Bronchial Epithelial Cells from Cystic Fibrosis Patients Express a Specific Long Non-coding RNA Signature upon Pseudomonas aeruginosa Infection

被引:39
作者
Balloy, Viviane [1 ]
Koshy, Remya [2 ]
Perra, Lea [1 ]
Corvol, Harriet [1 ,3 ]
Chignard, Michel [1 ]
Guillot, Loic [1 ]
Scaria, Vinod [2 ,4 ]
机构
[1] UPMC Univ Paris 06, Sorbonne Univ, INSERM, CRSA, Paris, France
[2] CSIR, Inst Genom & Integrat Biol, GN Ramachandran Knowledge Ctr Genome Informat, Delhi, India
[3] Hop Trousseau, AP HP, Pneumol Pediat, Paris, France
[4] CSIR, Inst Genom & Integrat Biol, Acad Sci & Innovat Res, Delhi, India
关键词
cystic fibrosis; lung; epithelium; Pseudomonas aeruginosa; IncRNA; NEGATIVE PROGNOSTIC-FACTOR; LINC-UBC1; NEST;
D O I
10.3389/fcimb.2017.00218
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pseudomonas aeruginosa (Pa) is the leading cause of chronic lung infection in Cystic Fibrosis (CF) patients. It is well recognized that CF epithelial cells fail to develop an appropriate response to infection, allowing bacterial colonization and a chronic inflammatory response. Since long non-coding RNAs (IncRNAs), are known to play a key role in regulating mammalian innate immune response, we hypothesized that CF cells exposed to Pa could express a specific IncRNA signature responsible of the maladaptative CF response. We analyzed transcriptomic datasets to compare the expression profiles of IncRNAs in primary CF and non-CF epithelial cells infected with Pa at 0, 2, 4, and 6 h of infection. Our analysis identified temporal expression signatures of 25, 73, 15, and 26 IncRNA transcripts differentially expressed at 0, 2, 4, and 6 h post-infection respectively, between CF and non-CF cells. In addition, we identified profiles specific to CF and non-CF cells. The differential expression of two candidate IncRNAs were independently validated using real-time PCR. We identified a specific CF signature of IncRNA expression in a context of Pa infection that could potentially play a role in the maladaptive immune response of CF patients.
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页数:9
相关论文
共 27 条
[1]   Normal and Cystic Fibrosis Human Bronchial Epithelial Cells Infected with Pseudomonas aeruginosa Exhibit Distinct Gene Activation Patterns [J].
Balloy, Viviane ;
Varet, Hugo ;
Dillies, Marie-Agnes ;
Proux, Caroline ;
Jagla, Bernd ;
Coppee, Jean-Yves ;
Tabary, Olivier ;
Corvol, Harriet ;
Chignard, Michel ;
Guillot, Loiec .
PLOS ONE, 2015, 10 (10)
[2]   Airway inflammation in cystic fibrosis: molecular mechanisms and clinical implications [J].
Cohen-Cymberknoh, Malena ;
Kerem, Eitan ;
Ferkol, Thomas ;
Elizur, Arnon .
THORAX, 2013, 68 (12) :1157-1162
[3]   Making a NeST for a Persistent Virus [J].
Cullen, Bryan R. .
CELL HOST & MICROBE, 2013, 13 (03) :241-242
[4]  
Elborn J. S., 2016, CYSTIC FI BROSIS, V388
[5]   Function and evolution of the long noncoding RNA circuitry orchestrating X-chromosome inactivation in mammals [J].
Furlan, Giulia ;
Rougeulle, Claire .
WILEY INTERDISCIPLINARY REVIEWS-RNA, 2016, 7 (05) :702-722
[6]   The NeST Long ncRNA Controls Microbial Susceptibility and Epigenetic Activation of the Interferon-γ Locus [J].
Gomez, J. Antonio ;
Wapinski, Orly L. ;
Yang, Yul W. ;
Bureau, Jean-Francois ;
Gopinath, Smita ;
Monack, Denise M. ;
Chang, Howard Y. ;
Brahic, Michel ;
Kirkegaard, Karla .
CELL, 2013, 152 (04) :743-754
[7]   linc-UBC1 physically associates with polycomb repressive complex 2 (PRC2) and acts as a negative prognostic factor for lymph node metastasis and survival in bladder cancer [J].
He, Wang ;
Cai, Qingqing ;
Sun, Fenyong ;
Zhong, Guangzheng ;
Wang, Pei ;
Liu, Hongyan ;
Luo, Junhua ;
Yu, Hao ;
Huang, Jian ;
Lin, Tianxin .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2013, 1832 (10) :1528-1537
[8]  
Hu YR, 2015, INT J CLIN EXP PATHO, V8, P594
[9]   Long Noncoding RNA NEAT1-Dependent SFPQ Relocation from Promoter Region to Paraspeckle Mediates IL8 Expression upon Immune Stimuli [J].
Imamura, Katsutoshi ;
Imamachi, Naoto ;
Akizuki, Gen ;
Kumakura, Michiko ;
Kawaguchi, Atsushi ;
Nagata, Kyosuke ;
Kato, Akihisa ;
Kawaguchi, Yasushi ;
Sato, Hiroki ;
Yoneda, Misako ;
Kai, Chieko ;
Yada, Tetsushi ;
Suzuki, Yutaka ;
Yamada, Toshimichi ;
Ozawa, Takeaki ;
Kaneki, Kiyomi ;
Inoue, Tsuyoshi ;
Kobayashi, Mika ;
Kodama, Tatsuhiko ;
Wada, Youichiro ;
Sekimizu, Kazuhisa ;
Akimitsu, Nobuyoshi .
MOLECULAR CELL, 2014, 53 (03) :393-406
[10]  
Li R., 2016, J IMMUNOL, V196