NLRP3 at the crossroads between immune/inflammatory responses and enteric neuroplastic remodelling in a mouse model of diet-induced obesity.

NLRP3 inflammasome colonic motility high-fat diet inflammation macrophages obesity substance P tachykinin neurotransmission

Journal

British journal of pharmacology
ISSN: 1476-5381
Titre abrégé: Br J Pharmacol
Pays: England
ID NLM: 7502536

Informations de publication

Date de publication:
10 2021
Historique:
revised: 26 04 2021
received: 17 07 2020
accepted: 29 04 2021
pubmed: 18 5 2021
medline: 26 10 2021
entrez: 17 5 2021
Statut: ppublish

Résumé

Enteric neurogenic/inflammation contributes to bowel dysmotility in obesity. We examined the role of NLRP3 in colonic neuromuscular dysfunctions in mice with high-fat diet (HFD)-induced obesity. Wild-type C57BL/6J and NLRP3-KO (Nlrp3 HFD mice displayed increased body and epididymal fat weight, cholesterol levels, plasma resistin levels and plasma and colonic IL-1β levels, colonic inflammasome adaptor protein apoptosis-associated speck-like protein containing caspase-recruitment domain (ASC) and caspase-1 mRNA expression and ASC immunopositivity in macrophages. Colonic tachykininergic contractions were enhanced in HFD mice. HFD NLRP3 In obesity, NLRP3 regulates an interplay between the shaping of enteric immune/inflammatory responses and the activation of substance P/NK

Sections du résumé

BACKGROUND AND PURPOSE
Enteric neurogenic/inflammation contributes to bowel dysmotility in obesity. We examined the role of NLRP3 in colonic neuromuscular dysfunctions in mice with high-fat diet (HFD)-induced obesity.
EXPERIMENTAL APPROACH
Wild-type C57BL/6J and NLRP3-KO (Nlrp3
KEY RESULTS
HFD mice displayed increased body and epididymal fat weight, cholesterol levels, plasma resistin levels and plasma and colonic IL-1β levels, colonic inflammasome adaptor protein apoptosis-associated speck-like protein containing caspase-recruitment domain (ASC) and caspase-1 mRNA expression and ASC immunopositivity in macrophages. Colonic tachykininergic contractions were enhanced in HFD mice. HFD NLRP3
CONCLUSION AND IMPLICATIONS
In obesity, NLRP3 regulates an interplay between the shaping of enteric immune/inflammatory responses and the activation of substance P/NK

Identifiants

pubmed: 34000757
doi: 10.1111/bph.15532
doi:

Substances chimiques

Inflammasomes 0
NLR Family, Pyrin Domain-Containing 3 Protein 0
Nlrp3 protein, mouse 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3924-3942

Informations de copyright

© 2021 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

Références

Alexander, S. P. H., Christopoulos, A., Davenport, A. P., Kelly, E., Mathie, A., Peters, J. A., Veale, E. L., Armstrong, J. F., Faccenda, E., Harding, S. D., Pawson, A. J., Sharman, J. L., Southan, C., Davies, J. A., & CGTP collaborators. (2019). The Concise Guide to PHARMACOLOGY 2019/20: G protein-coupled receptors. British Journal of Pharmacology, 176(Suppl 1), S21-S141. https://doi.org/10.1111/bph.14748
Alexander, S. P. H., Roberts, R. E., Broughton, B. R. S., Sobey, C. G., George, C. H., Stanford, S. C., Cirino, G., Docherty, J. R., Giembycz, M. A., Hoyer, D., Insel, P. A., Izzo, A. A., Ji, Y., MacEwan, D. J., Mangum, J., Wonnacott, S., & Ahluwalia, A. (2018). Goals and practicalities of immunoblotting and immunohistochemistry: A guide for submission to the British Journal of Pharmacology. British Journal of Pharmacology, 175, 407-411. https://doi.org/10.1111/bph.14112
Andersen, C. J., Murphy, K. E., & Fernandez, M. L. (2016). Impact of obesity and metabolic syndrome on immunity. Advances in Nutrition, 7, 66-75. https://doi.org/10.3945/an.115.010207
Antonioli, L., Caputi, V., Fornai, M., Pellegrini, C., Gentile, D., Giron, M. C., Orso, G., Bernardini, N., Segnani, C., Ippolito, C., Csóka, B., Haskó, G., Németh, Z. H., Scarpignato, C., Blandizzi, C., & Colucci, R. (2019). Interplay between colonic inflammation and tachykininergic pathways in the onset of colonic dysmotility in a mouse model of diet-induced obesity. International Journal of Obesity, 43, 331-343. https://doi.org/10.1038/s41366-018-0166-2
Antonioli, L., D'Antongiovanni, V., Pellegrini, C., Fornai, M., Benvenuti, L., Carlo, A., den Wijngaard, R., Caputi, V., Cerantola, S., Giron, M. C., Németh, Z. H., Haskó, G., Blandizzi, C., & Colucci, R. (2020). Colonic dysmotility associated with high-fat diet-induced obesity: Role of enteric glia. FASEB Journal: Official Publication of the Federation of American Societies for Experimental Biology, 34, 5512-5524. https://doi.org/10.1096/fj.201901844R
Antonioli, L., Fornai, M., Colucci, R., Awwad, O., Ghisu, N., Tuccori, M., del Tacca, M., & Blandizzi, C. (2011). Differential recruitment of high affinity A1 and A2A adenosine receptors in the control of colonic neuromuscular function in experimental colitis. European Journal of Pharmacology, 650, 639-649. https://doi.org/10.1016/j.ejphar.2010.10.041
Antonioli, L., Moriconi, D., Masi, S., Bottazzo, D., Pellegrini, C., Fornai, M., Anselmino, M., Ferrannini, E., Blandizzi, C., Taddei, S., & Nannipieri, M. (2020). Differential impact of weight loss and glycemic control on inflammasome signaling. Obesity, 28, 609-615. https://doi.org/10.1002/oby.22734
Antonioli, L., Pellegrini, C., Fornai, M., Tirotta, E., Gentile, D., Benvenuti, L., Giron, M. C., Caputi, V., Marsilio, I., Orso, G., Bernardini, N., Segnani, C., Ippolito, C., Csóka, B., Németh, Z. H., Haskó, G., Scarpignato, C., Blandizzi, C., & Colucci, R. (2017). Colonic motor dysfunctions in a mouse model of high-fat diet-induced obesity: An involvement of A2B adenosine receptors. Purinergic Signalling, 13, 497-510. https://doi.org/10.1007/s11302-017-9577-0
Bartho, L., Benko, R., Holzer-Petsche, U., Holzer, P., Undi, S., & Wolf, M. (2008). Role of extrinsic afferent neurons in gastrointestinal motility. European Review for Medical and Pharmacological Sciences, 12(Suppl 1), 21-31.
Beyak, M. J., Ramji, N., Krol, K. M., Kawaja, M. D., & Vanner, S. J. (2004). Two TTX-resistant Na+ currents in mouse colonic dorsal root ganglia neurons and their role in colitis-induced hyperexcitability. American Journal of Physiology. Gastrointestinal and Liver Physiology, 287(4), G845-G855. https://doi.org/10.1152/ajpgi.00154.2004
Bornstein, J. C., Costa, M., & Grider, J. R. (2004). Enteric motor and interneuronal circuits controlling motility. Neurogastroenterology and Motility: The Official Journal of the European Gastrointestinal Motility Society, 16(Suppl 1), 34-38. https://doi.org/10.1111/j.1743-3150.2004.00472.x
Bremner, J. D., Innis, R. B., Southwick, S. M., Staib, L., Zoghbi, S., & Charney, D. S. (2000). Decreased benzodiazepine receptor binding in prefrontal cortex in combat-related posttraumatic stress disorder. The American Journal of Psychiatry, 157(7), 1120-1126. https://doi.org/10.1176/appi.ajp.157.7.1120
Broderick, L., De Nardo, D., Franklin, B. S., Hoffman, H. M., & Latz, E. (2015). The inflammasomes and autoinflammatory syndromes. Annual Review of Pathology, 10, 395-424. https://doi.org/10.1146/annurev-pathol-012414-040431
Brown, I. A., McClain, J. L., Watson, R. E., Patel, B. A., & Gulbransen, B. D. (2016). Enteric glia mediate neuron death in colitis through purinergic pathways that require connexin-43 and nitric oxide. Cellular and Molecular Gastroenterology and Hepatology, 2(1), 77-91. https://doi.org/10.1016/j.jcmgh.2015.08.007
Casadesus, G., Shukitt-Hale, B., & Joseph, J. A. (2001). Automated measurement of age-related changes in the locomotor response to environmental novelty and home-cage activity. Mechanisms of Ageing and Development, 122, 1887-1897. https://doi.org/10.1016/S0047-6374(01)00324-4
Chanput, W., Mes, J. J., & Wichers, H. J. (2014). THP-1 cell line: An in vitro cell model for immune modulation approach. International Immunopharmacology, 23(1), 37-45. https://doi.org/10.1016/j.intimp.2014.08.002
Copel, C., Clerc, N., Osorio, N., Delmas, P., & Mazet, B. (2013). The Nav1.9 channel regulates colonic motility in mice. Frontiers in Neuroscience, 7(58), 1-8.
Csoka, B., Toro, G., Vindeirinho, J., Varga, Z. V., Koscso, B., Nemeth, Z. H., Kókai, E., Antonioli, L., Suleiman, M., Marchetti, P., Cseri, K., Deák, Á., Virág, L., Pacher, P., Bai, P., & Haskó, G. (2017). A2A adenosine receptors control pancreatic dysfunction in high-fat-diet-induced obesity. FASEB Journal: Official Publication of the Federation of American Societies for Experimental Biology, 31(11), 4985-4997. https://doi.org/10.1096/fj.201700398R
Cuesta, M. C., Quintero, L., Pons, H., & Suarez-Roca, H. (2002). Substance P and calcitonin gene-related peptide increase IL-1 beta, IL-6 and TNF alpha secretion from human peripheral blood mononuclear cells. Neurochemistry International, 40(4), 301-306. https://doi.org/10.1016/S0197-0186(01)00094-8
Cunin, P., Caillon, A., Corvaisier, M., Garo, E., Scotet, M., Blanchard, S., Delneste, Y., & Jeannin, P. (2011). The tachykinins substance P and hemokinin-1 favor the generation of human memory Th17 cells by inducing IL-1beta, IL-23, and TNF-like 1A expression by monocytes. Journal of Immunology, 186(7), 4175-4182. https://doi.org/10.4049/jimmunol.1002535
Curtis, M. J., Alexander, S., Cirino, G., Docherty, J. R., George, C. H., Giembycz, M. A., Hoyer, D., Insel, P. A., Izzo, A. A., Ji, Y., MacEwan, D. J., Sobey, C. G., Stanford, S. C., Teixeira, M. M., Wonnacott, S., & Ahluwalia, A. (2018). Experimental design and analysis and their reporting II: Updated and simplified guidance for authors and peer reviewers. British Journal of Pharmacology, 175, 987-993. https://doi.org/10.1111/bph.14153
Dalby, M. J., Aviello, G., Ross, A. W., Walker, A. W., Barrett, P., & Morgan, P. J. (2018). Diet induced obesity is independent of metabolic endotoxemia and TLR4 signalling, but markedly increases hypothalamic expression of the acute phase protein, SerpinA3N. Scientific Reports, 8(1), 15648. https://doi.org/10.1038/s41598-018-33928-4
D'Antongiovanni, V., Benvenuti, L., Fornai, M., Pellegrini, C., van den Wijngaard, R., Cerantola, S., Giron, M. C., Caputi, V., Colucci, R., Haskó, G., Németh, Z. H., Blandizzi, C., & Antonioli, L. (2020). Glial A2B adenosine receptors modulate abnormal tachykininergic responses and prevent enteric inflammation associated with high fat diet-induced obesity. Cell, 9(5), 1245.
D'Antongiovanni, V., Pellegrini, C., Fornai, M., Colucci, R., Blandizzi, C., Antonioli, L., & Bernardini, N. (2020). Intestinal epithelial barrier and neuromuscular compartment in health and disease. World Journal of Gastroenterology, 26(14), 1564-1579. https://doi.org/10.3748/wjg.v26.i14.1564
De Nardo, D., & Latz, E. (2011). NLRP3 inflammasomes link inflammation and metabolic disease. Trends in Immunology, 32, 373-379. https://doi.org/10.1016/j.it.2011.05.004
Ding, S., Chi, M. M., Scull, B. P., Rigby, R., Schwerbrock, N. M., Magness, S., Jobin, C., & Lund, P. K. (2010). High-fat diet: Bacteria interactions promote intestinal inflammation which precedes and correlates with obesity and insulin resistance in mouse. PLoS ONE, 5(8), e12191. https://doi.org/10.1371/journal.pone.0012191
Donath, M. Y., Boni-Schnetzler, M., Ellingsgaard, H., Halban, P. A., & Ehses, J. A. (2010). Cytokine production by islets in health and diabetes: Cellular origin, regulation and function. Trends in Endocrinology and Metabolism: TEM, 21(5), 261-267. https://doi.org/10.1016/j.tem.2009.12.010
Fazzini, A., D'Antongiovanni, V., Giusti, L., Da Valle, Y., Ciregia, F., Piano, I., Caputo, A., D'Ursi, A. M., Gargini, C., Lucacchini, A., & Mazzoni, M. R. (2014). Altered protease-activated receptor-1 expression and signaling in a malignant pleural mesothelioma cell line, NCI-H28, with homozygous deletion of the beta-catenin gene. PLoS ONE, 9(3), e111550. https://doi.org/10.1371/journal.pone.0111550
Fuchs, F., Damm, J., Gerstberger, R., Roth, J., & Rummel, C. (2013). Activation of the inflammatory transcription factor nuclear factor interleukin-6 during inflammatory and psychological stress in the brain. Journal of Neuroinflammation, 10(140), 1-16.
Fysekidis, M., Bouchoucha, M., Bihan, H., Reach, G., Benamouzig, R., & Catheline, J. M. (2012). Prevalence and co-occurrence of upper and lower functional gastrointestinal symptoms in patients eligible for bariatric surgery. Obesity Surgery, 22, 403-410. https://doi.org/10.1007/s11695-011-0396-z
Gallagher, T. K., Geoghegan, J. G., Baird, A. W., & Winter, D. C. (2007). Implications of altered gastrointestinal motility in obesity. Obesity Surgery, 17, 1399-1407. https://doi.org/10.1007/s11695-007-9221-0
Goode, T., O'Connor, T., Hopkins, A., Moriarty, D., O'Sullivan, G. C., Collins, J. K., O'Donoghue, D., Baird, A. W., O'Connell, J., & Shanahan, F. (2003). Neurokinin-1 receptor (NK-1R) expression is induced in human colonic epithelial cells by proinflammatory cytokines and mediates proliferation in response to substance P. Journal of Cellular Physiology, 197, 30-41. https://doi.org/10.1002/jcp.10234
Goverse, G., Stakenborg, M., & Matteoli, G. (2016). The intestinal cholinergic anti-inflammatory pathway. The Journal of Physiology, 594, 5771-5780. https://doi.org/10.1113/JP271537
Gulbransen, B. D., & Sharkey, K. A. (2009). Purinergic neuron-to-glia signaling in the enteric nervous system. Gastroenterology, 136, 1349-1358. https://doi.org/10.1053/j.gastro.2008.12.058
Gulbransen, B. D., & Sharkey, K. A. (2012). Novel functional roles for enteric glia in the gastrointestinal tract. Nature Reviews. Gastroenterology & Hepatology, 9, 625-632. https://doi.org/10.1038/nrgastro.2012.138
Ho, W. Z., Lai, J. P., Zhu, X. H., Uvaydova, M., & Douglas, S. D. (1997). Human monocytes and macrophages express substance P and neurokinin-1 receptor. Journal of Immunology, 159(11), 5654-5660.
Hume, D. A., Perry, V. H., & Gordon, S. (1984). The mononuclear phagocyte system of the mouse defined by immunohistochemical localisation of antigen F4/80: Macrophages associated with epithelia. The Anatomical Record, 210, 503-512. https://doi.org/10.1002/ar.1092100311
Ippolito, C., Colucci, R., Segnani, C., Errede, M., Girolamo, F., Virgintino, D., Dolfi, A., Tirotta, E., Buccianti, P., di Candio, G., Campani, D., Castagna, M., Bassotti, G., Villanacci, V., Blandizzi, C., & Bernardini, N. (2016). Fibrotic and vascular remodelling of colonic wall in patients with active ulcerative colitis. Journal of Crohn's & Colitis, 10, 1194-1204. https://doi.org/10.1093/ecco-jcc/jjw076
Javanmard Khameneh, H., Leong, K. W. K., Mencarelli, A., Vacca, M., Mambwe, B., Neo, K., Tay, A., Zolezzi, F., Lee, B., & Mortellaro, A. (2019). The Inflammasome adaptor ASC intrinsically limits CD4(+) T-cell proliferation to help maintain intestinal homeostasis. Frontiers in Immunology, 10, 1-15, 1566. https://doi.org/10.3389/fimmu.2019.01566
Kataoka, N., Shima, Y., Nakajima, K., & Nakamura, K. (2020). A central master driver of psychosocial stress responses in the rat. Science, 367, 1105-1112. https://doi.org/10.1126/science.aaz4639
Khan, W. I., & Collins, S. M. (2006). Gut motor function: Immunological control in enteric infection and inflammation. Clinical and Experimental Immunology, 143, 389-397. https://doi.org/10.1111/j.1365-2249.2005.02979.x
Kim, K. A., Gu, W., Lee, I. A., Joh, E. H., & Kim, D. H. (2012). High fat diet-induced gut microbiota exacerbates inflammation and obesity in mice via the TLR4 signaling pathway. PLoS ONE, 7, e47713. https://doi.org/10.1371/journal.pone.0047713
Lai, J. P., Ho, W. Z., Kilpatrick, L. E., Wang, X., Tuluc, F., Korchak, H. M., & Douglas, S. D. (2006). Full-length and truncated neurokinin-1 receptor expression and function during monocyte/macrophage differentiation. Proceedings of the National Academy of Sciences of the United States of America, 103(20), 7771-7776. https://doi.org/10.1073/pnas.0602563103
Lam, Y. Y., Ha, C. W., Campbell, C. R., Mitchell, A. J., Dinudom, A., Oscarsson, J., Cook, D. I., Hunt, N. H., Caterson, I. D., Holmes, A. J., & Storlien, L. H. (2012). Increased gut permeability and microbiota change associate with mesenteric fat inflammation and metabolic dysfunction in diet-induced obese mice. PLoS ONE, 7, e34233. https://doi.org/10.1371/journal.pone.0034233
Lee, H. M., Kim, J. J., Kim, H. J., Shong, M., Ku, B. J., & Jo, E. K. (2013). Upregulated NLRP3 inflammasome activation in patients with type 2 diabetes. Diabetes, 62(1), 194-204. https://doi.org/10.2337/db12-0420
Lieb, K., Fiebich, B. L., Busse-Grawitz, M., Hull, M., Berger, M., & Bauer, J. (1996). Effects of substance P and selected other neuropeptides on the synthesis of interleukin-1 beta and interleukin-6 in human monocytes: A re-examination. Journal of Neuroimmunology, 67, 77-81. https://doi.org/10.1016/0165-5728(96)00034-3
Lilley, E., Stanford, S. C., Kendall, D. E., Alexander, S. P., Cirino, G., Docherty, J. R., George, C. H., Insel, P. A., Izzo, A. A., Ji, Y., Panettieri, R. A., Sobey, C. G., Stefanska, B., Stephens, G., Teixeira, M., & Ahluwalia, A. (2020). ARRIVE 2.0 and the British Journal of Pharmacology: Updated guidance for 2020. British Journal of Pharmacology, 177(16), 3611-3616. https://bpspubs.onlinelibrary.wiley.com/doi/full/10.1111/bph.15178
Lin, H. H., Faunce, D. E., Stacey, M., Terajewicz, A., Nakamura, T., Zhang-Hoover, J., Kerley, M., Mucenski, M. L., Gordon, S., & Stein-Streilein, J. (2005). The macrophage F4/80 receptor is required for the induction of antigen-specific efferent regulatory T cells in peripheral tolerance. The Journal of Experimental Medicine, 201(10), 1615-1625. https://doi.org/10.1084/jem.20042307
Lopez-Castejon, G., Luheshi, N. M., Compan, V., High, S., Whitehead, R. C., Flitsch, S., Kirov, A., Prudovsky, I., Swanton, E., & Brough, D. (2013). Deubiquitinases regulate the activity of caspase-1 and interleukin-1beta secretion via assembly of the inflammasome. The Journal of Biological Chemistry, 288(4), 2721-2733. https://doi.org/10.1074/jbc.M112.422238
Luck, H., Tsai, S., Chung, J., Clemente-Casares, X., Ghazarian, M., Revelo, X. S., Lei, H., Luk, C. T., Shi, S. Y., Surendra, A., Copeland, J. K., Ahn, J., Prescott, D., Rasmussen, B. A., Chng, M. H. Y., Engleman, E. G., Girardin, S. E., Lam, T. K. T., Croitoru, K., … Winer, D. A. (2015). Regulation of obesity-related insulin resistance with gut anti-inflammatory agents. Cell Metabolism, 21(4), 527-542. https://doi.org/10.1016/j.cmet.2015.03.001
Margolis, K. G., & Gershon, M. D. (2009). Neuropeptides and inflammatory bowel disease. Current Opinion in Gastroenterology, 25, 503-511. https://doi.org/10.1097/MOG.0b013e328331b69e
Martin, F. C., Anton, P. A., Gornbein, J. A., Shanahan, F., & Merrill, J. E. (1993). Production of interleukin-1 by microglia in response to substance P: Role for a non-classical NK-1 receptor. Journal of Neuroimmunology, 42, 53-60. https://doi.org/10.1016/0165-5728(93)90212-H
Martin, F. C., Charles, A. C., Sanderson, M. J., & Merrill, J. E. (1992). Substance P stimulates IL-1 production by astrocytes via intracellular calcium. Brain Research, 599, 13-18. https://doi.org/10.1016/0006-8993(92)90846-2
Maslanik, T., Mahaffey, L., Tannura, K., Beninson, L., Greenwood, B. N., & Fleshner, M. (2013). The inflammasome and danger associated molecular patterns (DAMPs) are implicated in cytokine and chemokine responses following stressor exposure. Brain, Behavior, and Immunity, 28, 54-62. https://doi.org/10.1016/j.bbi.2012.10.014
Masumoto, J., Taniguchi, S., Nakayama, J., Shiohara, M., Hidaka, E., Katsuyama, T., Murase, S., & Sagara, J. (2001). Expression of apoptosis-associated speck-like protein containing a caspase recruitment domain, a pyrin N-terminal homology domain-containing protein, in normal human tissues. The Journal of Histochemistry and Cytochemistry: Official Journal of the Histochemistry Society, 49(10), 1269-1275. https://doi.org/10.1177/002215540104901009
Morimoto, A., Nakamori, T., Morimoto, K., Tan, N., & Murakami, N. (1993). The central role of corticotrophin-releasing factor (CRF-41) in psychological stress in rats. The Journal of Physiology, 460, 221-229. https://doi.org/10.1113/jphysiol.1993.sp019468
Mushref, M. A., & Srinivasan, S. (2013). Effect of high fat-diet and obesity on gastrointestinal motility. Annals of Translational Medicine, 1(2), 14.
Padilla, F., Couble, M. L., Coste, B., Maingret, F., Clerc, N., Crest, M., Ritter, A. M., Magloire, H., & Delmas, P. (2007). Expression and localization of the Nav1.9 sodium channel in enteric neurons and in trigeminal sensory endings: Implication for intestinal reflex function and orofacial pain. Molecular and Cellular Neurosciences, 35, 138-152. https://doi.org/10.1016/j.mcn.2007.02.008
Palazon-Riquelme, P., Worboys, J. D., Green, J., Valera, A., Martin-Sanchez, F., Pellegrini, C., Brough, D., & López-Castejón, G. (2018). USP7 and USP47 deubiquitinases regulate NLRP3 inflammasome activation. EMBO Reports, 19(10), e44766. https://doi.org/10.15252/embr.201744766
Pavillard, L. E., Canadas-Lozano, D., Alcocer-Gomez, E., Marin-Aguilar, F., Pereira, S., Robertson, A. A. B., Muntané, J., Ryffel, B., Cooper, M. A., Quiles, J. L., Bullón, P., Ruiz-Cabello, J., & Cordero, M. D. (2017). NLRP3-inflammasome inhibition prevents high fat and high sugar diets-induced heart damage through autophagy induction. Oncotarget, 8, 99740-99756. https://doi.org/10.18632/oncotarget.20763
Pelegrin, P., & Surprenant, A. (2009). Dynamics of macrophage polarization reveal new mechanism to inhibit IL-1beta release through pyrophosphates. The EMBO Journal, 28, 2114-2127. https://doi.org/10.1038/emboj.2009.163
Pellegrini, C., Antonioli, L., Lopez-Castejon, G., Blandizzi, C., & Fornai, M. (2017). Canonical and non-canonical activation of NLRP3 Inflammasome at the crossroad between immune tolerance and intestinal inflammation. Frontiers in Immunology, 25(8), 36.
Pellegrini, C., Fornai, M., Colucci, R., Tirotta, E., Blandini, F., Levandis, G., Cerri, S., Segnani, C., Ippolito, C., Bernardini, N., Cseri, K., Blandizzi, C., Haskó, G., & Antonioli, L. (2016). Alteration of colonic excitatory tachykininergic motility and enteric inflammation following dopaminergic nigrostriatal neurodegeneration. Journal of Neuroinflammation, 13(1), 146. https://doi.org/10.1186/s12974-016-0608-5
Percie du Sert, N., Hurst, V., Ahluwalia, A., Alam, S., Avey, M. T., Baker, M., Browne, W. J., Clark, A., Cuthill, I. C., Dirnagl, U., Emerson, M., Garner, P., Holgate, S. T., Howells, D. W., Karp, N. A., Lazic, S. E., Lidster, K., MacCallum, C. J., Macleod, M., … Würbel, H. (2020). The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research. PLoS Biology, 18(7), e3000410. https://doi.org/10.1371/journal.pbio.3000410
Pierantonelli, I., Rychlicki, C., Agostinelli, L., Giordano, D. M., Gaggini, M., Fraumene, C., Saponaro, C., Manghina, V., Sartini, L., Mingarelli, E., Pinto, C., Buzzigoli, E., Trozzi, L., Giordano, A., Marzioni, M., Minicis, S. D., Uzzau, S., Cinti, S., Gastaldelli, A., & Svegliati-Baroni, G. (2017). Lack of NLRP3-inflammasome leads to gut-liver axis derangement, gut dysbiosis and a worsened phenotype in a mouse model of NAFLD. Scientific Reports, 7(1), 12200. https://doi.org/10.1038/s41598-017-11744-6
Rajindrajith, S., Devanarayana, N. M., & Benninga, M. A. (2014). Obesity and functional gastrointestinal diseases in children. Journal of Neurogastroenterology and Motility, 20, 414-416. https://doi.org/10.5056/jnm14067
Raybould, H. E. (2012). Gut microbiota, epithelial function and derangements in obesity. The Journal of Physiology, 590, 441-446. https://doi.org/10.1113/jphysiol.2011.222133
Reichardt, F., Baudry, C., Gruber, L., Mazzuoli, G., Moriez, R., Scherling, C., Kollmann, P., Daniel, H., Kisling, S., Haller, D., Neunlist, M., & Schemann, M. (2013). Properties of myenteric neurones and mucosal functions in the distal colon of diet-induced obese mice. The Journal of Physiology, 591, 5125-5139. https://doi.org/10.1113/jphysiol.2013.262733
Rescigno, M. (2011). The intestinal epithelial barrier in the control of homeostasis and immunity. Trends in Immunology, 32, 256-264. https://doi.org/10.1016/j.it.2011.04.003
Rheinheimer, J., de Souza, B. M., Cardoso, N. S., Bauer, A. C., & Crispim, D. (2017). Current role of the NLRP3 inflammasome on obesity and insulin resistance: A systematic review. Metabolism, Clinical and Experimental, 74, 1-9. https://doi.org/10.1016/j.metabol.2017.06.002
Richter, S., D'Antongiovanni, V., Martinelli, S., Bechmann, N., Riverso, M., Poitz, D. M., Pacak, K., Eisenhofer, G., Mannelli, M., & Rapizzi, E. (2018). Primary fibroblast co-culture stimulates growth and metabolism in Sdhb-impaired mouse pheochromocytoma MTT cells. Cell and Tissue Research, 374(3), 473-485. https://doi.org/10.1007/s00441-018-2907-x
Rodriguez-Hernandez, H., Simental-Mendia, L. E., Rodriguez-Ramirez, G., & Reyes-Romero, M. A. (2013). Obesity and inflammation: Epidemiology, risk factors, and markers of inflammation. International Journal of Endocrinology, 2013, 678159.
Rugiero, F., Mistry, M., Sage, D., Black, J. A., Waxman, S. G., Crest, M., Clerc, N., Delmas, P., & Gola, M. (2003). Selective expression of a persistent tetrodotoxin-resistant Na+ current and NaV1.9 subunit in myenteric sensory neurons. The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, 23, 2715-2725. https://doi.org/10.1523/JNEUROSCI.23-07-02715.2003
Sage, D., Salin, P., Alcaraz, G., Castets, F., Giraud, P., Crest, M., Mazet, B., & Clerc, N. (2007). Na(v)1.7 and Na(v)1.3 are the only tetrodotoxin-sensitive sodium channels expressed by the adult guinea pig enteric nervous system. The Journal of Comparative Neurology, 504(4), 363-378. https://doi.org/10.1002/cne.21450
Schmid-Burgk, J. L., Gaidt, M. M., Schmidt, T., Ebert, T. S., Bartok, E., & Hornung, V. (2015). Caspase-4 mediates non-canonical activation of the NLRP3 inflammasome in human myeloid cells. European Journal of Immunology, 45, 2911-2917. https://doi.org/10.1002/eji.201545523
Shi, C. S., Shenderov, K., Huang, N. N., Kabat, J., Abu-Asab, M., Fitzgerald, K. A., Sher, A., & Kehrl, J. H. (2012). Activation of autophagy by inflammatory signals limits IL-1beta production by targeting ubiquitinated inflammasomes for destruction. Nature Immunology, 13(3), 255-263. https://doi.org/10.1038/ni.2215
Souza, A. C. P., Souza, C. M., Amaral, C. L., Lemes, S. F., Santucci, L. F., Milanski, M., Torsoni, A. S., & Torsoni, M. A. (2019). Short-term High-fat diet consumption reduces hypothalamic expression of the nicotinic acetylcholine receptor alpha7 subunit (alpha7nAChR) and affects the anti-inflammatory response in a mouse model of sepsis. Frontiers in Immunology, 10, 565. https://doi.org/10.3389/fimmu.2019.00565
Stenman, L. K., Holma, R., & Korpela, R. (2012). High-fat-induced intestinal permeability dysfunction associated with altered fecal bile acids. World Journal of Gastroenterology, 18, 923-929. https://doi.org/10.3748/wjg.v18.i9.923
Steppan, C. M., Bailey, S. T., Bhat, S., Brown, E. J., Banerjee, R. R., Wright, C. M., Patel, H. R., Ahima, R. S., & Lazar, M. A. (2001). The hormone resistin links obesity to diabetes. Nature, 409, 307-312. https://doi.org/10.1038/35053000
Stienstra, R., van Diepen, J. A., Tack, C. J., Zaki, M. H., van de Veerdonk, F. L., Perera, D., Neale, G. A., Hooiveld, G. J., Hijmans, A., Vroegrijk, I., van den Berg, S., Romijn, J., Rensen, P. C. N., Joosten, L. A. B., Netea, M. G., & Kanneganti, T. D. (2011). Inflammasome is a central player in the induction of obesity and insulin resistance. Proceedings of the National Academy of Sciences of the United States of America, 108, 15324-15329. https://doi.org/10.1073/pnas.1100255108
Stoffels, B., Hupa, K. J., Snoek, S. A., van Bree, S., Stein, K., Schwandt, T., Vilz, T. O., Lysson, M., van't Veer, C., Kummer, M. P., Hornung, V., Kalff, J. C., de Jonge, W. J., & Wehner, S. (2014). Postoperative ileus involves interleukin-1 receptor signaling in enteric glia. Gastroenterology, 146, 176-187, e171.
Strowig, T., Henao-Mejia, J., Elinav, E., & Flavell, R. (2012). Inflammasomes in health and disease. Nature, 481, 278-286. https://doi.org/10.1038/nature10759
Tejera, D., Mercan, D., Sanchez-Caro, J. M., Hanan, M., Greenberg, D., Soreq, H., Latz, E., Golenbock, D., & Heneka, M. T. (2019). Systemic inflammation impairs microglial Abeta clearance through NLRP3 inflammasome. The EMBO Journal, 38, e101064.
Troseid, M., Nestvold, T. K., Rudi, K., Thoresen, H., Nielsen, E. W., & Lappegard, K. T. (2013). Plasma lipopolysaccharide is closely associated with glycemic control and abdominal obesity: Evidence from bariatric surgery. Diabetes Care, 36, 3627-3632. https://doi.org/10.2337/dc13-0451
Vallejo, S., Palacios, E., Romacho, T., Villalobos, L., Peiro, C., & Sanchez-Ferrer, C. F. (2014). The interleukin-1 receptor antagonist anakinra improves endothelial dysfunction in streptozotocin-induced diabetic rats. Cardiovascular Diabetology, 13(1), 158. https://doi.org/10.1186/s12933-014-0158-z
Vandanmagsar, B., Youm, Y. H., Ravussin, A., Galgani, J. E., Stadler, K., Mynatt, R. L., Ravussin, E., Stephens, J. M., & Dixit, V. D. (2011). The NLRP3 inflammasome instigates obesity-induced inflammation and insulin resistance. Nature Medicine, 17(2), 179-188. https://doi.org/10.1038/nm.2279
Yang, G., Lee, H. E., & Lee, J. Y. (2016). A pharmacological inhibitor of NLRP3 inflammasome prevents non-alcoholic fatty liver disease in a mouse model induced by high fat diet. Scientific Reports, 6, 24399. https://doi.org/10.1038/srep24399
Yang, S. J., & Lim, Y. (2014). Resveratrol ameliorates hepatic metaflammation and inhibits NLRP3 inflammasome activation. Metabolism, Clinical and Experimental, 63, 693-701. https://doi.org/10.1016/j.metabol.2014.02.003

Auteurs

Carolina Pellegrini (C)

Department of Pharmacy, University of Pisa, Pisa, Italy.
Lydia Becker Institute of Immunology and Inflammation, Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.

Matteo Fornai (M)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Laura Benvenuti (L)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Rocchina Colucci (R)

Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Padua, Italy.

Valentina Caputi (V)

Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Padua, Italy.
APC Microbiome Ireland, University College Cork, Cork, Ireland.

Pablo Palazon-Riquelme (P)

Lydia Becker Institute of Immunology and Inflammation, Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.

Maria Cecilia Giron (MC)

Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Padua, Italy.

Anna Nericcio (A)

Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Padua, Italy.

Francesca Garelli (F)

Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Padua, Italy.

Vanessa D'Antongiovanni (V)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Cristina Segnani (C)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Chiara Ippolito (C)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Monica Nannipieri (M)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Gloria Lopez-Castejon (G)

Lydia Becker Institute of Immunology and Inflammation, Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.

Pablo Pelegrin (P)

Biomedical Research Institute of Murcia (IMIB-Arrixaca), Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.

György Haskó (G)

Department of Anesthesiology, Columbia University, New York, New York, USA.

Nunzia Bernardini (N)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Interdepartmental Research Center "Nutraceuticals and Food for Health", University of Pisa, Pisa, Italy.

Corrado Blandizzi (C)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Luca Antonioli (L)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Articles similaires

Humans Meals Time Factors Female Adult
Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice

Classifications MeSH