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PRECLINICAL PUBLICATION · 2014

Distinct CD11b+-monocyte subsets accelerate endothelial cell recovery after acute and chronic endothelial cell damage.

Mouse / Other

Evidence by therapy association

Study details and outcomes are extracted in the context of a specific intervention. Separate associations are retained rather than silently merged.

PMID 24602320 ↗2014Mixed findings

Distinct CD11b+-monocyte subsets accelerate endothelial cell recovery after acute and chronic endothelial cell damage.

MouseOtherCD11b-diphtheria toxin receptor mice and ApoE-/- CD11b-DTR mice; wild type donor cellsTransfusionAfter endothelial injury, with assessment at 7 days

Model: Acute carotid endothelial injury in monocyte-depleted CD11b-DTR mice and chronic hypercholesterolaemia-induced endothelial injury in ApoE-/- CD11b-DTR mice

CD11b+ monocytes improved endothelium-dependent vasoreactivity 7 days after acute injury and homed to the injury site, whereas CD11b-negative cells had no effect. In chronic hypercholesterolaemic injury, interferon-gamma stimulated monocytes decreased endothelial function while interleukin-4 stimul…

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