Targeting TGF-β as a therapy for Alzheimer's disease
Described herein are compositions and methods for enhancing peripheral macrophage Aβ phagocytosis activity. The methods include inhibiting the TGF-β signaling pathway and activating the BMP signaling pathway in peripheral macrophages to promote central nervous system infiltration and enhance macrophage Aβ phagocytosis activity. Inhibition of TGF-β signaling and activation of BMP signaling in peripheral macrophages represents an advantageous anti-amyloid therapeutic approach for Alzheimer's disease.
1. A method of enhancing macrophage Aβ phagocytosis activity of a peripheral macrophage of a mammal with Alzheimer's disease, the method comprising contacting the peripheral macrophage of the mammal with Alzheimer's disease with an inhibitor of a component of TGF-β signaling pathway and with an activator of a component of bone morphogenic protein-Smad1/5/8-PAK2 signaling pathway,
wherein the inhibitor of a component of TGF-β signaling pathway is at least one selected from the group consisting of dominant negative TGF-β receptor, a nucleic acid encoding a dominant negative TGF-β receptor, SB-505124 and SB-431542, and
wherein the activator of a component of bone morphogenic protein-Smad1/5/8-PAK2 signaling pathway is at least one selected from the group consisting of BMP-2, BMP-4, a nucleic acid encoding BMP-2, and a nucleic acid encoding BMP-4,
thereby inducing the peripheral macrophage to infiltrate the central nervous system (CNS) of the mammal.
2. The method of claim 1 , wherein said TGF-β signaling pathway is TGF-β-Smad2/3 signaling pathway.
3. The method of claim 1 , wherein said inhibitor of a component of TGF-β signaling pathway inhibits activin-like kinase 5 (ALK5).