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. 2020 Dec 9;146:110448. doi: 10.1016/j.mehy.2020.110448

Table 1.

Association of miR-146a downregulation/deficiency with vascular and autoimmune diseases.

Expression/Function Association with pathological condition/disease Reference
Human
Downregulation of plasma miR-146a Poor coronary collateral circulation in patients with coronary artery disease [31]
Downregulation of serum miR-146a Severe acute ischemic stroke [32]
Downregulation of serum miR-146a Acute exacerbation of chronic obstructive pulmonary disease and negative correlation with inflammatory cytokines: TNF-α, IL-1β, IL-6, IL-8 [33]
Downregulation of PBMCs-derived miR-146a Severe systemic lupus erythematosus and the induction of type I IFNs [34]



miR-146a-deficient mice
Knockout of the miR-146a gene in C57BL/6 mice Myeloproliferative disease (myeloid and lymphoid malignancies) due to a lack of NF-kB suppression [35]
Mice harboring miR-146a-deficient Treg cells Impaired function of Treg cells: no restraint of IFN-γ-mediated pathogenic Th1 responses and associated inflammation [36]
Model of myocardial ischemia and reperfusion injury Decreased heart function and increased myocardial infarction and apoptosis by targeting Med 1 gene [37]
Model of Atopic dermatitis Increased accumulation of infiltrating cells in the dermis, elevated expression of IFN-γ, CCL5 and CCL8 in the skin [38]