Research Article

hUC-MSCs Attenuate Acute Graft-Versus-Host Disease through Chi3l1 Repression of Th17 Differentiation

Figure 6

Chi3l1 deletion compromises hUC-MSCs and inhibits T cell proliferation. (a–c) CD3+ T cells obtained from the spleens of healthy C57BL/6J mice were stained with CFSE (5 μM) and then incubated in 24-well plates with hUC-MSCs, sh-Chi3l1-MSCs, and sh-NC-MSCs at a CD3+ T/hUC-MSC ratio of 20 : 1 for 72 hours. (a) Proliferation of CD3+ T cells analyzed by flow cytometry. (b) CD3+ T cell proliferation was measured after treatment with different hUC-MSCs. (c) mRNA expression levels of IFN-γ, IL-17A, and FOXP3 analyzed by qPCR (three independent experiments, one-way ANOVA, and Tukey’s multiple comparison test, ; ns: not significant).
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