UNC5C is required for spinal accessory motor neuron development

被引:37
作者
Dillon, A. K.
Jevince, A. R.
Hinck, L.
Ackerman, S. L.
Lu, X.
Tessier-Lavigne, M.
Kaprielian, Z.
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 10461 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
[3] Univ Calif Santa Cruz, Dept Mol Cell & Dev Biol, Santa Cruz, CA 95064 USA
[4] Jackson Lab, Bar Harbor, ME 04609 USA
[5] Howard Hughes Med Inst, Bar Harbor, ME 04609 USA
[6] Univ Virginia, Dept Cell Biol, Charlottesville, VA 22908 USA
[7] Genentech Inc, San Francisco, CA 94080 USA
关键词
D O I
10.1016/j.mcn.2007.04.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In both invertebrates and vertebrates, UNC5 receptors facilitate chemorepulsion away from a Netrin source. Unlike most motor neurons in the embryonic vertebrate spinal cord, spinal accessory motor neuron (SACMN) cell bodies and their axons translocate along a dorsally directed trajectory away from the floor plate/ventral midline and toward the lateral exit point (LEP). We have recently shown that Netrin-1 and DCC are required for the migration of SACMN cell bodies, in vivo. These observations raised the possibility that vertebrate UNC5 proteins mediate the presumed repulsion of SACMN away from the Netrin-rich ventral midline. Here, we show that SACMN are likely to express UNC5A and UNC5C. Whereas SACMN development proceeds normally in UNC5A null mice, many SACMN cell bodies fail to migrate away from the ventral midline and inappropriately cluster in the ventrolateral spinal cord of mouse embryos lacking UNC5C. These results support an important role for UNC5C in SACMN development. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:482 / 489
页数:8
相关论文
共 33 条
  • [21] A Cxcl12-Cxcr4 chemokine signaling pathway defines the initial trajectory of mammalian motor axons
    Lieberam, I
    Agalliu, D
    Nagasawa, T
    Ericson, J
    Jessell, TM
    [J]. NEURON, 2005, 47 (05) : 667 - 679
  • [22] Przyborski SA, 1998, DEVELOPMENT, V125, P41
  • [23] Motor axon migration: a long way to go
    Schneider, VA
    Granato, M
    [J]. DEVELOPMENTAL BIOLOGY, 2003, 263 (01) : 1 - 11
  • [24] Identification and characterization of a cell surface marker for embryonic rat spinal accessory motor neurons
    Schubert, W
    Kaprielian, Z
    [J]. JOURNAL OF COMPARATIVE NEUROLOGY, 2001, 439 (03) : 368 - 383
  • [25] MuSC, a novel member of the immunoglobulin superfamily, is expressed in neurons of a subset of cranial sensory ganglia in the mouse embryo
    Sekine-Aizawa, Y
    Omori, A
    Fujita, SC
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 1998, 10 (09) : 2810 - 2824
  • [26] Netrin-1 is required for commissural axon guidance in the developing vertebrate nervous system
    Serafini, T
    Colamarino, SA
    Leonardo, ED
    Wang, H
    Beddington, R
    Skarnes, WC
    TessierLavigne, M
    [J]. CELL, 1996, 87 (06) : 1001 - 1014
  • [27] EARLY AXON AND DENDRITIC OUTGROWTH OF SPINAL ACCESSORY MOTOR NEURONS STUDIED WITH DII IN FIXED TISSUES
    SNIDER, WD
    PALAVALI, V
    [J]. JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 297 (02) : 227 - 238
  • [28] Hierarchical guidance cues in the developing nervous system of C-elegans
    Wadsworth, WG
    Hedgecock, EM
    [J]. BIOESSAYS, 1996, 18 (05) : 355 - 362
  • [29] Dorsally derived netrin 1 provides an inhibitory cue and elaborates the 'waiting period' for primary sensory axons in the developing spinal cord
    Watanabe, K
    Tamamaki, N
    Furuta, T
    Ackerman, SL
    Ikenaka, K
    Ono, K
    [J]. DEVELOPMENT, 2006, 133 (07): : 1379 - 1387
  • [30] Axon fasciculation defects and retinal dysplasias in mice lacking the immunoglobulin superfamily adhesion molecule BEN/ALCAM/SC1
    Weiner, JA
    Koo, SJ
    Nicolas, S
    Fraboulet, S
    Pfaff, SL
    Pourquié, O
    Sanes, JR
    [J]. MOLECULAR AND CELLULAR NEUROSCIENCE, 2004, 27 (01) : 59 - 69