Robo2 determines subtype-specific axonal projections of trigeminal sensory neurons
Abstract
How neurons connect to form functional circuits is central to the understanding of the development and function of the nervous system. In the somatosensory system, perception of sensory stimuli to the head requires specific connections between trigeminal sensory neurons and their many target areas in the central nervous system. Different trigeminal subtypes have specialized functions and downstream circuits, but it has remained unclear how subtype-specific axonal projection patterns are formed. Using zebrafish as a model system, we followed the development of two trigeminal sensory neuron subtypes: one that expresses trpa1b, a nociceptive channel important for sensing environmental chemicals; and a distinct subtype labeled by an islet1 reporter (Isl1SS). We found that Trpa1b and Isl1SS neurons have overall similar axon trajectories but different branching morphologies and distributions of presynaptic sites. Compared with Trpa1b neurons, Isl1SS neurons display reduced branch growth and synaptogenesis at the hindbrain-spinal cord junction. The subtype-specific morphogenesis of Isl1SS neurons depends on the guidance receptor Robo2. robo2 is preferentially expressed in the Isl1SS subset and inhibits branch growth and synaptogenesis. In the absence of Robo2, Isl1SS afferents acquire many of the characteristics of Trpa1b afferents. These results reveal that subtype-specific activity of Robo2 regulates subcircuit morphogenesis in the trigeminal sensory system.
Additional Information
© 2012 Company of Biologists. Accepted December 1, 2011. We dedicate this study to C. B. Chien and thank him for the robo2 and Slit gene probes, robo2 (astray) mutant fish and for many thoughtful suggestions. We thank D. Yelon for the CHORI211-236I20 BAC clone; M. Meyer for the Syp:GFP-DSR plasmid; S. Zimmerman, J. Miller and K. Hurley for fish care; P. Huang, F. Imam, J. Kay, F. Merkle and X. Wang for critical comments on the manuscript; and members of the Schier laboratory for discussion. This work was supported by a National Research Service Award (NRSA) postdoctoral fellowship from the National Institutes of Health [F32 NS057870 to Y.A.P.]; and research grants from the National Institutes of Health [R01 HD067140 and R01 NS049319 to A.F.S.]. Deposited in PMC for release after 12 months. The authors declare no competing financial interests.Attached Files
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Supplemental Material - DEV076588FigS1.jpg
Supplemental Material - DEV076588FigS2.jpg
Supplemental Material - DEV076588FigS3.jpg
Supplemental Material - DEV076588FigS4.jpg
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Additional details
- PMCID
- PMC3252355
- Eprint ID
- 102557
- Resolver ID
- CaltechAUTHORS:20200415-105814073
- NIH Postdoctoral Fellowship
- F32 NS057870
- NIH
- R01 HD067140
- NIH
- R01 NS049319
- Created
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2020-04-15Created from EPrint's datestamp field
- Updated
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2021-11-16Created from EPrint's last_modified field