Document Detail


Microbial stimulation fully differentiates monocytes to DC-SIGN/CD209(+) dendritic cells for immune T cell areas.
MedLine Citation:
PMID:  21029863     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Dendritic cells (DCs), critical antigen-presenting cells for immune control, normally derive from bone marrow precursors distinct from monocytes. It is not yet established if the large reservoir of monocytes can develop into cells with critical features of DCs in vivo. We now show that fully differentiated monocyte-derived DCs (Mo-DCs) develop in mice and DC-SIGN/CD209a marks the cells. Mo-DCs are recruited from blood monocytes into lymph nodes by lipopolysaccharide and live or dead gram-negative bacteria. Mobilization requires TLR4 and its CD14 coreceptor and Trif. When tested for antigen-presenting function, Mo-DCs are as active as classical DCs, including cross-presentation of proteins and live gram-negative bacteria on MHC I in vivo. Fully differentiated Mo-DCs acquire DC morphology and localize to T cell areas via L-selectin and CCR7. Thus the blood monocyte reservoir becomes the dominant presenting cell in response to select microbes, yielding DC-SIGN(+) cells with critical functions of DCs.
Authors:
Cheolho Cheong; Ines Matos; Jae-Hoon Choi; Durga Bhavani Dandamudi; Elina Shrestha; M Paula Longhi; Kate L Jeffrey; Robert M Anthony; Courtney Kluger; Godwin Nchinda; Hyein Koh; Anthony Rodriguez; Juliana Idoyaga; Maggi Pack; Klara Velinzon; Chae Gyu Park; Ralph M Steinman
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Cell     Volume:  143     ISSN:  1097-4172     ISO Abbreviation:  Cell     Publication Date:  2010 Oct 
Date Detail:
Created Date:  2010-10-29     Completed Date:  2010-11-22     Revised Date:  2011-10-31    
Medline Journal Info:
Nlm Unique ID:  0413066     Medline TA:  Cell     Country:  United States    
Other Details:
Languages:  eng     Pagination:  416-29     Citation Subset:  IM    
Copyright Information:
Copyright © 2010 Elsevier Inc. All rights reserved.
Affiliation:
Chris Browne Center for Immunology and Immune Diseases, The Rockefeller University, New York, NY 10065, USA. ccheong@rockefeller.edu
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MeSH Terms
Descriptor/Qualifier:
Animals
Antigen Presentation
Antigens, CD14 / immunology
Cell Adhesion Molecules / immunology,  metabolism*
Cell Differentiation*
Dendritic Cells / cytology*,  immunology
Escherichia coli / immunology*
L-Selectin / immunology
Lectins, C-Type / immunology,  metabolism*
Lymph Nodes / cytology,  immunology
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Monocytes / cytology*,  immunology
Receptors, CCR7 / immunology
Receptors, Cell Surface / immunology,  metabolism*
T-Lymphocytes / immunology
Toll-Like Receptor 4 / agonists,  immunology
Grant Support
ID/Acronym/Agency:
AI40045/AI/NIAID NIH HHS; AI40874/AI/NIAID NIH HHS; GM62116/GM/NIGMS NIH HHS; R01 AI040874-13A1/AI/NIAID NIH HHS; R37 AI040045-15/AI/NIAID NIH HHS; UL1RR024143/RR/NCRR NIH HHS
Chemical
Reg. No./Substance:
0/Antigens, CD14; 0/Ccr7 protein, mouse; 0/Cell Adhesion Molecules; 0/DC-specific ICAM-3 grabbing nonintegrin; 0/Lectins, C-Type; 0/Receptors, CCR7; 0/Receptors, Cell Surface; 0/Toll-Like Receptor 4; 126880-86-2/L-Selectin
Comments/Corrections
Comment In:
Cell. 2010 Oct 29;143(3):339-40   [PMID:  21029856 ]
Nat Rev Immunol. 2010 Dec;10(12):808   [PMID:  21155170 ]

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