ABSTRACT
AIMS: Treatment strategies for breast cancer continue to evolve. No uniformity exists in the UK for the management of node-positive breast cancer patients. Most centres continue to use conventional histopathology of sampled sentinel lymph nodes (SLNs), which requires delayed axillary clearance in up to 25% of patients. Some use touch imprint cytology or frozen section for intraoperative testing, although both have inherent sensitivity issues. An intraoperative molecular diagnostic approach helps to overcome some of these limitations. The aim of this study was to assess the clinical effectiveness of Metasin, a molecular method for the intraoperative evaluation of SLNs. METHODS AND RESULTS: RNA from 3296 lymph nodes from 1836 patients undergoing SLN assessment was analysed with Metasin. Alternate slices of tissue were examined in parallel by histology. Cases deemed to be discordant were analysed by protein gel electrophoresis. There was concordance between Metasin and histology in 94.1% of cases, with a sensitivity of 92% [95% confidence interval (CI) 88-94%] and a specificity of 97% (95% CI 95-97%). Positive and negative predictive values were 88% and 98%, respectively. Over half of the discordant cases (4.4%) were ascribed to tissue allocation bias (TAB). CONCLUSIONS: Clinical validation of the Metasin assay suggests that it is sufficiently sensitive and specific to make it fit for purpose in the intraoperative setting.
Subject(s)
Biomarkers, Tumor/analysis , Breast Neoplasms/pathology , Lymphatic Metastasis/diagnosis , Real-Time Polymerase Chain Reaction/methods , Sentinel Lymph Node/pathology , Female , Humans , Intraoperative Period , Sentinel Lymph Node Biopsy/methodsABSTRACT
Nodal status is one of the most important prognostic factors in breast cancer. Established tests such as touch imprint cytology and frozen sections currently used in the intra-operative setting show variations in sensitivity and specificity. This limitation has led to the development of molecular alternatives, such as GeneSearch, a commercial intra-operative real-time quantitative Polymerase Chain Reaction (RT-qPCR) assay that allows the surgeon to carry out axillary clearance as a one-step process. Since GeneSearch has been discontinued, we have developed the replacement Metasin assay, which targets the breast epithelial cell markers CK19 and mammaglobin mRNA and identifies metastatic disease in sentinel lymph nodes. The optimised assay can be completed within 32 min (6 min for RNA preparation and 26 min instrument run time), making its use feasible in the intraoperative setting. An analysis by Metasin of 154 archived lymph node homogenates previously analysed by both parallel histology and GeneSearch showed concordance for 148 cases. The sensitivity and specificity of Metasin compared with GeneSearch were 95% (CI 83%-99%) and 97% (CI 91%-99%) respectively; compared with histology they were 95% (CI 83%-99%) and 97% (CI 91%-99%), respectively. The sensitivity and specificity of GeneSearch compared with histology were 90% (CI 77%-96%) and 97% (CI 93%-99%) respectively. The positive predictive value of Metasin was 90% and negative predictive value was 98% for both histology and GeneSearch. The positive predictive value of GeneSearch was 92% and the negative predictive value was 97% compared to histology. The discordance rates of Metasin with both GeneSearch and histology were 3.89%. In comparison, the discordance rate of GeneSearch with histology was 4.5%. Metasin's robustness was independently evaluated on 193 samples previously analysed by GeneSearch from the Jules Bordet Institute, where Metasin yielded comparable results.
Subject(s)
Lymphatic Metastasis , Sentinel Lymph Node Biopsy , Breast Neoplasms , Humans , Lymph Nodes , Mammaglobin A , Sensitivity and SpecificityABSTRACT
Axonal projections from the retina to the brain are regulated by molecules including the Slit family of ligands [Thompson, H., Barker, D., Camand, O., Erskine, L., 2006a. Slits contribute to the guidance of retinal ganglion cell axons in the mammalian optic tract. Dev. Biol. 296, 476-484, Thompson, H., Camand, O., Barker, D., Erskine, L., 2006b. Slit proteins regulate distinct aspects of retinal ganglion cell axon guidance within dorsal and ventral retina. J. Neurosci. 26, 8082-8091]. However, the roles of Slit receptors in mammals, (termed Robos), have not been investigated in visual system development. Here we examined Robo1 and 2 mutant mice and found that Robos regulate the correct targeting of retinal ganglion cell (RGC) axons along the entire visual projection. We noted aberrant projections of RGC axons into the cerebral cortex, an area not normally targeted by RGC axons. The optic chiasm was expanded along the rostro-caudal axis (similar to Slit mutant mice, Plump, A.S., Erskine, L., Sabatier, C., Brose, K., Epstein, C.J., Goodman, C.S., Mason, C.A., Tessier-Lavigne, M., 2002. Slit1 and Slit2 cooperate to prevent premature midline crossing of retinal axons in the mouse visual system. Neuron 33, 219-232), with ectopic crossing points, and some axons projecting caudally toward the corticospinal tract. Further, we found that axons exuberantly projected into the diencephalon. These defects were more pronounced in Robo2 than Robo1 knockout animals, implicating Robo2 as the predominant Robo receptor in visual system development.
Subject(s)
Axons/physiology , Brain/physiology , Nerve Tissue Proteins/physiology , Receptors, Immunologic/physiology , Retinal Ganglion Cells/physiology , Visual Pathways/cytology , Visual Pathways/physiology , Animals , Brain/cytology , Brain/embryology , Cell Movement/genetics , Female , Mice , Mice, Knockout , Mice, Transgenic , Nerve Tissue Proteins/deficiency , Nerve Tissue Proteins/genetics , Pregnancy , Receptors, Immunologic/deficiency , Receptors, Immunologic/genetics , Retinal Ganglion Cells/cytology , Visual Pathways/embryology , Roundabout ProteinsABSTRACT
Cortical interneurons in rodents are generated in the ventral telencephalon and migrate tangentially into the cortex. This process requires the coordinated action of many intrinsic and extrinsic factors. Here we show that Robo1 and Robo2 receptor proteins are dynamically expressed throughout the period of corticogenesis and colocalize with interneuronal markers, suggesting that they play a role in the migration of these cells. Analysis of Robo mutants showed a marked increase in the number of interneurons in the cortices of Robo1(-/-), but not Robo2(-/-), animals throughout the period of corticogenesis and in adulthood; this excess number of interneurons was observed in all layers of the developing cortex. Using BrdU incorporation in dissociated cell cultures and phosphohistone-3 labeling in vivo, we demonstrated that the increased number of interneurons in Robo1(-/-) mice is, at least in part, due to increased proliferation. Interestingly, a similar increase in proliferation was observed in Slit1(-/-)/Slit2(-/-) mutant mice, suggesting that cell division is influenced by Slit-Robo signaling mechanisms. Morphometric analysis of migrating interneurons in Robo1(-/-), Robo2(-/-) and Slit1(-/-)/Slit2(-/-), but not in Slit1(-/-) mice, showed a differential increase in neuronal process length and branching suggesting that Slit-Robo signaling also plays an important role in the morphological differentiation of these neurons.
Subject(s)
Cerebral Cortex/cytology , Intercellular Signaling Peptides and Proteins/physiology , Interneurons/physiology , Nerve Tissue Proteins/physiology , Receptors, Immunologic/physiology , Signal Transduction , Animals , Biomarkers , Calbindins , Cell Culture Techniques , Cell Differentiation , Cell Movement , Cell Proliferation , Cells, Cultured , DNA, Complementary , Electroporation , Embryo, Mammalian , Embryonic Stem Cells/chemistry , Embryonic Stem Cells/metabolism , Genetic Markers , Genetic Vectors , Genomic Library , Immunohistochemistry , Integrases/metabolism , Intercellular Signaling Peptides and Proteins/genetics , Intercellular Signaling Peptides and Proteins/metabolism , Interneurons/cytology , Kinetics , Mice , Mice, Inbred C57BL , Mice, Knockout , Mice, Transgenic , Mutation , Nerve Tissue Proteins/genetics , Nerve Tissue Proteins/metabolism , Receptors, Immunologic/genetics , Receptors, Immunologic/metabolism , S100 Calcium Binding Protein G/metabolism , Selection, Genetic , Telencephalon/cytology , Transfection , Roundabout ProteinsABSTRACT
Congenital anomalies of the kidney and urinary tract (CAKUT) include vesicoureteral reflux (VUR). VUR is a complex, genetically heterogeneous developmental disorder characterized by the retrograde flow of urine from the bladder into the ureter and is associated with reflux nephropathy, the cause of 15% of end-stage renal disease in children and young adults. We investigated a man with a de novo translocation, 46,X,t(Y;3)(p11;p12)dn, who exhibits multiple congenital abnormalities, including severe bilateral VUR with ureterovesical junction defects. This translocation disrupts ROBO2, which encodes a transmembrane receptor for SLIT ligand, and produces dominant-negative ROBO2 proteins that abrogate SLIT-ROBO signaling in vitro. In addition, we identified two novel ROBO2 intracellular missense variants that segregate with CAKUT and VUR in two unrelated families. Adult heterozygous and mosaic mutant mice with reduced Robo2 gene dosage also exhibit striking CAKUT-VUR phenotypes. Collectively, these results implicate the SLIT-ROBO signaling pathway in the pathogenesis of a subset of human VUR.
Subject(s)
Chromosomes, Human, Pair 3/genetics , Chromosomes, Human, Y/genetics , Genetic Predisposition to Disease , Receptors, Immunologic/genetics , Signal Transduction/genetics , Translocation, Genetic/genetics , Urinary Tract/abnormalities , Vesico-Ureteral Reflux/genetics , Amino Acid Sequence , Animals , Blotting, Southern , Blotting, Western , Cell Line , DNA Mutational Analysis , DNA Primers , Humans , In Situ Hybridization, Fluorescence , Male , Mice , Molecular Sequence Data , Mutation, Missense/genetics , Nerve Tissue Proteins/metabolism , Pedigree , Receptors, Immunologic/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Vesico-Ureteral Reflux/pathologyABSTRACT
The Slit genes encode secreted ligands that regulate axon branching, commissural axon pathfinding and neuronal migration. The principal identified receptor for Slit is Robo (Roundabout in Drosophila). To investigate Slit signalling in forebrain development, we generated Robo1 knockout mice by targeted deletion of exon 5 of the Robo1 gene. Homozygote knockout mice died at birth, but prenatally displayed major defects in axon pathfinding and cortical interneuron migration. Axon pathfinding defects included dysgenesis of the corpus callosum and hippocampal commissure, and abnormalities in corticothalamic and thalamocortical targeting. Slit2 and Slit1/2 double mutants display malformations in callosal development, and in corticothalamic and thalamocortical targeting, as well as optic tract defects. In these animals, corticothalamic axons form large fasciculated bundles that aberrantly cross the midline at the level of the hippocampal and anterior commissures, and more caudally at the medial preoptic area. Such phenotypes of corticothalamic targeting were not observed in Robo1 knockout mice but, instead, both corticothalamic and thalamocortical axons aberrantly arrived at their respective targets at least 1 day earlier than controls. By contrast, in Slit mutants, fewer thalamic axons actually arrive in the cortex during development. Finally, significantly more interneurons (up to twice as many at E12.5 and E15.5) migrated into the cortex of Robo1 knockout mice, particularly in both rostral and parietal regions, but not caudal cortex. These results indicate that Robo1 mutants have distinct phenotypes, some of which are different from those described in Slit mutants, suggesting that additional ligands, receptors or receptor partners are likely to be involved in Slit/Robo signalling.
Subject(s)
Axons/metabolism , Cell Movement , Interneurons/cytology , Interneurons/metabolism , Nerve Tissue Proteins/metabolism , Prosencephalon/cytology , Prosencephalon/embryology , Receptors, Immunologic/metabolism , Animals , Cells, Cultured , Cerebral Cortex/cytology , Cerebral Cortex/embryology , Cerebral Cortex/metabolism , Corpus Callosum/cytology , Corpus Callosum/embryology , Corpus Callosum/metabolism , Gene Expression Regulation, Developmental , Mice , Mice, Knockout , Nerve Tissue Proteins/deficiency , Nerve Tissue Proteins/genetics , Neuroglia/cytology , Neuroglia/metabolism , Prosencephalon/metabolism , Receptors, Immunologic/deficiency , Receptors, Immunologic/genetics , Roundabout ProteinsABSTRACT
Robo3 is a member of the roundabout (Robo) family of proteins that plays a key role in axon guidance and cell migration in the developing nervous system. Recent studies have shown that Robo3 plays a crucial role in controlling axon guidance at the midline of the CNS. Here we describe and compare two human Robo3 isoforms, Robo3A and Robo3B, which differ by the insertion of 26 amino acids at the N-terminus, and these forms appear to be evolutionary conserved. We investigated the bioactivity of these isoforms and show that they have different binding properties to Slit, and that orthologs of these forms are expressed in the mouse embryo. In addition, we show that, like other members of the Robo family, Robo3 can bind homophilically, but it is also capable of binding heterophilically to Robo1 and NCAM. We propose that these properties of Robo3 may contribute to its function at the midline of the CNS.
Subject(s)
Nerve Tissue Proteins/metabolism , Receptors, Immunologic/metabolism , Amino Acid Sequence , Animals , Central Nervous System/embryology , Central Nervous System/metabolism , Conserved Sequence , Humans , Mice , Mice, Inbred C57BL , Molecular Sequence Data , Nerve Tissue Proteins/chemistry , Neural Cell Adhesion Molecules/metabolism , Protein Binding , Protein Isoforms/chemistry , Protein Isoforms/metabolism , Receptors, Cell Surface , Receptors, Immunologic/chemistry , Sequence Homology, Amino Acid , Subcellular Fractions , Roundabout ProteinsABSTRACT
The floor plate is known to be a source of repellent signals for cranial motor axons, preventing them from crossing the midline of the hindbrain. However, it is unknown which molecules mediate this effect in vivo. We show that Slit and Robo proteins are candidate motor axon guidance molecules, as Robo proteins are expressed by cranial motoneurons, and Slit proteins are expressed by the tissues that delimit motor axon trajectories, i.e. the floor plate and the rhombic lip. We present in vitro evidence showing that Slit1 and Slit2 proteins are selective inhibitors and repellents for dorsally projecting, but not for ventrally projecting, cranial motor axons. Analysis of mice deficient in Slit and Robo function shows that cranial motor axons aberrantly enter the midline, while ectopic expression of Slit1 in chick embryos leads to specific motor axon projection errors. Expression of dominant-negative Robo receptors within cranial motoneurons in chick embryos strikingly perturbs their projections, causing some motor axons to enter the midline, and preventing dorsally projecting motor axons from exiting the hindbrain. These data suggest that Slit proteins play a key role in guiding dorsally projecting cranial motoneurons and in facilitating their neural tube exit.
Subject(s)
Axons/metabolism , Glycoproteins/metabolism , Motor Neurons/metabolism , Nerve Tissue Proteins/metabolism , Rhombencephalon/embryology , Rhombencephalon/metabolism , Animals , Cell Line , Cells, Cultured , Chick Embryo , Electroporation , Gene Expression Regulation, Developmental , Genotype , Glycoproteins/genetics , Humans , Mice , Mutation/genetics , Nerve Tissue Proteins/genetics , Rats , Receptors, Immunologic/genetics , Receptors, Immunologic/metabolism , Roundabout ProteinsABSTRACT
The ventral midline of the central nervous system is an important intermediate target where growing commissural axons either cross and project contralaterally or remain on the same side of the body. New studies on mice and humans show that this decision by commissural axons is largely dependent on Slits, extracellular matrix proteins that are widely expressed in the midline of the nervous system, and their receptors, Robos (Long et al. [2004] Neuron 42:213-223; Sabatier et al. [2004] Cell 117:157-169; Jen et al. [2004] Science 304:1509-1513). Here, we show that the Robo family proteins Robo1 and Rig-1 exhibit differential expression patterns on commissural axons as they approach, cross, and leave the midline of the developing mouse spinal cord and demonstrate that Robo1 and Robo2 bind Slit1 and Slit2, but Rig-1 does not. In addition, we show that cultured chick commissural axons are repelled by a source of Slit protein, and the soluble Robo-Fc proteins are capable of neutralizing this repulsion. Finally, we exploit the large size and accessibility of the early chick embryo to analyze the function of Slit/Robo signaling in midline commissural axon guidance, and we demonstrate that the in vivo perturbation of Robo-Slit interaction at the floor plate causes consistent guidance defects of commissural axons during midline crossing. These findings demonstrate the evolutionarily conserved role for Robo-Slit interaction in the control of midline crossing axons in vertebrates.
Subject(s)
Glycoproteins/metabolism , Nerve Tissue Proteins/genetics , Nerve Tissue Proteins/metabolism , Neurons/metabolism , Receptors, Immunologic/genetics , Spinal Cord/metabolism , Animals , Axons/metabolism , Mice , Nerve Tissue Proteins/biosynthesis , Neurons/cytology , Receptors, Immunologic/biosynthesis , Spinal Cord/embryology , Roundabout ProteinsABSTRACT
Robo, the receptor for the midline repellent Slit, is a member of the cell adhesion molecule (CAM) Ig superfamily. We have recently demonstrated that members of the Robo family (Robo1 and Robo2) interact homophilically and heterophilically, thereby functioning to promote neurite outgrowth. Here, we describe a series of in vitro experiments to dissect the Robo ligand-interacting domains by deleting specific extracellular regions of the Robo1 molecule, generating a series of mutant proteins. Using these, we demonstrate that Ig domains 1 and 2 of Robo1 are important for Robo-Slit interaction and provide functional data using the Slit-mediated olfactory bulb repulsion assay. To investigate whether homophilic binding properties of Robo are domain specific, we used Robo1-Fc mutant deletion proteins in an aggregation assay and observed a reduction in homophilic binding when any one Ig or all the fibronectin domains were deleted, although homophilic binding was never completely abolished.
Subject(s)
Cell Differentiation/physiology , Central Nervous System/embryology , Growth Cones/metabolism , Nerve Tissue Proteins/metabolism , Receptors, Immunologic/metabolism , Animals , Binding Sites/genetics , Biological Assay , Cell Membrane/genetics , Cell Membrane/metabolism , Cells, Cultured , Central Nervous System/cytology , Central Nervous System/metabolism , Coculture Techniques , Down-Regulation/genetics , Fetus , Fibronectins/genetics , Growth Cones/ultrastructure , Immunoglobulin Variable Region/genetics , Intercellular Signaling Peptides and Proteins , Ligands , Mutation/genetics , Nerve Tissue Proteins/genetics , Olfactory Bulb/cytology , Olfactory Bulb/embryology , Olfactory Bulb/metabolism , Protein Binding/genetics , Protein Structure, Tertiary/genetics , Rats , Receptors, Immunologic/genetics , Roundabout ProteinsABSTRACT
The Robo family of molecules is important for axon guidance across the midline during central nervous system (CNS) development in invertebrates and vertebrates. Here we describe the patterns of Robo protein expression in the developing mouse CNS from embryonic day (E) 9.5 to postnatal day (P) 4, as determined by immunohistochemical labeling with an antibody (S3) raised against a common epitope present in the Robo ectodomain of Robos 1 and 2. In the spinal cord, midline-crossing axons are initially (at E11) S3-positive. At later times, midline Robo expression disappears, but is strongly upregulated in longitudinally running postcrossing axons. It is also strongly expressed in noncrossing longitudinal axons. Differential expression of Robo along axons was also found in axons cultured from E14 spinal cord. These findings resemble those from the Drosophila ventral nerve cord and indicate that in vertebrates a low level of Robo expression occurs in the initial crossing of the midline, while a high level of expression in the postcrossing fibers prevents recrossing. Likewise, Robo-positive ipsilateral axons are prevented from crossing at all. However, in the brain different rules appear to apply. Most commissural axons including those of the corpus callosum are strongly S3-positive along their whole length from their time of formation to postnatal life, but some have more complex age-dependent expression patterns. S3 labeling of the optic pathway is also complex, being initially strong in the retinal ganglion cells, optic tract, and chiasma but thereafter being lost except in a proportion of postchiasmal axons. The corticospinal tract is strongly positive throughout its course at all stages examined, including its decussation, formed at about P2 in the central part of the medulla oblongata.
Subject(s)
Cell Differentiation/physiology , Central Nervous System/embryology , Growth Cones/metabolism , Neural Pathways/embryology , Receptors, Immunologic/metabolism , Aging/physiology , Animals , Animals, Newborn , Central Nervous System/growth & development , Central Nervous System/metabolism , Epitopes/immunology , Female , Fetus , Functional Laterality/physiology , Gene Expression Regulation, Developmental/physiology , Immunohistochemistry , Mice , Mice, Inbred C57BL , Nerve Tissue Proteins , Neural Pathways/growth & development , Neural Pathways/metabolism , Protein Structure, Tertiary/physiology , Pyramidal Tracts/embryology , Pyramidal Tracts/growth & development , Pyramidal Tracts/metabolism , Spinal Cord/embryology , Spinal Cord/growth & development , Spinal Cord/metabolism , Visual Pathways/embryology , Visual Pathways/growth & development , Visual Pathways/metabolism , Roundabout ProteinsABSTRACT
The Robo genes encode a family of proteins that are the receptors for the midline repellent Slits and play a role in axon guidance. In addition to Robo1 and Robo2, Rig-1 has been recently identified in mouse as a novel member of the Robo family of proteins. As a first step in elucidating the role of Rig-1 during vertebrate development, we characterised the expression of Rig-1 by in situ hybridisation together with Robo1 and Robo2 in the spinal cord and other tissues of the mouse embryo. Our results show that Rig-1 has a dynamic pattern of expression in the developing CNS. In the spinal cord Rig-1 shows overlapping but distinct pattern of expression with Robo1 and Robo2.
Subject(s)
Embryo, Mammalian/metabolism , Gene Expression Profiling , Membrane Proteins/genetics , Nerve Tissue Proteins/genetics , Animals , Brain/embryology , Brain/metabolism , Embryo, Mammalian/embryology , Gene Expression Regulation, Developmental , In Situ Hybridization , Mice , Receptors, Cell Surface , Receptors, Immunologic/genetics , Spinal Cord/embryology , Spinal Cord/metabolism , Roundabout ProteinsABSTRACT
Commissural axons generally cross the midline only once. In the Drosophila nerve cord and mouse spinal cord, commissural axons are guided by Slit only after they cross the midline, where Slit prevents these axons from recrossing the midline. In the developing corpus callosum, Slit2 expressed by the glial wedge guides callosal axons before they cross the midline, as they approach the corticoseptal boundary. These data highlighted a potential difference between the role of Slit2 in guiding commissural axons in the brain compared with the spinal cord. Here, we investigate whether Slit2 also guides callosal axons after they cross the midline. Because such questions cannot be addressed in conventional gene knock-out animals, we used in utero injections of antisense oligonucleotides to specifically deplete Slit2 on only one side of the brain. We used this technique together with a novel in vitro assay of hemisected brain slices to specifically analyze postcrossing callosal axons. We find that in the brain, unlike the spinal cord, Slit2 mediates both precrossing and postcrossing axonal guidance. Depletion of Slit2 on one side of the brain causes axons to defasciculate and, in some cases, to aberrantly enter the septum. Because these axons do not recross the midline, we conclude that the principle function of Slit2 at the cortical midline may be to channel the axons along the correct path and possibly repel them away from the midline. We find no evidence that Slit2 prevents axons from recrossing the midline in the brain.
Subject(s)
Axons/physiology , Corpus Callosum/cytology , Corpus Callosum/physiology , Nerve Tissue Proteins/physiology , Animals , Axons/drug effects , Cells, Cultured , Cerebral Cortex/cytology , Cerebral Cortex/embryology , Coculture Techniques , Corpus Callosum/embryology , Immunohistochemistry , Intercellular Signaling Peptides and Proteins , Mice , Mice, Inbred C57BL , Nerve Tissue Proteins/antagonists & inhibitors , Nerve Tissue Proteins/genetics , Neuroglia/cytology , Oligonucleotides, Antisense/pharmacology , Receptors, Cell Surface/biosynthesis , Receptors, Immunologic/physiology , Spinal Cord/cytology , Spinal Cord/embryology , Roundabout ProteinsABSTRACT
The vomeronasal projection conveys information provided by pheromones and detected by neurones in the vomeronasal organ (VNO) to the accessory olfactory bulb (AOB) and thence to other regions of the brain such as the amygdala. The VNO-AOB projection is topographically organised such that axons from apical and basal parts of the VNO terminate in the anterior and posterior AOB respectively. We provide evidence that the Slit family of axon guidance molecules and their Robo receptors contribute to the topographic targeting of basal vomeronasal axons. Robo receptor expression is confined largely to basal VNO axons, while Slits are differentially expressed in the AOB with a higher concentration in the anterior part, which basal axons do not invade. Immunohistochemistry using a Robo-specific antibody reveals a zone-specific targeting of VNO axons in the AOB well before cell bodies of these neurones in the VNO acquire their final zonal position. In vitro assays show that Slit1-Slit3 chemorepel VNO axons, suggesting that basal axons are guided to the posterior AOB due to chemorepulsive activity of Slits in the anterior AOB. These data in combination with recently obtained other data suggest a model for the topographic targeting in the vomeronasal projection where ephrin-As and neuropilins guide apical VNO axons, while Robo/Slit interactions are important components in the targeting of basal VNO axons.
Subject(s)
Axons/metabolism , Chemotaxis/physiology , Glycoproteins/metabolism , Nerve Tissue Proteins/metabolism , Olfactory Bulb/anatomy & histology , Receptors, Immunologic/metabolism , Vomeronasal Organ/cytology , Afferent Pathways , Animals , Ephrins/metabolism , Glycoproteins/genetics , In Situ Hybridization , Mice , Nerve Tissue Proteins/genetics , Olfactory Bulb/growth & development , Olfactory Bulb/metabolism , Receptors, Immunologic/genetics , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Semaphorins/metabolism , Vomeronasal Organ/growth & development , Vomeronasal Organ/metabolism , Roundabout ProteinsABSTRACT
In the present study we show that following transfection in 3T3 cells, human Robo1 and Robo2 stimulate neurite outgrowth from Robo-positive neurons (retinal neurons and olfactory neurons), but have no effect on Robo-negative neurons (cerebellar granule cells). The neurite outgrowth response was inhibited by an antibody raised against the first Ig domain of Robo1/2 or by soluble Robo-Fc chimera. Furthermore, we show that the extracellular domains of Robo1 and Robo2 are homophilic adhesion molecules that can also interact with each other. These data suggest a wider range of functions for the Robo family in the development of the nervous system and provide novel insights into the molecular basis for the phenotypes observed in Robo mutants in Drosophila, C. elegans, and zebrafish.