Erratum: A primary human macrophage-enteroid co-culture model to investigate mucosal gut physiology and host-pathogen interactions (Scientific Reports (2017) 7 (45270) DOI: 10.1038/srep45270);A primary human macrophage-enteroid co-culture model to investigate mucosal gut physiology and host-pathogen interactions

Scientific Reports

Volumn 7, Issue , 2017, Pages

  Noel, Gaelle ^a   Baetz, Nicholas W ^b   Staab, Janet F ^b   Donowitz, Mark ^b   Kovbasnjuk, Olga ^b   Pasetti, Marcela F ^a   Zachos, Nicholas C ^b  

^a University of Maryland School of Medicine Center for Vaccine Development   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKINE;

BACTERIUM; BIOLOGICAL MODEL; CELL COMMUNICATION; CELL CULTURE; COCULTURE; EPITHELIUM CELL; GROWTH, DEVELOPMENT AND AGING; HOST PATHOGEN INTERACTION; HUMAN; IMMUNOLOGY; INTESTINE MUCOSA; MACROPHAGE; PHYSIOLOGY; PROCEDURES; SECRETION (PROCESS);

BACTERIA; CELL COMMUNICATION; CELLS, CULTURED; COCULTURE TECHNIQUES; CYTOKINES; EPITHELIAL CELLS; HOST-PATHOGEN INTERACTIONS; HUMANS; INTESTINAL MUCOSA; MACROPHAGES; MODELS, BIOLOGICAL;

EID: 85016300809     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep46790     Document Type: Erratum

References (59)

1. Peterson, L. W. & Artis, D. Intestinal epithelial cells: regulators of barrier function and immune homeostasis. Nat Rev Immunol 14, 141-153, doi: 10.1038/nri3608 (2014).
2. Duell, B. L., Cripps, A. W., Schembri, M. A. & Ulett, G. C. Epithelial Cell Coculture Models for Studying Infectious Diseases: Benefits and Limitations. Journal of Biomedicine and Biotechnology 2011, 852419, doi: 10.1155/2011/852419 (2011).
3. Gibbons, D. L. & Spencer, J. Mouse and human intestinal immunity: same ballpark, different players; different rules, same score. Mucosal Immunol 4, 148-157 (2011).
4. Tsilingiri, K. et al. Probiotic and postbiotic activity in health and disease: comparison on a novel polarised ex-vivo organ culture model. Gut 61, 1007-1015, doi: 10.1136/gutjnl-2011-300971 (2012).
5. Bimczok, D. et al. Human gastric epithelial cells contribute to gastric immune regulation by providing retinoic acid to dendritic cells. Mucosal Immunol 8, 533-544, doi: 10.1038/mi.2014.86 (2015).
6. Bisping, G. et al. Patients with inflammatory bowel disease (IBD) reveal increased induction capacity of intracellular interferongamma (IFN-gamma) in peripheral CD8+ lymphocytes co-cultured with intestinal epithelial cells. Clin Exp Immunol 123, 15-22 (2001).
7. Leonard, F., Collnot, E.-M. & Lehr, C.-M. A Three-Dimensional Coculture of Enterocytes, Monocytes and Dendritic Cells To Model Inflamed Intestinal Mucosa in Vitro. Molecular Pharmaceutics 7, 2103-2119, doi: 10.1021/mp1000795 (2010).
8. McKay, D. M., Croitoru, K. & Perdue, M. H. T cell-monocyte interactions regulate epithelial physiology in a coculture model of inflammation. Am J Physiol 270, C418-428 (1996).
9. Parkos, C. A., Delp, C., Arnaout, M. A. & Madara, J. L. Neutrophil migration across a cultured intestinal epithelium. Dependence on a CD11b/CD18-mediated event and enhanced efficiency in physiological direction. Journal of Clinical Investigation 88, 1605-1612 (1991).
10. Nanthakumar, N. N., Fusunyan, R. D., Sanderson, I. & Walker, W. A. Inflammation in the developing human intestine: A possible pathophysiologic contribution to necrotizing enterocolitis. Proc Natl Acad Sci USA 97, 6043-6048 (2000).
11. Trapecar, M., Goropevsek, A., Gorenjak, M., Gradisnik, L. & Slak Rupnik, M. A Co-Culture Model of the Developing Small Intestine Offers New Insight in the Early Immunomodulation of Enterocytes and Macrophages by italic Lactobacillus spp. italic through STAT1 and NF-kB p65 Translocation. PLoS ONE 9, e86297, doi: 10.1371/journal.pone.0086297 (2014).
12. Bermudez-Brito, M., Plaza-Diaz, J., Fontana, L., Munoz-Quezada, S. & Gil, A. In vitro cell and tissue models for studying hostmicrobe interactions: a review. Br J Nutr 109 Suppl 2, S27-34, doi: 10.1017/S0007114512004023 (2013).
13. Foulke-Abel, J. et al. Human Enteroids as a Model of Upper Small Intestinal Ion Transport Physiology and Pathophysiology. Gastroenterology 150, 638-649 e638, doi: 10.1053/j.gastro.2015.11.047 (2016).
14. In, J. G. et al. Human mini-guts: new insights into intestinal physiology and host-pathogen interactions. Nat Rev Gastroenterol Hepatol 13, 633-642, doi: 10.1038/nrgastro.2016.142 (2016).
15. Sato, T. & Clevers, H. Growing self-organizing mini-guts from a single intestinal stem cell: mechanism and applications. Science 340, 1190-1194, doi: 10.1126/science.1234852 (2013).
16. Zachos, N. C. et al. Human Enteroids/Colonoids and Intestinal Organoids Functionally Recapitulate Normal Intestinal Physiology and Pathophysiology. J Biol Chem 291, 3759-3766, doi: 10.1074/jbc.R114.635995 (2016).
17. Stelzner, M. et al. A nomenclature for intestinal in vitro cultures. Am J Physiol Gastrointest Liver Physiol 302, G1359-1363, doi: 10.1152/ajpgi.00493.2011 (2012).
18. Barker, N. & Clevers, H. Lineage tracing in the intestinal epithelium. Curr Protoc Stem Cell Biol Chapter 5, Unit5A 4, doi: 10.1002/9780470151808.sc05a04s13 (2010).
19. Mukherjee, S. & Hooper, L. V. Antimicrobial defense of the intestine. Immunity 42, 28-39, doi: 10.1016/j.immuni.2014.12.028 (2015).
20. Foulke-Abel, J. et al. Human enteroids as an ex-vivo model of host-pathogen interactions in the gastrointestinal tract. Exp Biol Med (Maywood) 239, 1124-1134, doi: 10.1177/1535370214529398 (2014).
21. In, J. et al. Enterohemorrhagic Escherichia coli Reduces Mucus and Intermicrovillar Bridges in Human Stem Cell-Derived Colonoids. Cellular and Molecular Gastroenterology and Hepatology 2, 48-62.e43, doi: 10.1016/j.jcmgh.2015.10.001 (2016).
22. Sato, T. et al. Long-term expansion of epithelial organoids from human colon, adenoma, adenocarcinoma, and Barrett's epithelium. Gastroenterology 141, 1762-1772, doi: 10.1053/j.gastro.2011.07.050 (2011).
23. Schuijers, J. et al. Ascl2 acts as an R-spondin/Wnt-responsive switch to control stemness in intestinal crypts. Cell Stem Cell 16, 158-170, doi: 10.1016/j.stem.2014.12.006 (2015).
24. Durand, A. et al. Functional intestinal stem cells after Paneth cell ablation induced by the loss of transcription factor Math1 (Atoh1). Proc Natl Acad Sci USA 109, 8965-8970, doi: 10.1073/pnas.1201652109 (2012).
25. Smythies, L. E. et al. Mucosal IL-8 and TGF-beta recruit blood monocytes: evidence for cross-talk between the lamina propria stroma and myeloid cells. J Leukoc Biol 80, 492-499, doi: 10.1189/jlb.1005566 (2006).
26. Tabbaa, M. G., Axon, A. T. R. & Dixon, M. F. Enterocyte dimensions in patients with abnormal intestinal permeability. European Journal of Gastroenterology and Hepatology 6, 607-610 (1994).
27. Grant, C. N., Nellis, E. D. & Chahine, A. A. A case of small intestinal cast causing SBO in complicated intestinal graft-versus-host disease. Pediatr Surg Int 30, 685-688, doi: 10.1007/s00383-014-3515-9 (2014).
28. Mizutani, T. et al. Real-time analysis of P-glycoprotein-mediated drug transport across primary intestinal epithelium threedimensionally cultured in vitro. Biochem Biophys Res Commun 419, 238-243, doi: 10.1016/j.bbrc.2012.01.155 (2012).
29. Sato, T. et al. Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche. Nature 459, 262-265, doi: 10.1038/nature07935 (2009).
30. Walker, N. M. et al. Cellular chloride and bicarbonate retention alters intracellular pH regulation in Cftr KO crypt epithelium. Am J Physiol Gastrointest Liver Physiol 310, G70-80, doi: 10.1152/ajpgi.00236.2015 (2016).
31. Spottl, T. et al. A new organotypic model to study cell interactions in the intestinal mucosa. Eur J Gastroenterol Hepatol 18, 901-909 (2006).
32. Barrila, J. et al. Organotypic 3D cell culture models: using the rotating wall vessel to study host-pathogen interactions. Nat Rev Microbiol 8, 791-801, doi: 10.1038/nrmicro2423 (2010).
33. Carvalho, H. M., Teel, L. D., Goping, G. & O'Brien, A. D. A three-dimensional tissue culture model for the study of attach and efface lesion formation by enteropathogenic and enterohaemorrhagic Escherichia coli. Cell Microbiol 7, 1771-1781, doi: 10.1111/j.1462-5822.2004.00594.x (2005).
34. Nickerson, C. A. et al. Three-dimensional tissue assemblies: novel models for the study of Salmonella enterica serovar Typhimurium pathogenesis. Infect Immun 69, 7106-7120, doi: 10.1128/IAI.69.11.7106-7120.2001 (2001).
35. Barker, N. Adult intestinal stem cells: critical drivers of epithelial homeostasis and regeneration. Nat Rev Mol Cell Biol 15, 19-33, doi: 10.1038/nrm3721 (2014).
36. Middendorp, S. et al. Adult stem cells in the small intestine are intrinsically programmed with their location-specific function. Stem Cells 32, 1083-1091, doi: 10.1002/stem.1655 (2014).
37. VanDussen, K. L. et al. Development of an enhanced human gastrointestinal epithelial culture system to facilitate patient-based assays. Gut 64, 911-920, doi: 10.1136/gutjnl-2013-306651 (2015).
38. Smith, P. D. et al. Intestinal macrophages and response to microbial encroachment. Mucosal Immunol 4, 31-42, doi: 10.1038/ mi.2010.66 (2011).
39. Smythies, L. E. et al. Inflammation anergy in human intestinal macrophages is due to Smad-induced IkappaBalpha expression and NF-kappaB inactivation. J Biol Chem 285, 19593-19604, doi: 10.1074/jbc.M109.069955 (2010).
40. Italiani, P. & Boraschi, D. From Monocytes to M1/M2 Macrophages: Phenotypical vs. Functional Differentiation. Front Immunol 5, 514, doi: 10.3389/fimmu.2014.00514 (2014).
41. Saxena, K. et al. Human Intestinal Enteroids: a New Model To Study Human Rotavirus Infection, Host Restriction, and Pathophysiology. J Virol 90, 43-56, doi: 10.1128/JVI.01930-15 (2015).
42. Zhang, Y. G., Wu, S., Xia, Y. & Sun, J. Salmonella-infected crypt-derived intestinal organoid culture system for host-bacterial interactions. Physiol Rep 2, doi: 10.14814/phy2.12147 (2014).
43. Gonzales-Siles, L. & Sjoling, A. The different ecological niches of enterotoxigenic Escherichia coli. Environ Microbiol 18, 741-751, doi: 10.1111/1462-2920.13106 (2016).
44. Humphries, R. M. & Armstrong, G. D. Sticky situation: localized adherence of enteropathogenic Escherichia coli to the small intestine epithelium. Future Microbiol 5, 1645-1661, doi: 10.2217/fmb.10.124 (2010).
45. Rescigno, M., Rotta, G., Valzasina, B. & Ricciardi-Castagnoli, P. Dendritic cells shuttle microbes across gut epithelial monolayers. Immunobiology 204, 572-581, doi: 10.1078/0171-2985-00094 (2001).
46. Strisciuglio, C. et al. Impaired autophagy leads to abnormal dendritic cell-epithelial cell interactions. J Crohns Colitis 7, 534-541, doi: 10.1016/j.crohns.2012.08.009 (2012).
47. Yin, Y. et al. CpG DNA assists the whole inactivated H9N2 influenza virus in crossing the intestinal epithelial barriers via transepithelial uptake of dendritic cell dendrites. Mucosal Immunol 8, 799-814, doi: 10.1038/mi.2014.110 (2014).
48. Chieppa, M., Rescigno, M., Huang, A. Y. & Germain, R. N. Dynamic imaging of dendritic cell extension into the small bowel lumen in response to epithelial cell TLR engagement. J Exp Med 203, 2841-2852, doi: 10.1084/jem.20061884 (2006).
49. Kim, H. J., Li, H., Collins, J. J. & Ingber, D. E. Contributions of microbiome and mechanical deformation to intestinal bacterial overgrowth and inflammation in a human gut-on-a-chip. Proc Natl Acad Sci USA 113, E7-15, doi: 10.1073/pnas.1522193112 (2016).
50. Mazzini, E., Massimiliano, L., Penna, G. & Rescigno, M. Oral tolerance can be established via gap junction transfer of fed antigens from CX3CR1(+ ) macrophages to CD103(+ ) dendritic cells. Immunity 40, 248-261, doi: 10.1016/j.immuni.2013.12.012 (2014).
51. Travis, M. A. et al. Loss of integrin alpha(v)beta8 on dendritic cells causes autoimmunity and colitis in mice. Nature 449, 361-365, doi: 10.1038/nature06110 (2007).
52. Wang, Y. P. et al. Effects of Wnt3a on proliferation, activation and the expression of TGFb/Smad in rat hepatic stellate cells. Zhonghua Gan Zang Bing Za Zhi 21, 111-115 (2013).
53. Shi, M. et al. Latent TGF-beta structure and activation. Nature 474, 343-349, doi: 10.1038/nature10152 (2011).
54. Petruccelli, B. P., Kollaritsch, H. & Taylor, D. N. Treatment of travelers' diarrhea, 92-100 (BC Decker, 1997).
55. Mills, M. & Estes, M. K. Physiologically relevant human tissue models for infectious diseases. Drug Discov Today 21, 1540-1552, doi: 10.1016/j.drudis.2016.06.020 (2016).
56. Evans, D. G., Silver, R. P., Evans, D. J. Jr., Chase, D. G. & Gorbach, S. L. Plasmid-controlled colonization factor associated with virulence in Esherichia coli enterotoxigenic for humans. Infect Immun 12, 656-667 (1975).
57. Evans, D. J. Jr. & Evans, D. G. Three characteristics associated with enterotoxigenic Escherichia coli isolated from man. Infect Immun 8, 322-328 (1973).
58. Levine, M. M. et al. Escherichia coli strains that cause diarrhoea but do not produce heat-labile or heat-stable enterotoxins and are non-invasive. Lancet 1, 1119-1122 (1978).
59. Cleary, J. et al. Enteropathogenic Escherichia coli (EPEC) adhesion to intestinal epithelial cells: role of bundle-forming pili (BFP), EspA filaments and intimin. Microbiology 150, 527-538, doi: 10.1099/mic.0.26740-0 (2004).