Key result
Mitochondrial damage-associated molecular patterns activate immune pathways linked to vascular dysfunction and CVD.
Why the study?
Cell death releases mitochondrial damage-associated molecular patterns that may induce vascular changes by mechanisms that are currently not well understood.
This review summarizes the emerging evidence linking mitochondrial damage-associated molecular patterns (mtDAMPs) to immune system activation, vascular dysfunction, and cardiovascular disease.
Answers are grounded in this paper and cite their sources.
mtDAMPs may promote vascular dysfunction via innate immunity; leaves open whether targeting them alters cardiovascular outcomes.
Immune system activation occurs not only due to foreign stimuli, but also due to endogenous molecules. As such, endogenous molecules that are released into the circulation due to cell death and/or injury alarm the immune system that something has disturbed homeostasis and a response is needed. Collectively, these molecules are known as damage-associated molecular patterns (DAMPs). Mitochondrial DAMPs (mtDAMPs) are potent immunological activators due to the bacterial ancestry of mitochondria. Mitochondrial DAMPs are recognized by specific pattern recognition receptors of the innate immune system, some of which are expressed in the cardiovascular system. Cell death leads to release of mtDAMPs that may induce vascular changes by mechanisms that are currently not well understood. This review will focus on recently published evidence linking mtDAMPs and immune system activation to vascular dysfunction and cardiovascular disease.
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Wenceslau et al. (2014) conducted a review in Vascular dysfunction and cardiovascular disease. Mitochondrial damage-associated molecular patterns (mtDAMPs) was evaluated. Mitochondrial damage-associated molecular patterns released during cell death act as potent immunological activators linked to vascular dysfunction and cardiovascular disease.
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