2006, Number 1
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Rev Mex Neuroci 2006; 7 (1)
Genic apoptosis regulation via p38 in neurotoxicity processes
Segura TJE, Flores SME, Román RF
Language: Spanish
References: 54
Page: 55-68
PDF size: 230.61 Kb.
ABSTRACT
A lot of studies have show that GMS induces two kinds of cellular death: a fast death of necrotic kind which produces the liberation of excitatory neurotransmitters like Glutamate and GABA (at postnatal age), this provokes a second kind of cellular death by apoptosis (slow dead), that eventually produces the activation of the MAPKs pathway, which are: ERK, JNK and p38. These promote the activation of early gen that under conditions of stress produce alterations in the profiles of transcription factors; therefore, alterations in the genic expression. Nevertheless, it is important to know the participation of the p38 pathway, in neurototoxicity; which could be associated with possible changes in the levels of expression of early genes correlationated with the apoptotic process of neuronal death; throughout the identification of these responsible genes (participant) in the process of neuronal death; they could contribute to the design of new therapeutic strategies to prevent the neuroexcitotoxicity common phenomenon in different chronical neurodegenerative diseases.
REFERENCES
Orrego F, Villanueva S. The chemical nature of the main central excitatory transmitter. A critical appraisal based upon release studies and synaptic vesicle localization. Neuroscience 1993; 56: 539-55.
Dingledine R, McBain CJ. Glutamate and aspartate. In Siegel JG, Agranoff BW, Albers RW, Fisher SK, Uhler MD (Eds). Basic neurochemistry. Lippincott-Raven Press, PH; 1999, pp. 315-33.
Südhof T. Intracellular trafficking. In Siegel GJ, Agranoff BW, Uhler ME (Eds.). Basic neurochemistry. Philadelphia: Lippincott Raven Press; 1999, pp. 174-88.
Rodríguez A, López AM. Características farmacológicas de las subunidades de los receptores del glutamato del tipo N-metil-D-aspartato (NMDA). Salud Mental 1997; 20: 39-47.
Ozawa SO, Kamiya H, Tsuzuki K. Glutamate receptors in the mammalian central nervous system. Prog Neurobiol 1998; 54: 581-618.
Doble A. The role of excitotoxicity in neurodegenerative disease: implications for therapy. Pharmacol Ther 1999; 81: 163-221.
Michaelis EK. Molecular biology of glutamate receptors in the central nervous system and their role in excitotoxicity, oxidative stress and aging. Progress in Neurobiology 1998; 54: 369-415.
Cull-Candy S, Brickley S, Farrant M. NMDA receptors subunits: diversity, development and disease. Curr Opin Neurobiol 2001; 11: 327-35.
Feldmeyer D, Cull Candy S. Functional consequences of changes in NMDA receptor subunit expression during development. Journal of Neurocitology 1996; 25: 857-67.
Takai H, Katayama K, Uetsuka K, Nakayama H, Doi K. Distribution of N-methyl-D-aspartate receptors (NMDARs) in the developing rat brain. Exp Mol Pathol 2003; 75: 89-94.
Olsen RW, DeLorey TM. GABA and glycine. In Siegel JG, Agranoff BW, Albers RW, Fisher SK, Uhler MD (Eds). Basic neurochemistry. Lippincott-Raven Press, PH; 1999, pp. 315-33.
Mitrovic MM, Nung Jan Y, Yeh Jan L. Ligand-induced signal transduction within hweterodimeric GABAB receptor. Proceedings of the National Academy of Sciences of the United States of America 2001; 987: 14643-8.
Gutiérrez R. The GABAergic phenotype of the “glutamatergic” granule cells of the dentate gyrus. Progress in Neurobiology 2003; 71: 337-58.
Olney JW. New insights and new issues in developmental neurotoxicology. Neuro Toxicology 2003; 23: 659-68.
Lapouble E, Montecot C, Sevestre A, Pichon J. Phosphinothricin induces epileptic activity via nitric oxide production through NMDA receptor activation in adult mice. Brain Research 2002; 6: 46-52.
Nishizawa Y. Glutamate release and neuronal damage in ischemia. Life Sciences 2001; 69: 369-81.
Mattson MP. Apoptosis in neurodegenerative disorders. Nature 2000a; 1: 120-307.
Martin LJ, Al-Abdulla NA, Brambrink AM, Kirsch JR, Sieberand FE, Portera-Cailliau C. Neurodegeneration in excitotoxicity, global cerebralischemia, and target deprivation: a perspective on the contributions of apoptosis and necrosis. Brain Research Bulletin 1998; 1: 281-309.
Mattson MP, Culmsee C, Zai FY. Apoptotic and antiapoptotic mechanisms in stroke. Springer-Verlag 2000b; 30: 173-87.
Mattson MP, LaFerla FM, Chan SL, Leissring MA, Shepel PN, Geiger JD. Calcium signaling in the ER: its role in neuronal plasticity and neurodegenerative disorders. Trends Neuroscience 2000c; 23: 222-9.
Chakrabort T, Das S, Mondal M, Roychoudhury S, Chakrabortis S. Oxidant, mitochondria and calcium: an overview. Cellular Signaling 1999; 11: 77-85.
Segura T, Galindo MF, Rallo-Gutiérrez B, Ceña V, Jordán J. Dianas farmacológicas en las enfermedades neurodegenerativas. Rev Neurol 2003; 36: 1047-57.
Zimmermann KC, Bonzon C, Green DR. The machinery of programmed cell death. Pharmacology & Therapeutics 2001; 92: 57-70.
Herlaar E, Brown Z. p38 MAPK signalling cascades in inflammatory disease. Molecular Medicine Today 1999; 5: 439-47.
Arbabi S, Maier RV. Mitogen-activated protein kinases. Critic Care Medical; 1: S74-9.
Hagemann C, Blank JL. The ups and downs of MEK kinase interactions. Cellular Signaling 2001; 13: 863-75.
Seger R, Krebs EG. The MAPK signaling cascade. FASEB J 1995; 9: 726-35.
Davis RJ. Signal transduction by the JNK group of MAP kinases. Cell 2000; 103: 239-52.
Gum RJ, McLaughlin MM, Kumar S, Wang Z, Bower MJ, Lee JC, Adams JL, Livi GP, Goldsmith EJ, Young PR. Acquisition of sensitivity of stress-activated protein kinases to the p38 inhibitor, SB 203580, by alteration of one or more amino acids within the ATP binding pocket. The Journal of Biological Chemistry 1998; 273: 15605-10.
Shapiro L, Dinarello CA. Osmotic regulation of cytoline sintesis in vitro. Proc Natl Acad Sci USA 1995; 92: 12230-4.
Zarubin T, Han J. Activation and signaling of the p38 MAP kinase pathway. Cell Research 2005; 15: 11-8.
Obata T, Brown GE, Yaffe MB. MAP kinase pathways activated by stress: The p38 MAPK pathway. Crit Care Med 2000; 28: 334-40.
Garrintong TP, Johnson GL. Organization and regulation of mitogen-activaded protein kinase signalling pathways. Current Opinion in Cell Biology 1999; 11: 211-8.
Schaeffer HJ, Weber MJ. Mitogen-activated protein kinases messages from ubiquitous messengers. Molecular and Cellular Biologya 1999; 19: 2435-44.
Su B, Karin M. Mitogen-activated protein kinase cascades and regulation of gene expresión. Current Opinion in Immunology 1996; 8: 402-11.
Ono K, Han J. The p38 signal transduction pathway activation and fuction. Cellular Signalling 2000; 12: 1-13.
Li J, Gorospe M, Hutter D, Barnes J, Keyse SM, Liu Y. Transcriptional induction of MKP-1 in response to stress is associated with histone H3 phosphorylation-acetylation. Molecular and Cellular Biology 2001; 21: 8213-24.
Clayton AL, Mahadevan LC. MAP kinase-mediated phosphoacetylation of histone H3 and inducible gene regulation. FEBS Letters 2003; 546: 51-8.
Frevel MAE, Bakheet T, Silva AM, Hissong JG, Khabar KSA, Williams BRG. p38 mitogen-activated protein kinase-dependent and independent signaling of mRNA stability of AU-Rich element-containing transcripts. Molecular and Cellular Biology 2003; 23: 425-36.
Bakheet T, Frevel M, Williams BRG, Greer W, Khabar KSA. ARED: human AU-rich element an unexpectedly diverse functional repertoire of encoded proteins. Nucleic Acids Research 2001; 29: 246-54.
Bevilacqua A, Ceriani MC, Capaccioli S, Nicolin A. Post-transcriptional regulation of gene expression by degradation of messenger RNAs. Journal of Cellular Physiology 2003; 195: 356-72.
Dean JLE, Sully G, Clark AR, Saklatvala J. The involvement of AU-rich element-binding proteins in p38 mitogen-activated protein kinase pathway-mediated mRNA stabilisation. Cell Signal 2004; 16: 1113-21.
Chen RW, Qin ZH, Ren M, Kanai H, Chalecka-Franaszek E, Leeds P, Chuang DM. Regulation of c-Jun N-terminal kinase, p38 kinase and AP-1 DNA binding in cultured brain neurons: roles in glutamate excitotoxicity and lithium neuroprotection. J Neurochem 2003; 84: 566-75.
Mukherjee PK, DeCoster MA, Campbell FZ, Davis RJ, Bazan NG. Glutamate receptor aignaling interplay modulates stress-sensitive mitogen-activaded protein kinases and neuronal cell death. The Journal of Biological Chemistry 1998; 5: 6493-8.
Willaime-Morawek S, Brami-Cherrier K, Mariani J, Caboche J, Brugg B. c-Jun N-terminal kinases/c-Jun and p38 pathways cooperate in ceramide-induced neuronal apoptosis. Neuroscience 2003; 119: 387-97.
Willaime S, Vanhoutte P, Caboche J, Lemaigre-Dubreuil Y, Mariani J, Brugg B. Ceramide-induced apoptosis in cortical neurons is mediated by an increase in p38 phosphorylation and not by the decrease in ERK phosphorylation. Eur J Neurosci 2001; 13: 2037-46.
Namgung U, Zhengui X. Arsenic induces apoptosis in rat cerebellar neurons via activation of JNK3 and p38 MAP kinases. Toxicology and Applied Pharmacology 2001; 174: 130-8.
Yamagishi S, Yamada M, Ishikawa Y, Matsumoto T, Ikeuchi, Hatanaka H. p38 Mitogen-activated protein kinase regulates low potassium-induced c-Jun phosphorylation and apoptosis in cultured cerebellar granule neurons. The Journal of Biological Chemistry 2001; 16: 5129-33.
Kumar S, Jiang MS, Adams JL, Lee JC. Pyridinylimidazole compound SB 203580 inhibits the activity but not the activation of p38 mitogen-activated protein kinase. Biochemical and Biophysical Research Communications 1999; 263: 825-31.
Persengiev SP, Green MR. The role of ATF/CREB family members in cell growth, survival and apoptosis 2003; 8(3): 225-8.
Sano Y, Harada J, Tashiro S, Gotoh-Mandeville R, Maekawa T, Ishii S. ATF-2 is a common nuclear target of smad and TAK1 pathways in transforming growth factor-beta signaling. J Biol Chem 1999; 26; 274(13): 8949-57.
Rivera MC, Segura JE, Feria A, Armendáriz J, Beas-Zarate C. NMDA and AMPA receptor expression and cortical neuronal death are associated with p38 in glutamate-induced excitotoxicity in vivo. Journal of Neuroscience Research 2004; 76: 678-87.
Mori T, Wang X, Jung JC, Sumii T, Singhal AB, Fini ME, Dixon CE, Alessandrini A, Lo EH. Mitogen-activated protein kinase inhibition in traumatic brain injury: in vitro and in vivo effects. J Cereb Blood Flow Metab 2002; 22(4): 444-52.
Chaparro V, Rivera MC, Flores ME, Gómez U, Beas C. Proinflammatory cytokines and apoptosis following glutamate-induced excitotoxicity mediated by p38 MAPK in the hippocampus of neonatal rats. J Neuroimmunol 2005; 165(1-2): 53-62.