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Microbial stimulation fully differentiates monocytes to DC-SIGN/CD209(+) dendritic cells for immune T cell areas

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 
Citation
 CELL, Vol.143(3) : 416-429, 2010 
Journal Title
 CELL 
ISSN
 0092-8674 
Issue Date
2010
MeSH
Animals ; Antigen Presentation ; Cell Adhesion Molecules/immunology ; Cell Adhesion Molecules/metabolism* ; Cell Differentiation* ; Dendritic Cells/cytology* ; Dendritic Cells/immunology ; Escherichia coli/immunology* ; L-Selectin/immunology ; Lectins, C-Type/immunology ; Lectins, C-Type/metabolism* ; Lipopolysaccharide Receptors/immunology ; Lymph Nodes/cytology ; Lymph Nodes/immunology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Monocytes/cytology* ; Monocytes/immunology ; Receptors, CCR7/immunology ; Receptors, Cell Surface/immunology ; Receptors, Cell Surface/metabolism* ; T-Lymphocytes/immunology ; Toll-Like Receptor 4/agonists ; Toll-Like Receptor 4/immunology
Abstract
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
Files in This Item:
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DOI
10.1016/j.cell.2010.09.039
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
Yonsei Authors
Park, Chae Gyu(박채규) ORCID logo https://orcid.org/0000-0003-1906-1308
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/103281
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