Figure 5From: Mesenchymal stem cells promote alveolar epithelial cell wound repair in vitro through distinct migratory and paracrine mechanismsAEC and SAEC wound repair stimulation by individual hMSC paracrine factors. (A) Recombinant human plasma Fibronectin did not enhance AEC wound in serum-free condition (open bars) but required 0.2% FBS supplementation (black bars) (n = 6; **p < 0.01, ***p < 0.001) (B) Recombinant human plasma Fibronectin significantly increased SAEC wound repair at 100 ng/ml concentration in SF-SABM (grey bar) vs. negative control (NC) (black bar) (n = 6; *p < 0.05). (C) Recombinant human Lumican did not enhance AEC wound in serum-free condition (open bars) but required 0.2% FBS supplementation (black bars) (n = 9; **p < 0.01, ***p < 0.001). (D) Recombinant human Lumican significantly increased SAEC wound repair (n = 6; **p < 0.01, ***p < 0.001). (E) Recombinant human Periostin enhanced AEC wound repair (n = 10, **p < 0.01, ***p < 0.001; $p < 0.001 vs corresponding serum-free NC). (F) Periostin increased SAEC wound repair at 1 μg/ml in SF-SABM (n = 6; *p < 0.05). (G) Human recombinant IGFBP-7 did not stimulate AEC wound repair in serum-free (open bars) or 0.2% FBS supplemented conditions (black bars) (n = 9; *p < 0.001 vs 0.2% FBS supplemented NC, $p < 0.001 vs serum-free NC). (H) Recombinant human IGFBP-7 significantly stimulated SAEC wound repair (n = 6; **p < 0.01, ***p < 0.001). NC (negative control) represents wound repair with DMEM for AEC and serum-free SABM for SAEC. PC (positive control) represents wound repair with 10% FBS supplemented DMEM for AEC and complete SAGM for SAEC. Data presented as mean ± SD. ns = not significant. Scale bar, 200 μm.Back to article page