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Chemokine signaling guides axons within the retina in zebrafish

Authors :
Ichiro Masai
Bernard Thisse
Hitoshi Okamoto
Komei Shirabe
John Y. Kuwada
Qin Li
Christine Thisse
Institut de génétique et biologie moléculaire et cellulaire (IGBMC)
Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Louis Pasteur - Strasbourg I
Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Source :
Journal of Neuroscience, Journal of Neuroscience, Society for Neuroscience, 2005, 25 (7), pp.1711-7. ⟨10.1523/JNEUROSCI.4393-04.2005⟩
Publication Year :
2005
Publisher :
HAL CCSD, 2005.

Abstract

International audience; Chemokines are a large family of secreted proteins that play an important role in the migration of leukocytes during hematopoiesis and inflammation. Chemokines and their receptors are also widely distributed in the CNS. Although recent investigations are beginning to elucidate chemokine function within the CNS, relatively little is known about the CNS function of this important class of molecules. To better appreciate the CNS function of chemokines, the role of signaling by stromal cell-derived factor-1 (SDF-1) through its receptor, chemokine (CXC motif) receptor 4 (CXCR4), was analyzed in zebrafish embryos. The SDF-1/CXCR4 expression pattern suggested that SDF-1/CXCR4 signaling was important for guiding retinal ganglion cell axons within the retina to the optic stalk to exit the retina. Antisense knockdown of the ligand and/or receptor and a genetic CXCR4 mutation both induced retinal axons to follow aberrant pathways within the retina. Furthermore, retinal axons deviated from their normal pathway and extended to cells ectopically expressing SDF-1 within the retina. These data suggest that chemokine signaling is both necessary and sufficient for directing retinal growth cones within the retina.

Details

Language :
English
ISSN :
02706474 and 15292401
Database :
OpenAIRE
Journal :
Journal of Neuroscience, Journal of Neuroscience, Society for Neuroscience, 2005, 25 (7), pp.1711-7. ⟨10.1523/JNEUROSCI.4393-04.2005⟩
Accession number :
edsair.doi.dedup.....fcc4c54cf15b062b821ba7dd3610021c
Full Text :
https://doi.org/10.1523/JNEUROSCI.4393-04.2005⟩