Medical Journals

Stromal Cell-derived Factor-1 Antagonizes Slit/Robo Signaling in Vivo.

Authors:
  • Chalasani Sreekanth H
  • Sabol Angela
  • Xu Hong
  • Gyda Michael A
  • Rasband Kendall
  • Granato Michael
  • Chien Chi-Bin
  • Raper Jonathan A

From: Neuroscience Department, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.

The Journal of neuroscience : the official journal of the Society for Neuroscience

  • Publish Date: Jan 2007
  • ISSN: 1529-2401
  • Volume: 27
  • Issue: 5
  • Pages: 973-80
  • Medium: Internet
  • Language: English
  • Citation (JAMA): Chalasani Sreekanth H, Sabol Angela, Xu Hong, et al. Stromal Cell-derived Factor-1 Antagonizes Slit/Robo Signaling in Vivo.. J. Neurosci. Jan 2007;27:973-80

Abstract

Retinal ganglion cell axons exit the eye, enter the optic stalk, cross the ventral midline at the optic chiasm, and terminate in the optic tectum of the zebrafish. While in the optic stalk, they grow immediately adjacent to cells expressing the powerful retinal axon repellent slit2. The chemokine stromal cell-derived factor-1 (SDF1) is expressed within the optic stalk and its receptor CXCR4 is expressed in retinal ganglion cells. SDF1 makes cultured retinal axons less responsive to slit2. Here, we show that reducing SDF1 signaling in vivo rescues retinal axon pathfinding errors in zebrafish mutants that have a partial functional loss of the slit receptor robo2. In contrast, reducing SDF1 signaling in animals that completely lack the robo2 receptor does not rescue retinal guidance errors. These results demonstrate that endogenous levels of SDF1 antagonize the repellent effects of slit/robo signaling in vivo and that this antagonism is important during axonal pathfinding.

Mesh Headings (Keywords): Animals, Cells, Cultured, Chemokine CXCL12, Chemokines, CXC, Gene Expression Regulation, Developmental, Intracellular Signaling Peptides and Proteins, Receptors, CXCR4, Receptors, Immunologic, Retinal Ganglion Cells, Signal Transduction, Zebrafish, Zebrafish Proteins


Check for Full Text / PubMed Unique Identifier (PMID): 17267551


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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