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. Author manuscript; available in PMC: 2018 Aug 1.
Published in final edited form as: Transplantation. 2017 Aug;101(8):1793–1800. doi: 10.1097/TP.0000000000001529

Figure 3. Migration pattern of the systemically administered MDSC.

Figure 3

(A) MDSC preferably migrate to islet allografts. 2 × 106 MDSC generated from normal B6 mice (CD45.2) mice were i.v. injected into the congenic mice (CD45.1) immediately after transplantation of BALB/c islets. Leukocytes were isolated on POD 1, 2, 4 and 7 from islet allografts, draining lymph node (dLN) and spleen, and stained for CD11b and CD45.2 for flow analysis gated on CD11b+ population. The data show mean percentage of CD45.2+ cells ± SD (n=3) (p<0.05, graft vs. spleen or dLN at all time points). (B) Migration of MDSC to islet allografts requires CCR2. In a separate study, MDSC were generated from CCR2−/− mice, instead of WT mice, and i.v. injected into the congenic mice (CD45.1) immediately after transplantation of BALB/c islets. Leukocytes were isolated on POD 1, 2, 4 and 7 from islet allografts, and stained with anti-CD11b, CD45.1 and CD45.2 mAbs for low analysis. The number is percentage of CD45.1+ or CD45.2+ cells gated on CD11b+ cell population. The data are representative of three separate experiments.