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      Coronary heart disease alters intercellular communication by modifying microparticle-mediated microRNA transport.

      Febs Letters
      Adolescent, Adult, Binding Sites, Biological Transport, physiology, Carrier Proteins, genetics, metabolism, Cell Communication, Coronary Disease, Female, Human Umbilical Vein Endothelial Cells, Humans, Male, MicroRNAs, Middle Aged, Real-Time Polymerase Chain Reaction

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          Abstract

          Coronary heart disease (CHD) is characterized by abnormal intercellular communication and circulating microRNAs (miRNAs) are likely involved in this process. Here, we show that CHD was associated with changes in the transport of circulating miRNA, particularly decreased miRNA enrichment in microparticles (MPs). Additionally, MPs from CHD patients were less efficient at transferring miRNA to cultured HUVECs, which correlated with their diminished capacity to bind developmental endothelial locus-1 (Del-1). In summary, CHD was associated with distinct changes in circulating miRNA transport and these changes may contribute to the abnormal intercellular communication that underlies CHD initiation and progression. Published by Elsevier B.V.

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