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Emerging role of damage-associated molecular patterns derived from mitochondria in inflammation

Journal

TRENDS IN IMMUNOLOGY
Volume 32, Issue 4, Pages 157-164

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.it.2011.01.005

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Funding

  1. FWO-Vlaanderen [3G072810, 31507110]
  2. VIB, Ghent University (GROUPID consortium of the UGent MRP initiative)
  3. Research Foundation Flanders (FWO-Vlaanderen) [G.0875.11, G.0973.11]
  4. Federal Research Program [IAP 6/18]
  5. European Research Program FP6 ApopTrain [MRTN-CT-035624]
  6. Euregional PACTII
  7. Flemish Government [BOF09/01M00709]
  8. [Apo-Sys 200767]

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Cell death and injury often lead to release or exposure of intracellular molecules called damage-associated molecular patterns (DAMPs) or cell death-associated molecules. These molecules are recognized by the innate immune system by pattern recognition receptors the same receptors that detect pathogen-associated molecular patterns, thus revealing similarities between pathogen-induced and non-infectious inflammatory responses. Many DAMPs are derived from the plasma membrane, nucleus, endoplasmic reticulum and cytosol. Recently, mitochondria have emerged as other organelles that function as a source of DAMPs. Here, we highlight the significance of mitochondria! DAMPs and discuss their contribution to inflammation and development of human pathologies.

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