Runx3 controls the axonal projection of proprioceptive dorsal root ganglion neurons

被引:257
作者
Inoue, K
Ozaki, S
Shiga, T
Ito, K
Masuda, T
Okado, N
Iseda, T
Kawaguchi, S
Ogawa, M
Bae, SC
Yamashita, N
Itohara, S
Kudo, N
Ito, Y [1 ]
机构
[1] Kyoto Univ, Inst Virus Res, Dept Viral Oncol, Lab Cell Regulat,Sakyo Ku, Kyoto 6068507, Japan
[2] Univ Tsukuba, Inst Basic Med Sci, Dept Physiol, Tsukuba, Ibaraki 3058575, Japan
[3] Univ Tsukuba, Inst Basic Med Sci, Dept Anat, Tsukuba, Ibaraki 3058575, Japan
[4] Kyoto Univ, Grad Sch Med, Dept Integrat Brain Sci, Kyoto 6068501, Japan
[5] RIKEN, Brain Sci Inst, Lab Cell Culture Dev, Wako, Saitama 3510198, Japan
[6] Chungbuk Natl Univ, Inst Med Res, Coll Med, Dept Biochem, Cheongju 361763, South Korea
[7] RIKEN, Brain Sci Inst, Lab Behav Genet, Wako, Saitama 3510198, Japan
[8] Inst Mol & Cell Biol, Singapore 117609, Singapore
关键词
D O I
10.1038/nn925
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dorsal root ganglion (DRG) neurons specifically project axons to central and peripheral targets according to their sensory modality. The Runt-related genes Runx1 and Runx3 are expressed in DRG neuronal subpopulations, suggesting that they may regulate the trajectories of specific axons. Here we report that Runx3-deficient (Runx3(-/-)) mice displayed severe motor discoordination and that few DRG neurons synthesized the proprioceptive neuronal marker parvalbumin. Proprioceptive afferent axons failed to project to their targets in the spinal cord as well as those in the muscle. NT-3-responsive Runx3(-/-) DRG neurons showed less neurite outgrowth in vitro. However, we found no changes in the fate specification of Runx3(-/-) DRG neurons or in the number of DRG neurons that expressed trkC. Our data demonstrate that Runx3 is critical in regulating the axonal projections of a specific subpopulation of DRG neurons.
引用
收藏
页码:946 / 954
页数:9
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