze’ev, A. (https://doi.org/10.1073/pnas.96.10.5522>
26. 1999) β-Catenin regulates expression of cyclin D1 in colon carcinoma cells. Nature 398, 422-426.
< , O., McCormick, F. (https://doi.org/10.1038/18884>
27. 1995) The retinoblastoma protein and cell cycle control. Cell 81, 323-330.
< , R. A. (https://doi.org/10.1016/0092-8674(95)90385-2>
28. 2006) Wnt signaling: is the party in the nucleus? Genes Dev. 20, 1394-1404.
< , K., Jones, K. A. (https://doi.org/10.1101/gad.1424006>
29. 2003) β-Catenin signals regulate cell growth and the balance between progenitor cell expansion and differentiation in the nervous system. Dev. Biol. 258, 406-418.
< , D., Fujita, Y., Hulsken, J., Müller, T., Walther, I., Taketo, M. M., Crenshaw, E. B., Birchmeier, W., Birchmeier, C. (https://doi.org/10.1016/S0012-1606(03)00123-4>