CD11c+ Cells Partially Mediate the Renoprotective Effect Induced by Bone Marrow-Derived Mesenchymal Stem Cells
Figure 4
In vitro co-culture with MSCs induced a phenotypic change in the CD11c+ cells.
The spleen-derived CD11c+ cells were isolated by magnetic sorting and co-cultured with the vehicle (media) or MSCs either in direct contact or separated by trans-well insets for 72 h. Subsequently, their phenotypes were assessed by flow cytometry. (A) Left, expression of CD11c; right, expression of CD11b. CD11c-MSC, same chamber; CD11c//MSC, lower/upper separation. The isolated CD11c+ cells can be divided into CD11chigh or CD11clow and CD11bhigh CD11blow populations. The phenotypic changes were semi-quantitatively assessed by calculating and comparing the ratios of cell types (CD11chigh/CD11clow or CD11bhigh/CD11blow). * p < 0.05 compared to CD11c+//media. (B) Expression of the maturation marker CD80 in the CD11c+ cells. (C) Intracellular IL-10 in the CD11c+ cells. (D) Intracellular TNF-α in the CD11c+ cells. * p < 0.05 compared to the PBS-treated CD11c+ cells. All in vitro experiments were performed in triplicate and repeated 3 times.