fig1

Delivery of miR-214 via extracellular vesicles downregulates <i>Xbp1</i> expression and <InlineParagraph>pro-inflammatory</InlineParagraph> cytokine genes in macrophages

Figure 1. Engineering pCMV-MIR-214 and generation of iEV-214. (A) Sequence of pre-miR-214 minigene that was cloned into pCMV-MIR to generate pCMV-MIR-214; (B) Restriction mapping of pCMV-MIR (empty) and pCMV-MIR-214. Plasmids were double digested with SgfI and XhoI and fragments were resolved via electrophoresis; (C) Schematic representation depicting the generation of iEV-214; (D) Quantification of iEVs purified from the conditioned media of J558L cells that were untransfected (-) or transfected with pCMV-MIR-scr or pCMV-MIR-214. iEV protein content was quantified using the BCA assay.

Extracellular Vesicles and Circulating Nucleic Acids
ISSN 2767-6641 (Online)
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