Immunomodulatory potential of gut microbiome-derived short-chain fatty acids (SCFAs)

被引:440
作者
Ratajczak, Weronika [1 ]
Ryl, Aleksandra [2 ]
Mizerski, Arnold [3 ]
Walczakiewicz, Kinga [1 ]
Sipak, Olimpia [4 ]
Laszczynska, Maria [1 ]
机构
[1] Pomeranian Med Univ, Dept Histol & Dev Biol, Szczecin, Poland
[2] Pomeranian Med Univ, Dept Med Rehabil & Clin Physiotherapy, Szczecin, Poland
[3] Pomeranian Med Univ, Dept Gen Pharmacol & Pharmacoecon, Szczecin, Poland
[4] Pomeranian Med Univ, Dept Obstet & Pathol Pregnancy, Szczecin, Poland
关键词
intestinal microbiota; dysbiosis; short-chain fatty acids (SCFAs); inflammation; inflammasome; REGULATORY T-CELLS; HISTONE DEACETYLASE INHIBITORS; INTESTINAL MICROBIOTA; OXIDATIVE STRESS; DIETARY FIBER; RECEPTORS; METABOLITES; DISEASE; INFLAMMASOME; PATHWAYS;
D O I
10.18388/abp.2018_2648
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intestinal microbiota is an element of the bacterial ecosystem in all mammalian organisms. These microorganisms play a very important part in the development, functioning, and modulation of the immune system from the moment of birth. In recent years, owing to the use of modern sequencing techniques, the microbiome composition in healthy people has been identified based on bacterial 16S rRNA analysis. Currently, more and more attention is being given to the influence of microorganisms on the host's cellular metabolism. Analysis of microbial metabolites, among them short-chain fatty acids (SCFAs), and disruption of intestinal microbiota homeostasis in terms of their effects on molecular regulatory mechanisms of immune reactions will surely improve the understanding of the etiology of many common diseases. SCFAs, mainly butyrate, propionate, and acetate, occur in specific amounts, and their proportions can change, depending on the diet, age and diseases. The levels of SCFAs are substantially influenced by the ratio of commensal intestinal bacteria, the disturbance of which (dysbiosis) can lead to a disproportion between the SCFAs produced. SCFAs are regarded as mediators in the communication between the intestinal microbiome and the immune system. The signal they produce is transferred, among others, in immune cells via free fatty acid receptors (FFARs), which belong to the family of G protein-coupled receptors (GPCRs). It has been also confirmed that SCFAs inhibit the activity of histone deacetylase (HDAC) - an enzyme involved in post-translational modifications, namely the process of deacetylation and, what is new, the process of histone crotonylation. These properties of SCFAs have an effect on their immunomodulatory potential i.e. maintaining the anti/pro-inflammatory balance. SCFAs act not only locally in the intestines colonized by commensal bacteria, but also influence the intestinal immune cells, and modulate immune response by multi-protein inflammasome complexes. SCFAs have been confirmed to contribute to the maintenance of the immune homeostasis of the urinary system (kidneys), respiratory system (lungs), central nervous system, and the sight organ.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 107 条
[41]   Short-chain fatty acids and ketones directly regulate sympathetic nervous system via G protein-coupled receptor 41 (GPR41) [J].
Kimura, Ikuo ;
Inoue, Daisuke ;
Maeda, Takeshi ;
Hara, Takafumi ;
Ichimura, Atsuhiko ;
Miyauchi, Satoshi ;
Kobayashi, Makio ;
Hirasawa, Akira ;
Tsujimoto, Gozoh .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (19) :8030-8035
[42]   Short-chain fatty acids, GPR41 and GPR43 ligands, inhibit TNF-α-induced MCP-1 expression by modulating p38 and JNK signaling pathways in human renal cortical epithelial cells [J].
Kobayashi, Mamiko ;
Mikami, Daisuke ;
Kimura, Hideki ;
Kamiyama, Kazuko ;
Morikawa, Yukie ;
Yokoi, Seiji ;
Kasuno, Kenji ;
Takahashi, Naoki ;
Taniguchi, Takanobu ;
Iwano, Masayuki .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2017, 486 (02) :499-505
[43]   From Dietary Fiber to Host Physiology: Short-Chain Fatty Acids as Key Bacterial Metabolites [J].
Koh, Ara ;
De Vadder, Filipe ;
Kovatcheva-Datchary, Petia ;
Backhed, Fredrik .
CELL, 2016, 165 (06) :1332-1345
[44]  
Komiya Y, 2018, GUT, DOI [10.1136/gut-jnl-2018-316661, DOI 10.1136/GUT-JNL-2018-316661]
[45]   Novel adipokines: their potential role in the pathogenesis of obesity and metabolic disorders [J].
Korek, Emilia ;
Krauss, Hanna .
POSTEPY HIGIENY I MEDYCYNY DOSWIADCZALNEJ, 2015, 69 :799-810
[46]   MICROBIOME Growth dynamics of gut microbiota in health and disease inferred from single metagenomic samples [J].
Korem, Tal ;
Zeevi, David ;
Suez, Jotham ;
Weinberger, Adina ;
Avnit-Sagi, Tali ;
Pompan-Lotan, Maya ;
Matot, Elad ;
Jona, Ghil ;
Harmelin, Alon ;
Cohen, Nadav ;
Sirota-Madi, Alexandra ;
Thaiss, Christoph A. ;
Pevsner-Fischer, Meirav ;
Sorek, Rotem ;
Xavier, Ramnik J. ;
Elinav, Eran ;
Segal, Eran .
SCIENCE, 2015, 349 (6252) :1101-1106
[47]   Microbial shifts in the aging mouse gut [J].
Langille, Morgan Gi ;
Meehan, Conor J. ;
Koenig, Jeremy E. ;
Dhanani, Akhilesh S. ;
Rose, Robert A. ;
Howlett, Susan E. ;
Beiko, Robert G. .
MICROBIOME, 2014, 2
[48]   Richness of human gut microbiome correlates with metabolic markers [J].
Le Chatelier, Emmanuelle ;
Nielsen, Trine ;
Qin, Junjie ;
Prifti, Edi ;
Hildebrand, Falk ;
Falony, Gwen ;
Almeida, Mathieu ;
Arumugam, Manimozhiyan ;
Batto, Jean-Michel ;
Kennedy, Sean ;
Leonard, Pierre ;
Li, Junhua ;
Burgdorf, Kristoffer ;
Grarup, Niels ;
Jorgensen, Torben ;
Brandslund, Ivan ;
Nielsen, Henrik Bjorn ;
Juncker, Agnieszka S. ;
Bertalan, Marcelo ;
Levenez, Florence ;
Pons, Nicolas ;
Rasmussen, Simon ;
Sunagawa, Shinichi ;
Tap, Julien ;
Tims, Sebastian ;
Zoetendal, Erwin G. ;
Brunak, Soren ;
Clement, Karine ;
Dore, Joel ;
Kleerebezem, Michiel ;
Kristiansen, Karsten ;
Renault, Pierre ;
Sicheritz-Ponten, Thomas ;
de Vos, Willem M. ;
Zucker, Jean-Daniel ;
Raes, Jeroen ;
Hansen, Torben ;
Bork, Peer ;
Wang, Jun ;
Ehrlich, S. Dusko ;
Pedersen, Oluf .
NATURE, 2013, 500 (7464) :541-+
[49]   Functional characterization of human receptors for short chain fatty acids and their role in polymorphonuclear cell activation [J].
Le Poul, E ;
Loison, C ;
Struyf, S ;
Springael, JY ;
Lannoy, V ;
Decobecq, ME ;
Brezillon, S ;
Dupriez, V ;
Vassart, G ;
Van Damme, J ;
Parmentier, M ;
Detheux, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (28) :25481-25489
[50]   Microbiota in T-cell homeostasis and inflammatory diseases [J].
Lee, Naeun ;
Kim, Wan-Uk .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2017, 49 :e340-e340