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Genetic Analysis of Ephrin-A2 and Ephrin-A5 Show Their Requirement in Multiple Aspects of Retinocollicular Mapping Interdisciplinary Program in Brain Science Eye movement & Vision Lab. Hwang, JaeWon
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Introduction Topographic Maps Chemoaffinity Theory Eph receptor and Ephrin Gradient vs Competition Model Neuraxis
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Topographic Maps Axon projections in the vertebrate nervous system are typically organized with nearest neighbor relationships of the projecting neurons maintained in their connections within the target.
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Chemoaffinity Theory There are labels in gradients across the projecting and target fields and that axons find their correct location by matching up the labels. (Sperry, 1963)
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Eph receptor and Ephrin Eph receptor - RTK - At least 14 members Ephrin - Eph ligand - At least 8 members - A family & B family - Repellant activity
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Gradient vs Competition Dual-gradient model There may be two opposing gradients, for example a repellent and an attractant, with each axon identifying its correct place as the point where the opposing forces cancel out. Axon-axon competition There may be axon-axon competition for limiting positive factors in the target or by direct axon-axon interactions.
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Neuraxis
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Experiment Methods Results
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Methods Mice with a disruption in the ephrin-A2 and ephrin-A5 gene. (using homologous recombination in ES cells) A focal injection of DiI was made in one retina followed by examination of the contralateral midbrain.
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Result - Single Mutant Temporal axons - an additional more posterior arborization Nasal axons - no defects in ephrin-A2 - /- mice - an additional more anterior arborization in ephrin-A5 -/- mice
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Result – Double Mutant Homozygote - the ectopic termination extended over all regions Heterozygote - similar to single mutant
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Result – Double Mutant 2
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Result - Ephrin Expression Ephrin RNA distribution Ephrin(protein) distribution (Wild Type)
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Result - Ephrin Expression 2
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Result - EphA Expression EphA RNA expression Ephrin-A2 protein EphA5 protein
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Result – Stripe Assays Axon preference for anterior SC lanes no preference strong preference ABCD
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Result - Summary Fig 8. Schmatic illustration of retinocollicular mapping phenotypes in mice with disrupted ephrin-A2 or ephrin-A5 genes.
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Discussion Discussion 1 Discussion 2 Discussion 3 Discussion 4 Discussion 5
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Discussion 1-1 Simple repulsion model and two counterbalanced gradients cannot account for the behavior of nasal axons and double mutant phenotype. ⇒ An alternative is a model involving a repellent gradient of ephrins, in combination with axon-axon competition.
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Discussion 1-2 Incorporating competiton in the model can explain several aspects of data. Nasal axons shift anteriorly. Axons are not respecified to a specific ectopic position. Retinal axons fill the available space in the target.
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Discussion 2 The termination zones always took the form of punctate spots in the SC. But why? ⇒ There may be a mechanism that causes neighboring axons in the retina to cluster together in the SC, such as Hebbian activity-dependent refinement.
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Discussion 3 Do axons detect absolute or relative ephrin levels? ⇒ Data in double heterozygotes show neither of them correct. The ability of axons to discriminate between any two points on the tectum would depend on those two points having a sufficiently great difference in ephrin concentration.
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Discussion 4 Additive and Distinct function of ephrin-A2 and ephrin-A5 - Double homozygous mutant shows a synergistic phenotype. (Additive) - Ephrin-A5 is dominant in posterior tectum. (Distinct) - Ephrin-A2 -/-, ephrin-A5 -/-, and ephrin-A2 +/- ;ephrin-A5 +/- mice all show a similar temporal axon phenotype in anterior SC. (Additive)
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Discussion 5 Two possible model of dorsoventral mapping errors in double homozygous mutant. Ephrin acting directly as dorsoventral labels. A secondary effect to the anteroposterior defect.
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