“…Surface markers were used to determine the ratio of MSCs and hematopoietic stem cells in the culture after three passages, and the cells were analyzed by flow cytometry (FACSCalibur; BD Pharmingen, San Diego, CA, USA). Positive and negative markers (monoclonal antibodies) for 2 × 10 5 MSCs included the following: CD73 (purified mouse anti-rat CD73; clone 5 F/B9, BD Pharmingen, San Diego, CA, USA); CD90 (anti-CD90/Thy1-FITC, clone FITC.MRC OX-7; Abcam, Cambridge, MA, USA); CD44 (anti-CD44-PE, clone OX-50; Abcam, Cambridge, MA, USA); ICAM-I (anti-ICAM-I-FITC, clone 1A29; Abcam, Cambridge, MA, USA); RT1 (anti-RT1-Aw2-FITC, clone MRC OX-18; Abcam, Cambridge, MA, USA); CD34 (anti-CD34-PE, clone ICO-115; Abcam, Cambridge, MA,USA); CD11b (anti-CD11b-PE, clone ED8; Abcam, Cambridge, MA, USA); CD45 (anti-CD45-FITC, clone MRC OX-1; Abcam, Cambridge, MA, USA); and MHCII (anti-rat MHC CLASS II RT1D-PE, clone MRC OX-17; Abcam, Cambridge, MA, USA) [ 38 – 41 ]. The isotype controls were secondary antibody anti-mouse IgG, isotype control IgG1-FITC, isotype control IgG1-PE, and MSCs.…”