참고문헌
- Heinonen, K. M. and C. Perreault. 2008. Development and functional properties of thymic and extrathymic T lymphocytes. Crit. Rev. Immunol. 28: 441-466. https://doi.org/10.1615/CritRevImmunol.v28.i5.40
- Bhandoola, A., B. H. von, H. T. Petrie, and J. C. Zuniga-Pflucker. 2007. Commitment and developmental potential of extrathymic and intrathymic T cell precursors: plenty to choose from. Immunity 26: 678-689. https://doi.org/10.1016/j.immuni.2007.05.009
- Gapin, L. 2014. Check MAIT. J. Immunol. 192: 4475-4480. https://doi.org/10.4049/jimmunol.1400119
- Rossjohn, J., D. G. Pellicci, O. Patel, L. Gapin, and D. I. Godfrey. 2012. Recognition of CD1d-restricted antigens by natural killer T cells. Nat. Rev. Immunol. 12: 845-857. https://doi.org/10.1038/nri3328
- Wan, Y. Y. 2010. Multi-tasking of helper T cells. Immunology 130: 166-171. https://doi.org/10.1111/j.1365-2567.2010.03289.x
- Li, P., R. Spolski, W. Liao, and W. J. Leonard. 2014. Complex interactions of transcription factors in mediating cytokine biology in T cells. Immunol. Rev. 261: 141-156. https://doi.org/10.1111/imr.12199
- Gratz, I. K., and D. J. Campbell. 2014. Organ-specific and memory treg cells: specificity, development, function, and maintenance. Front Immunol. 5: 333.
- Liston, A., and D. H. Gray. 2014. Homeostatic control of regulatory T cell diversity. Nat. Rev. Immunol. 14: 154-165. https://doi.org/10.1038/nri3605
- Liu, X., R. I. Nurieva, and C. Dong. 2013. Transcriptional regulation of follicular T-helper (Tfh) cells. Immunol. Rev. 252: 139-145. https://doi.org/10.1111/imr.12040
- Tripathi, S. K. and R. Lahesmaa. 2014. Transcriptional and epigenetic regulation of T-helper lineage specification. Immunol. Rev. 261: 62-83. https://doi.org/10.1111/imr.12204
- Bonelli, M., H. Y. Shih, K. Hirahara, K. Singelton, A. Laurence, A. Poholek, T. Hand, Y. Mikami, G. Vahedi, Y. Kanno, and J. J. O'Shea. 2014. Helper T cell plasticity: impact of extrinsic and intrinsic signals on transcriptomes and epigenomes. Curr. Top. Microbiol. Immunol. 381: 279-326.
- Kara, E. E., I. Comerford, K. A. Fenix, C. R. Bastow, C. E. Gregor, D. R. McKenzie, and S. R. McColl. 2014. Tailored immune responses: novel effector helper T cell subsets in protective immunity. PLoS. Pathog. 10: e1003905. https://doi.org/10.1371/journal.ppat.1003905
- Man, K., M. Miasari, W. Shi, A. Xin, D. C. Henstridge, S. Preston, M. Pellegrini, G. T. Belz, G. K. Smyth, M. A. Febbraio, S. L. Nutt, and A. Kallies. 2013. The transcription factor IRF4 is essential for TCR affinity-mediated metabolic programming and clonal expansion of T cells. Nat. Immunol. 14: 1155-1165. https://doi.org/10.1038/ni.2710
- Nakayama, T., and M. Yamashita. 2010. The TCR-mediated signaling pathways that control the direction of helper T cell differentiation. Semin. Immunol. 22: 303-309. https://doi.org/10.1016/j.smim.2010.04.010
- Nurieva, R. I., X. Liu, and C. Dong. 2009. Yin-Yang of costimulation: crucial controls of immune tolerance and function. Immunol. Rev. 229: 88-100. https://doi.org/10.1111/j.1600-065X.2009.00769.x
- Ishii N., T. Takahashi, P. Soroosh, and K. Sugamura. 2010. OX40-OX40 ligand interaction in T-cell-mediated immunity and immunopathology. Adv. Immunol. 105: 63-98. https://doi.org/10.1016/S0065-2776(10)05003-0
- Ford, M. L., and C. P. Larsen. 2009. Translating costimulation blockade to the clinic: lessons learned from three pathways. Immunol. Rev. 229: 294-306. https://doi.org/10.1111/j.1600-065X.2009.00776.x
- Mace, T. A., S. A. King, Z. Ameen, O. Elnaggar, G. Young, K. M. Riedl, S. J. Schwartz, S. K. Clinton, T. J. Knobloch, C. M. Weghorst, and G. B. Lesinski. 2014. Bioactive compounds or metabolites from black raspberries modulate T lymphocyte proliferation, myeloid cell differentiation and Jak/STAT signaling. Cancer Immunol. Immunother. 63: 889-900. https://doi.org/10.1007/s00262-014-1564-5
- Nicolaou, A., C. Mauro, P. Urquhart, and F. Marelli-Berg. 2014. Polyunsaturated Fatty Acid-derived lipid mediators and T cell function. Front Immunol. 5: 75.
- Arpaia, N., C. Campbell, X. Fan, S. Dikiy, d. van, V, P. deRoos, H. Liu, J. R. Cross, K. Pfeffer, P. J. Coffer, and A. Y. Rudensky. 2013. Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation. Nature 504: 451-455. https://doi.org/10.1038/nature12726
- Benson, M. J., K. Pino-Lagos, M. Rosemblatt, and R. J. Noelle. 2007. All-trans retinoic acid mediates enhanced T reg cell growth, differentiation, and gut homing in the face of high levels of co-stimulation. J. Exp. Med. 204: 1765-1774. https://doi.org/10.1084/jem.20070719
-
Kang, S. G., H. W. Lim, O. M. Andrisani, H. E. Broxmeyer, and C. H. Kim. 2007. Vitamin A metabolites induce gut-homing
$FoxP3^+$ regulatory T cells. J. Immunol. 179: 3724-3733. https://doi.org/10.4049/jimmunol.179.6.3724 - Mucida, D., Y. Park, G. Kim, O. Turovskaya, I. Scott, M. Kronenberg, and H. Cheroutre. 2007. Reciprocal TH17 and regulatory T cell differentiation mediated by retinoic acid. Science 317: 256-260. https://doi.org/10.1126/science.1145697
- Park, J., M. Kim, S. G. Kang, A. H. Jannasch, B. Cooper, J. Patterson, and C. H. Kim. 2014. Short-chain fatty acids induce both effector and regulatory T cells by suppression of histone deacetylases and regulation of the mTOR-S6K pathway. Mucosal. Immunol. doi: 10.1038/mi.2014.44.
- Smith, P. M., M. R. Howitt, N. Panikov, M. Michaud, C. A. Gallini, Y. Bohlooly, J. N. Glickman, and W. S. Garrett. 2013. The microbial metabolites, short-chain fatty acids, regulate colonic Treg cell homeostasis. Science 341: 569-573. https://doi.org/10.1126/science.1241165
- Furusawa, Y., Y. Obata, S. Fukuda, T. A. Endo, G. Nakato, D. Takahashi, Y. Nakanishi, C. Uetake, K. Kato, T. Kato, M. Takahashi, N. N. Fukuda, S. Murakami, E. Miyauchi, S. Hino, K. Atarashi, S. Onawa, Y. Fujimura, T. Lockett, J. M. Clarke, D. L. Topping, M. Tomita, S. Hori, O. Ohara, T. Morita, H. Koseki, J. Kikuchi, K. Honda, K. Hase, and H. Ohno. 2013. Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells. Nature 504: 446-450. https://doi.org/10.1038/nature12721
- Macfarlane, S., and G. T. Macfarlane. 2003. Regulation of short-chain fatty acid production. Proc. Nutr. Soc. 62: 67-72. https://doi.org/10.1079/PNS2002207
- Barcenilla, A., S. E. Pryde, J. C. Martin, S. H. Duncan, C. S. Stewart, C. Henderson, and H. J. Flint. 2000. Phylogenetic relationships of butyrate-producing bacteria from the human gut. Appl. Environ. Microbiol. 66: 1654-1661. https://doi.org/10.1128/AEM.66.4.1654-1661.2000
- Charrier, C., G. J. Duncan, M. D. Reid, G. J. Rucklidge, D. Henderson, P. Young, V. J. Russell, R. I. Aminov, H. J. Flint, and P. Louis. 2006. A novel class of CoA-transferase involved in short-chain fatty acid metabolism in butyrate-producing human colonic bacteria. Microbiology 152: 179-185. https://doi.org/10.1099/mic.0.28412-0
- Miller, T. L., and M. J. Wolin. 1996. Pathways of acetate, propionate, and butyrate formation by the human fecal microbial flora. Appl. Environ. Microbiol. 62: 1589-1592.
- Reichardt, N., S. H. Duncan, P. Young, A. Belenguer, L. C. McWilliam, K. P. Scott, H. J. Flint, and P. Louis. 2014. Phylogenetic distribution of three pathways for propionate production within the human gut microbiota. ISME. J. 8: 1323-1335. https://doi.org/10.1038/ismej.2014.14
- Louis, P., G. L. Hold, and H. J. Flint. 2014. The gut microbiota, bacterial metabolites and colorectal cancer. Nat. Rev. Microbiol. 12: 661-672. https://doi.org/10.1038/nrmicro3344
- Li, H., L. Myeroff, D. Smiraglia, M. F. Romero, T. P. Pretlow, L. Kasturi, J. Lutterbaugh, R. M. Rerko, G. Casey, J. P. Issa, J. Willis, J. K. Willson, C. Plass, and S. D. Markowitz. 2003. SLC5A8, a sodium transporter, is a tumor suppressor gene silenced by methylation in human colon aberrant crypt foci and cancers. Proc. Natl. Acad. Sci. U. S. A. 100: 8412-8417. https://doi.org/10.1073/pnas.1430846100
- Miyauchi, S., E. Gopal, Y. J. Fei, and V. Ganapathy. 2004. Functional identification of SLC5A8, a tumor suppressor down-regulated in colon cancer, as a Na(+)-coupled transporter for short-chain fatty acids. J. Biol. Chem. 279: 13293-13296. https://doi.org/10.1074/jbc.C400059200
- Yanase, H., K. Takebe, J. Nio-Kobayashi, H. Takahashi-Iwanaga, and T. Iwanaga. 2008. Cellular expression of a sodium-dependent monocarboxylate transporter (Slc5a8) and the MCT family in the mouse kidney. Histochem. Cell Biol. 130: 957-966. https://doi.org/10.1007/s00418-008-0490-z
- Halestrap, A. P., X. Wang, R. C. Poole, V. N. Jackson, and N. T. Price. 1997. Lactate transport in heart in relation to myocardial ischemia. Am. J. Cardiol. 80: 17A-25A. https://doi.org/10.1016/S0002-9149(97)00454-2
- Eberle, J. A., P. Widmayer, and H. Breer. 2014. Receptors for short-chain fatty acids in brush cells at the "gastric groove". Front Physiol. 5: 152.
- Tazoe, H., Y. Otomo, S. Karaki, I. Kato, Y. Fukami, M. Terasaki, and A. Kuwahara. 2009. Expression of short-chain fatty acid receptor GPR41 in the human colon. Biomed. Res. 30: 149-156. https://doi.org/10.2220/biomedres.30.149
- Nohr, M. K., M. H. Pedersen, A. Gille, K. L. Egerod, M. S. Engelstoft, A. S. Husted, R. M. Sichlau, K. V. Grunddal, S. S. Poulsen, S. Han, R. M. Jones, S. Offermanns, and T. W. Schwartz. 2013. GPR41/FFAR3 and GPR43/FFAR2 as co-sensors for short-chain fatty acids in enteroendocrine cells vs FFAR3 in enteric neurons and FFAR2 in enteric leukocytes. Endocrinology 154: 3552-3564. https://doi.org/10.1210/en.2013-1142
- Kim, M. H., S. G. Kang, J. H. Park, M. Yanagisawa, and C. H. Kim. 2013. Short-chain fatty acids activate GPR41 and GPR43 on intestinal epithelial cells to promote inflammatory responses in mice. Gastroenterology 145: 396-406. https://doi.org/10.1053/j.gastro.2013.04.056
- Wang, A., R. M. Akers, and H. Jiang. 2012. Short communication: Presence of G protein-coupled receptor 43 in rumen epithelium but not in the islets of Langerhans in cattle. J. Dairy Sci. 95: 1371-1375. https://doi.org/10.3168/jds.2011-4886
- Xiong, Y., N. Miyamoto, K. Shibata, M. A. Valasek, T. Motoike, R. M. Kedzierski, and M. Yanagisawa. 2004. Short-chain fatty acids stimulate leptin production in adipocytes through the G protein-coupled receptor GPR41. Proc. Natl. Acad. Sci. U. S. A. 101: 1045-1050. https://doi.org/10.1073/pnas.2637002100
- Zaibi, M. S., C. J. Stocker, J. O'Dowd, A. Davies, M. Bellahcene, M. A. Cawthorne, A. J. Brown, D. M. Smith, and J. R. Arch. 2010. Roles of GPR41 and GPR43 in leptin secretory responses of murine adipocytes to short chain fatty acids. FEBS Lett. 584: 2381-2386. https://doi.org/10.1016/j.febslet.2010.04.027
- Bahar, H. K., A. Veprik, N. Rubins, O. Naaman, and M. D. Walker. 2012. GPR41 gene expression is mediated by internal ribosome entry site (IRES)-dependent translation of bicistronic mRNA encoding GPR40 and GPR41 proteins. J. Biol. Chem. 287: 20154-20163. https://doi.org/10.1074/jbc.M112.358887
- Sina, C., O. Gavrilova, M. Forster, A. Till, S. Derer, F. Hildebrand, B. Raabe, A. Chalaris, J. Scheller, A. Rehmann, A. Franke, S. Ott, R. Hasler, S. Nikolaus, U. R. Folsch, S. Rose-John, H. P. Jiang, J. Li, S. Schreiber, and P. Rosenstiel. 2009. G protein-coupled receptor 43 is essential for neutrophil recruitment during intestinal inflammation. J. Immunol. 183: 7514-7522. https://doi.org/10.4049/jimmunol.0900063
- Brown, A. J., S. M. Goldsworthy, A. A. Barnes, M. M. Eilert, L. Tcheang, D. Daniels, A. I. Muir, M. J. Wigglesworth, I. Kinghorn, N. J. Fraser, N. B. Pike, J. C. Strum, K. M. Steplewski, P. R. Murdock, J. C. Holder, F. H. Marshall, P. G. Szekeres, S. Wilson, D. M. Ignar, S. M. Foord, A. Wise, and S. J. Dowell. 2003. The Orphan G protein-coupled receptors GPR41 and GPR43 are activated by propionate and other short chain carboxylic acids. J. Biol. Chem. 278: 11312-11319. https://doi.org/10.1074/jbc.M211609200
- Voltolini, C., S. Battersby, S. L. Etherington, F. Petraglia, J. E. Norman, and H. N. Jabbour. 2012. A novel antiinflammatory role for the short-chain fatty acids in human labor. Endocrinology 153: 395-403. https://doi.org/10.1210/en.2011-1457
- Thangaraju, M., G. A. Cresci, K. Liu, S. Ananth, J. P. Gnanaprakasam, D. D. Browning, J. D. Mellinger, S. B. Smith, G. J. Digby, N. A. Lambert, P. D. Prasad, and V. Ganapathy. 2009. GPR109A is a G-protein-coupled receptor for the bacterial fermentation product butyrate and functions as a tumor suppressor in colon. Cancer Res. 69: 2826-2832. https://doi.org/10.1158/0008-5472.CAN-08-4466
- Pluznick, J. L., R. J. Protzko, H. Gevorgyan, Z. Peterlin, A. Sipos, J. Han, I. Brunet, L. X. Wan, F. Rey, T. Wang, S. J. Firestein, M. Yanagisawa, J. I. Gordon, A. Eichmann, J. Peti-Peterdi, and M. J. Caplan. 2013. Olfactory receptor responding to gut microbiota-derived signals plays a role in renin secretion and blood pressure regulation. Proc. Natl. Acad. Sci. U. S. A. 110: 4410-4415. https://doi.org/10.1073/pnas.1215927110
- McCrudden, F. H., and H. L. Fales. 1913. The cause of the excessive calcium excretion through the feces in infantilism. J. Exp. Med. 17: 24-28. https://doi.org/10.1084/jem.17.1.24
- Zoller, H. F., and W. M. Clark. 1921. The production of volatile fatty acids by bacteria of the dysentery group. J. Gen. Physiol. 3: 325-330. https://doi.org/10.1085/jgp.3.3.325
- Topping, D. L., and P. M. Clifton. 2001. Short-chain fatty acids and human colonic function: roles of resistant starch and nonstarch polysaccharides. Physiol. Rev. 81: 1031-1064. https://doi.org/10.1152/physrev.2001.81.3.1031
- Finnie, I. A., A. D. Dwarakanath, B. A. Taylor, and J. M. Rhodes. 1995. Colonic mucin synthesis is increased by sodium butyrate. Gut 36: 93-99. https://doi.org/10.1136/gut.36.1.93
- Tan, J., C. McKenzie, M. Potamitis, A. N. Thorburn, C. R. Mackay, and L. Macia. 2014. The role of short-chain fatty acids in health and disease. Adv. Immunol. 121: 91-119. https://doi.org/10.1016/B978-0-12-800100-4.00003-9
- Tazoe, H., Y. Otomo, I. Kaji, R. Tanaka, S. I. Karaki, and A. Kuwahara. 2008. Roles of short-chain fatty acids receptors, GPR41 and GPR43 on colonic functions. J. Physiol. Pharmacol. 59 Suppl 2: 251-262.
- Wang, A., Z. Gu, B. Heid, R. M. Akers, and H. Jiang. 2009. Identification and characterization of the bovine G protein-coupled receptor GPR41 and GPR43 genes. J. Dairy Sci. 92: 2696-2705. https://doi.org/10.3168/jds.2009-2037
- Tazoe, H., Y. Otomo, S. Karaki, I. Kato, Y. Fukami, M. Terasaki, and A. Kuwahara. 2009. Expression of short-chain fatty acid receptor GPR41 in the human colon. Biomed. Res. 30: 149-156. https://doi.org/10.2220/biomedres.30.149
- Le, P. E., C. Loison, S. Struyf, J. Y. Springael, V. Lannoy, M. E. Decobecq, S. Brezillon, V. Dupriez, G. Vassart, D. J. Van, M. Parmentier, and M. Detheux. 2003. Functional characterization of human receptors for short chain fatty acids and their role in polymorphonuclear cell activation. J. Biol. Chem. 278: 25481-25489. https://doi.org/10.1074/jbc.M301403200
- Vinolo, M. A., G. J. Ferguson, S. Kulkarni, G. Damoulakis, K. Anderson, Y. Bohlooly, L. Stephens, P. T. Hawkins, and R. Curi. 2011. SCFAs induce mouse neutrophil chemotaxis through the GPR43 receptor. PLoS. One 6: e21205. https://doi.org/10.1371/journal.pone.0021205
- Cani, P. D., A. Everard, and T. Duparc. 2013. Gut microbiota, enteroendocrine functions and metabolism. Curr. Opin. Pharmacol. 13: 935-940. https://doi.org/10.1016/j.coph.2013.09.008
- Licciardi, P. V., K. Ververis, and T. C. Karagiannis. 2011. Histone deacetylase inhibition and dietary short-chain Fatty acids. ISRN. Allergy 2011: 869647.
- Yin, L., G. Laevsky, and C. Giardina. 2001. Butyrate suppression of colonocyte NF-kappa B activation and cellular proteasome activity. J. Biol. Chem. 276: 44641-44646. https://doi.org/10.1074/jbc.M105170200
- Eftimiadi, C., E. Buzzi, M. Tonetti, P. Buffa, D. Buffa, M. T. van Steenbergen, G. J. de, and G. A. Botta. 1987. Short-chain fatty acids produced by anaerobic bacteria alter the physiological responses of human neutrophils to chemotactic peptide. J. Infect. 14: 43-53. https://doi.org/10.1016/S0163-4453(87)90808-5
- Carretta, M. D., I. Conejeros, M. A. Hidalgo, and R. A. Burgos. 2013. Propionate induces the release of granules from bovine neutrophils. J. Dairy Sci. 96: 2507-2520. https://doi.org/10.3168/jds.2012-6111
- Luhrs, H., T. Gerke, J. G. Muller, R. Melcher, J. Schauber, F. Boxberge, W. Scheppach, and T. Menzel. 2002. Butyrate inhibits NF-kappaB activation in lamina propria macrophages of patients with ulcerative colitis. Scand. J. Gastroenterol. 37: 458-466. https://doi.org/10.1080/003655202317316105
- Millard, A. L., P. M. Mertes, D. Ittelet, F. Villard, P. Jeannesson, and J. Bernard. 2002. Butyrate affects differentiation, maturation and function of human monocyte-derived dendritic cells and macrophages. Clin. Exp. Immunol. 130: 245-255. https://doi.org/10.1046/j.0009-9104.2002.01977.x
- Park, J. S., E. J. Lee, J. C. Lee, W. K. Kim, and H. S. Kim. 2007. Anti-inflammatory effects of short chain fatty acids in IFN-gamma-stimulated RAW 264.7 murine macrophage cells: involvement of NF-kappaB and ERK signaling pathways. Int. Immunopharmacol. 7: 70-77. https://doi.org/10.1016/j.intimp.2006.08.015
- Kendrick, S. F., G. O'Boyle, J. Mann, M. Zeybel, J. Palmer, D. E. Jones, and C. P. Day. 2010. Acetate, the key modulator of inflammatory responses in acute alcoholic hepatitis. Hepatology 51: 1988-1997. https://doi.org/10.1002/hep.23572
- Arora, T., R. Sharma, and G. Frost. 2011. Propionate. Anti-obesity and satiety enhancing factor? Appetite 56: 511-515. https://doi.org/10.1016/j.appet.2011.01.016
- Hong, Y. H., Y. Nishimura, D. Hishikawa, H. Tsuzuki, H. Miyahara, C. Gotoh, K. C. Choi, D. D. Feng, C. Chen, H. G. Lee, K. Katoh, S. G. Roh, and S. Sasaki. 2005. Acetate and propionate short chain fatty acids stimulate adipogenesis via GPCR43. Endocrinology 146: 5092-5099. https://doi.org/10.1210/en.2005-0545
- Ge, H., X. Li, J. Weiszmann, P. Wang, H. Baribault, J. L. Chen, H. Tian, and Y. Li. 2008. Activation of G protein-coupled receptor 43 in adipocytes leads to inhibition of lipolysis and suppression of plasma free fatty acids. Endocrinology 149: 4519-4526. https://doi.org/10.1210/en.2008-0059
- Kimura, I., D. Inoue, T. Maeda, T. Hara, A. Ichimura, S. Miyauchi, M. Kobayashi, A. Hirasawa, and G. Tsujimoto. 2011. Short-chain fatty acids and ketones directly regulate sympathetic nervous system via G protein-coupled receptor 41 (GPR41). Proc. Natl. Acad. Sci. U. S. A. 108: 8030-8035. https://doi.org/10.1073/pnas.1016088108
- Nancey, S., J. Bienvenu, B. Coffin, F. Andre, L. Descos, and B. Flourie. 2002. Butyrate strongly inhibits in vitro stimulated release of cytokines in blood. Dig. Dis. Sci. 47: 921-928. https://doi.org/10.1023/A:1014781109498
- Cavaglieri, C. R., A. Nishiyama, L. C. Fernandes, R. Curi, E. A. Miles, and P. C. Calder. 2003. Differential effects of short-chain fatty acids on proliferation and production of pro- and anti-inflammatory cytokines by cultured lymphocytes. Life Sci. 73: 1683-1690. https://doi.org/10.1016/S0024-3205(03)00490-9
- Kurita-Ochiai, T., K. Fukushima, and K. Ochiai. 1995. Volatile fatty acids, metabolic by-products of periodontopathic bacteria, inhibit lymphocyte proliferation and cytokine production. J. Dent. Res. 74: 1367-1373. https://doi.org/10.1177/00220345950740070801
- Zimmerman, M. A., N. Singh, P. M. Martin, M. Thangaraju, V. Ganapathy, J. L. Waller, H. Shi, K. D. Robertson, D. H. Munn, and K. Liu. 2012. Butyrate suppresses colonic inflammation through HDAC1-dependent Fas upregulation and Fas-mediated apoptosis of T cells. Am. J. Physiol. Gastrointest. Liver Physiol. 302: G1405-G1415. https://doi.org/10.1152/ajpgi.00543.2011
- Furusawa, Y., Y. Obata, S. Fukuda, T. A. Endo, G. Nakato, D. Takahashi, Y. Nakanishi, C. Uetake, K. Kato, T. Kato, M. Takahashi, N. N. Fukuda, S. Murakami, E. Miyauchi, S. Hino, K. Atarashi, S. Onawa, Y. Fujimura, T. Lockett, J. M. Clarke, D. L. Topping, M. Tomita, S. Hori, O. Ohara, T. Morita, H. Koseki, J. Kikuchi, K. Honda, K. Hase, and H. Ohno. 2013. Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells. Nature 504: 446-450. https://doi.org/10.1038/nature12721
- Atarashi, K., T. Tanoue, K. Oshima, W. Suda, Y. Nagano, H. Nishikawa, S. Fukuda, T. Saito, S. Narushima, K. Hase, S. Kim, J. V. Fritz, P. Wilmes, S. Ueha, K. Matsushima, H. Ohno, B. Olle, S. Sakaguchi, T. Taniguchi, H. Morita, M. Hattori, and K. Honda. 2013. Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota. Nature 500: 232-236. https://doi.org/10.1038/nature12331
- Dennis, P. B., A. Jaeschke, M. Saitoh, B. Fowler, S. C. Kozma, and G. Thomas. 2001. Mammalian TOR: a homeostatic ATP sensor. Science 294: 1102-1105. https://doi.org/10.1126/science.1063518
- Delgoffe, G. M., T. P. Kole, Y. Zheng, P. E. Zarek, K. L. Matthews, B. Xiao, P. F. Worley, S. C. Kozma, and J. D. Powell. 2009. The mTOR kinase differentially regulates effector and regulatory T cell lineage commitment. Immunity 30: 832-844. https://doi.org/10.1016/j.immuni.2009.04.014
- Chen, S., D. Liu, J. Wu, B. Xu, K. Lu, W. Zhu, and M. Chen. 2014. Effect of inhibiting the signal of mammalian target of rapamycin on memory T cells. Transplant. Proc. 46: 1642-1648. https://doi.org/10.1016/j.transproceed.2013.10.063
- Hinnebusch, B. F., S. Meng, J. T. Wu, S. Y. Archer, and R. A. Hodin. 2002. The effects of short-chain fatty acids on human colon cancer cell phenotype are associated with histone hyperacetylation. J. Nutr. 132: 1012-1017. https://doi.org/10.1093/jn/132.5.1012
- Haberland, M., R. L. Montgomery, and E. N. Olson. 2009. The many roles of histone deacetylases in development and physiology: implications for disease and therapy. Nat. Rev. Genet. 10: 32-42. https://doi.org/10.1038/nrg2485
- Yu, X., A. M. Shahir, J. Sha, Z. Feng, B. Eapen, S. Nithianantham, B. Das, J. Karn, A. Weinberg, N. F. Bissada, and F. Ye. 2014. Short-chain fatty acids from periodontal pathogens suppress histone deacetylases, EZH2, and SUV39H1 to promote Kaposi's sarcoma-associated herpesvirus replication. J. Virol. 88: 4466-4479. https://doi.org/10.1128/JVI.03326-13
- Fenton, T. R., J. Gwalter, J. Ericsson, and I. T. Gout. 2010. Histone acetyltransferases interact with and acetylate p70 ribosomal S6 kinases in vitro and in vivo. Int. J. Biochem. Cell Biol. 42: 359-366. https://doi.org/10.1016/j.biocel.2009.11.022
- Singh, N., M. Thangaraju, P. D. Prasad, P. M. Martin, N. A. Lambert, T. Boettger, S. Offermanns, and V. Ganapathy. 2010. Blockade of dendritic cell development by bacterial fermentation products butyrate and propionate through a transporter (Slc5a8)-dependent inhibition of histone deacetylases. J. Biol. Chem. 285: 27601-27608. https://doi.org/10.1074/jbc.M110.102947
- Wang, B., A. Morinobu, M. Horiuchi, J. Liu, and S. Kumagai. 2008. Butyrate inhibits functional differentiation of human monocyte-derived dendritic cells. Cell Immunol. 253: 54-58. https://doi.org/10.1016/j.cellimm.2008.04.016
- Nascimento, C. R., C. G. Freire-de-Lima, O. A. da Silva de, F. D. Rumjanek, and V. M. Rumjanek. 2011. The short chain fatty acid sodium butyrate regulates the induction of CD1a in developing dendritic cells. Immunobiology 216: 275-284. https://doi.org/10.1016/j.imbio.2010.07.004
- Berndt, B. E., M. Zhang, S. Y. Owyang, T. S. Cole, T. W. Wang, J. Luther, N. A. Veniaminova, J. L. Merchant, C. C. Chen, G. B. Huffnagle, and J. Y. Kao. 2012. Butyrate increases IL-23 production by stimulated dendritic cells. Am. J. Physiol. Gastrointest. Liver Physiol. 303: G1384-G1392. https://doi.org/10.1152/ajpgi.00540.2011
- Frikeche, J., T. Simon, E. Brissot, M. Gregoire, B. Gaugler, and M. Mohty. 2012. Impact of valproic acid on dendritic cells function. Immunobiology 217: 704-710. https://doi.org/10.1016/j.imbio.2011.11.010
- Singh, N., A. Gurav, S. Sivaprakasam, E. Brady, R. Padia, H. Shi, M. Thangaraju, P. D. Prasad, S. Manicassamy, D. H. Munn, J. R. Lee, S. Offermanns, and V. Ganapathy. 2014. Activation of Gpr109a, receptor for niacin and the commensal metabolite butyrate, suppresses colonic inflammation and carcinogenesis. Immunity 40: 128-139. https://doi.org/10.1016/j.immuni.2013.12.007
- Ananthakrishnan, A. N., H. Khalili, G. G. Konijeti, L. M. Higuchi, S. P. de, J. R. Korzenik, C. S. Fuchs, W. C. Willett, J. M. Richter, and A. T. Chan. 2013. A prospective study of long-term intake of dietary fiber and risk of Crohn's disease and ulcerative colitis. Gastroenterology 145: 970-977. https://doi.org/10.1053/j.gastro.2013.07.050
- Amre, D. K., S. D'Souza, K. Morgan, G. Seidman, P. Lambrette, G. Grimard, D. Israel, D. Mack, P. Ghadirian, C. Deslandres, V. Chotard, B. Budai, L. Law, E. Levy, and E. G. Seidman. 2007. Imbalances in dietary consumption of fatty acids, vegetables, and fruits are associated with risk for Crohn's disease in children. Am. J. Gastroenterol. 102: 2016-2025. https://doi.org/10.1111/j.1572-0241.2007.01411.x
- Hou, J. K., B. Abraham, and H. El-Serag. 2011. Dietary intake and risk of developing inflammatory bowel disease: a systematic review of the literature. Am. J. Gastroenterol. 106: 563-573. https://doi.org/10.1038/ajg.2011.44
- Vieira, E. L., A. J. Leonel, A. P. Sad, N. R. Beltrao, T. F. Costa, T. M. Ferreira, A. C. Gomes-Santos, A. M. Faria, M. C. Peluzio, D. C. Cara, and J. I. varez-Leite. 2012. Oral administration of sodium butyrate attenuates inflammation and mucosal lesion in experimental acute ulcerative colitis. J. Nutr. Biochem. 23: 430-436. https://doi.org/10.1016/j.jnutbio.2011.01.007
- Tarrerias, A. L., M. Millecamps, A. Alloui, C. Beaughard, J. L. Kemeny, S. Bourdu, G. Bommelaer, A. Eschalier, M. Dapoigny, and D. Ardid. 2002. Short-chain fatty acid enemas fail to decrease colonic hypersensitivity and inflammation in TNBS-induced colonic inflammation in rats. Pain 100: 91-97. https://doi.org/10.1016/S0304-3959(02)00234-8
- Maslowski, K. M., A. T. Vieira, A. Ng, J. Kranich, F. Sierro, D. Yu, H. C. Schilter, M. S. Rolph, F. Mackay, D. Artis, R. J. Xavier, M. M. Teixeira, and C. R. Mackay. 2009. Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43. Nature 461: 1282-1286. https://doi.org/10.1038/nature08530
- Masui, R., M. Sasaki, Y. Funaki, N. Ogasawara, M. Mizuno, A. Iida, S. Izawa, Y. Kondo, Y. Ito, Y. Tamura, K. Yanamoto, H. Noda, A. Tanabe, N. Okaniwa, Y. Yamaguchi, T. Iwamoto, and K. Kasugai. 2013. G protein-coupled receptor 43 moderates gut inflammation through cytokine regulation from mononuclear cells. Inflamm. Bowel. Dis. 19: 2848-2856. https://doi.org/10.1097/01.MIB.0000435444.14860.ea
- Hamer, H. M., D. M. Jonkers, S. A. Vanhoutvin, F. J. Troost, G. Rijkers, B. A. de, A. Bast, K. Venema, and R. J. Brummer. 2010. Effect of butyrate enemas on inflammation and antioxidant status in the colonic mucosa of patients with ulcerative colitis in remission. Clin. Nutr. 29: 738-744. https://doi.org/10.1016/j.clnu.2010.04.002
- Scheppach, W., H. Sommer, T. Kirchner, G. M. Paganelli, P. Bartram, S. Christl, F. Richter, G. Dusel, and H. Kasper. 1992. Effect of butyrate enemas on the colonic mucosa in distal ulcerative colitis. Gastroenterology 103: 51-56. https://doi.org/10.1016/0016-5085(92)91094-K
- Vernia, P., A. Marcheggiano, R. Caprilli, G. Frieri, G. Corrao, D. Valpiani, M. C. Di Paolo, P. Paoluzi, and A. Torsoli. 1995. Short-chain fatty acid topical treatment in distal ulcerative colitis. Aliment. Pharmacol. Ther. 9: 309-313.
- Vernia, P., G. Monteleone, G. Grandinetti, G. Villotti, G. E. Di, G. Frieri, A. Marcheggiano, F. Pallone, R. Caprilli, and A. Torsoli. 2000. Combined oral sodium butyrate and mesalazine treatment compared to oral mesalazine alone in ulcerative colitis: randomized, double-blind, placebo-controlled pilot study. Dig. Dis. Sci. 45: 976-981. https://doi.org/10.1023/A:1005537411244
- Di, S. A., R. Morera, R. Ciccocioppo, P. Cazzola, S. Gotti, F. P. Tinozzi, S. Tinozzi, and G. R. Corazza. 2005. Oral butyrate for mildly to moderately active Crohn's disease. Aliment. Pharmacol. Ther. 22: 789-794. https://doi.org/10.1111/j.1365-2036.2005.02639.x
- Steinhart, A. H., T. Hiruki, A. Brzezinski, and J. P. Baker. 1996. Treatment of left-sided ulcerative colitis with butyrate enemas: a controlled trial. Aliment. Pharmacol. Ther. 10: 729-736. https://doi.org/10.1046/j.1365-2036.1996.d01-509.x
- Breuer, R. I., K. H. Soergel, B. A. Lashner, M. L. Christ, S. B. Hanauer, A. Vanagunas, J. M. Harig, A. Keshavarzian, M. Robinson, J. H. Sellin, D. Weinberg, D. E. Vidican, K. L. Flemal, and A. W. Rademaker. 1997. Short chain fatty acid rectal irrigation for left-sided ulcerative colitis: a randomised, placebo controlled trial. Gut 40: 485-491. https://doi.org/10.1136/gut.40.4.485
- Trompette, A., E. S. Gollwitzer, K. Yadava, A. K. Sichelstiel, N. Sprenger, C. Ngom-Bru, C. Blanchard, T. Junt, L. P. Nicod, N. L. Harris, and B. J. Marsland. 2014. Gut microbiota metabolism of dietary fiber influences allergic airway disease and hematopoiesis. Nat. Med. 20: 159-166. https://doi.org/10.1038/nm.3444
- Hadjiagapiou, C., L. Schmidt, P. K. Dudeja, T. J. Layden, and K. Ramaswamy. 2000. Mechanism(s) of butyrate transport in Caco-2 cells: role of monocarboxylate transporter 1. Am. J. Physiol. Gastrointest. Liver Physiol. 279: G775-G780. https://doi.org/10.1152/ajpgi.2000.279.4.G775
- Alrefai, W. A., S. Tyagi, R. Gill, S. Saksena, C. Hadjiagapiou, F. Mansour, K. Ramaswamy, and P. K. Dudeja. 2004. Regulation of butyrate uptake in Caco-2 cells by phorbol 12-myristate 13-acetate. Am. J. Physiol. Gastrointest. Liver Physiol. 286: G197-G203. https://doi.org/10.1152/ajpgi.00144.2003
- Ritzhaupt, A., A. Ellis, K. B. Hosie, and S. P. Shirazi-Beechey. 1998. The characterization of butyrate transport across pig and human colonic luminal membrane. J. Physiol. 507(Pt 3): 819-830. https://doi.org/10.1111/j.1469-7793.1998.819bs.x
- Gopal, E., Y. J. Fei, S. Miyauchi, L. Zhuang, P. D. Prasad, and V. Ganapathy. 2005. Sodium-coupled and electrogenic transport of B-complex vitamin nicotinic acid by slc5a8, a member of the Na/glucose co-transporter gene family. Biochem. J. 388: 309-316. https://doi.org/10.1042/BJ20041916
- Miyauchi, S., E. Gopal, E. Babu, S. R. Srinivas, Y. Kubo, N. S. Umapathy, S. V. Thakkar, V. Ganapathy, and P. D. Prasad. 2010. Sodium-coupled electrogenic transport of pyroglutamate (5-oxoproline) via SLC5A8, a monocarboxylate transporter. Biochim. Biophys. Acta 1798: 1164-1171. https://doi.org/10.1016/j.bbamem.2010.03.002
- Thangaraju, M., G. Cresci, S. Itagaki, J. Mellinger, D. D. Browning, F. G. Berger, P. D. Prasad, and V. Ganapathy. 2008. Sodium-coupled transport of the short chain fatty acid butyrate by SLC5A8 and its relevance to colon cancer. J. Gastrointest. Surg. 12: 1773-1781. https://doi.org/10.1007/s11605-008-0573-0
- Gopal, E., Y. J. Fei, M. Sugawara, S. Miyauchi, L. Zhuang, P. Martin, S. B. Smith, P. D. Prasad, and V. Ganapathy. 2004. Expression of slc5a8 in kidney and its role in Na(+)-coupled transport of lactate. J. Biol. Chem. 279: 44522-44532. https://doi.org/10.1074/jbc.M405365200
- Martin, P. M., Y. Dun, B. Mysona, S. Ananth, P. Roon, S. B. Smith, and V. Ganapathy. 2007. Expression of the sodium-coupled monocarboxylate transporters SMCT1 (SLC5A8) and SMCT2 (SLC5A12) in retina. Invest. Ophthalmol. Vis. Sci. 48: 3356-3363. https://doi.org/10.1167/iovs.06-0888
-
Martin, P. M., E. Gopal, S. Ananth, L. Zhuang, S. Itagaki, B. M. Prasad, S. B. Smith, P. D. Prasad, and V. Ganapathy. 2006. Identity of SMCT1 (SLC5A8) as a neuron-specific
$Na^+$ -coupled transporter for active uptake of L-lactate and ketone bodies in the brain. J. Neurochem. 98: 279-288. https://doi.org/10.1111/j.1471-4159.2006.03878.x - Tolhurst, G., H. Heffron, Y. S. Lam, H. E. Parker, A. M. Habib, E. Diakogiannaki, J. Cameron, J. Grosse, F. Reimann, and F. M. Gribble. 2012. Short-chain fatty acids stimulate glucagon-like peptide-1 secretion via the G-protein-coupled receptor FFAR2. Diabetes 61: 364-371. https://doi.org/10.2337/db11-1019
- Hong, Y. H., Y. Nishimura, D. Hishikawa, H. Tsuzuki, H. Miyahara, C. Gotoh, K. C. Choi, D. D. Feng, C. Chen, H. G. Lee, K. Katoh, S. G. Roh, and S. Sasaki. 2005. Acetate and propionate short chain fatty acids stimulate adipogenesis via GPCR43. Endocrinology 146: 5092-5099. https://doi.org/10.1210/en.2005-0545
- Dewulf, E. M., Q. Ge, L. B. Bindels, F. M. Sohet, P. D. Cani, S. M. Brichard, and N. M. Delzenne. 2013. Evaluation of the relationship between GPR43 and adiposity in human. Nutr. Metab. (Lond) 10: 11. https://doi.org/10.1186/1743-7075-10-11
- Tang, Y., Y. Chen, H. Jiang, G. T. Robbins, and D. Nie. 2011. G-protein-coupled receptor for short-chain fatty acids suppresses colon cancer. Int. J. Cancer 128: 847-856. https://doi.org/10.1002/ijc.25638
- Karaki, S., R. Mitsui, H. Hayashi, I. Kato, H. Sugiya, T. Iwanaga, J. B. Furness, and A. Kuwahara. 2006. Short-chain fatty acid receptor, GPR43, is expressed by enteroendocrine cells and mucosal mast cells in rat intestine. Cell Tissue Res. 324: 353-360. https://doi.org/10.1007/s00441-005-0140-x
- Nilsson, N. E., K. Kotarsky, C. Owman, and B. Olde. 2003. Identification of a free fatty acid receptor, FFA2R, expressed on leukocytes and activated by short-chain fatty acids. Biochem. Biophys. Res. Commun. 303: 1047-1052. https://doi.org/10.1016/S0006-291X(03)00488-1
- Wanders, D., E. C. Graff, and R. L. Judd. 2012. Effects of high fat diet on GPR109A and GPR81 gene expression. Biochem. Biophys. Res. Commun. 425: 278-283. https://doi.org/10.1016/j.bbrc.2012.07.082
- Taggart, A. K., J. Kero, X. Gan, T. Q. Cai, K. Cheng, M. Ippolito, N. Ren, R. Kaplan, K. Wu, T. J. Wu, L. Jin, C. Liaw, R. Chen, J. Richman, D. Connolly, S. Offermanns, S. D. Wright, and M. G. Waters. 2005. (D)-beta-Hydroxybutyrate inhibits adipocyte lipolysis via the nicotinic acid receptor PUMA-G. J. Biol. Chem. 280: 26649-26652. https://doi.org/10.1074/jbc.C500213200
- Ingersoll, M. A., S. Potteaux, D. Alvarez, S. B. Hutchison, R. N. van, and G. J. Randolph. 2012. Niacin inhibits skin dendritic cell mobilization in a GPR109A independent manner but has no impact on monocyte trafficking in atherosclerosis. Immunobiology 217: 548-557. https://doi.org/10.1016/j.imbio.2011.05.014
- Li, X., J. S. Millar, N. Brownell, F. Briand, and D. J. Rader. 2010. Modulation of HDL metabolism by the niacin receptor GPR109A in mouse hepatocytes. Biochem. Pharmacol. 80: 1450-1457. https://doi.org/10.1016/j.bcp.2010.07.023
- Bermudez, Y., C. A. Benavente, R. G. Meyer, W. R. Coyle, M. K. Jacobson, and E. L. Jacobson. 2011. Nicotinic acid receptor abnormalities in human skin cancer: implications for a role in epidermal differentiation. PLoS. One 6: e20487. https://doi.org/10.1371/journal.pone.0020487
- Xu, L. L., B. G. Stackhouse, K. Florence, W. Zhang, N. Shanmugam, I. A. Sesterhenn, Z. Zou, V. Srikantan, M. Augustus, V. Roschke, K. Carter, D. G. McLeod, J. W. Moul, D. Soppett, and S. Srivastava. 2000. PSGR, a novel prostate-specific gene with homology to a G protein-coupled receptor, is overexpressed in prostate cancer. Cancer Res. 60: 6568-6572.
- Weber, M., U. Pehl, H. Breer, and J. Strotmann. 2002. Olfactory receptor expressed in ganglia of the autonomic nervous system. J. Neurosci. Res. 68: 176-184. https://doi.org/10.1002/jnr.10164
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- Diet, Gut Microbiota, and Obesity: Links with Host Genetics and Epigenetics and Potential Applications vol.10, pp.1, 2014, https://doi.org/10.1093/advances/nmy078
- The Differential Roles of T Cells in Non-alcoholic Fatty Liver Disease and Obesity vol.10, pp.None, 2014, https://doi.org/10.3389/fimmu.2019.00082
- T-Cell-Driven Inflammation as a Mediator of the Gut-Brain Axis Involved in Parkinson's Disease vol.10, pp.None, 2019, https://doi.org/10.3389/fimmu.2019.00239
- Impact of Gut Dysbiosis on Neurohormonal Pathways in Chronic Kidney Disease vol.7, pp.1, 2014, https://doi.org/10.3390/diseases7010021
- 16S rRNA gene profiling and genome reconstruction reveal community metabolic interactions and prebiotic potential of medicinal herbs used in neurodegenerative disease and as nootropics vol.14, pp.3, 2014, https://doi.org/10.1371/journal.pone.0213869
- Mikrobiom, Diabetes und Herz: neue Zusammenhänge? vol.44, pp.3, 2014, https://doi.org/10.1007/s00059-019-4791-x
- Role of the intestinal microbiome in autoimmune diseases and its use in treatments vol.339, pp.None, 2014, https://doi.org/10.1016/j.cellimm.2018.10.005
- Gut microbiota and health: connecting actors across the metabolic system vol.78, pp.2, 2019, https://doi.org/10.1017/s0029665118002719
- Man and the Microbiome: A New Theory of Everything? vol.15, pp.None, 2019, https://doi.org/10.1146/annurev-clinpsy-050718-095432
- Short Chain Fatty Acids, pancreatic dysfunction and type 2 diabetes vol.19, pp.4, 2014, https://doi.org/10.1016/j.pan.2019.04.013
- Infection-Induced Intestinal Dysbiosis Is Mediated by Macrophage Activation and Nitrate Production vol.10, pp.3, 2014, https://doi.org/10.1128/mbio.00935-19
- Roles of short-chain fatty acids in kidney diseases vol.132, pp.10, 2019, https://doi.org/10.1097/cm9.0000000000000228
- Gut Microbiome, Short-Chain Fatty Acids, and Mucosa Injury in Young Adults with Human Immunodeficiency Virus Infection vol.64, pp.7, 2014, https://doi.org/10.1007/s10620-018-5428-2
- The addition of cactus flour (Opuntia ficus indica) to the Western-style diet attenuates the onset of metabolic disorders in rats vol.49, pp.4, 2019, https://doi.org/10.1108/nfs-08-2018-0231
- Microbiota Metabolite Short-Chain Fatty Acids Facilitate Mucosal Adjuvant Activity of Cholera Toxin through GPR43 vol.203, pp.1, 2014, https://doi.org/10.4049/jimmunol.1801068
- Role of SCFAs in gut microbiome and glycolysis for colorectal cancer therapy vol.234, pp.10, 2014, https://doi.org/10.1002/jcp.28436
- Microbiota Alterations in Alzheimer’s Disease: Involvement of the Kynurenine Pathway and Inflammation vol.36, pp.2, 2014, https://doi.org/10.1007/s12640-019-00057-3
- The role of short-chain fatty acids in microbiota-gut-brain communication vol.16, pp.8, 2014, https://doi.org/10.1038/s41575-019-0157-3
- The long-term consequences of antibiotic therapy: Role of colonic short-chain fatty acids (SCFA) system and intestinal barrier integrity vol.14, pp.8, 2014, https://doi.org/10.1371/journal.pone.0220642
- Role of Personalized Nutrition in Chronic-Degenerative Diseases vol.11, pp.8, 2014, https://doi.org/10.3390/nu11081707
- Microbiota Metabolite Butyrate Differentially Regulates Th1 and Th17 Cells’ Differentiation and Function in Induction of Colitis vol.25, pp.9, 2014, https://doi.org/10.1093/ibd/izz046
- The Mediterranean Diet and Cancer: What Do Human and Molecular Studies Have to Say about It? vol.11, pp.9, 2014, https://doi.org/10.3390/nu11092155
- The Microbiota-Gut-Brain Axis vol.99, pp.4, 2014, https://doi.org/10.1152/physrev.00018.2018
- Effects of Gas Production Recording System and Pig Fecal Inoculum Volume on Kinetics and Variation of In Vitro Fermentation using Corn Distiller’s Dried Grains with Solubles and Soybean Hulls vol.9, pp.10, 2014, https://doi.org/10.3390/ani9100773
- Obesity during pregnancy results in maternal intestinal inflammation, placental hypoxia, and alters fetal glucose metabolism at mid-gestation vol.9, pp.1, 2014, https://doi.org/10.1038/s41598-019-54098-x
- Impact of microbiota on central nervous system and neurological diseases: the gut-brain axis vol.16, pp.None, 2019, https://doi.org/10.1186/s12974-019-1434-3
- Invariant NKT Cells Functionally Link Microbiota-Induced Butyrate Production and Joint Inflammation vol.203, pp.12, 2014, https://doi.org/10.4049/jimmunol.1801314
- Application of Polymeric Nano-Materials in Management of Inflammatory Bowel Disease vol.20, pp.None, 2014, https://doi.org/10.2174/1568026620666200320113322
- The Microbiome and Alzheimer’s Disease: Potential and Limitations of Prebiotic, Synbiotic, and Probiotic Formulations vol.8, pp.None, 2020, https://doi.org/10.3389/fbioe.2020.537847
- Exploring the Molecular Mechanisms Underlying the Protective Effects of Microbial SCFAs on Intestinal Tolerance and Food Allergy vol.11, pp.None, 2014, https://doi.org/10.3389/fimmu.2020.01225
- Alterations in Circulating Fatty Acid Are Associated With Gut Microbiota Dysbiosis and Inflammation in Multiple Sclerosis vol.11, pp.None, 2014, https://doi.org/10.3389/fimmu.2020.01390
- The Impact of Milk and Its Components on Epigenetic Programming of Immune Function in Early Life and Beyond: Implications for Allergy and Asthma vol.11, pp.None, 2014, https://doi.org/10.3389/fimmu.2020.02141
- Butyrate: A Review on Beneficial Pharmacological and Therapeutic Effect vol.16, pp.None, 2014, https://doi.org/10.2174/1573401316999201029210912
- Adipose Tissue Distribution, Inflammation and Its Metabolic Consequences, Including Diabetes and Cardiovascular Disease vol.7, pp.None, 2014, https://doi.org/10.3389/fcvm.2020.00022
- Microbial insight into dietary protein source affects intestinal function of pigs with intrauterine growth retardation vol.59, pp.1, 2020, https://doi.org/10.1007/s00394-019-01910-z
- Diet complexity and l-threonine supplementation: effects on growth performance, immune response, intestinal barrier function, and microbial metabolites in nursery pigs vol.98, pp.5, 2014, https://doi.org/10.1093/jas/skaa125
- Microbiota Modulating Nutritional Approaches to Countering the Effects of Viral Respiratory Infections Including SARS-CoV-2 through Promoting Metabolic and Immune Fitness with Probiotics and Plant Bio vol.8, pp.6, 2014, https://doi.org/10.3390/microorganisms8060921
- Nutritional psychiatry in the treatment of psychotic disorders: Current hypotheses and research challenges vol.5, pp.None, 2014, https://doi.org/10.1016/j.bbih.2020.100070
- Physiological, antimicrobial, intestine morphological, and immunological effects of fructooligosaccharides in pigs vol.63, pp.2, 2014, https://doi.org/10.5194/aab-63-325-2020
- The dichotomous role of the gut microbiome in exacerbating and ameliorating neurodegenerative disorders vol.20, pp.7, 2014, https://doi.org/10.1080/14737175.2020.1775585
- Anti-neuroinflammatory Effect of Short-Chain Fatty Acid Acetate against Alzheimer’s Disease via Upregulating GPR41 and Inhibiting ERK/JNK/NF-κB vol.68, pp.27, 2014, https://doi.org/10.1021/acs.jafc.0c02807
- Influence of a 3-month low-calorie Mediterranean diet compared to the vegetarian diet on human gut microbiota and SCFA: the CARDIVEG Study vol.59, pp.5, 2014, https://doi.org/10.1007/s00394-019-02050-0
- Impact of Protein Intake in Older Adults with Sarcopenia and Obesity: A Gut Microbiota Perspective vol.12, pp.8, 2014, https://doi.org/10.3390/nu12082285
- Gut Microbiota and Disorders of the Central Nervous System vol.26, pp.5, 2014, https://doi.org/10.1177/1073858420918826
- Microbiota and Diabetes Mellitus: Role of Lipid Mediators vol.12, pp.10, 2014, https://doi.org/10.3390/nu12103039
- Metabolism of short‐chain fatty acid propionate induces surface expression of NKG2D ligands on cancer cells vol.34, pp.11, 2014, https://doi.org/10.1096/fj.202000162r
- Do the Bugs in Your Gut Eat Your Memories? Relationship between Gut Microbiota and Alzheimer’s Disease vol.10, pp.11, 2014, https://doi.org/10.3390/brainsci10110814
- How does spaceflight affect the acquired immune system? vol.6, pp.None, 2014, https://doi.org/10.1038/s41526-020-0104-1
- Adiponectin Role in Neurodegenerative Diseases: Focus on Nutrition Review vol.21, pp.23, 2020, https://doi.org/10.3390/ijms21239255
- Blautia-a new functional genus with potential probiotic properties? vol.13, pp.1, 2021, https://doi.org/10.1080/19490976.2021.1875796
- Biological Function of Short-Chain Fatty Acids and Its Regulation on Intestinal Health of Poultry vol.8, pp.None, 2014, https://doi.org/10.3389/fvets.2021.736739
- A New Formulation of Probiotics Attenuates Calcipotriol-Induced Dermatitis by Inducing Regulatory Dendritic Cells vol.12, pp.None, 2014, https://doi.org/10.3389/fimmu.2021.775018
- Changes in gut microbiota composition and their associations with cortisol, melatonin and interleukin 6 in patients with chronic insomnia vol.2021, pp.2021, 2014, https://doi.org/10.24075/brsmu.2021.017
- Altered Fecal Microbiota Correlated With Systemic Inflammation in Male Subjects With Methamphetamine Use Disorder vol.11, pp.None, 2014, https://doi.org/10.3389/fcimb.2021.783917
- The Role of the Gut Microbiome in Pathogenesis, Biology, and Treatment of Plasma Cell Dyscrasias vol.11, pp.None, 2014, https://doi.org/10.3389/fonc.2021.741376
- The Role of Gut Bacterial Metabolites in Brain Development, Aging and Disease vol.13, pp.3, 2014, https://doi.org/10.3390/nu13030732
- In the Age of Viral Pandemic, Can Ingredients Inspired by Human Milk and Infant Nutrition Be Repurposed to Support the Immune System? vol.13, pp.3, 2021, https://doi.org/10.3390/nu13030870
- Detrimental effect on the gut microbiota of 1,2-dicarbonyl compounds after in vitro gastro-intestinal and fermentative digestion vol.341, pp.1, 2014, https://doi.org/10.1016/j.foodchem.2020.128237
- Gastroprotective Effects of Polyphenols against Various Gastro-Intestinal Disorders: A Mini-Review with Special Focus on Clinical Evidence vol.26, pp.7, 2014, https://doi.org/10.3390/molecules26072090
- Short-Chain Fatty Acids, Maternal Microbiota and Metabolism in Pregnancy vol.13, pp.4, 2014, https://doi.org/10.3390/nu13041244
- Control of lymphocyte functions by gut microbiota-derived short-chain fatty acids vol.18, pp.5, 2014, https://doi.org/10.1038/s41423-020-00625-0
- Isovaleric acid ameliorates ovariectomy‐induced osteoporosis by inhibiting osteoclast differentiation vol.25, pp.9, 2014, https://doi.org/10.1111/jcmm.16482
- Food intake and its effect on the species and abundance of intestinal flora in colorectal cancer and healthy individuals vol.36, pp.3, 2014, https://doi.org/10.3904/kjim.2019.373
- Butyrate: A Link between Early Life Nutrition and Gut Microbiome in the Development of Food Allergy vol.11, pp.5, 2021, https://doi.org/10.3390/life11050384
- Role of Gut Microbiota and Probiotics in Colorectal Cancer: Onset and Progression vol.9, pp.5, 2014, https://doi.org/10.3390/microorganisms9051021
- Neuro-Signals from Gut Microbiota: Perspectives for Brain Glioma vol.13, pp.11, 2014, https://doi.org/10.3390/cancers13112810
- Combination of Bifidobacterium longum and Galacto-Oligosaccharide Protects the Skin from Photoaging vol.24, pp.6, 2014, https://doi.org/10.1089/jmf.2021.k.0032
- Lactobacillus strains derived from human gut ameliorate metabolic disorders via modulation of gut microbiota composition and short-chain fatty acids metabolism vol.12, pp.3, 2014, https://doi.org/10.3920/bm2020.0148
- Importance of “muscle” and “intestine” training before major HPB surgery: A review vol.28, pp.7, 2021, https://doi.org/10.1002/jhbp.835
- Obesity-Induced Dysbiosis Exacerbates IFN-γ Production and Pulmonary Inflammation in the Mycobacterium tuberculosis Infection vol.10, pp.7, 2014, https://doi.org/10.3390/cells10071732
- Leaky Gut: Effect of Dietary Fiber and Fats on Microbiome and Intestinal Barrier vol.22, pp.14, 2014, https://doi.org/10.3390/ijms22147613
- Lactobacillus plantarum HAC01 ameliorates type 2 diabetes in high-fat diet and streptozotocin-induced diabetic mice in association with modulating the gut microbiota vol.12, pp.14, 2014, https://doi.org/10.1039/d1fo00698c
- Ginsenoside Rk3 alleviates gut microbiota dysbiosis and colonic inflammation in antibiotic-treated mice vol.146, pp.None, 2021, https://doi.org/10.1016/j.foodres.2021.110465
- Intestinal microbiota and kidney diseases vol.40, pp.3, 2021, https://doi.org/10.23876/j.krcp.21.053
- The consequences of altered microbiota in immune-related chronic kidney disease vol.36, pp.10, 2014, https://doi.org/10.1093/ndt/gfaa087
- Microbiomics in Collusion with the Nervous System in Carcinogenesis: Diagnosis, Pathogenesis and Treatment vol.9, pp.10, 2021, https://doi.org/10.3390/microorganisms9102129
- The Interplay between Gut Microbiota and the Immune System in Liver Transplant Recipients and Its Role in Infections vol.89, pp.11, 2014, https://doi.org/10.1128/iai.00376-21
- Melatonin-Mediated Colonic Microbiota Metabolite Butyrate Prevents Acute Sleep Deprivation-Induced Colitis in Mice vol.22, pp.21, 2021, https://doi.org/10.3390/ijms222111894
- A Citrus Fruit Extract High in Polyphenols Beneficially Modulates the Gut Microbiota of Healthy Human Volunteers in a Validated In Vitro Model of the Colon vol.13, pp.11, 2014, https://doi.org/10.3390/nu13113915
- Expanded catalog of microbial genes and metagenome-assembled genomes from the pig gut microbiome vol.12, pp.1, 2021, https://doi.org/10.1038/s41467-021-21295-0
- Intestinal Barrier and Permeability in Health, Obesity and NAFLD vol.10, pp.1, 2014, https://doi.org/10.3390/biomedicines10010083
- Dual role of microbiota-derived short-chain fatty acids on host and pathogen vol.145, pp.None, 2014, https://doi.org/10.1016/j.biopha.2021.112352
- Effect of dehydration and butter-frying on chinicuil (Comadia redtenbacheri Hammershmidt) and maguey white worm (Aegiale hesperiaris Walker) vol.8, pp.1, 2014, https://doi.org/10.3920/jiff2020.0154
- The role of short-chain fatty acids in immunity, inflammation and metabolism vol.62, pp.1, 2014, https://doi.org/10.1080/10408398.2020.1854675