Figure 1From: Administered circulating microparticles derived from lung cancer patients markedly improved angiogenesis, blood flow and ischemic recovery in rat critical limb ischemia Upper Panel) Matrigel Assay for angiogenesis with and without Patient’s Lung cancer- derived microparticles (Lc- MPs) treatment (n =  6). A to C) After 5-hour cell culture [1.0 × 104 human umbilical vein endothelial cells (HUVECs)], Matrigel-assay angiogenesis was observed by microscopic findings (100×) in without (A) and with Lc-MPs treatment [3.0 × 105 (B) and 6.0 × 105 (C) MPs, respectively]. D) Analytical results of number of tubules (white arrows), * vs. other groups with different symbols (*, †, ‡), p < 0.001. E) Analytical results of total tubular length, * vs. other groups with different symbols (*, †, ‡), p < 0.001. F) Analytical results of cluster formation (black arrows), * vs. other groups with different symbols (*, †, ‡), p < 0.001. G) Analytical results of network formation (blue dot line), * vs. other groups with different symbols (*, †, ‡), p < 0.001. All statistical analyses were performed by one-way ANOVA, followed by Bonferroni multiple comparison post hoc test. Lower Panel) Aortic-ring (AR) angiogenesis and nitric oxide (NO) production after lung-cancer microparticles (Lc-MPs) treatment (n = 6). H & I) By day-5 cell culturing, the angiogenesis did not differ between with and without Lc-MPs treatment. J & K) By day-12 cell culturing, the AR angiogenesis was significantly enhanced in with (K) than in without (J) Lc-MP treatment. N) Mean sprouting length, p < 0.0001, * vs. control group; O) Number of sprouts around aortic ring, p < 0.0001, * vs. control group. L & M) Immunofluorescent microscopic finding of NO production by 6-hour after cell culture; P) The statistically analytic results of fluorescent intensity of NO expression, p < 0.0001, * vs. control group.Back to article page