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Tytuł artykułu
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Warianty tytułu
Języki publikacji
Abstrakty
Down syndrome (DS) is the most common chromosomal disorder. It is featured by intellectual disability and is caused by trisomy 21. People with DS can develop some traits of Alzheimer disease at an earlier age than subjects without trisomy 21. Apoptosis is a programmed cell death process under both normal physiological and pathological conditions. Poly (ADP-ribose) polymerase 1 is a mediator of programmed-necrotic cell death and appears to be also involved in the apoptosis. The aim of the present work was to detect the intracellular distribution of PARP-1 protein using immunofluorescence techniques and the expression of PARP-1 mRNA in culture of fibroblasts of DS subjects. The analysis of the intracellular distribution of PARP-1 show a signal at the nuclear level in about 75 % of the cells of DS subjects with a slight uniformly fluorescent cytoplasm. In contrast, in about 65% of the analyzed fibroblasts of the normal subjects only a slight fluorescent was found. These observations have been confirmed by PARP-1 gene mRNA expression evaluation. The data obtained from this study strengthen the hypothesis that the over-expression of PARP-1 gene could have a role in the activation of the apoptotic pathways acting in the neurodegenerative processes in DS.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Numer
Strony
762-765
Opis fizyczny
Daty
wydano
2013-12-01
online
2013-12-06
Twórcy
autor
- IRCCS Associazione Oasi Maria SS Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy, micezia@tiscali.it
autor
- IRCCS Associazione Oasi Maria SS Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy
autor
- IRCCS Associazione Oasi Maria SS Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy
autor
- IRCCS Associazione Oasi Maria SS Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy
autor
- IRCCS Associazione Oasi Maria SS Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy
autor
- IRCCS Associazione Oasi Maria SS Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy
autor
- IRCCS Associazione Oasi Maria SS Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy
autor
- ANFFAS, Catania, Italy
autor
- IRCCS Associazione Oasi Maria SS Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy
autor
- IRCCS Associazione Oasi Maria SS Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy
autor
- IRCCS Associazione Oasi Maria SS Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy
Bibliografia
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- [4] Wisniewski KE, Dalton AJ, McLachlan C, Wen GY, Wisniewski HM. Alzheimer’s disease in Down’s syndrome: clinicopathologic studies. Neurology 1985;35:957–961 http://dx.doi.org/10.1212/WNL.35.7.957[Crossref]
- [5] Elmore S. Apoptosis: a review of programmed cell death. Toxicol Pathol 2007;35:495–516 http://dx.doi.org/10.1080/01926230701320337[WoS][Crossref]
- [6] Hassa PO, Hottiger MO. The diverse biological roles of mammalian PARPs, a small but powerful family of poly-ADP-ribose polymerases. Front Biosci 2008;13:3046–3082 http://dx.doi.org/10.2741/2909[Crossref][WoS]
- [7] Yu SW, Wang H, Poitras MF, Coombs C, Bowers WJ, Federoff HJ. Mediation of poly(ADP-ribose) polymerase-1-dependent cell death by apoptosis-inducing factor. Science 2002;297:259–263 http://dx.doi.org/10.1126/science.1072221
- [8] Andrabi SA, Kim NS, Yu SW. Poly(ADP-ribose) (PAR) polymer is a death signal. Proc Natl Acad Sci USA 2006;103:18308–183013 http://dx.doi.org/10.1073/pnas.0606526103[Crossref]
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- [10] Li CM, Guo M, Salas M, Schupf N, Silverman W, Zigman WB, Husain S, Warburton D, Thaker H, Tycko B. Cell type-specific over-expression of chromosome 21 genes in fibroblasts and fetal hearts with trisomy 21. BMC Med Genet 2006;7:24 http://dx.doi.org/10.1186/1471-2350-7-24[Crossref]
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- [12] Eustermann S, Videler H, Yang JC, Cole PT, Gruszka D, Veprintsev D, Neuhaus D. The DNA-binding domain of human PARP-1 interacts with DNA single-strand breaks as a monomer through its second zinc finger. J Mol Biol 2011;407:149–170 http://dx.doi.org/10.1016/j.jmb.2011.01.034[Crossref]
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- [14] Sahaboglu A, Tanimoto N, Kaur J, Sancho-Pelluz J, Huber G, Fahl E. PARP1 gene knock-out increases resistance to retinal degeneration without affecting retinal function. PLoS One 2010;11:e15495 http://dx.doi.org/10.1371/journal.pone.0015495[WoS][Crossref]
- [15] Hassa PO, Haenni SS, Elser M, Hottiger MO. Nuclear ADP-ribosylation reactions in mammalian cells: where are we today and where are we going? Microbiol Mol Biol Rev 2006;70:789–829 http://dx.doi.org/10.1128/MMBR.00040-05[Crossref]
- [16] Barone C, Romano C, Ridolfo F, Gulotta E, Scavuzzo C, Salluzzo MG, Giambirtone MC, Caraci F, Romano C, Bosco P. Differential expression of PARP1 mRNA in leucocytes of patients with Down syndrome. J Genet 2011;90:469–472 http://dx.doi.org/10.1007/s12041-011-0074-x[Crossref]
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Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_s11536-013-0225-y