Abstract

BackgroundOlfactory Sensory Neuron (OSN) axons project from the zebrafish olfactory epithelium to reproducible intermediate target locations in the olfactory bulb called protoglomeruli at early stages in development. Two classes of OSNs expressing either OMP or TRPC2 exclusively target distinct, complementary protoglomeruli. Using RNAseq, we identified axon guidance receptors nrp2a and nrp2b, and their ligand sema3fa, as potential guidance factors that are differentially expressed between these two classes of OSNs.MethodsTo investigate their role in OSN axon guidance, we assessed the protoglomerular targeting fidelity of OSNs labeled by OMP:RFP and TRPC2:Venus transgenes in nrp2a, nrp2b, or sema3fa mutants. We used double mutant and genetic interaction experiments to interrogate the relationship between the three genes. We used live time-lapse imaging to compare the dynamic behaviors of OSN growth cones during protoglomerular targeting in heterozygous and mutant larvae.ResultsThe fidelity of protoglomerular targeting of TRPC2-class OSNs is degraded in nrp2a, nrp2b, or sema3fa mutants, as axons misproject into OMP-specific protoglomeruli and other ectopic locations in the bulb. These misprojections are further enhanced in nrp2a;nrp2b double mutants suggesting that nrp2s work at least partially in parallel in the same guidance process. Results from genetic interaction experiments are consistent with sema3fa acting in the same biological pathway as both nrp2a and nrp2b. Live time-lapse imaging was used to examine the dynamic behavior of TRPC2-class growth cones in nrp2a mutants compared to heterozygous siblings. Some TRPC2-class growth cones ectopically enter the dorsal-medial region of the bulb in both groups, but in fully mutant embryos, they are less likely to correct the error through retraction. The same result was observed when TRPC2-class growth cone behavior was compared between sema3fa heterozygous and sema3fa mutant larvae.ConclusionsOur results suggest that nrp2a and nrp2b expressed in TRPC2-class OSNs help prevent their mixing with axon projections in OMP-specific protoglomeruli, and further, that sema3fa helps to exclude TRPC2-class axons by repulsion from the dorsal-medial bulb.

Highlights

  • The precise wiring together of olfactory circuitry is essential for its proper function

  • Expression patterns of nrp2a, nrp2b, and sema3fa in the develo ping zebrafish olfactory system A striking feature of the zebrafish olfactory projection is that axons originating from Olfactory Marker Protein (OMP)-expressing Olfactory Sensory Neuron (OSN) and from TRPC2-expressing OSNs terminate in distinct and separate protoglomerular neuropils in the Olfactory Bulb (OB) (Fig. 1A, Additional file 1)

  • We reasoned that axonal guidance receptors that are differentially expressed in OMP-class as compared to TRPC2-class OSNs are candidates for mediating this differential targeting

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Summary

Introduction

The precise wiring together of olfactory circuitry is essential for its proper function. OSNs predominantly expressing the same OR are stochastically distributed within the OE while their axons converge on a single glomerulus at a stereotypical location within the OB [5, 6] This pattern of stereotyped convergence converts a diffuse odorant experience into a stereotypical map of neuronal activity in the bulb [7,8,9]. OSNs first project axons to a set of distinct and identifiable intermediate neuropil targets in the olfactory bulb, known as protoglomeruli. Olfactory Sensory Neuron (OSN) axons project from the zebrafish olfactory epithelium to reproducible intermediate target locations in the olfactory bulb called protoglomeruli at early stages in development. Using RNAseq, we identified axon guidance receptors nrp2a and nrp2b, and their ligand sema3fa, as potential guidance factors that are differentially expressed between these two classes of OSNs

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