Specific induction of the unique GPR15 expression in heterogeneous blood lymphocytes by tobacco smoking

被引:14
作者
Bauer, Mario [1 ]
Hackermueller, Joerg [2 ]
Schor, Jana [2 ]
Schreiber, Stephan [2 ]
Fink, Beate [1 ]
Pierzchalski, Arkadiusz [1 ]
Herberth, Gunda [1 ]
机构
[1] Helmholtz Ctr Environm Res GmbH UFZ, Dept Environm Immunol, Leipzig, Germany
[2] Helmholtz Ctr Environm Res GmbH UFZ, Young Investigators Grp Bioinformat & Transcript, Leipzig, Germany
关键词
GPR15; MAIT; Th17; Treg; smoking; RECEPTOR GPR15; MAIT CELLS; DISEASE; INNATE;
D O I
10.1080/1354750X.2018.1539769
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Purpose: In the peripheral blood, it has been shown that smoking is, to date, the only specific condition leading to an increase in GPR15+ T cells. We, therefore, aimed to characterize GPR15-expressing blood T cells in more detail. Materials and Methods: The whole transcriptome by RNAseq as a proxy for protein expression was analyzed in GPR15+ and GPR15- T cells. A deep immuno-phenotyping was conducted for the identification of T cell subtypes. Results: The expression of GPR15 seemed to be unique, not concomitantly accompanied with the expression of another protein. According to different T cell subtypes, there is no single cell type prominently represented in GPR15+ T cells. The individually different proportions of GPR15+ cells among each GPR15-expressing T cell subtypes in blood were strongly associated with chronic smoking. Indeed, the frequency of GPR15+ T cell subtypes can be effectively used as a highly convincing biomarker for tobacco smoking. Conclusions: While the chronic smoking-induced enrichment of GPR15+ T cells in blood might indicate a systemic inflammation, by the widespread presence in different T cell subtypes, GPR15 could feature a general impact on maintaining the systemic homeostasis to putatively prevent harm from smoking.
引用
收藏
页码:217 / 224
页数:8
相关论文
共 33 条
[1]   Differential expression of GPR15 on T cells during ulcerative colitis [J].
Adamczyk, Alexandra ;
Gageik, Daniel ;
Frede, Annika ;
Pastille, Eva ;
Hansen, Wiebke ;
Rueffer, Andreas ;
Buer, Jan ;
Buening, Juergen ;
Langhorst, Jost ;
Westendorf, Astrid M. .
JCI INSIGHT, 2017, 2 (08)
[2]   Tobacco smoking-associated genome-wide DNA methylation changes in the EPIC study [J].
Ambatipudi, Srikant ;
Cuenin, Cyrille ;
Hernandez-Vargas, Hector ;
Ghantous, Akram ;
Le Calvez-Kelm, Florence ;
Kaaks, Rudolf ;
Barrdahl, Myrto ;
Boeing, Heiner ;
Aleksandrova, Krasimira ;
Trichopoulou, Antonia ;
Lagiou, Pagona ;
Naska, Androniki ;
Palli, Domenico ;
Krogh, Vittorio ;
Polidoro, Silvia ;
Tumino, Rosario ;
Panico, Salvatore ;
Bueno-de-Mesquita, Bas ;
Peeters, Petra H. M. ;
Quiros, Jose Ramon ;
Navarro, Carmen ;
Ardanaz, Eva ;
Dorronsoro, Miren ;
Key, Tim ;
Vineis, Paolo ;
Murphy, Neil ;
Riboli, Elio ;
Romieu, Isabelle ;
Herceg, Zdenko .
EPIGENOMICS, 2016, 8 (05) :599-618
[3]   Smoking reduces circulating CD26hiCD161hi MAIT cells in healthy individuals and patients with multiple sclerosis [J].
Ammitzboll, Cecilie ;
Bornsen, Lars ;
Christensen, Jeppe Romme ;
Ratzer, Rikke ;
Nielsen, Birgitte Romme ;
Sondergaard, Helle B. ;
von Essen, Marina R. ;
Sellebjerg, Finn .
JOURNAL OF LEUKOCYTE BIOLOGY, 2017, 101 (05) :1211-1220
[4]   HTSeq-a Python']Python framework to work with high-throughput sequencing data [J].
Anders, Simon ;
Pyl, Paul Theodor ;
Huber, Wolfgang .
BIOINFORMATICS, 2015, 31 (02) :166-169
[5]   Tobacco-smoking induced GPR15-expressing T cells in blood do not indicate pulmonary damage [J].
Bauer, Mario ;
Fink, Beate ;
Seyfarth, Hans-Juergen ;
Wirtz, Hubert ;
Frille, Armin .
BMC PULMONARY MEDICINE, 2017, 17
[6]  
Bauer M, 2016, CLIN EPIGENETICS, V8, DOI [10.1186/s13148-015-0113-1, 10.1186/s13148-016-0249-7]
[7]  
Bottcher K., 2018, HEPATOLOGY
[8]   In siblings with similar genetic susceptibility for inflammatory bowel disease, smokers tend to develop Crohn's disease and non-smokers develop ulcerative colitis [J].
Bridger, S ;
Lee, JCW ;
Bjarnason, I ;
Jones, JEL ;
Macpherson, AJ .
GUT, 2002, 51 (01) :21-25
[9]   Global transcriptional analysis of psoriatic skin and blood confirms known disease-associated pathways and highlights novel genomic "hot spots" for differentially expressed genes [J].
Coda, Alvin B. ;
Icen, Murat ;
Smith, Jason R. ;
Sinha, Animesh A. .
GENOMICS, 2012, 100 (01) :18-26
[10]   Expression cloning of new receptors used by simian and human immunodeficiency viruses [J].
Deng, HK ;
Unutmaz, D ;
KewalRamani, VN ;
Littman, DR .
NATURE, 1997, 388 (6639) :296-300