Abstract
It is unclear if naïve T cells require dendritic cell ICAMs to proliferate inside lymph nodes. To check if and when CD4 lymphocytes use ICAMs on migratory DCs, wild-type and ICAM-1 and 2 double knock out bone marrow-derived DCs pulsed with saturating levels of an OT-II transgene-specific ovalbumin-derived peptide were co-transferred into skin-draining lymph nodes. Intravital imaging of OT-II lymphocytes entering these lymph nodes revealed that ICAM-1 and -2 deficient migratory DCs formed fewer stable conjugates with OT-II lymphocytes but promoted normal T cell proliferation. DC ICAMs were also not required for unstable TCR-dependent lymphocyte arrests on antigen presenting migratory DCs. Thus, rare antigen-stimulated ICAM-stabilized T-DC conjugates are dispensable for CD4 lymphocyte proliferation inside lymph nodes.
Keywords:
Lymph nodes; T cell activation; dendritic cells; integrins; vaccination.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antigens, CD / genetics
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Antigens, CD / metabolism*
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CD4-Positive T-Lymphocytes / cytology
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CD4-Positive T-Lymphocytes / immunology*
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Cell Adhesion Molecules / genetics
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Cell Adhesion Molecules / metabolism*
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Cell Movement / physiology
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Cell Proliferation / physiology
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Dendritic Cells / cytology
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Dendritic Cells / immunology*
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Intercellular Adhesion Molecule-1 / genetics
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Intercellular Adhesion Molecule-1 / metabolism*
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Lipopolysaccharides / immunology
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Lymph Nodes / cytology
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Lymph Nodes / metabolism*
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Lymphocyte Activation / immunology
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Mice
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Mice, Inbred C57BL
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Mice, Knockout
Substances
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Antigens, CD
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Cell Adhesion Molecules
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ICAM-2 protein, mouse
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Icam1 protein, mouse
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Lipopolysaccharides
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Intercellular Adhesion Molecule-1
Grants and funding
This work was supported by the Israel Science Foundation under Grant 791/17; the German Israeli Foundation under Grant I-1470-412.13/2018, and a grant from Mr. and Mrs. William Glied.