Toll-like receptor 8 functions as a negative regulator of neurite outgrowth and inducer of neuronal apoptosis

Author:

Ma Yinghua123,Li Jianxue1,Chiu Isaac4,Wang Yawen123,Sloane Jacob A.123,Lü Jining5,Kosaras Bela1,Sidman Richard L.12,Volpe Joseph J.26,Vartanian Timothy123

Affiliation:

1. Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA 02115

2. Program in Neuroscience

3. Center for Neurodegeneration and Repair,

4. Center for Blood Research, Graduate Program in Immunology, Harvard Medical School, Boston, MA 02115

5. Pulmonary Center, Boston University School of Medicine, Boston, MA 02118

6. Department of Neurology, Children's Hospital, Boston, MA 02115

Abstract

Toll receptors in Drosophila melanogaster function in morphogenesis and host defense. Mammalian orthologues of Toll, the Toll-like receptors (TLRs), have been studied extensively for their essential functions in controlling innate and adaptive immune responses. We report that TLR8 is dynamically expressed during mouse brain development and localizes to neurons and axons. Agonist stimulation of TLR8 in cultured cortical neurons causes inhibition of neurite outgrowth and induces apoptosis in a dissociable manner. Our evidence indicates that such TLR8-mediated neuronal responses do not involve the canonical TLR–NF-κB signaling pathway. These findings reveal novel functions for TLR8 in the mammalian nervous system that are distinct from the classical role of TLRs in immunity.

Publisher

Rockefeller University Press

Subject

Cell Biology

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