The Recombinant Protein EphB4-Fc Changes the Ti Particle-Mediated Imbalance of OPG/RANKL via EphrinB2/EphB4 Signaling Pathway and Inhibits the Release of Proinflammatory Factors In Vivo

<div>Histological staining of calvaria sections and immunohistochemistry of ephrinB2. (a–p) Show that hematoxylin and eosin (H&amp;E) and tartrate-resistant acid phosphatase- (TRAP-) stained with low and high ephB4-Fc. (q–t) Show that the expression of ephrinB2 protein with low and high ephB4-Fc. (u) Quantitative analysis of the number of TRAP-positive multinuclear macrophages on the surface of the sections. (v) Quantification of positive staining and mean density of positive staining. 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Oxidative Medicine and Cellular Longevity

fig7

Figure 7

Figure 7: The Recombinant Protein EphB4-Fc Changes the Ti Particle-Mediated Imbalance of OPG/RANKL via EphrinB2/EphB4 Signaling Pathway and Inhibits the Release of Proinflammatory Factors In Vivo 

Figure 7 | The Recombinant Protein EphB4-Fc Changes the Ti Particle-Mediated Imbalance of OPG/RANKL via EphrinB2/EphB4 Signaling Pathway and Inhibits the Release of Proinflammatory Factors In Vivo 