دورية أكاديمية

Endocytosis of commensal antigens by intestinal epithelial cells regulates mucosal T cell homeostasis.

التفاصيل البيبلوغرافية
العنوان: Endocytosis of commensal antigens by intestinal epithelial cells regulates mucosal T cell homeostasis.
المؤلفون: Ladinsky MS; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA., Araujo LP; Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA., Zhang X; Department of Biological Sciences, Rutgers University, Newark, NJ 07102, USA., Veltri J; Department of Pharmacology, Physiology and Neurosciences, Rutgers University, Newark, NJ 07103, USA., Galan-Diez M; Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA., Soualhi S; Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA., Lee C; Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA., Irie K; Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.; Department of Preventive Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan., Pinker EY; Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA., Narushima S; RIKEN Center for Integrative Medical Sciences, Kanagawa 230-0045, Japan., Bandyopadhyay S; Department of Biological Sciences, Rutgers University, Newark, NJ 07102, USA., Nagayama M; RIKEN Center for Integrative Medical Sciences, Kanagawa 230-0045, Japan.; Department of Medicine, Division of Gastroenterology, Jichi Medical University, Tochigi 329-0498, Japan., Elhenawy W; Department of Biochemistry & Biomedical Sciences, Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, Canada., Coombes BK; Department of Biochemistry & Biomedical Sciences, Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, Canada., Ferraris RP; Department of Pharmacology, Physiology and Neurosciences, Rutgers University, Newark, NJ 07103, USA., Honda K; RIKEN Center for Integrative Medical Sciences, Kanagawa 230-0045, Japan.; Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo 160-8582, Japan., Iliev ID; Department of Microbiology and Immunology and The Jill Roberts Institute for Research in Inflammatory Bowel Disease, Weill Cornell Medicine, New York, NY 10065, USA., Gao N; Department of Biological Sciences, Rutgers University, Newark, NJ 07102, USA., Bjorkman PJ; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA. bjorkman@caltech.edu ii2137@cumc.columbia.edu., Ivanov II; Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA. bjorkman@caltech.edu ii2137@cumc.columbia.edu.
المصدر: Science (New York, N.Y.) [Science] 2019 Mar 08; Vol. 363 (6431).
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: American Association for the Advancement of Science Country of Publication: United States NLM ID: 0404511 Publication Model: Print Cited Medium: Internet ISSN: 1095-9203 (Electronic) Linking ISSN: 00368075 NLM ISO Abbreviation: Science
أسماء مطبوعة: Publication: : Washington, DC : American Association for the Advancement of Science
Original Publication: New York, N.Y. : [s.n.] 1880-
مواضيع طبية MeSH: Antigens, Bacterial/*immunology , Endocytosis/*immunology , Gastrointestinal Microbiome/*immunology , Host Microbial Interactions/*immunology , Intestinal Mucosa/*immunology , Intraepithelial Lymphocytes/*immunology , Th17 Cells/*immunology, Animals ; Bacteria/immunology ; Endocytosis/genetics ; Homeostasis/genetics ; Lymphocyte Activation ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Inbred NOD ; Symbiosis ; cdc42 GTP-Binding Protein/genetics ; cdc42 GTP-Binding Protein/physiology
مستخلص: Commensal bacteria influence host physiology, without invading host tissues. We show that proteins from segmented filamentous bacteria (SFB) are transferred into intestinal epithelial cells (IECs) through adhesion-directed endocytosis that is distinct from the clathrin-dependent endocytosis of invasive pathogens. This process transfers microbial cell wall-associated proteins, including an antigen that stimulates mucosal T helper 17 (T H 17) cell differentiation, into the cytosol of IECs in a cell division control protein 42 homolog (CDC42)-dependent manner. Removal of CDC42 activity in vivo led to disruption of endocytosis induced by SFB and decreased epithelial antigen acquisition, with consequent loss of mucosal T H 17 cells. Our findings demonstrate direct communication between a resident gut microbe and the host and show that under physiological conditions, IECs acquire antigens from commensal bacteria for generation of T cell responses to the resident microbiota.
(Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.)
References: Infect Immun. 1999 Apr;67(4):1992-2000. (PMID: 10085047)
Infect Immun. 2000 Nov;68(11):6496-504. (PMID: 11035767)
Am J Physiol Regul Integr Comp Physiol. 2001 Oct;281(4):R1274-82. (PMID: 11557636)
Genesis. 2004 Jul;39(3):186-93. (PMID: 15282745)
J Struct Biol. 2005 Oct;152(1):36-51. (PMID: 16182563)
Proc Natl Acad Sci U S A. 2007 Mar 20;104(12):5091-6. (PMID: 17360364)
Nat Rev Mol Cell Biol. 2007 Aug;8(8):603-12. (PMID: 17609668)
J Microsc. 2008 May;230(Pt 2):212-7. (PMID: 18445149)
Cell Host Microbe. 2008 Oct 16;4(4):337-49. (PMID: 18854238)
Immunity. 2009 Oct 16;31(4):677-89. (PMID: 19833089)
Cell. 2009 Oct 30;139(3):485-98. (PMID: 19836068)
Nat Rev Immunol. 2010 Mar;10(3):159-69. (PMID: 20182457)
Mucosal Immunol. 2011 Jan;4(1):15-21. (PMID: 20944557)
Gut Microbes. 2010 Nov-Dec;1(6):367-72. (PMID: 21468217)
Cell Host Microbe. 2011 Sep 15;10(3):260-72. (PMID: 21925113)
Cell Host Microbe. 2011 Sep 15;10(3):273-84. (PMID: 21925114)
J Clin Invest. 2012 Mar;122(3):1052-65. (PMID: 22354172)
Cell Host Microbe. 2012 Oct 18;12(4):509-20. (PMID: 22999859)
Science. 2013 Aug 2;341(6145):569-73. (PMID: 23828891)
Nature. 2013 Dec 19;504(7480):446-50. (PMID: 24226770)
Nature. 2013 Dec 19;504(7480):451-5. (PMID: 24226773)
Immunity. 2014 Apr 17;40(4):594-607. (PMID: 24684957)
Nature. 2014 Jun 5;510(7503):152-6. (PMID: 24739972)
J Immunol. 2014 Jul 1;193(1):431-8. (PMID: 24899505)
Am J Physiol Gastrointest Liver Physiol. 2014 Oct 15;307(8):G824-35. (PMID: 25059827)
Proc Natl Acad Sci U S A. 2014 Sep 23;111(38):13942-7. (PMID: 25201978)
J Immunol Methods. 2015 Jun;421:104-111. (PMID: 25858227)
Cell Rep. 2015 Aug 25;12(8):1314-24. (PMID: 26279572)
Cell. 2015 Oct 8;163(2):367-80. (PMID: 26411289)
Science. 2016 May 27;352(6289):1116-20. (PMID: 27230380)
Nature. 2016 Nov 24;539(7630):565-569. (PMID: 27828940)
Proc Natl Acad Sci U S A. 2016 Dec 13;113(50):E8141-E8150. (PMID: 27911839)
Sci Immunol. 2017 Jul 21;2(13):null. (PMID: 28733471)
Nature. 2018 Feb 15;554(7692):373-377. (PMID: 29414937)
Infect Immun. 1974 Oct;10(4):948-56. (PMID: 4426712)
J Bacteriol. 1978 Jun;134(3):1099-107. (PMID: 659364)
Infect Immun. 1993 Sep;61(9):4001-4. (PMID: 8359925)
Lab Anim. 1993 Apr;27(2):141-50. (PMID: 8501895)
J Struct Biol. 1996 Jan-Feb;116(1):71-6. (PMID: 8742726)
J Bacteriol. 1976 Jul;127(1):572-83. (PMID: 931952)
معلومات مُعتمدة: P50 GM082545 United States GM NIGMS NIH HHS; F31 DK121428 United States DK NIDDK NIH HHS; R21 AI126305 United States AI NIAID NIH HHS; R21 AI146817 United States AI NIAID NIH HHS; R01 DK102934 United States DK NIDDK NIH HHS; R01 AT010243 United States AT NCCIH NIH HHS; P50 AI150464 United States AI NIAID NIH HHS; R01 DK098378 United States DK NIDDK NIH HHS
المشرفين على المادة: 0 (Antigens, Bacterial)
0 (Cdc42 protein, mouse)
EC 3.6.5.2 (cdc42 GTP-Binding Protein)
تواريخ الأحداث: Date Created: 20190309 Date Completed: 20190819 Latest Revision: 20230930
رمز التحديث: 20230930
مُعرف محوري في PubMed: PMC6708280
DOI: 10.1126/science.aat4042
PMID: 30846568
قاعدة البيانات: MEDLINE
الوصف
تدمد:1095-9203
DOI:10.1126/science.aat4042