miR-338-3p is over-expressed in blood, CFS, serum and spinal cord from sporadic amyotrophic lateral sclerosis patients

被引:0
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作者
Bruna De Felice
Anna Annunziata
Giuseppe Fiorentino
Marco Borra
Elio Biffali
Cinzia Coppola
Roberto Cotrufo
Johannes Brettschneider
Maria Luisa Giordana
Tamas Dalmay
Guy Wheeler
Raffaella D’Alessandro
机构
[1] University of Naples II,DISTABIF—Department of Environmental, Biological and Pharmaceutical Sciences and Technologies
[2] Monaldi Hospital,Division of Respiratory Physiopathology
[3] Stazione Zoologica “Anton Dohrn”,First Division of Neurology, Department of Clinical and Experimental Medicine “F. Magrassi and A. Lanzara”
[4] University of Naples II,Department of Neurology
[5] Regional Interuniversity Center for Research in Neuroscience (CIRN),Department of Neuroscience
[6] University of Ulm,School of Biological Sciences
[7] University of Turin,undefined
[8] University of East Anglia,undefined
来源
neurogenetics | 2014年 / 15卷
关键词
MicroRNAs; sALS; Leukocytes; CSF; Spinal cord; Real-time PCR;
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学科分类号
摘要
Amyotrophic lateral sclerosis (ALS) is a progressive and seriously disabling adult-onset neurological disease. Ninety percent of ALS patients are sporadic cases (sALS) with no clear genetic linkage. Accumulating evidence indicates that various microRNAs (miRNAs), expressed in a spatially and temporally controlled manner in the brain, play a key role in neuronal development. In addition, microRNA dysregulation contributes to some mental disorders and neurodegeneration diseases. In our research, the expression of one selected miRNA, miR-338-3p, which previously we have found over-expressed in blood leukocytes, was studied in several different tissues from sALS patients. For the first time, we detected a specific microRNA disease-related upregulation, miR-338-3p, in blood leukocytes as well in cerebrospinal fluid, serum, and spinal cord from sALS patients. Besides, staining of in situ hybridization showed that the signals of miR-338-3p were localized in the grey matter of spinal cord tissues from sALS autopsied patients. We propose that miRNA profiles found in tissue samples from sALS patients can be relevant to understand sALS pathogenesis and lead to set up effective biomarkers for sALS early diagnosis.
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页码:243 / 253
页数:10
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