Figure 3.
Figure 3. Lactadherin reduced MPs and its deficiency increased TBI-induced BDMV release and coagulopathy. (A) A schematic illustration of lactadherin-mediated MV clearance. (B) Levels of circulating NSE+ (scale on the left) and mtMVs (MitoTracker Green+, scale on the right) measured 3 hours after injury of sham mice and FPI mice preconditioned with PBS or lactadherin (n = 15, 1-way ANOVA). (C) Levels of circulating NSE+ MVs (scale on the left) and mtMVs (scale on the right) in noninjured mice infused with 1.5 × 107/mouse of BDMVs followed by lactadherin or PBS (n = 12, 1-way ANOVA). Plasma samples from lactadherin−/− mice and their wild-type littermates were examined for dynamic changes in plasma levels of (D) NSE+ MVs, (E) annexin V-binding MVs, (F) clotting time, and (G) plasma levels of d-dimer (n = 24, repeated-measures ANOVA; *P < .001).

Lactadherin reduced MPs and its deficiency increased TBI-induced BDMV release and coagulopathy. (A) A schematic illustration of lactadherin-mediated MV clearance. (B) Levels of circulating NSE+ (scale on the left) and mtMVs (MitoTracker Green+, scale on the right) measured 3 hours after injury of sham mice and FPI mice preconditioned with PBS or lactadherin (n = 15, 1-way ANOVA). (C) Levels of circulating NSE+ MVs (scale on the left) and mtMVs (scale on the right) in noninjured mice infused with 1.5 × 107/mouse of BDMVs followed by lactadherin or PBS (n = 12, 1-way ANOVA). Plasma samples from lactadherin−/− mice and their wild-type littermates were examined for dynamic changes in plasma levels of (D) NSE+ MVs, (E) annexin V-binding MVs, (F) clotting time, and (G) plasma levels of d-dimer (n = 24, repeated-measures ANOVA; *P < .001).

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