Microarray analysis of long non-coding RNAs in COPD lung tissue

被引:70
作者
Bi, Hui [1 ]
Zhou, Ji [1 ]
Wu, Dandan [1 ]
Gao, Wei [1 ]
Li, Lingling [1 ]
Yu, Like [2 ]
Liu, Feng [2 ]
Huang, Mao [1 ]
Adcock, Ian M. [3 ]
Barnes, Peter J. [3 ]
Yao, Xin [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Resp Med, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Chest Hosp, Dept Resp Med, Nanjing, Jiangsu, Peoples R China
[3] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, Airway Dis Sect, London, England
基金
中国国家自然科学基金;
关键词
Long noncoding RNA; COPD; Microarray analysis; Inflammation; OBSTRUCTIVE PULMONARY-DISEASE; CIGARETTE-SMOKE; XIST GENE; FOLLOW-UP; T-CELLS; MODEL;
D O I
10.1007/s00011-014-0790-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Long noncoding RNAs (lncRNAs) play an important role in the pathogenesis of many human diseases. In this study, we provide the description of genome-wide lncRNA expression in the lung tissue of non-smokers without Chronic obstructive pulmonary disease (COPD), of smokers without COPD and of smokers with COPD. RNA was extracted from human lung tissue and analysed using an Agilent Human lncRNA + mRNA Array v2.0 system. 39,253 distinct lncRNA transcripts were detected in the lung tissues of all subjects. In smokers without COPD 87 lncRNAs were significantly up-regulated and 244 down-regulated compared to non-smokers without COPD with RNA50010|UCSC-9199-1005 and RNA58351| CombinedLit_316_550, the most over- and under-regulated, respectively. In contrast, in COPD patients 120 lncRNAs were over-expressed and 43 under-expressed compared with smokers without COPD with RNA44121|UCSC-2000-3182 and RNA43510|UCSC-1260-3754 being the most over- and under-regulated, respectively. Gene Ontology (GO) and pathway analysis indicated that cigarette smoking was associated with activation of metabolic pathways, whereas COPD transcripts were associated with 'hematopoietic cell lineage', intermediary metabolism and immune system processes. We conclude that the altered expression of lncRNAs might play partial role in pathways implicated in COPD onset and progression such as intermediary metabolism and the immune response.
引用
收藏
页码:119 / 126
页数:8
相关论文
共 31 条
  • [1] [Anonymous], 2014, Global Strategy for the Diagnosis, Management and Prevention of COPD, Global Initiative for Chronic Obstructive Lung Disease
  • [2] Network biology:: Understanding the cell's functional organization
    Barabási, AL
    Oltvai, ZN
    [J]. NATURE REVIEWS GENETICS, 2004, 5 (02) : 101 - U15
  • [3] Chronic obstructive pulmonary disease: molecular and cellular mechanisms
    Barnes, PJ
    Shapiro, SD
    Pauwels, RA
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (04) : 672 - 688
  • [4] THE PRODUCT OF THE MOUSE XIST GENE IS A 15 KB INACTIVE X-SPECIFIC TRANSCRIPT CONTAINING NO CONSERVED ORF AND LOCATED IN THE NUCLEUS
    BROCKDORFF, N
    ASHWORTH, A
    KAY, GF
    MCCABE, VM
    NORRIS, DP
    COOPER, PJ
    SWIFT, S
    RASTAN, S
    [J]. CELL, 1992, 71 (03) : 515 - 526
  • [5] THE HUMAN XIST GENE - ANALYSIS OF A 17 KB INACTIVE X-SPECIFIC RNA THAT CONTAINS CONSERVED REPEATS AND IS HIGHLY LOCALIZED WITHIN THE NUCLEUS
    BROWN, CJ
    HENDRICH, BD
    RUPERT, JL
    LAFRENIERE, RG
    XING, Y
    LAWRENCE, J
    WILLARD, HF
    [J]. CELL, 1992, 71 (03) : 527 - 542
  • [6] Carr SJ, 2009, J CARDIOPULM REHABIL, V29, P318, DOI 10.1097/HCR.0b013e3181ac7bb8
  • [7] Non-coding RNAs, epigenetics and complexity
    Costa, Fabricio F.
    [J]. GENE, 2008, 410 (01) : 9 - 17
  • [8] Plasma markers of inflammation and incidence of hospitalisations for COPD: results from a population-based cohort study
    Engstrom, G.
    Segelstorm, N.
    Ekberg-Aronsson, M.
    Nilsson, P. M.
    Lindgarde, F.
    Lofdahl, C-G
    [J]. THORAX, 2009, 64 (03) : 211 - 215
  • [9] Regulatory roles of natural antisense transcripts
    Faghihi, Mohammad Ali
    Wahlestedt, Claes
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (09) : 637 - 643
  • [10] Three-year follow-up of Interleukin 6 and C-reactive protein in chronic obstructive pulmonary disease
    Ferrari, Renata
    Tanni, Suzana E.
    Caram, Laura M. O.
    Correa, Corina
    Correa, Camila R.
    Godoy, Irma
    [J]. RESPIRATORY RESEARCH, 2013, 14