Differential requirement for Plexin-A3 and -A4 in mediating responses of sensory and sympathetic neurons to distinct class 3 Semaphorins

被引:183
作者
Yaron, A
Huang, PH
Cheng, HJ [1 ]
Tessier-Lavigne, M
机构
[1] Stanford Univ, Dept Biol Sci, Howard Hughes Med Inst, Stanford, CA 94305 USA
[2] Genentech Inc, San Francisco, CA USA
[3] Univ Calif Davis, Ctr Neurosci, Sect Neurobiol Physiol & Behav, Div Biol Sci, Davis, CA 95616 USA
[4] Univ Calif Davis, Dept Pathol & Lab Med, Sch Med, Davis, CA 95616 USA
关键词
D O I
10.1016/j.neuron.2005.01.013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The class 3 Semaphorins Sema3A and Sema3F are potent axonal repellents that cause repulsion by binding Neuropilin-1 and Neuropilin-2, respectively. Plexins are implicated as signaling coreceptors for the Neuropilins, but the identity of the Plexins that transduce Sema3A and Sema3F responses in vivo is uncertain. Here, we show that Plexin-A3 and -A4 are key determinants of these responses, through analysis of a Plexin-A3/Plexin-A4 double mutant mouse. Sensory and sympathetic neurons from the double mutant are insensitive to Sema3A and Sema3F in vitro, and defects in axonal projections in vivo correspond to those seen in Neuropilin-1 and -2 mutants. Interestingly, we found a differential requirement for these two Plexins: signaling via Neuropilin-1 is mediated principally by Plexin-A4, whereas signaling via Neuropilin-2 is mediated principally by Plexin-A3. Thus, Plexin-A3 and -A4 contribute to the specificity of axonal responses to class 3 Semaphorins.
引用
收藏
页码:513 / 523
页数:11
相关论文
共 50 条
[1]   Stereotyped pruning of long hippocampal axon branches triggered by retraction inducers of the semaphorin family [J].
Bagri, A ;
Cheng, HJ ;
Yaron, A ;
Pleasure, SJ ;
Tessier-Lavigne, M .
CELL, 2003, 113 (03) :285-299
[2]  
Bagri A, 2002, ADV EXP MED BIOL, V515, P13
[3]   Semaphorin III Is needed for normal patterning and growth of nerves, bones and heart [J].
Behar, O ;
Golden, JA ;
Mashimo, H ;
Schoen, FJ ;
Fishman, MC .
NATURE, 1996, 383 (6600) :525-528
[4]  
Brown CB, 2001, DEVELOPMENT, V128, P3071
[5]   Semaphorin 3A elicits stage-dependent collapse, turning, and branching in Xenopus retinal growth cones [J].
Campbell, DS ;
Regan, AG ;
Lopez, JS ;
Tannahill, D ;
Harris, WA ;
Holt, CE .
JOURNAL OF NEUROSCIENCE, 2001, 21 (21) :8538-8547
[6]   Analysis of the L1-deficient mouse phenotype reveals cross-talk between Sema3A and L1 signaling pathways in axonal guidance [J].
Castellani, V ;
Chédotal, A ;
Schachner, M ;
Faivre-Sarrailh, C ;
Rougon, G .
NEURON, 2000, 27 (02) :237-249
[7]   Semaphorin-neuropilin interactions underlying sympathetic axon responses to class III semaphorins [J].
Chen, H ;
He, ZG ;
Bagri, A ;
Tessier-Lavigne, M .
NEURON, 1998, 21 (06) :1283-1290
[8]   Neuropilin-2, a novel member of the neuropilin family, is a high affinity receptor for the semaphorins Sema E and Sema IV but not Sema III [J].
Chen, H ;
Chedotal, A ;
He, ZG ;
Goodman, CS ;
TessierLavigne, M .
NEURON, 1997, 19 (03) :547-559
[9]   Neuropilin-2 regulates the development of select cranial and sensory nerves and hippocampal mossy fiber projections [J].
Chen, H ;
Bagri, A ;
Zupicich, JA ;
Zou, YM ;
Stoeckli, E ;
Pleasure, SJ ;
Lowenstein, DH ;
Skarnes, WC ;
Chédotal, A ;
Tessier-Lavigne, M .
NEURON, 2000, 25 (01) :43-56
[10]   Plexin-A3 mediates semaphorin signaling and regulates the development of hippocampal axonal projections [J].
Cheng, HJ ;
Bagri, A ;
Yaron, A ;
Stein, E ;
Pleasure, SJ ;
Tessier-Lavigne, M .
NEURON, 2001, 32 (02) :249-263