Ephrin-A5 (AL-1/RAGS) is essential for proper retinal axon guidance and topographic mapping in the mammalian visual system

Neuron. 1998 Feb;20(2):235-43. doi: 10.1016/s0896-6273(00)80452-3.


Ephrin-A5 (AL-1/RAGS), a ligand for Eph receptor tyrosine kinases, repels retinal axons in vitro and has a graded expression in the superior colliculus (SC), the major midbrain target of retinal ganglion cells. These properties implicate ephrin-A5 in the formation of topographic maps, a fundamental organizational feature of the nervous system. To test this hypothesis, we generated mice lacking ephrin-A5. The majority of ephrin-A5-/- mice develop to adulthood, are morphologically intact, and have normal anterior-posterior patterning of the midbrain. However, within the SC, retinal axons establish and maintain dense arborizations at topographically incorrect sites that correlate with locations of low expression of the related ligand ephrin-A2. In addition, retinal axons transiently overshoot the SC and extend aberrantly into the inferior colliculus (IC). This defect is consistent with the high level of ephrin-A5 expression in the IC and the finding that retinal axon growth on membranes from wild-type IC is inhibited relative to that on membranes from ephrin-A5-/- IC. These findings show that ephrin-A5 is required for the proper guidance and mapping of retinal axons in the mammalian midbrain.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Axons / physiology*
  • Brain Mapping
  • Ephrin-A2
  • Gene Expression Regulation, Developmental
  • Inferior Colliculi / cytology
  • Inferior Colliculi / embryology
  • Mammals
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • Mutagenesis
  • Optic Nerve / cytology*
  • Optic Nerve / embryology
  • Retinal Ganglion Cells / chemistry
  • Retinal Ganglion Cells / cytology*
  • Retinal Ganglion Cells / ultrastructure
  • Superior Colliculi / cytology*
  • Superior Colliculi / embryology
  • Transcription Factors / genetics*


  • Ephrin-A2
  • Transcription Factors