Abstract
Apoptosis in the immune system is critical for maintaining self-tolerance and preventing autoimmunity. Nevertheless, inhibiting apoptosis in lymphocytes is not alone sufficient to break self-tolerance, suggesting the involvement of other cell types. We investigated whether apoptosis in dendritic cells (DCs) helps regulate self-tolerance by generating transgenic mice expressing the baculoviral caspase inhibitor, p35, in DCs (DC-p35). DC-p35 mice displayed defective DC apoptosis, resulting in their accumulation and, in turn, chronic lymphocyte activation and systemic autoimmune manifestations. The observation that a defect in DC apoptosis can independently lead to autoimmunity is consistent with a central role for these cells in maintaining immune self-tolerance.
Original language | English (US) |
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Pages (from-to) | 1160-4 |
Number of pages | 5 |
Journal | Science (New York, N.Y.) |
Volume | 311 |
Issue number | 5764 |
DOIs | |
State | Published - Feb 24 2006 |
Keywords
- Adoptive Transfer
- Aging
- Animals
- Antibodies, Antinuclear
- Apoptosis
- Autoimmunity
- B-Lymphocytes
- Caspase Inhibitors
- Cell Survival
- Dendritic Cells
- Kidney
- Lung
- Lymphocyte Activation
- Mice
- Mice, Inbred BALB C
- Mice, Inbred C57BL
- Mice, Transgenic
- Self Tolerance
- Spleen
- T-Lymphocytes
- Viral Proteins
- Journal Article
- Research Support, N.I.H., Extramural
- Research Support, Non-U.S. Gov't