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. 2017 Sep 19;75(3):547–561. doi: 10.1007/s00018-017-2641-7

Fig. 7.

Fig. 7

Chemotactic migration of PDGFR-β+ MSCs. a, b Transwell migration assay showed that the migration of unsorted MSCs, PDGFR-β+ MSCs and PDGFR-β MSCs in response to PDGF-BB or fresh wound tissue extracts. Nuclei were stained with DAPI (a). The average number of cells migrated across the pores per microscopic field was quantified by Image J (b). Pre-treatment of PDGFR-β+ MSCs with a functional blocking antibody against PDGFR-β significantly reduced their migration toward PDGF-BB or the fresh wound tissue extracts (a, b). Experiments were performed in triplicate wells. c, d Real-time PCR analysis of the expression of PDGFB after wounding in mice (c). d Immunofluorescence analysis of a day-3 wound showed the expression of PDGF-B (red), which showed higher levels in the wound bed tissue and the tissue adjacent to the wound. Nuclei were stained with DAPI. Scale bars 50 µm. ***P < 0.001, **P < 0.01, *P < 0.05