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Article type: Research Article
Authors: Villa, Chiaraa; * | Ridolfi, Elisaa | Fenoglio, Chiaraa | Ghezzi, Lauraa | Vimercati, Robertoa | Clerici, Francescab | Marcone, Alessandrac | Gallone, Salvatored | Serpente, Mariaa | Cantoni, Claudiaa | Bonsi, Rossanaa | Cioffi, Saraa | Cappa, Stefanoc; e | Franceschi, Massimof | Rainero, Innocenzod | Mariani, Claudiob | Scarpini, Elioa | Galimberti, Danielaa
Affiliations: [a] “Neurology Unit”, Department of Pathophysiology and Transplantation “Dino Ferrari” Center, University of Milan, Fondazione Cà Granda, IRCCS Ospedale Maggiore Policlinico, Milan, Italy | [b] Center for Research and Treatment on Cognitive Dysfunctions, Chair of Neurology, University of Milan, “Luigi Sacco” Hospital, Milan, Italy | [c] Division of Neurology, San Raffaele Turro Hospital, San Raffaele Scientific Institute, Milan, Italy | [d] Department of Neuroscience, University of Turin, Turin, Italy | [e] Neurorehabilitation Unit, Department of Clinical Neurosciences, San Raffaele Scientific Institute and Università Vita-Salute San Raffaele, Milan, Italy | [f] IRCCS Multimedica, Milan, Italy
Correspondence: [*] Correspondence to: Chiara Villa, Department of Pathophysiology and Transplantation “Dino Ferrari” Center, University of Milan, Fondazione Cà Granda, IRCCS Ospedale Maggiore Policlinico, Milan, Italy. Tel: +39 025503887; Fax: +39 0250320430; E-mail: chiara.villa1@unimi.it.
Abstract: Altered gene expression occurs in central nervous system disorders, including Alzheimer's disease (AD). Transcription factor Sp1 (specificity protein 1) can regulate the expression of several AD-related proteins, including amyloid-β protein precursor and tau. Sp1 is regulated by oxidative stress, and Sp1 mRNA was found to be upregulated in AD cortex and hippocampus. The distribution of three single nucleotide polymorphisms (SNPs), including rs7300593, rs17695156, and rs12821290, covering 100% Sp1 genetic variability, has been determined in a population of 393 AD patients as compared with 412 controls. In addition, expression analysis of Sp1 and its regulatory microRNAs (hsa-miR-29b and hsa-miR-375) has been performed in peripheral blood mononuclear cells (PBMCs), together with Sp1 protein analysis. No differences in all three SNP distributions were observed in AD patients as compared with controls. Stratifying according to gender, a significantly decreased frequency of Sp1 rs17695156 T allele was observed in male patients versus male controls. Significantly increased Sp1 relative expression levels were observed in PBMCs from AD patients as compared with controls. Western blot analysis paralleled mRNA increase in AD patients versus controls and correlated positively with Sp1 mRNA levels. Significantly decreased relative expression levels of hsa-miR-29b, but not of hsa-miR-375, were observed in AD patients versus controls and correlated negatively with Sp1 mRNA levels. According to these results, Sp1 and its regulatory hsa-miR-29b are deregulated in AD patients, possibly leading to aberrant production of downstream target genes involved in the pathogenesis. Moreover, Sp1 rs176951056 T allele is likely a protective factor in the male population.
Keywords: Alzheimer's disease, expression, gene regulation, microRNAs, peripheral blood mononuclear cells, risk factor, Sp1
DOI: 10.3233/JAD-122263
Journal: Journal of Alzheimer's Disease, vol. 35, no. 3, pp. 487-494, 2013
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