MicroRNA expression in the aging mouse thymus

被引:19
作者
Ye, Yaqiong [1 ]
Li, Daotong [1 ]
Ouyang, Dan [1 ]
Deng, Li [1 ]
Zhang, Yuan [1 ]
Ma, Yongjiang [1 ]
Li, Yugu [1 ]
机构
[1] South China Agr Univ, Coll Vet Med, Guangzhou 510642, Guangdong, Peoples R China
关键词
MicroRNA; Aging; Thymus; Mice; Cancer; Signaling pathway; AGE-ASSOCIATED CHANGES; INSULIN-RECEPTOR; CELL-PROLIFERATION; BONE-MARROW; YOUNG-ADULT; LIFE-SPAN; APOPTOSIS; FAMILY; GENES; SENESCENCE;
D O I
10.1016/j.gene.2014.06.039
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
MicroRNAs (miRNAs) have been implicated in the process of aging in many model organisms, such as Caenorhabitis elegans, and in many organs, such as the mouse lung and human epididymis. However, the role of miRNAs in the thymus tissues of the aging mouse remains unclear. To address this question, we investigated the miRNA expression profiles in the thymuses of 1-, 10- and 19-month-old mice using miRNA array and qRT-PCR assays. A total of 223 mouse miRNAs were screened, and the expression levels of those miRNAs exhibited gradual increases and decreases over the course of thymus aging. Fifty miRNAs in the 10-month-old thymus and 81 miRNAs in the 19-month-old thymus were defined as differentially expressed miRNAs (p < 0.05) in comparison with their levels in the 1-month-old mouse, and approximately one-third of these miRNAs were grouped within 11 miRNA clusters. Each miRNA cluster contained 2 to 5 miRNA genes, and most of the cluster members displayed similar expression patterns, being either increased or decreased. In addition, Ingenuity Pathway Analysis (IPA) software and the IPA database were used to analyze the 12 miRNAs that exhibited significant expression changes, revealing that as many as 15 pathways may be involved. Thus, our current study determined the expression profiles of miRNAs in the mouse thymus during the process of aging. The results suggested that these miRNAs could become meaningful biomarkers for studying thymus aging and that the aging-related alternations in miRNA expression may be involved in the regulation of cell proliferation, apoptosis, development and carcinogenesis/tumorigenesis. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:218 / 225
页数:8
相关论文
共 59 条
[31]   MicroRNAs: Novel Diagnostic and Therapeutic Tools for Pancreatic Ductal Adenocarcinoma? [J].
Mardin, Wolf Arif ;
Mees, Soeren Torge .
ANNALS OF SURGICAL ONCOLOGY, 2009, 16 (11) :3183-3189
[32]   Epithelial framework reorganization during human thymus involution [J].
Marinova, TT .
GERONTOLOGY, 2005, 51 (01) :14-18
[33]   MicroRNA Profiling of Epstein-Barr Virus-Associated NK/T-Cell Lymphomas by Deep Sequencing [J].
Motsch, Natalie ;
Alles, Julia ;
Imig, Jochen ;
Zhu, Jiayun ;
Barth, Stephanie ;
Reineke, Tanja ;
Tinguely, Marianne ;
Cogliatti, Sergio ;
Dueck, Anne ;
Meister, Gunter ;
Renner, Christoph ;
Graesser, Friedrich A. .
PLOS ONE, 2012, 7 (08)
[34]   MicroRNAs linking inflamm-aging, cellular senescence and cancer [J].
Olivieri, Fabiola ;
Rippo, Maria Rita ;
Monsurro, Vladia ;
Salvioli, Stefano ;
Capri, Miriam ;
Procopio, Antonio Domenico ;
Franceschi, Claudio .
AGEING RESEARCH REVIEWS, 2013, 12 (04) :1056-1068
[35]   13q14 deletions in CLL involve cooperating tumor suppressors [J].
Palamarchuk, Alexey ;
Efanov, Alexey ;
Nazaryan, Natalya ;
Santanam, Urmila ;
Alder, Hansjuerg ;
Rassenti, Laura ;
Kipps, Thomas ;
Croce, Carlo M. ;
Pekarsky, Yuri .
BLOOD, 2010, 115 (19) :3916-3922
[36]   Age-Associated Changes in MicroRNA Expression in Bone Marrow Derived Dendritic Cells [J].
Park, Seungbum ;
Kang, Soowon ;
Min, Kyung Hoon ;
Hwang, Kwang Woo ;
Min, Hyeyoung .
IMMUNOLOGICAL INVESTIGATIONS, 2013, 42 (03) :179-190
[37]   The miR-200 family determines the epithelial phenotype of cancer cells by targeting the E-cadherin repressors ZEB1 and ZEB2 [J].
Park, Sun-Mi ;
Gaur, Arti B. ;
Lengyel, Ernst ;
Peter, Marcus E. .
GENES & DEVELOPMENT, 2008, 22 (07) :894-907
[38]   MicroRNA function: Multiple mechanisms for a tiny RNA? [J].
Pillai, RS .
RNA, 2005, 11 (12) :1753-1761
[39]   Clinical implications of physiological changes in the aging heart [J].
Pugh, KG ;
Wei, JY .
DRUGS & AGING, 2001, 18 (04) :263-276
[40]   Inflammatory signaling and cellular senescence [J].
Ren, Jian-Lin ;
Pan, Jin-Shui ;
Lu, Ya-Pi ;
Sun, Peiqing ;
Han, Jiahuai .
CELLULAR SIGNALLING, 2009, 21 (03) :378-383