Figure 7
Figure 7. Increased canonical Wnt signaling in osteogenic cells in myelomatous bones treated with Wnt3a. Myelomatous human bone sections were immunohistochemically stained with 8E7 antibody that reacts with the active form of β-catenin. (A,B) Bones were engrafted with H929/EV (A) and H929/W3A (B) MM cells. Note expression of active form of β-catenin in certain vascular endothelial cells (VECs) and in cellular components along the bone surface. Bones engrafted with H929/W3A had increased numbers of cells expressing the active form of β-catenin along the bone surface. (C,D) Primary myelomatous bones treated with Wnt3a had an increased number of osteoblastic (OB) cells expressing the active form of β-catenin. Osteoclasts (OCs) as well as MM cells expressed very low levels of β-catenin.

Increased canonical Wnt signaling in osteogenic cells in myelomatous bones treated with Wnt3a. Myelomatous human bone sections were immunohistochemically stained with 8E7 antibody that reacts with the active form of β-catenin. (A,B) Bones were engrafted with H929/EV (A) and H929/W3A (B) MM cells. Note expression of active form of β-catenin in certain vascular endothelial cells (VECs) and in cellular components along the bone surface. Bones engrafted with H929/W3A had increased numbers of cells expressing the active form of β-catenin along the bone surface. (C,D) Primary myelomatous bones treated with Wnt3a had an increased number of osteoblastic (OB) cells expressing the active form of β-catenin. Osteoclasts (OCs) as well as MM cells expressed very low levels of β-catenin.

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