Ephrin-As and Patterned Retinal Activity Act Together in the Development of Topographic Maps in the Primary Visual System

The development of topographic maps in the primary visual system is thought to rely on a combination of EphA/ephrin-A interactions and patterned neural activity. Here, we characterize the retinogeniculate and retinocollicular maps of mice mutant for ephrins-A2, -A3, and -A5 (the three ephrin-As expressed in the mouse visual system), mice mutant for the β2 subunit of the nicotinic acetylcholine receptor (that lack early patterned retinal activity), and mice mutant for both ephrin-As and β2. We also provide the first comprehensive anatomical description of the topographic connections between the retina and the dorsal lateral geniculate nucleus. We find that, although ephrin-A2/A3/A5 triple knock-out mice have severe mapping defects in both projections, they do not completely lack topography. Mice lacking β2-dependent retinal activity have nearly normal topography but fail to refine axonal arbors. Mice mutant for both ephrin-As and β2 have synergistic mapping defects that result in a near absence of map in the retinocollicular projection; however, the retinogeniculate projection is not as severely disrupted as the retinocollicular projection is in these mutants. These results show that ephrin-As and patterned retinal activity act together to establish topographic maps, and demonstrate that midbrain and forebrain connections have a differential requirement for ephrin-As and patterned retinal activity in topographic map development.

[1]  M. Feller,et al.  Retinogeniculate Axons Undergo Eye-Specific Segregation in the Absence of Eye-Specific Layers , 2002, The Journal of Neuroscience.

[2]  M. Stryker,et al.  Prenatal tetrodotoxin infusion blocks segregation of retinogeniculate afferents. , 1988, Science.

[3]  W. Levick,et al.  The determination of the projection of the visual field on to the lateral geniculate nucleus in the cat , 1962, The Journal of physiology.

[4]  Arthur L. Beaudet,et al.  Multiorgan Autonomic Dysfunction in Mice Lacking the β2 and the β4 Subunits of Neuronal Nicotinic Acetylcholine Receptors , 1999, The Journal of Neuroscience.

[5]  M Sur,et al.  Blockade of afferent impulse activity disrupts on/off sublamination in the ferret lateral geniculate nucleus. , 1997, Brain research. Developmental brain research.

[6]  John G Flanagan,et al.  Ephrin-As and neural activity are required for eye-specific patterning during retinogeniculate mapping , 2005, Nature Neuroscience.

[7]  Matthew S. Grubb,et al.  Abnormal Functional Organization in the Dorsal Lateral Geniculate Nucleus of Mice Lacking the β2 Subunit of the Nicotinic Acetylcholine Receptor , 2003, Neuron.

[8]  D. Copenhagen,et al.  Development of Precise Maps in Visual Cortex Requires Patterned Spontaneous Activity in the Retina , 2005, Neuron.

[9]  G. Schneider,et al.  The morphology of optic tract axons arborizing in the superior colliculus of the hamster , 1984, The Journal of comparative neurology.

[10]  G. Lemke,et al.  Retinotectal mapping: new insights from molecular genetics. , 2005, Annual review of cell and developmental biology.

[11]  Ian D. Thompson,et al.  Opposing Gradients of Ephrin-As and EphA7 in the Superior Colliculus Are Essential for Topographic Mapping in the Mammalian Visual System , 2005, Neuron.

[12]  R E Beitel,et al.  Relation of the visual field to the lateral geniculate body of the albino rat. , 1968, Journal of neurophysiology.

[13]  Philippe Soriano,et al.  Ephrin signaling in vivo: Look both ways , 2005, Developmental dynamics : an official publication of the American Association of Anatomists.

[14]  M. Hanson,et al.  Normal Patterns of Spontaneous Activity Are Required for Correct Motor Axon Guidance and the Expression of Specific Guidance Molecules , 2004, Neuron.

[15]  John G Flanagan,et al.  Topographic Guidance Labels in a Sensory Projection to the Forebrain , 1998, Neuron.

[16]  John G. Flanagan,et al.  Genetic Analysis of Ephrin-A2 and Ephrin-A5 Shows Their Requirement in Multiple Aspects of Retinocollicular Mapping , 2000, Neuron.

[17]  Rachel O.L. Wong,et al.  Failure to Maintain Eye-Specific Segregation in nob, a Mutant with Abnormally Patterned Retinal Activity , 2006, Neuron.

[18]  C. Holt,et al.  Topographic Mapping in Dorsoventral Axis of the Xenopus Retinotectal System Depends on Signaling through Ephrin-B Ligands , 2002, Neuron.

[19]  M. Stryker,et al.  Ephrin-As Guide the Formation of Functional Maps in the Visual Cortex , 2005, Neuron.

[20]  A. Huberman,et al.  Ephrin-As mediate targeting of eye-specific projections to the lateral geniculate nucleus , 2005, Nature Neuroscience.

[21]  John G Flanagan,et al.  Neural map specification by gradients , 2006, Current Opinion in Neurobiology.

[22]  C. Holt,et al.  The transcription factor Engrailed-2 guides retinal axons , 2005, Nature.

[23]  J P Changeux,et al.  Requirement of the nicotinic acetylcholine receptor β2 subunit for the anatomical and functional development of the visual system , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[24]  D. O'Leary,et al.  Retinotopic Map Refinement Requires Spontaneous Retinal Waves during a Brief Critical Period of Development , 2003, Neuron.

[25]  Marla B. Feller,et al.  Spontaneous patterned retinal activity and the refinement of retinal projections , 2005, Progress in Neurobiology.

[26]  A. Schmitt,et al.  Wnt–Ryk signalling mediates medial–lateral retinotectal topographic mapping , 2006, Nature.

[27]  Michael C Crair,et al.  Evidence for an Instructive Role of Retinal Activity in Retinotopic Map Refinement in the Superior Colliculus of the Mouse , 2005, The Journal of Neuroscience.

[28]  John G Flanagan,et al.  Loss-of-Function Analysis of EphA Receptors in Retinotectal Mapping , 2004, The Journal of Neuroscience.

[29]  D. O'Leary,et al.  EphB Forward Signaling Controls Directional Branch Extension and Arborization Required for Dorsal-Ventral Retinotopic Mapping , 2002, Neuron.

[30]  Andrew D Huberman,et al.  Decoupling Eye-Specific Segregation from Lamination in the Lateral Geniculate Nucleus , 2002, The Journal of Neuroscience.

[31]  D. O'Leary,et al.  Development of topographic order in the mammalian retinocollicular projection , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  E. S. Ruthazer,et al.  Insights into activity-dependent map formation from the retinotectal system: a middle-of-the-brain perspective. , 2004, Journal of neurobiology.

[33]  R. W. Guillery,et al.  Generation of cat retinal ganglion cells in relation to central pathways , 1983, Nature.

[34]  D. O'Leary,et al.  Molecular gradients and development of retinotopic maps. , 2005, Annual review of neuroscience.

[35]  R. Heintzmann,et al.  Silencing of EphA3 through a cis interaction with ephrinA5 , 2006, Nature Neuroscience.

[36]  Richard Axel,et al.  Axonal Ephrin-As and Odorant Receptors Coordinate Determination of the Olfactory Sensory Map , 2003, Cell.

[37]  A. Beaudet,et al.  Mice Lacking Specific Nicotinic Acetylcholine Receptor Subunits Exhibit Dramatically Altered Spontaneous Activity Patterns and Reveal a Limited Role for Retinal Waves in Forming ON and OFF Circuits in the Inner Retina , 2000, The Journal of Neuroscience.

[38]  Jonas Frisén,et al.  Ephrin-A5 (AL-1/RAGS) Is Essential for Proper Retinal Axon Guidance and Topographic Mapping in the Mammalian Visual System , 1998, Neuron.

[39]  C. Shatz,et al.  Competition in retinogeniculate patterning driven by spontaneous activity. , 1998, Science.

[40]  J. Lund,et al.  The organization of the retinal projection to the dorsal lateral geniculate nucleus in pigmented and albino rats , 1974, The Journal of comparative neurology.

[41]  P. Garraghty Connectional specificity in the cat's retinogeniculate system. , 1995, The International journal of neuroscience.

[42]  F. Valverde,et al.  The neuropil in superficial layers of the superior colliculus of the mouse , 1973, Zeitschrift für Anatomie und Entwicklungsgeschichte.