A Cxcl12-Cxcr4 chemokine signaling pathway defines the initial trajectory of mammalian motor axons

被引:141
作者
Lieberam, I
Agalliu, D
Nagasawa, T
Ericson, J
Jessell, TM [1 ]
机构
[1] Columbia Univ, Howard Hughes Med Inst, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[2] Columbia Univ, Dept Genet & Dev, New York, NY 10032 USA
[3] Kyoto Univ, Dept Med Syst Control, Inst Frontier Med Sci, Kyoto 6068507, Japan
[4] Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden
关键词
D O I
10.1016/j.neuron.2005.08.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Motor neurons, alone among neurons in the vertebrate CNS, extend axons out of the neural tube to innervate peripheral targets. Two classes of motor neurons, termed vMNs and dMNs, extend axons out of the neural tube via ventral and dorsal exit points, respectively, in accord with their homeodomain transcription factor repertoire. Downstream of these transcriptional codes, the cell surface receptors that shape initial motor axon trajectories have not been identified. We show here that the chemokine receptor Cxcr4 is expressed on the axons of vMNs as they follow their ventral trajectory, whereas its ligand, Cxcl12, is expressed by mesenchymal cells surrounding the ventral neural tube. Genetic studies reveal that Cxcl12-Cxcr4 signaling directs the ventral trajectory of spinal vMNs. In its absence, these neurons adopt a dMN-like trajectory, despite preservation of their vMN transcriptional identity. Thus, the status of Cxcr4 signaling helps to determine the initial axonal trajectory of mammalian motor neurons.
引用
收藏
页码:667 / 679
页数:13
相关论文
共 56 条
  • [1] T134, a small-molecule CXCR4 inhibitor, has no cross-drug resistance with AMD3100, a CXCR4 antagonist with a different structure
    Arakaki, R
    Tamamura, H
    Premanathan, M
    Kanbara, K
    Ramanan, S
    Mochizuki, K
    Baba, M
    Fujii, N
    Nakashima, H
    [J]. JOURNAL OF VIROLOGY, 1999, 73 (02) : 1719 - 1723
  • [2] Control of axon elongation via an SDF-1α/Rho/mDia pathway in cultured cerebellar granule neurons
    Arakawa, Y
    Bito, H
    Furuyashiki, T
    Tsuji, T
    Takemoto-Kimura, S
    Kimura, K
    Nozaki, K
    Hashimoto, N
    Narumiya, S
    [J]. JOURNAL OF CELL BIOLOGY, 2003, 161 (02) : 381 - 391
  • [3] Requirement for the homeobox gene Hb9 in the consolidation of motor neuron identity
    Arber, S
    Han, B
    Mendelsohn, M
    Smith, M
    Jessell, TM
    Sockanathan, S
    [J]. NEURON, 1999, 23 (04) : 659 - 674
  • [4] Slit proteins bind robe receptors and have an evolutionarily conserved role in repulsive axon guidance
    Brose, K
    Bland, KS
    Wang, KH
    Arnott, D
    Henzel, W
    Goodman, CS
    Tessier-Lavigne, M
    Kidd, T
    [J]. CELL, 1999, 96 (06) : 795 - 806
  • [5] The development of vestibulocochlear efferents and cochlear afferents in mice
    Bruce, LL
    Kingsley, J
    Nichols, DH
    Fritzsch, B
    [J]. INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 1997, 15 (4-5) : 671 - 692
  • [6] Caton A, 2000, DEVELOPMENT, V127, P1751
  • [7] A chemokine, SDF-1, reduces the effectiveness of multiple axonal repellents and is required for normal axon pathfinding
    Chalasani, SH
    Sabelko, KA
    Sunshine, MJ
    Littman, DR
    Raper, JA
    [J]. JOURNAL OF NEUROSCIENCE, 2003, 23 (04) : 1360 - 1371
  • [8] THE AXONAL CHEMOATTRACTANT NETRIN-1 IS ALSO A CHEMOREPELLENT FOR TROCHLEAR MOTOR AXONS
    COLAMARINO, SA
    TESSIERLAVIGNE, M
    [J]. CELL, 1995, 81 (04) : 621 - 629
  • [9] EphB2 guides axons at the midline and is necessary for normal vestibular function
    Cowan, CA
    Yokoyama, N
    Bianchi, LM
    Henkemeyer, M
    Fritzsch, B
    [J]. NEURON, 2000, 26 (02) : 417 - 430
  • [10] Hepatocyte growth factor scatter factor is an axonal chemoattractant and a neurotrophic factor for spinal motor neurons
    Ebens, A
    Brose, K
    Leonardo, ED
    Hanson, MG
    Bladt, F
    Birchmeier, C
    Barres, BA
    TessierLavigne, M
    [J]. NEURON, 1996, 17 (06) : 1157 - 1172