期刊
JOURNAL OF IMMUNOLOGY
卷 183, 期 2, 页码 945-952出版社
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0900921
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资金
- National Institutes of Health
Although it has long been known that human CD4(+) T cells can express functional class II MHC molecules, the role of lysosomal proteases in the T cell class II MHC processing and presentation pathway is unknown. Using CD4(+) T cell clones that constitutively express class II MHC, we determined that cathepsin S is necessary for invariant chain proteolysis in T cells. CD4(+)HLA-DR+ T cells down-regulated cathepsin S expression and activity 18 h after activation, thereby ceasing nascent class II MHC product formation. This blockade resulted in the loss of the invariant chain fragment CLIP from the cell surface, suggesting that-like professional APC-CD4(+) HLA-DR+ cells modulate self-Ag presentation as a consequence of activation. Furthermore, cathepsin S expression and activity, and concordantly cell surface CLIP expression, was reduced in HLA-DR+ CD4(+) T cells as compared with B cells both in vitro and ex vivo. The Journal of Immunology, 2009, 183: 945-952.
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