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

被引:211
作者
Ma, Yinghua
Li, Jianxue
Chiu, Isaac
Wang, Yawen
Sloane, Jacob A.
Lu, Jining
Kosaras, Bela
Sidman, Richard L.
Volpe, Joseph J.
Vartanian, Timothy [1 ]
机构
[1] Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Ctr Neurodegenerat & Repair, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Grad Program Immunol, Ctr Blood Res, Boston, MA 02115 USA
[5] Boston Univ, Sch Med, Ctr Pulm, Boston, MA 02118 USA
[6] Childrens Hosp, Dept Neurol, Boston, MA 02115 USA
关键词
D O I
10.1083/jcb.200606016
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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-kappa B 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.
引用
收藏
页码:209 / 215
页数:7
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