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Migrating Lymph Dendritic Cells Contain Intracellular CD40 That Is Mobilized to the Immunological Synapse during Interactions with Antigen-Specific T Lymphocytes
被引:6
作者:

Foster, Neil
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Univ Nottingham, Sch Vet Sci & Med, Bonington NG7 2NR, Leics, England Univ Nottingham, Sch Vet Sci & Med, Bonington NG7 2NR, Leics, England

Turnbull, Emma L.
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Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 2JD, England Univ Nottingham, Sch Vet Sci & Med, Bonington NG7 2NR, Leics, England

Macpherson, Gordon
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Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 2JD, England Univ Nottingham, Sch Vet Sci & Med, Bonington NG7 2NR, Leics, England
机构:
[1] Univ Nottingham, Sch Vet Sci & Med, Bonington NG7 2NR, Leics, England
[2] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 2JD, England
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D O I:
10.4049/jimmunol.1202010
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Steady state migrating rat lymph dendritic cells (LDC) are semimature, expressing high levels of surface MHC class II, but low levels of surface costimulatory molecules. In this study, we show that surface CD40 is not detectable, but LDC contain intracellular CD40. Multiple isoforms of CD40 were detected, including the type 1 isoform required for signal transduction. Culture of LDC with syngeneic T cells does not induce redistribution of cytoplasmic CD40. When LDC were cultured with naive allogeneic CD4(+) T lymphocytes, polarization of CD40 to the immune synapse occurred between 3 and 6 h postculture. By 24 h, although large numbers of T cells were engaged with LDC, CD40 could not be detected in LDC or at the synapses. We conclude that migrating LDC contain stores of CD40 that can be mobilized rapidly to the sites of interaction with Ag-specific T cells. The disappearance of CD40 by 24 h may help in the regulation of T cell activation. The Journal of Immunology, 2012, 189: 5632-5637.
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页码:5632 / 5637
页数:6
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