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

被引:101
作者
De Felice, Bruna [1 ]
Annunziata, Anna [2 ]
Fiorentino, Giuseppe [2 ]
Borra, Marco [3 ]
Biffali, Elio [3 ]
Coppola, Cinzia [4 ,5 ]
Cotrufo, Roberto [4 ,5 ]
Brettschneider, Johannes [6 ]
Giordana, Maria Luisa [7 ]
Dalmay, Tamas [8 ]
Wheeler, Guy [8 ]
D'Alessandro, Raffaella [1 ]
机构
[1] Univ Naples 2, DISTABIF Dept Environm Biol & Pharmaceut Sci & Te, I-81100 Caserta, Italy
[2] Monaldi Hosp, Div Resp Physiopathol, I-80131 Naples, Italy
[3] Stn Zool Anton Dohrn, I-80121 Naples, Italy
[4] Univ Naples 2, Dept Clin & Expt Med F Magrassi & A Lanzara, Div Neurol 1, I-81100 Caserta, Italy
[5] Reg Interuniv Ctr Res Neurosci CIRN, Naples, Italy
[6] Univ Ulm, Dept Neurol, D-89081 Ulm, Germany
[7] Univ Turin, Dept Neurosci, I-10126 Turin, Italy
[8] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
关键词
MicroRNAs; sALS; Leukocytes; CSF; Spinal cord; Real-time PCR; ALZHEIMERS-DISEASE; MICRORNA EXPRESSION; HEXANUCLEOTIDE REPEAT; UP-REGULATION; PROGRESSION; MICROARRAY; BRAIN; IDENTIFICATION; BIOMARKERS; LEUKOCYTES;
D O I
10.1007/s10048-014-0420-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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.
引用
收藏
页码:243 / 253
页数:11
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