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Characterization of MSC-exo. ( A ) surface markers of bone marrow MSC detected by flow cytometry were shown as CD45 − CD11 − CD90 + CD29 + . ( B ) Representative Western blot images of exosomal protein markers (Alix and Tsg101) and MSC markers (CD73). ( C ) MSC-exo and MSC NIC -exo manifested cup-shaped morphology under TEM. Scale bar = 200 μm. ( D ) The particle size and concentration were analyzed by <t>nanoparticle</t> tracking analysis. No significant difference was found between MSC-exo and MSC NIC -exo. ( E ) Representative confocal images suggested that exosomes were endocytosed by BMDM. Scale bar = 10 μm.
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a Transmission electron microscopy (TEM) and <t>nanoparticle</t> tracking analysis (NTA) of the circulating sEVs purified from the plasma of normal weight healthy human subjects (NC) and human subjects with obesity or overweight (OB). b Volcano plot, c heatmap showing the differential expressed proteins (DEPs) in the sEVs. d Pathway enrichments analysis of the DEPs in the sEVs. e TEM and NTA of the circulating sEVs purified from plasma of the mouse models. f GO analysis of the DEPs in the sEVs of the mouse models. g Overlapping DEPs in the human and mouse sEVs. h ECM1 protein levels in the circulating sEVs in CD mice (C-sEVs) and DIO mice (D-sEVs). i ECM1 protein levels in the plasma and sEVs-depleted plasma of DIO mice. Shown is the mean ± SD; two-sided unpaired t -test for ( b , d , h , i ); n = 3 independent experiments for ( a , e ); n = 6 mice in each group; p values were indicated in graphs. C-sEVs, circulating sEVs in control diet mice; D-sEVs, circulating sEVs in high-fat diet-induced obesity mice; sEV-depleted, sEVs-depleted plasma in high-fat diet-induced obesity mice; ECM1 extracellular matrix protein 1. Source data are provided in Source Data file.
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a Transmission electron microscopy (TEM) and <t>nanoparticle</t> tracking analysis (NTA) of the circulating sEVs purified from the plasma of normal weight healthy human subjects (NC) and human subjects with obesity or overweight (OB). b Volcano plot, c heatmap showing the differential expressed proteins (DEPs) in the sEVs. d Pathway enrichments analysis of the DEPs in the sEVs. e TEM and NTA of the circulating sEVs purified from plasma of the mouse models. f GO analysis of the DEPs in the sEVs of the mouse models. g Overlapping DEPs in the human and mouse sEVs. h ECM1 protein levels in the circulating sEVs in CD mice (C-sEVs) and DIO mice (D-sEVs). i ECM1 protein levels in the plasma and sEVs-depleted plasma of DIO mice. Shown is the mean ± SD; two-sided unpaired t -test for ( b , d , h , i ); n = 3 independent experiments for ( a , e ); n = 6 mice in each group; p values were indicated in graphs. C-sEVs, circulating sEVs in control diet mice; D-sEVs, circulating sEVs in high-fat diet-induced obesity mice; sEV-depleted, sEVs-depleted plasma in high-fat diet-induced obesity mice; ECM1 extracellular matrix protein 1. Source data are provided in Source Data file.
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a Transmission electron microscopy (TEM) and <t>nanoparticle</t> tracking analysis (NTA) of the circulating sEVs purified from the plasma of normal weight healthy human subjects (NC) and human subjects with obesity or overweight (OB). b Volcano plot, c heatmap showing the differential expressed proteins (DEPs) in the sEVs. d Pathway enrichments analysis of the DEPs in the sEVs. e TEM and NTA of the circulating sEVs purified from plasma of the mouse models. f GO analysis of the DEPs in the sEVs of the mouse models. g Overlapping DEPs in the human and mouse sEVs. h ECM1 protein levels in the circulating sEVs in CD mice (C-sEVs) and DIO mice (D-sEVs). i ECM1 protein levels in the plasma and sEVs-depleted plasma of DIO mice. Shown is the mean ± SD; two-sided unpaired t -test for ( b , d , h , i ); n = 3 independent experiments for ( a , e ); n = 6 mice in each group; p values were indicated in graphs. C-sEVs, circulating sEVs in control diet mice; D-sEVs, circulating sEVs in high-fat diet-induced obesity mice; sEV-depleted, sEVs-depleted plasma in high-fat diet-induced obesity mice; ECM1 extracellular matrix protein 1. Source data are provided in Source Data file.
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a Transmission electron microscopy (TEM) and <t>nanoparticle</t> tracking analysis (NTA) of the circulating sEVs purified from the plasma of normal weight healthy human subjects (NC) and human subjects with obesity or overweight (OB). b Volcano plot, c heatmap showing the differential expressed proteins (DEPs) in the sEVs. d Pathway enrichments analysis of the DEPs in the sEVs. e TEM and NTA of the circulating sEVs purified from plasma of the mouse models. f GO analysis of the DEPs in the sEVs of the mouse models. g Overlapping DEPs in the human and mouse sEVs. h ECM1 protein levels in the circulating sEVs in CD mice (C-sEVs) and DIO mice (D-sEVs). i ECM1 protein levels in the plasma and sEVs-depleted plasma of DIO mice. Shown is the mean ± SD; two-sided unpaired t -test for ( b , d , h , i ); n = 3 independent experiments for ( a , e ); n = 6 mice in each group; p values were indicated in graphs. C-sEVs, circulating sEVs in control diet mice; D-sEVs, circulating sEVs in high-fat diet-induced obesity mice; sEV-depleted, sEVs-depleted plasma in high-fat diet-induced obesity mice; ECM1 extracellular matrix protein 1. Source data are provided in Source Data file.
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Characterization of MSC-exo. ( A ) surface markers of bone marrow MSC detected by flow cytometry were shown as CD45 − CD11 − CD90 + CD29 + . ( B ) Representative Western blot images of exosomal protein markers (Alix and Tsg101) and MSC markers (CD73). ( C ) MSC-exo and MSC NIC -exo manifested cup-shaped morphology under TEM. Scale bar = 200 μm. ( D ) The particle size and concentration were analyzed by nanoparticle tracking analysis. No significant difference was found between MSC-exo and MSC NIC -exo. ( E ) Representative confocal images suggested that exosomes were endocytosed by BMDM. Scale bar = 10 μm.

Journal: International Journal of Nanomedicine

Article Title: Nicorandil-Pretreated Mesenchymal Stem Cell-Derived Exosomes Facilitate Cardiac Repair After Myocardial Infarction via Promoting Macrophage M2 Polarization by Targeting miR-125a-5p/TRAF6/IRF5 Signaling Pathway

doi: 10.2147/IJN.S441307

Figure Lengend Snippet: Characterization of MSC-exo. ( A ) surface markers of bone marrow MSC detected by flow cytometry were shown as CD45 − CD11 − CD90 + CD29 + . ( B ) Representative Western blot images of exosomal protein markers (Alix and Tsg101) and MSC markers (CD73). ( C ) MSC-exo and MSC NIC -exo manifested cup-shaped morphology under TEM. Scale bar = 200 μm. ( D ) The particle size and concentration were analyzed by nanoparticle tracking analysis. No significant difference was found between MSC-exo and MSC NIC -exo. ( E ) Representative confocal images suggested that exosomes were endocytosed by BMDM. Scale bar = 10 μm.

Article Snippet: Exosomes were detected using a transmission electron microscope (Tecnai G2 Spirit BioTwin, FEI, USA) and Nanoparticle Tracking Analysis (ZetaVIEW S/N 17–310, PARTICLE METRIX, Germany).

Techniques: Flow Cytometry, Western Blot, Concentration Assay

a Transmission electron microscopy (TEM) and nanoparticle tracking analysis (NTA) of the circulating sEVs purified from the plasma of normal weight healthy human subjects (NC) and human subjects with obesity or overweight (OB). b Volcano plot, c heatmap showing the differential expressed proteins (DEPs) in the sEVs. d Pathway enrichments analysis of the DEPs in the sEVs. e TEM and NTA of the circulating sEVs purified from plasma of the mouse models. f GO analysis of the DEPs in the sEVs of the mouse models. g Overlapping DEPs in the human and mouse sEVs. h ECM1 protein levels in the circulating sEVs in CD mice (C-sEVs) and DIO mice (D-sEVs). i ECM1 protein levels in the plasma and sEVs-depleted plasma of DIO mice. Shown is the mean ± SD; two-sided unpaired t -test for ( b , d , h , i ); n = 3 independent experiments for ( a , e ); n = 6 mice in each group; p values were indicated in graphs. C-sEVs, circulating sEVs in control diet mice; D-sEVs, circulating sEVs in high-fat diet-induced obesity mice; sEV-depleted, sEVs-depleted plasma in high-fat diet-induced obesity mice; ECM1 extracellular matrix protein 1. Source data are provided in Source Data file.

Journal: Nature Communications

Article Title: Elevated extracellular matrix protein 1 in circulating extracellular vesicles supports breast cancer progression under obesity conditions

doi: 10.1038/s41467-024-45995-5

Figure Lengend Snippet: a Transmission electron microscopy (TEM) and nanoparticle tracking analysis (NTA) of the circulating sEVs purified from the plasma of normal weight healthy human subjects (NC) and human subjects with obesity or overweight (OB). b Volcano plot, c heatmap showing the differential expressed proteins (DEPs) in the sEVs. d Pathway enrichments analysis of the DEPs in the sEVs. e TEM and NTA of the circulating sEVs purified from plasma of the mouse models. f GO analysis of the DEPs in the sEVs of the mouse models. g Overlapping DEPs in the human and mouse sEVs. h ECM1 protein levels in the circulating sEVs in CD mice (C-sEVs) and DIO mice (D-sEVs). i ECM1 protein levels in the plasma and sEVs-depleted plasma of DIO mice. Shown is the mean ± SD; two-sided unpaired t -test for ( b , d , h , i ); n = 3 independent experiments for ( a , e ); n = 6 mice in each group; p values were indicated in graphs. C-sEVs, circulating sEVs in control diet mice; D-sEVs, circulating sEVs in high-fat diet-induced obesity mice; sEV-depleted, sEVs-depleted plasma in high-fat diet-induced obesity mice; ECM1 extracellular matrix protein 1. Source data are provided in Source Data file.

Article Snippet: Human and mouse plasma sEVs particle sizes were analyzed by nanoparticle tracking analysis (NTA, PARTICLE METRIX, ZetaVIEW S/N 22–756) at Shanghai Hwayen Biotechnological, Inc., China, and the protein expressions of human sEVs markers including CD63, CD9, TST10 and calnexin were examined.

Techniques: Transmission Assay, Electron Microscopy, Purification, Clinical Proteomics, Control