Prosurvival Effect of DHCR24/Seladin-1 in Acute and Chronic Responses to Oxidative Stress

REFERENCES

• Banker, G., and K. Goslin. 1991. Culturing nerve cells. MIT Press, Cambridge, MA.
   Google Scholar
• Benvenuti, S., P. Luciani, G. B. Vannelli, S. Gelmini, E. Franceschi, M. Serio, and A. Peri. 2005. Estrogen and selective estrogen receptor modulators exert neuroprotective effects and stimulate the expression of selective Alzheimer's disease indicator-1, a recently discovered antiapoptotic gene, in human neuroblast long-term cell cultures. J. Clin. Endocrinol. Metab. 90:1775–1782.
   PubMedGoogle Scholar
• Benvenuti, S., R. Saccardi, P. Luciani, S. Urbani, C. Deledda, I. Cellai, F. Francini, R. Squecco, F. Rosati, G. Danza, S. Gelmini, I. Greeve, M. Rossi, R. Maggi, M. Serio, and A. Peri. 2006. Neuronal differentiation of human mesenchymal stem cells: changes in the expression of the Alzheimer's disease-related gene seladin-1. Exp. Cell Res. 312:2592–2604.
   PubMedGoogle Scholar
• Bishop, G. J., T. Nomura, T. Yokota, K. Harrison, T. Noguchi, S. Fujioka, S. Takatsuto, J. D. Jones, and Y. Kamiya. 1999. The tomato DWARF enzyme catalyses C-6 oxidation in brassinosteroid biosynthesis. Proc. Natl. Acad. Sci. USA 96:1761–1766.
   PubMedGoogle Scholar
• Bligh, E. G., and W. J. Dyer. 1959. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 37:911–917.
   PubMedGoogle Scholar
• Crameri, A., E. Biondi, K. Kuehnle, D. Lutjohann, K. M. Thelen, S. Perga, C. G. Dotti, R. M. Nitsch, M. D. Ledesma, and M. H. Mohajeri. 2006. The role of seladin-1/DHCR24 in cholesterol biosynthesis, APP processing and Abeta generation in vivo. EMBO J. 25:432–443.
   PubMedGoogle Scholar
• Culmsee, C., and M. P. Mattson. 2005. p53 in neuronal apoptosis. Biochem. Biophys. Res. Commun. 331:761–777.
   PubMed Web of Science ®Google Scholar
• de Kruijff, B. 1990. Cholesterol as a target for toxins. Biosci. Rep. 10:127–130.
   PubMedGoogle Scholar
• Di Stasi, D., V. Vallacchi, V. Campi, T. Ranzani, M. Daniotti, E. Chiodini, S. Fiorentini, I. Greeve, A. Prinetti, L. Rivoltini, M. A. Pierotti, and M. Rodolfo. 2005. DHCR24 gene expression is upregulated in melanoma metastases and associated to resistance to oxidative stress-induced apoptosis. Int. J. Cancer 115:224–230.
   PubMed Web of Science ®Google Scholar
• Girotti, A. W. 1998. Lipid hydroperoxide generation, turnover, and effector action in biological systems. J. Lipid Res. 39:1529–1542.
   PubMed Web of Science ®Google Scholar
• Greeve, I., I. Hermans-Borgmeyer, C. Brellinger, D. Kasper, T. Gomez-Isla, C. Behl, B. Levkau, and R. M. Nitsch. 2000. The human DIMINUTO/DWARF1 homolog seladin-1 confers resistance to Alzheimer's disease-associated neurodegeneration and oxidative stress. J. Neurosci. 20:7345–7352.
   PubMed Web of Science ®Google Scholar
• Kinsky, S. C. 1970. Antibiotic interaction with model membranes. Annu. Rev. Pharmacol. 10:119–142.
   PubMedGoogle Scholar
• Li, Y. C., M. J. Park, S. K. Ye, C. W. Kim, and Y. N. Kim. 2006. Elevated levels of cholesterol-rich lipid rafts in cancer cells are correlated with apoptosis sensitivity induced by cholesterol-depleting agents. Am. J. Pathol. 168:1107-1118, 1404-1405.
   PubMed Web of Science ®Google Scholar
• Lu, X., F. Kambe, X. Cao, T. Yoshida, S. Ohmori, K. Murakami, T. Kaji, T. Ishii, D. Zadworny, and H. Seo. 2006. DHCR24-knockout embryonic fibroblasts are susceptible to serum withdrawal-induced apoptosis because of dysfunction of caveolae and insulin-Akt-Bad signaling. Endocrinology 147:3123–3132.
   PubMedGoogle Scholar
• Luciani, P., P. Ferruzzi, G. Arnaldi, C. Crescioli, S. Benvenuti, G. Nesi, A. Valeri, I. Greeve, M. Serio, M. Mannelli, and A. Peri. 2004. Expression of the novel adrenocorticotropin-responsive gene selective Alzheimer's disease indicator-1 in the normal adrenal cortex and in adrenocortical adenomas and carcinomas. J. Clin. Endocrinol. Metab. 89:1332–1339.
   PubMed Web of Science ®Google Scholar
• Luciani, P., S. Gelmini, E. Ferrante, A. Lania, S. Benvenuti, S. Baglioni, G. Mantovani, I. Cellai, F. Ammannati, A. Spada, M. Serio, and A. Peri. 2005. Expression of the antiapoptotic gene seladin-1 and octreotide-induced apoptosis in growth hormone-secreting and nonfunctioning pituitary adenomas. J. Clin. Endocrinol. Metab. 90:6156–6161.
   PubMedGoogle Scholar
• Martindale, J. L., and N. J. Holbrook. 2002. Cellular response to oxidative stress: signaling for suicide and survival. J. Cell Physiol. 192:1–15.
   PubMed Web of Science ®Google Scholar
• McMorris, T. C. 1997. Recent developments in the field of plant steroid hormones. Lipids 32:1303–1308.
   PubMedGoogle Scholar
• McNeill-Blue, C., B. A. Wetmore, J. F. Sanchez, W. J. Freed, and B. A. Merrick. 2006. Apoptosis mediated by p53 in rat neural AF5 cells following treatment with hydrogen peroxide and staurosporine. Brain Res. 1112:1–15.
   PubMedGoogle Scholar
• Ohyama, Y., S. Meaney, M. Heverin, L. Ekstrom, A. Brafman, M. Shafir, U. Andersson, M. Olin, G. Eggertsen, U. Diczfalusy, E. Feinstein, and I. Bjorkhem. 2006. Studies on the transcriptional regulation of cholesterol 24-hydroxylase (CYP46A1): marked insensitivity toward different regulatory axes. J. Biol. Chem. 281:3810–3820.
   PubMed Web of Science ®Google Scholar
• Pai, J. T., M. S. Brown, and J. L. Goldstein. 1996. Purification and cDNA cloning of a second apoptosis-related cysteine protease that cleaves and activates sterol regulatory element binding proteins. Proc. Natl. Acad. Sci. USA 93:5437–5442.
   PubMedGoogle Scholar
• Song, B. L., N. B. Javitt, and R. A. DeBose-Boyd. 2005. Insig-mediated degradation of HMG CoA reductase stimulated by lanosterol, an intermediate in the synthesis of cholesterol. Cell Metab. 1:179–189.
   PubMed Web of Science ®Google Scholar
• Takahashi, T., A. Gasch, N. Nishizawa, and N. H. Chua. 1995. The DIMINUTO gene of Arabidopsis is involved in regulating cell elongation. Genes Dev. 9:97–107.
   PubMedGoogle Scholar
• Wang, X., J. L. Martindale, Y. Liu, and N. J. Holbrook. 1998. The cellular response to oxidative stress: influences of mitogen-activated protein kinase signalling pathways on cell survival. Biochem. J. 333:291–300.
   PubMed Web of Science ®Google Scholar
• Wang, X., N. G. Zelenski, J. Yang, J. Sakai, M. S. Brown, and J. L. Goldstein. 1996. Cleavage of sterol regulatory element binding proteins (SREBPs) by CPP32 during apoptosis. EMBO J. 15:1012–1020.
   PubMed Web of Science ®Google Scholar
• Waterham, H. R., J. Koster, G. J. Romeijn, R. C. Hennekam, P. Vreken, H. C. Andersson, D. R. FitzPatrick, R. I. Kelley, and R. J. Wanders. 2001. Mutations in the 3β-hydroxysterol Δ24-reductase gene cause desmosterolosis, an autosomal recessive disorder of cholesterol biosynthesis. Am. J. Hum. Genet. 69:685–694.
   PubMed Web of Science ®Google Scholar
• Wechsler, A., A. Brafman, M. Shafir, M. Heverin, H. Gottlieb, G. Damari, S. Gozlan-Kelner, I. Spivak, O. Moshkin, E. Fridman, Y. Becker, R. Skaliter, P. Einat, A. Faerman, I. Bjorkhem, and E. Feinstein. 2003. Generation of viable cholesterol-free mice. Science 302:2087.
   PubMed Web of Science ®Google Scholar
• Wu, C., I. Miloslavskaya, S. Demontis, R. Maestro, and K. Galaktionov. 2004. Regulation of cellular response to oncogenic and oxidative stress by Seladin-1. Nature 432:640–645.
   PubMedGoogle Scholar
• Yang, B., T. N. Oo, and V. Rizzo. 2006. Lipid rafts mediate H2O2 prosurvival effects in cultured endothelial cells. FASEB J. 20:1501–1503.
   PubMed Web of Science ®Google Scholar
• Yokoyama, C., X. Wang, M. R. Briggs, A. Admon, J. Wu, X. Hua, J. L. Goldstein, and M. S. Brown. 1993. SREBP-1, a basic-helix-loop-helix-leucine zipper protein that controls transcription of the low density lipoprotein receptor gene. Cell 75:187–197.
   PubMed Web of Science ®Google Scholar