4.8 Article

Optic Chiasm Presentation of Semaphorin6D in the Context of Plexin-A1 and Nr-CAM Promotes Retinal Axon Midline Crossing

Journal

NEURON
Volume 74, Issue 4, Pages 676-690

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2012.03.025

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Funding

  1. National Institutes of Health [EY12736, NS065048]
  2. Howard Hughes Medical Institute
  3. Uehara Foundation
  4. Ministry of Health, Labour and Welfare
  5. National Institute of Biomedical Innovation
  6. Japan Science and Technology Agency
  7. Ministry of Education, Culture, Sports, Science and Technology of Japan
  8. Japan Society for the Promotion of Science

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At the optic chiasm, retinal ganglion cells (RGCs) project ipsi- or contralaterally to establish the circuitry for binocular vision. Ipsilateral guidance programs have been characterized, but contralateral guidance programs are not well understood. Here, we identify a tripartite molecular system for contralateral RGC projections: Semaphorin6D (Sema6D) and Nr-CAM are expressed on midline radial glia and Plexin-A1 on chiasm neurons, and Plexin-A1 and Nr-CAM are also expressed on contralateral RGCs. Sema6D is repulsive to contralateral RGCs, but Sema6D in combination with Nr-CAM and Plexin-A1 converts repulsion to growth promotion. Nr-CAM functions as a receptor for Sema6D. Sema6D, Plexin-A1, and Nr-CAM are all required for efficient RGC decussation at the optic chiasm. These findings suggest a mechanism by which a complex of Sema6D, Nr-CAM, and Plexin-A1 at the chiasm midline alters the sign of Sema6D and signals Nr-CAM/Plexin-A1 receptors on RGCs to implement the contralateral RGC projection.

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