Abstract:
:Sterile inflammation can be initiated by innate immune recognition of markers of tissue injury termed damage-associated molecular patterns (DAMPs). DAMP recognition by dendritic cells (DCs) has also been postulated to lead to T cell responses to foreign antigens in tumors or allografts. Many DAMPs represent intracellular contents that are released upon cell damage, notably after necrosis. In this regard, we have previously described DNGR-1 (CLEC9A) as a DC-restricted receptor specific for an unidentified DAMP that is exposed by necrotic cells and is necessary for efficient priming of cytotoxic T cells against dead cell-associated antigens. Here, we have shown that the DNGR-1 ligand is preserved from yeast to man and corresponds to the F-actin component of the cellular cytoskeleton. The identification of F-actin as a DNGR-1 ligand suggests that cytoskeletal exposure is a universal sign of cell damage that can be targeted by the innate immune system to initiate immunity.
journal_name
Immunityjournal_title
Immunityauthors
Ahrens S,Zelenay S,Sancho D,Hanč P,Kjær S,Feest C,Fletcher G,Durkin C,Postigo A,Skehel M,Batista F,Thompson B,Way M,Reis e Sousa C,Schulz Odoi
10.1016/j.immuni.2012.03.008subject
Has Abstractpub_date
2012-04-20 00:00:00pages
635-45issue
4eissn
1074-7613issn
1097-4180pii
S1074-7613(12)00126-4journal_volume
36pub_type
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