MicroRNA and Gut Microbiota: Tiny but Mighty-Novel Insights into Their Cross-talk in Inflammatory Bowel Disease Pathogenesis and Therapeutics

被引:52
作者
Casado-Bedmar, Maite [1 ]
Viennois, Emilie [1 ]
机构
[1] Univ Paris, Ctr Res Inflammat, U1149, INSERM, F-75018 Paris, France
关键词
MicroRNA; microbiota; inflammatory bowel disease; INTESTINAL BARRIER DYSFUNCTION; ENDOPLASMIC-RETICULUM STRESS; COLI NISSLE 1917; ULCERATIVE-COLITIS; EXPRESSION PROFILES; FECAL MICROBIOTA; EPITHELIAL-CELLS; PLANT MICRORNAS; ILEAL MUCOSA; MIR-155;
D O I
10.1093/ecco-jcc/jjab223
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
MicroRNAs [miRNAs], small non-coding RNAs, have recently been described as crucial contributors to intestinal homeostasis. They can interact with the gut microbiota in a reciprocal manner and deeply affect host health status, leading to several disorders when unbalanced. Inflammatory bowel disease [IBD] is a chronic inflammation of the gastrointestinal tract that co-occurs with alterations of the gut microbiota, and whose aetiology remains largely unclear. On one hand, host miRNA could be playing a relevant role in IBD pathophysiology by shaping the gut microbiota. The gut microbiome, on the other hand, may regulate the expression of host miRNAs, resulting in intestinal epithelial dysfunction, altered autophagy, and immune hyperactivation. Interestingly, it has been hypothesised that their reciprocal impact may be used for therapeutic goals. This review describes the latest research and suggests mechanisms through which miRNA and intestinal microbiota, as joint actors, may participate specifically in IBD pathophysiology. Furthermore, we discuss the diagnostic power and therapeutic potential resulting from their bidirectional communication after faecal transplantation, probiotics intake, or anti-miRNAs or miRNA mimics administration. The current literature is summarised in the present work in a comprehensive manner, hoping to provide a better understanding of the miRNA-microbiota cross-talk and to facilitate their application in IBD.
引用
收藏
页码:992 / 1005
页数:14
相关论文
共 158 条
[1]  
Ahmed Hassan Elham, 2020, Gastroenterol Hepatol Bed Bench, V13, P147
[2]   The global, regional, and national burden of inflammatory bowel disease in 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017 [J].
Alatab, Sudabeh ;
Sepanlou, Sadaf G. ;
Ikuta, Kevin ;
Vahedi, Homayoon ;
Bisignano, Catherine ;
Safiri, Saeid ;
Sadeghi, Anahita ;
Nixon, Molly R. ;
Abdoli, Amir ;
Abolhassani, Hassan ;
Alipour, Vahid ;
Almadi, Majid A. H. ;
Almasi-Hashiani, Amir ;
Anushiravani, Amir ;
Arabloo, Jalal ;
Atique, Suleman ;
Awasthi, Ashish ;
Badawi, Alaa ;
Baig, Atif A. A. ;
Bhala, Neeraj ;
Bijani, Ali ;
Biondi, Antonio ;
Borzi, Antonio M. ;
Burke, Kristin E. ;
Carvalho, Felix ;
Daryani, Ahmad ;
Dubey, Manisha ;
Eftekhari, Aziz ;
Fernandes, Eduarda ;
Fernandes, Joao C. ;
Fischer, Florian ;
Haj-Mirzaian, Arvin ;
Haj-Mirzaian, Arya ;
Hasanzadeh, Amir ;
Hashemian, Maryam ;
Hay, Simon, I ;
Hoang, Chi L. ;
Househ, Mowafa ;
Ilesanmi, Olayinka S. ;
Balalami, Nader Jafari ;
James, Spencer L. ;
Kengne, Andre P. ;
Malekzadeh, Masoud M. ;
Merat, Shahin ;
Meretoja, Tuomo J. ;
Mestrovic, Tomislav ;
Mirrakhimov, Erkin M. ;
Mirzaei, Hamed ;
Mohammad, Karzan A. ;
Mokdad, Ali H. .
LANCET GASTROENTEROLOGY & HEPATOLOGY, 2020, 5 (01) :17-30
[3]   Discovery of inflammatory bowel disease-associated miRNAs using a novel bipartite clustering approach [J].
Altaf-Ul-Amin, Md. ;
Karim, Mohammad Bozlul ;
Hu, Pingzhao ;
Ono, Naoaki ;
Kanaya, Shigehiko .
BMC MEDICAL GENOMICS, 2020, 13 (Suppl 3)
[4]   European evidence based consensus for endoscopy in inflammatory bowel disease [J].
Annese, Vito ;
Daperno, Marco ;
Rutter, Matthew D. ;
Amiot, Aurelien ;
Bossuyt, Peter ;
East, James ;
Ferrante, Marc ;
Goetz, Martin ;
Katsanos, Konstantinos H. ;
Kiesslich, Ralf ;
Ordas, Ingrid ;
Repici, Alessandro ;
Rosa, Bruno ;
Sebastian, Shaji ;
Kucharzik, Torsten ;
Eliakim, Rami .
JOURNAL OF CROHNS & COLITIS, 2013, 7 (12) :982-1018
[5]   The Intestinal Microbiota Interferes with the microRNA Response upon Oral Listeria Infection [J].
Archambaud, Cristel ;
Sismeiro, Odile ;
Toedling, Joern ;
Soubigou, Guillaume ;
Becavin, Christophe ;
Lechat, Pierre ;
Lebreton, Alice ;
Ciaudo, Constance ;
Cossart, Pascale .
MBIO, 2013, 4 (06)
[6]   Mucosal Gene Expression of Antimicrobial Peptides in Inflammatory Bowel Disease Before and After First Infliximab Treatment [J].
Arijs, Ingrid ;
De Hertogh, Gert ;
Lemaire, Katleen ;
Quintens, Roel ;
Van Lommel, Leentje ;
Van Steen, Kristel ;
Leemans, Peter ;
Cleynen, Isabelle ;
Van Assche, Gert ;
Vermeire, Severine ;
Geboes, Karel ;
Schuit, Frans ;
Rutgeerts, Paul .
PLOS ONE, 2009, 4 (11)
[7]   Personalizing Treatment in IBD: Hype or Reality in 2020? Can We Predict Response to Anti-TNF? [J].
Atreya, Raja ;
Neurath, Markus F. ;
Siegmund, Britta .
FRONTIERS IN MEDICINE, 2020, 7
[8]   Faecal microbiota transplantation for recurrent Clostridioides difficile infection: An updated systematic review and meta-analysis [J].
Baunwall, Simon Mark Dahl ;
Lee, Mads Ming ;
Eriksen, Marcel Kjaersgaard ;
Mullish, Benjamin H. ;
Marchesi, Julian R. ;
Dahlerup, Jens Frederik ;
Hvas, Christian Lodberg .
ECLINICALMEDICINE, 2020, 29-30
[9]   Role of Altered Expression of miR-146a, miR-155, and miR-122 in Pediatric Patients with Inflammatory Bowel Disease [J].
Beres, Nora J. ;
Szabo, Doloresz ;
Kocsis, Dorottya ;
Szucs, Daniel ;
Kiss, Zoltan ;
Mueller, Katalin E. ;
Lendvai, Gabor ;
Kiss, Andras ;
Arato, Andras ;
Sziksz, Erna ;
Vannay, Adam ;
Szabo, Attila J. ;
Veres, Gabor .
INFLAMMATORY BOWEL DISEASES, 2016, 22 (02) :327-335
[10]   miR-146a is a significant brake on autoimmunity, myeloproliferation, and cancer in mice [J].
Boldin, Mark P. ;
Taganov, Konstantin D. ;
Rao, Dinesh S. ;
Yang, Lili ;
Zhao, Jimmy L. ;
Kalwani, Manorama ;
Garcia-Flores, Yvette ;
Luong, Mui ;
Devrekanli, Asli ;
Xu, Jessica ;
Sun, Guizhen ;
Tay, Jia ;
Linsley, Peter S. ;
Baltimore, David .
JOURNAL OF EXPERIMENTAL MEDICINE, 2011, 208 (06) :1189-1201