fig7

Impact of exosomes derived from adipose stem cells on lymphocyte proliferation and phenotype in mouse skin grafts

Figure 7. Flow cytometry of CD3+T cells, B cells, NK cells, DC cells, and macrophages. (A) Flow cytometry gating strategy for cutaneous lymphoid subsets; (B) Changes in the proportions of T cells, B cells, NK cells, DC cells, and macrophages in the spleen in models treated with PBS, 0.5 × 108 Exosomes, 1 × 108 Exosomes, 1.5 × 108 Exosomes, and ASCs; (C) Changes in the proportions of T cells, B cells, NK cells, DC cells, and macrophages in the blood in models treated with PBS, 0.5 × 108 Exosomes, 1 × 108 Exosomes, 1.5 × 108 Exosomes, and ASCs; (D) Changes in the proportions of T cells, B cells, NK cells, DC cells, and macrophages in the dLN in models treated with PBS, 0.5 × 108 Exosomes, 1 × 108 Exosomes, 1.5 × 108 Exosomes, and ASCs. DCs: Dendritic cells; NK cells: natural killer cell; ASCs: adipose-derived stem cells. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001.

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

Portico

All published articles are preserved here permanently:

https://www.portico.org/publishers/oae/

Portico

All published articles are preserved here permanently:

https://www.portico.org/publishers/oae/