Toll-like receptor 3 is a potent negative regulator of axonal growth in mammals

被引:176
作者
Cameron, Jill S.
Alexopoulou, Lena
Sloane, Jacob A.
DiBernardo, Allitia B.
Ma, Yinghua
Kosaras, Bela
Flavell, Richard
Strittmatter, Stephen M.
Volpe, Joseph
Sidman, Richard
Vartanian, Timothy
机构
[1] Beth Israel Deaconess Med Ctr, Program Neurosci & Ctr Neurodegenerat & Repair, Dept Neurol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Childrens Hosp, Dept Neurol, Boston, MA 02115 USA
[3] Yale Univ, Sch Med, Immunobiol Sect, New Haven, CT 06520 USA
[4] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
[5] Yale Univ, Sch Med, Dept Neurol & Sect Neurobiol, New Haven, CT 06510 USA
关键词
toll-like receptor-3; axon; polyinosine : polycytidylic acid; poly I : C; RNA; CNS; danger theory;
D O I
10.1523/JNEUROSCI.4290-06.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Toll is a cell surface receptor with well described roles in the developmental patterning of invertebrates and innate immunity in adult Drosophila. Mammalian toll-like receptors represent a family of Toll orthologs that function in innate immunity by recognizing molecular motifs unique to pathogens or injured tissue. One member in this family of pattern recognition receptors, toll-like receptor 3 (TLR3), recognizes viral double-stranded RNA and host mRNA. We examined the expression and function of TLRs in the nervous system and found that TLR3 is expressed in the mouse central and peripheral nervous systems and is concentrated in the growth cones of neurons. Activation of TLR3 by the synthetic ligand polyinosine: polycytidylic acid (poly I:C) or by mRNA rapidly causes growth cone collapse and irreversibly inhibits neurite extension independent of nuclear factor kappa B. Mice lacking functional TLR3 were resistant to the neurodegenerative effects of poly I:C. Neonatal mice injected with poly I:C were found to have fewer axons exiting dorsal root ganglia and displayed related sensorimotor deficits. No effect of poly I:C was observed in mice lacking functional TLR3. Together, these findings provide evidence that an innate immune pattern recognition receptor functions autonomously in neurons to regulate axonal growth and advances a novel hypothesis that this class of receptors may contribute to injury and limited CNS regeneration.
引用
收藏
页码:13033 / 13041
页数:9
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