RESUMEN
Interneurons are inhibitory neurons, which protect neural tissue from excessive excitation. They are interconnected with glutamatergic pyramidal neurons in the cerebral cortex and regulate their function. Particularly in the prefrontal cortex (PFC), interneurons have been strongly implicated in regulating pathological states which display deficits in the PFC. The aim of this study is to investigate the adaptations in the adult glutamatergic system, when defects in interneuron development do not allow adequate numbers of interneurons to reach the cerebral cortex. To this end, we used a mouse model that displays ~50% fewer cortical interneurons due to the Rac1 protein loss from Nkx2.1/Cre expressing cells (Rac1 conditional knockout (cKO) mice), to examine how the developmental loss of interneurons may affect basal synaptic transmission, synaptic plasticity and neuronal morphology in the adult PFC. Despite the decrease in the number of interneurons, basal synaptic transmission, as examined by recording field excitatory postsynaptic potentials (fEPSPs) from layer II networks, is not altered in the PFC of Rac1 cKO mice. However, there is decreased paired-pulse ratio (PPR) and decreased long-term potentiation (LTP), in response to tetanic stimulation, in the layer II PFC synapses of Rac1 cKO mice. Furthermore, expression of N-methyl-d-aspartate (NMDA) subunits is decreased and dendritic morphology is altered, changes that could underlie the decrease in LTP in the Rac1 cKO mice. Finally, we find that treating Rac1 cKO mice with diazepam in early postnatal life can reverse changes in dendritic morphology observed in non-treated Rac1 cKO mice. Therefore, our data show that disruption in GABAergic inhibition alters glutamatergic function in the adult PFC, an effect that could be reversed by enhancement of GABAergic function during an early postnatal period.
Asunto(s)
Interneuronas/fisiología , Plasticidad Neuronal/fisiología , Corteza Prefrontal/crecimiento & desarrollo , Corteza Prefrontal/fisiopatología , Animales , Espinas Dendríticas/efectos de los fármacos , Espinas Dendríticas/patología , Espinas Dendríticas/fisiología , Diazepam/farmacología , Potenciales Postsinápticos Excitadores/efectos de los fármacos , Potenciales Postsinápticos Excitadores/fisiología , Moduladores del GABA/farmacología , Interneuronas/efectos de los fármacos , Interneuronas/patología , Masculino , Ratones Noqueados , Plasticidad Neuronal/efectos de los fármacos , Neuropéptidos/genética , Neuropéptidos/metabolismo , Proteínas Nucleares/genética , Proteínas Nucleares/metabolismo , Corteza Prefrontal/efectos de los fármacos , Corteza Prefrontal/patología , Receptores de N-Metil-D-Aspartato/metabolismo , Factor Nuclear Tiroideo 1 , Técnicas de Cultivo de Tejidos , Factores de Transcripción/genética , Factores de Transcripción/metabolismo , Proteína de Unión al GTP rac1/genética , Proteína de Unión al GTP rac1/metabolismoRESUMEN
Several studies have proposed that the nervous system participates in nociception and tendon healing process. The neural cell adhesion molecule L1 (L1—CAM), which has an important role in neural development and nociceptive pathways, has been described in the past in the skeletal muscles and tendino—muscular junction. The role of this protein in tendon pathology is unknown. Here, we show that L1—CAM is expressed in human tendons. Samples of the long head of the biceps tendon (LHB) from six patients undergoing shoulder surgery were studied. Both Western blot and immunofluorescence revealed a strong expression pattern of L1—CAM. These L1—CAM positive cells were also Tuj1 positive, suggesting a neuronal origin. To our knowledge this is the first unequivocal evidence of the presence of L1 CAM in human tendons suggesting that it may play a role in organization of extracellular matrix and tendon pain.
Asunto(s)
Molécula L1 de Adhesión de Célula Nerviosa/metabolismo , Tendones/metabolismo , Anciano , Femenino , Humanos , Masculino , Molécula L1 de Adhesión de Célula Nerviosa/inmunología , Hombro/cirugía , Dolor de Hombro/etiología , Tendones/patología , Tubulina (Proteína)/metabolismoRESUMEN
Recent work has uncovered a large number of imprinted genes, many of which are thought to play a role in neurodevelopment and behavior. In order to begin to understand the role of specific genes in these processes, their expression patterns will be key. In this study we used in situ hybridization to study the developmental expression of Gtl2 in the forebrain from E12.5 to adulthood, since preliminary data from a microarray study indicated differential expression between the ventral and dorsal telencephalon of the mouse at a critical time point in the generation and migration of cortical neuronal populations. Strong expression was observed in the diencephalon, ventral telencephalon, post mitotic cell layers of the neocortex and pyramidal cell layer of the hippocampus. Additionally, heavily labeled subpopulations of laminar restricted cells were seen in the latter two areas.
Asunto(s)
Regulación del Desarrollo de la Expresión Génica , Impresión Genómica , Prosencéfalo/embriología , Prosencéfalo/crecimiento & desarrollo , Proteínas/metabolismo , Animales , Femenino , Técnica del Anticuerpo Fluorescente Indirecta , Inmunohistoquímica , Hibridación in Situ , Ratones , Ratones Endogámicos C57BL , Ratones Endogámicos CBA , Embarazo , Proteínas/genética , ARN Largo no Codificante , Distribución TisularRESUMEN
Neurons destined to form several precerebellar nuclei are generated in the dorsal neuroepithelium (rhombic lip) of caudal hindbrain. They form two ventrally directed migratory streams, which behave differently. While neurons in the superficial migration migrate in a subpial position and cross the midline to settle into the contralateral hindbrain, neurons in the olivary migration travel deeper in the parenchyma and stop ipsilaterally against the floor plate. In the present study, we compared the behavior of the two neuronal populations in an organotypic culture system that preserves several aspects of their in vivo environment. Both migrations occurred in mouse hindbrain explants dissected at E11.5 even when the floor plate was ablated at the onset of the culture period, indicating that they could rely on dorsoventral cues already distributed in the neural tube. Nevertheless, the local constraints necessary for the superficial migration were more specific than for the olivary migration. Distinct chemoattractive and chemorespulsive signal were found to operate on the migrations. The floor plate exhibited a strong chemoattractive influence on both migrations, which deviated from their normal path in the direction of ectopic floor plate fragments. It was also found to produce a short-range stop signal and to induce inferior olive aggregation. The ventral neural tube was also found to inhibit or slow down the migration of olivary neurons. Interestingly, while ectopic sources of netrin were found to influence both migrations, this effect was locally modulated and affected differentially the successive phases of migration. Consistent with this observation, while neurons in the superficial migration expressed the Dcc-netrin receptor, the migrating olivary neurons did not express Dcc before they reached the midline. Our observations provide a clearer picture of the hierarchy of environmental cues that influence the morphogenesis of these precerebellar nuclei.
Asunto(s)
Movimiento Celular/fisiología , Cerebelo/embriología , Proteínas de Homeodominio , Bulbo Raquídeo/embriología , Factores de Crecimiento Nervioso/metabolismo , Neuronas/efectos de los fármacos , Neuronas/fisiología , Animales , Bromodesoxiuridina/metabolismo , Células COS , Moléculas de Adhesión Celular Neuronal/metabolismo , Cerebelo/citología , Cerebelo/fisiología , Factores Quimiotácticos/metabolismo , Contactina 2 , Técnicas de Cultivo , Proteínas de Unión al ADN/metabolismo , Femenino , Inmunohistoquímica , Hibridación in Situ , Bulbo Raquídeo/citología , Bulbo Raquídeo/crecimiento & desarrollo , Bulbo Raquídeo/fisiología , Ratones , Morfogénesis , Factores de Crecimiento Nervioso/genética , Factores de Crecimiento Nervioso/farmacología , Netrina-1 , Neuronas/citología , Embarazo , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/metabolismo , Trasplante de Tejidos , Factor de Transcripción Brn-3B , Factores de Transcripción/metabolismo , Proteínas Supresoras de TumorRESUMEN
Cortical nonpyramidal cells, the GABA-containing interneurons, originate mostly in the medial ganglionic eminence of the ventral telencephalon and follow tangential migratory routes to reach the dorsal telencephalon. Although several genes that play a role in this migration have been identified, the underlying cellular and molecular cues are not fully understood. We provide evidence that the neural cell adhesion molecule TAG-1 mediates the migration of cortical interneurons. We show that the migration of these neurons occurs along the TAG-1-expressing axons of the developing corticofugal system. The spatial and temporal pattern of expression of TAG-1 on corticofugal fibers coincides with the order of appearance of GABAergic cells in the developing cortex. Blocking the function of TAG-1, but not of L1, another adhesion molecule and binding partner of TAG-1, results in a marked reduction of GABAergic neurons in the cortex. These observations reveal a mechanism by which the adhesion molecule TAG-1, known to be involved in axonal pathfinding, also takes part in neuronal migration.
Asunto(s)
Encéfalo/embriología , Moléculas de Adhesión Celular Neuronal/metabolismo , Corteza Cerebral/embriología , Interneuronas/fisiología , Moléculas de Adhesión de Célula Nerviosa/metabolismo , Animales , Moléculas de Adhesión Celular Neuronal/antagonistas & inhibidores , Moléculas de Adhesión Celular Neuronal/aislamiento & purificación , Movimiento Celular , Corteza Cerebral/citología , Contactina 2 , Vías Eferentes , Complejo de Antígeno L1 de Leucocito , Glicoproteínas de Membrana/aislamiento & purificación , Glicoproteínas de Membrana/metabolismo , Ratones , Modelos Neurológicos , Fibras Nerviosas , Moléculas de Adhesión de Célula Nerviosa/antagonistas & inhibidores , Moléculas de Adhesión de Célula Nerviosa/aislamiento & purificación , Ratas , Ratas Sprague-Dawley , Tálamo/citología , Ácido gamma-AminobutíricoRESUMEN
Rat cerebellar granule cells differentiated in culture were fed [1-(3)H]sphingosine, allowing the metabolic radiolabelling of all cell sphingolipids and phosphatidylethanolamine. A detergent-insoluble sphingolipid-enriched membrane fraction, containing about 60% of cell sphingolipids, but only trace amounts of phosphatidylethanolamine, was prepared from [1-(3)H]sphingosine-fed cells by sucrose gradient centrifugation. This fraction was enriched in the Src family protein tyrosine kinases c-Src, Lyn and Fyn and in the GPI-anchored neuronal adhesion molecule TAG-1. The cell lysate and the sphingolipid-enriched membrane fraction were subjected to immunoprecipitation with anti-GD3 ganglioside monoclonal antibody R24, under experimental conditions designed to preserve the integrity of the domain. The radioactive lipid composition of the immunoprecipitates obtained from the cell lysate and from the sphingolipid-enriched fraction were very similar, and closely resembled the sphingolipid composition of the whole sphingolipid-enriched membrane fraction. In fact, the immunoprecipitates contained, together with GD3 ganglioside, all cell glycosphingolipids and sphingomyelin, whereas they did not contain phosphatidylethanolamine. Moreover, cholesterol and phosphatidylcholine were detected in the immunoprecipitates by qualitative TLC analysis followed by colourimetric visualization. c-Src, Lyn, Fyn and TAG-1 were associated with the anti-GD3 antibody immunoprecipitate. These proteins were not detected in the immunoprecipitates obtained under experimental conditions different from those designed to preserve the integrity of the domain. These data suggest that a membrane domain containing cholesterol, phosphatidylcholine, sphingolipids and proteins can be separated from the total cell membranes by anti-GD3 antibody immunoprecipitation, and that the association of c-Src, Fyn, Lyn, and TAG-1 with the sphingolipid-enriched domain is mediated by the interaction with a complex lipid environment, rather than by specific interactions with a single sphingolipid species.
Asunto(s)
Moléculas de Adhesión Celular Neuronal , Gangliósidos/aislamiento & purificación , Glicoproteínas de Membrana/aislamiento & purificación , Microdominios de Membrana/enzimología , Neuronas/enzimología , Pruebas de Precipitina/métodos , Familia-src Quinasas/aislamiento & purificación , Animales , Anticuerpos Monoclonales , Proteína Tirosina Quinasa CSK , Fraccionamiento Celular/métodos , Células Cultivadas , Cerebelo/citología , Contactina 2 , Gangliósidos/inmunología , Neuronas/citología , Proteínas Tirosina Quinasas/aislamiento & purificación , Proteínas Proto-Oncogénicas/aislamiento & purificación , Proteínas Proto-Oncogénicas c-fyn , Ratas , Ratas Sprague-Dawley , Esfingosina/aislamiento & purificación , TritioRESUMEN
Mox1 and Mox2 homeobox genes have been shown to be critical in axial skeleton and in limb muscle development respectively. Pax1 and Pax3 gene products are also implicated in these processes. Mox and Pax expression patterns are highly overlapping both spatially and temporally during embryonic development. We show here for the first time that Mox proteins physically interact with Pax1 and Pax3 using the yeast two-hybrid protein interaction assay as well as in vitro biochemical assays. There is a strong preference of Mox1 to associate with Pax1 rather than Pax3 and of Mox2 to associate with Pax3 rather than Pax1. The observed interactions are mediated through the homeodomain of Mox.
Asunto(s)
Antígenos de Superficie/metabolismo , Proteínas de Unión al ADN/metabolismo , NADH NADPH Oxidorreductasas/metabolismo , NADPH Oxidasas , Factores de Transcripción/metabolismo , Animales , Antígenos CD , Escherichia coli , Genes Homeobox/fisiología , Ratones , Factor de Transcripción PAX3 , Factores de Transcripción Paired Box , Proteínas Recombinantes/metabolismo , Técnicas del Sistema de Dos HíbridosRESUMEN
We have isolated the cDNA of avian Mox2 and analyzed its expression pattern during somitogenesis and limb bud formation. Mox2 plays an important role in limb muscle differentiation in the mouse. Mox2 is expressed in the somites of developing chick embryos and in presumptive migrating myoblasts from the dermomyotome to the limb buds. It is also expressed in the ventral and dorsal part of limb buds and is associated with non-proliferating myoblasts. Significant differences were observed in chick and mouse expression patterns, namely in the chick dermomyotome and limb.
Asunto(s)
Antígenos de Superficie/genética , Secuencia de Aminoácidos , Animales , Antígenos CD , Bromodesoxiuridina/metabolismo , Embrión de Pollo , Clonación Molecular , ADN Complementario/metabolismo , Proteínas de Unión al ADN/biosíntesis , Extremidades/embriología , Humanos , Inmunohistoquímica , Hibridación in Situ , Ratones , Datos de Secuencia Molecular , Factor de Transcripción PAX3 , Factores de Transcripción Paired Box , Ratas , Homología de Secuencia de Aminoácido , Factores de Tiempo , Distribución Tisular , Factores de Transcripción/biosíntesisRESUMEN
The expression of the mouse axonal adhesive glycoprotein F3 and of its mRNA was studied on sections of mouse cerebellar cortex, cerebral cortex, hippocampus, and olfactory bulb from postnatal days 0 (P0) to 30 (P30). In cerebellar cortex, a differential expression of F3 in granule versus Purkinje neurons was observed. F3 was highly expressed during migration of and initial axonal growth from cerebellar granule cells. The molecule was then downregulated on cell bodies and remained expressed, although at low levels, on their axonal extensions. On Purkinje cells, F3 was strongly expressed on cell bodies and processes at the beginning of the second postnatal week; by P16 it was restricted to neurites of Purkinje cells subpopulations. In the cerebral cortex, the molecule was highly expressed on migrating neurons at P0; by P16, it was found essentially within the neuropil with a diffuse pattern. In the hippocampal formation, where F3 was expressed on both pyramidal and granule neurons, a clear shift from the cell bodies to neurite extensions was observed on P3. In the olfactory pathway, F3 was expressed mainly on olfactory nerve fibers, mitral cells, and the synaptic glomeruli from P0 to P3, with a sharp decline from P11 to P16. As a whole, the data show that F3 protein expression is regulated at the regional, cellular, and subcellular levels and suggest that, in different regions, it can be proposed as a reliable neuronal differentiation marker.
Asunto(s)
Envejecimiento/metabolismo , Encéfalo/metabolismo , Moléculas de Adhesión Celular Neuronal/genética , Regulación del Desarrollo de la Expresión Génica , Neuronas/metabolismo , Animales , Animales Recién Nacidos , Axones/fisiología , Encéfalo/crecimiento & desarrollo , Corteza Cerebelosa/metabolismo , Corteza Cerebral/metabolismo , Contactinas , Hipocampo/metabolismo , Ratones , Bulbo Olfatorio/crecimiento & desarrollo , Bulbo Olfatorio/metabolismo , Células de Purkinje/metabolismo , ARN Mensajero/genética , Transcripción GenéticaRESUMEN
Neural cell adhesion molecules (CAMs) of the immunoglobulin (Ig) superfamily mediate not only cell aggregation but also growth cone guidance and neurite outgrowth. In this study we demonstrate that two neural CAMs, L1-CAM and TAG-1, induce the homophilic aggregation of Drosophila S2 cells but are unable to interact with each other when expressed on different cells (trans-interaction). However, immunoprecipitations from cells co-expressing L1-CAM and TAG-1 showed a strong cis-interaction between the two molecules in the plane of the plasma membrane. TAG-1 is linked to the membrane by a glycosylphosphatidylinositol (GPI) anchor and therefore is unable to directly interact with cytoplasmic proteins. In contrast, L1-CAM-mediated homophilic cell adhesion induces the selective recruitment of the membrane skeleton protein ankyrin to areas of cell contact. Immunolabeling experiments in which S2 cells expressing TAG-1 were mixed with cells co-expressing L1-CAM and TAG-1 demonstrated that the homophilic interaction between TAG-1 molecules results in the cis-activation of L1-CAM to bind ankyrin. This TAG-1-dependent recruitment of the membrane skeleton provides an example of how GPI-anchored CAMs are able to transduce signals to the cytoplasm. Furthermore, such interactions might ultimately result in the recruitment and the activation of other signaling molecules at sites of cell contacts.
Asunto(s)
Ancirinas/metabolismo , Moléculas de Adhesión Celular Neuronal , Adhesión Celular , Glicoproteínas de Membrana/metabolismo , Moléculas de Adhesión de Célula Nerviosa/metabolismo , Animales , Línea Celular , Membrana Celular/metabolismo , Contactina 2 , Drosophila/genética , Complejo de Antígeno L1 de Leucocito , Glicoproteínas de Membrana/genéticaRESUMEN
Studies of postnatal neurogenesis have benefited from the use of a relatively non-invasive method for chronic delivery of bioactive substances to a restricted area of cortex. This method consists of the implantation of an Elvax polymer microsource of active substances close to the targeted brain surface. Receptor ligands, as well as macromolecules such as proteins, peptides and enzymes have been shown to be released by the implants in a sustained manner over weeks. Here we describe the kinetics and immunoreactivity of different immunoglobulins released in vitro and in vivo by Elvax polymer. In vitro, the immunoglobulins first diffuse during a burst phase from the pore network of the polymer matrix. Release continues during a slow phase depending on loading, porosity and volume of the matrix but also on intrinsic properties of immunoglobulins. Elvax microsources loaded either with anti-TAG-1 or with anti-HNK-1 antibodies according to the release data in vitro, are implanted on the posterior cerebellar cortex of postnatal rats during the period when the targeted antigens are expressed by the differentiating cells. After several days, the released immunoreactive antibodies are located at the antigenic sites within the cerebellar cortex close to the implants. The sustained local delivery of immunoglobulins using the Elvax implant method allows access to cell surface and matrix molecules and thereby to the mechanisms they control during postnatal neurogenesis.
Asunto(s)
Antígenos CD57/análisis , Moléculas de Adhesión Celular Neuronal , Corteza Cerebelosa/crecimiento & desarrollo , Inmunoglobulina G/administración & dosificación , Inmunoglobulina M/administración & dosificación , Glicoproteínas de Membrana/análisis , Envejecimiento , Animales , Antígenos CD57/biosíntesis , Antígenos CD57/inmunología , Corteza Cerebelosa/citología , Contactina 2 , Preparaciones de Acción Retardada , Portadores de Fármacos , Implantes de Medicamentos , Inmunohistoquímica/métodos , Glicoproteínas de Membrana/biosíntesis , Glicoproteínas de Membrana/inmunología , Polivinilos , Ratas , Ratas WistarRESUMEN
Sensory organs of the vertebrate inner ear contain two major cell types: hair cells (HCs) and supporting cells (SCs). To study the lineage relationships between these two populations, replication-defective retroviral vectors encoding marker genes were delivered to the otic vesicle of the chicken embryo. The resulting labeled clones were analyzed in the hearing organ of the chicken, called the basilar papilla (BP), after cellular differentiation. BPs were allowed to develop for 2 weeks after delivery of the retrovirus, were removed, and were processed histochemically as whole mounts to identify clones of cells. Clusters of labeled cells were evident in the sensory epithelium, the nonsensory epithelium, and in adjacent tissues. Labeled cell types included HCs, two morphologically distinct types of SCs, homogene cells, border cells, hyaline cells, ganglion cells, and connective tissue cells. Each clone was sectioned and cell-type identification was performed on sensory clones expressing retrovirally transduced beta-galactosidase. Cell composition was determined for 41 sensory clones, most of which contained both HCs and SCs. Clones containing one HC and one SC were observed, suggesting that a common progenitor exists that can remain bipotential up to its final mitotic division. The possibility that these two cell types may also arise from a mitotic precursor during HC regeneration in the mature basilar papilla is consistent with their developmental history.
Asunto(s)
Células Ciliadas Auditivas/citología , Células Ciliadas Auditivas/embriología , Células Madre/citología , Animales , Recuento de Células , División Celular/fisiología , Embrión de Pollo , Células Clonales/citología , Genes Reporteros , Mitosis/fisiología , Retroviridae , Transfección , beta-Galactosidasa/genéticaRESUMEN
F3 and TAG-1 are two closely related adhesion glycoproteins of the Ig superfamily that are both expressed by the axons of cerebellar granule cells. In an in vitro system in which cerebellar granule cells were cultured on monolayers of transfected Chinese hamster ovary (CHO) cells, we show that F3 and TAG-1 interact functionally. F3 transfectants have been shown to inhibit outgrowth and induce fasciculation of granule cell neurites. By contrast TAG-1 transfectants have no effect on these events. However, when TAG-1 is coexpressed with F3, the inhibitory effect of F3 is blocked. Two possible mechanisms may account for this functional interaction: (1) either TAG-1 and F3 compete for the same neuronal receptor, and in favor of this we observed that binding sites for microspheres conjugated with F3 and TAG-1 are colocalized on the granule cell growth cones, (2) or alternatively, F3 and TAG-1 associate in a multimolecular complex after their binding to independent receptors. Extensive co-clustering of F3 with TAG-1 can in fact be achieved by anti-TAG-1 antibody-mediated cross-linking in double-transfected CHO cells. Moreover, F3 coimmunoprecipitates with TAG-1 in Triton X-100-insoluble microdomains purified from newborn brain. These data strongly suggest that F3 and TAG-1 may associate under physiological conditions to modulate neurite outgrowth and fasciculation of the cerebellar granule cells.
Asunto(s)
Moléculas de Adhesión Celular Neuronal/fisiología , Cerebelo/fisiología , Fasciculación , Glicoproteínas de Membrana/fisiología , Neuritas/fisiología , Animales , Animales Recién Nacidos , Células CHO , Células Cultivadas , Cerebelo/citología , Contactina 2 , Cricetinae , Detergentes , Octoxinol , Pruebas de Precipitina , Unión Proteica , Solubilidad , TransfecciónRESUMEN
The adhesion molecule BEN/SC1/DM-GRASP (BEN) is a marker in the developing chicken nervous system that is also expressed on the surface of embryonic and adult hematopoietic cells such as immature thymocytes, myeloid progenitors, and erythroid progenitors. F84.1 and KG-CAM, two monoclonal antibodies to rat neuronal glycoproteins with similarity to BEN, cross-react with an antigen on rat hematopoietic progenitors, but F84.1 only also recognizes human blood cell progenitors. We have defined the antigen recognized by F84.1 as the hematopoietic cell antigen (HCA). HCA expression was detected on 40% to 70% of CD34+ fetal and adult bone marrow cells and mobilized peripheral blood cells. Precursor cell activity for long-term in vitro bone marrow cell culture was confined to the subset of CD34+ cells that coexpress HCA. HCA is expressed by the most primitive subsets of CD34+ cells, including all rhodamine 123(lo), Thy-1+, and CD38(-/lo) CD34+ adult bone marrow cells. HCA was also detected on myeloid progenitors but not on early B-cell progenitors. We also describe here the cloning and characterization of cDNAs encoding two variants of the human HCA antigen (huHCA-1 and huHCA-2) and of a cDNA clone encoding rat HCA (raHCA). The deduced amino acid sequences of huHCA and raHCA are homologous to that of chicken BEN. Recombinant proteins produced from either human or rat HCA cDNAs were recognized by F84.1, whereas rat HCA but not human HCA was recognized by antirat KG-CAM. Expression of either form of huHCA in CHO cells conferred homophilic adhesion that could be competed with soluble recombinant huHCA-Fc. The molecular cloning of HCA and the availability of recombinant HCA should permit further evaluation of its role in human and rodent hematopoiesis.
Asunto(s)
Antígenos de Superficie/aislamiento & purificación , Células de la Médula Ósea , Moléculas de Adhesión Celular Neuronal , Células Madre Hematopoyéticas/inmunología , Adulto , Secuencia de Aminoácidos , Animales , Anticuerpos Monoclonales/inmunología , Antígenos CD , Antígenos CD34/análisis , Antígenos de Superficie/biosíntesis , Antígenos de Superficie/genética , Médula Ósea/embriología , Pollos , Clonación Molecular , Secuencia de Consenso , ADN Complementario/genética , Proteínas Fetales/biosíntesis , Proteínas Fetales/genética , Proteínas Fetales/aislamiento & purificación , Regulación del Desarrollo de la Expresión Génica , Células Madre Hematopoyéticas/metabolismo , Humanos , Datos de Secuencia Molecular , Proteínas del Tejido Nervioso/biosíntesis , Proteínas del Tejido Nervioso/genética , Proteínas del Tejido Nervioso/aislamiento & purificación , Neuronas/inmunología , Neuronas/metabolismo , Especificidad de Órganos , Ratas , Proteínas Recombinantes de Fusión/inmunología , Homología de Secuencia de Aminoácido , Especificidad de la EspecieRESUMEN
We have studied the expression pattern of two cell adhesion proteins of the immunoglobin (Ig) superfamily, BEN/SC1/DM-GRASP (BEN) and the transient axonal glycoprotein TAG-1, during the development of the human nervous system. This study was performed by immunocytochemistry on sections of human embryos ranging from 4 to 13 weeks postconception. The overall distribution of the two proteins during development is very similar to that reported in other vertebrate species, but several important differences have been observed. Both proteins exhibit a transient expression on selected neuronal populations, which include the motor and the sensory neurons. In addition, BEN was also detected on virtually all neurons derived from the neural crest as well as in nonneuronal tissues. A major difference of expression with the chick embryo is that, in the motor neurons, BEN expression was not observed at early stages of development, thus arguing against a role of this molecule in pathfinding and fasciculation. BEN was observed to be restricted to subsets of motor neurons, such as the medial column at the upper limb level. Expression was also detected in a laterodorsal population of the ventral horn cells, which are likely to correspond to migrating preganglionic neurons that originate from the motor pool at the thoracic level. TAG-1 was found on commissural neurons and weakly on the sympathetic neurons; it was also detected on restricted nonneuronal populations. In addition, we observed TAG-1 expression in fibers that could correspond either to subsets of dorsal root ganglia (DRGs) central afferences (including the Ia fibers) or to the axons of association interneurons and in scattered motoneurons likely to correspond either to preganglionic neurons, to gamma-motoneurons, or to late-born motoneurons. Therefore, our results indicate that the molecular strategies used to establish the axonal scaffolding of the nervous system in humans are extremely conserved among the different vertebrates.
Asunto(s)
Axones/metabolismo , Moléculas de Adhesión Celular Neuronal/metabolismo , Glicoproteínas/metabolismo , Médula Espinal/metabolismo , Humanos , Inmunohistoquímica , Médula Espinal/crecimiento & desarrolloRESUMEN
Cell adhesion molecules belonging to the immunoglobulin superfamily promote cell aggregation and neurite outgrowth. These proteins are multidomain molecules comprising a number of distinct modules, notably Ig domains of the C2 class and fibronectin type III repeats. A subgroup of these neural adhesion molecules are linked to the membrane with a glycosylphosphatidylinositol anchor and show a more restricted pattern of expression in the embryo. Among them, the human homologue of the transient axonal glycoprotein, named TAX-1, shares a great degree of similarity at the protein level with rodent TAG-1. In the present study we set out to determine which domains of TAX-1 are involved in promoting the homophilic, adhesive properties of the molecule. We established stable Schneider-2 cell lines expressing the intact molecule, the fibronectin, or the immunoglobulin domains. The fibronectin domains were necessary and sufficient to mediate homophilic binding and induce cell aggregation, a response also observed with cells expressing the intact TAX-1 molecule. Aggregation was inhibited by the secreted form of the TAG-1 protein. On the other hand, the immunoglobulin domains by themselves were not able to induce cell aggregation. In addition, TAX-1 was localized in areas of cell contact among aggregating cells, justifying its role as an adhesion molecule.
Asunto(s)
Moléculas de Adhesión Celular Neuronal/metabolismo , Fibronectinas/metabolismo , Sustancias de Crecimiento/metabolismo , Glicoproteínas de Membrana/metabolismo , Moléculas de Adhesión Celular Neuronal/genética , Línea Celular , Contactina 2 , ADN Complementario , Sustancias de Crecimiento/genética , Humanos , Inmunoglobulinas/metabolismo , Glicoproteínas de Membrana/genética , Fosfatidilinositol Diacilglicerol-Liasa , Hidrolasas Diéster Fosfóricas/metabolismo , Unión ProteicaRESUMEN
In the external granular layer of the cerebellum, the granule cell precursors express the transient axonal glycoprotein TAG-1, a molecule involved in adhesion and neurite outgrowth. Granule cells express TAG-1 transiently, just as they extend neurites before migrating over the radial glia. The present study aims to investigate whether the expression pattern of TAG-1 is altered when granule cells develop abnormally. We studied in vivo models in which Purkinje and/or granule cell defects occur during postnatal development. These include the cerebellar mutant mice staggerer and lurcher as well as rats irradiated during postnatal development. Neither alterations in Purkinje cell differentiation nor the related granule cell loss in the mouse mutants impairs the ability of the surviving granule cell precursors to express TAG-1. Also, early granule cell loss in the X-irradiated rats do not disturb the TAG-1 expression phase in the patches of surviving granule cell precursors. Ectopic granule cells found in the adult cerebellum of X-irradiated rats do not bear the molecule, although they are located in the most superficial part of the molecular layer, occupied by the immunopositive cells a few days earlier. Thus, TAG-1 marks a very precise stage of granule cell differentiation, and the inward migration process itself is not required for the cessation of the expression. We postulate that TAG-1 may be involved in local differentiation steps restricted to the deep external granular layer such as parallel migratory routes or synchrony of axonal growth.
Asunto(s)
Moléculas de Adhesión Celular Neuronal , Cerebelo/citología , Glicoproteínas de Membrana/análisis , Proteínas del Tejido Nervioso/análisis , Neuronas/citología , Roedores/anatomía & histología , Animales , Diferenciación Celular/genética , Diferenciación Celular/efectos de la radiación , Cerebelo/efectos de la radiación , Contactina 2 , Ratones , Ratones Endogámicos C57BL , Ratones Endogámicos CBA , Ratones Mutantes Neurológicos , Neuronas/efectos de la radiación , Ratas , Ratas Wistar , Roedores/genéticaRESUMEN
We have isolated and characterized cDNA clones encoding a novel human homeobox gene, MOX2, the homologue of the murine mox-2 gene. The MOX2 protein contains all of the characteristic features of Mox-2 proteins of other vertebrate species, namely the homeobox, the polyhistidine stretch, and a number of potential serine/threonine phosphorylation sites. The homeodomain of MOX2 protein is identical to all other vertebrate species reported so far (rodents and amphibians). Outside the homeodomain, Mox-2 proteins share a high degree of identity, except for a few amino acid differences encountered between the human and the rodent polypeptides. A polyhistidine stretch of 12 amino acids in the N terminal region of the protein is also conserved among humans, rodents, and (only partly) amphibians. The chromosomal position of MOX2 was assigned to 7p22.1-p21.3.
Asunto(s)
Cromosomas Humanos Par 7 , Genes Homeobox , Proteínas de Homeodominio/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Mapeo Cromosómico , ADN Complementario , Humanos , Ratones , Datos de Secuencia Molecular , Hibridación de Ácido Nucleico , Alineación de SecuenciaRESUMEN
Chimeric polypeptides composed of the homeodomain of Antennapedia and of the C-terminus of several low molecular weight GTP-binding proteins of the rab family have been found to translocate through the membrane of cells in culture and to accumulate in the cytoplasm and nucleus. We have used these chimeric peptides to study, in intact endocrine cells, a putative role for the C-terminal domain of rab proteins in the exocytotic process. We show that the internalization of 33- and 32-amino acid polypeptides corresponding to the C-terminal domains of rab3A and rab3B blocks calcium-triggered PRL release from adult rat anterior pituitary cells maintained in primary culture. This effect is specific to rab3 since it is not observed after internalization of either rab1 or rab2 C-terminal peptides. In addition, we demonstrate that this inhibition does not require the geranylgeranylation of the internalized C-termini. As rab3B normally shows a permissive effect on exocytosis in PRL-secreting cells, we suggest that the C-terminal domains of rab3A and rab3B contain structural elements that compete with endogenous rab3 necessary for calcium-induced exocytosis.
Asunto(s)
Proteínas de Unión al GTP/fisiología , Proteínas de Homeodominio , Proteínas Nucleares , Fragmentos de Péptidos/farmacología , Adenohipófisis/efectos de los fármacos , Prolactina/metabolismo , Factores de Transcripción , Secuencia de Aminoácidos , Animales , Proteína con Homeodominio Antennapedia , Secuencia de Bases , Proteínas de Unión al ADN/genética , Proteínas de Unión al ADN/metabolismo , Exocitosis/efectos de los fármacos , Femenino , Proteínas de Unión al GTP/genética , Proteínas de Unión al GTP/metabolismo , Ionomicina/antagonistas & inhibidores , Datos de Secuencia Molecular , Adenohipófisis/metabolismo , Prenilación de Proteína , Procesamiento Proteico-Postraduccional , Ratas , Ratas Wistar , Proteínas Recombinantes de Fusión/metabolismo , Proteínas Recombinantes de Fusión/farmacología , Tasa de Secreción/efectos de los fármacos , Alineación de Secuencia , Homología de Secuencia de Aminoácido , Proteínas de Unión al GTP rab3RESUMEN
The R15 neuropeptides have been identified in the marine mollusc Aplysia californica. They compose a new family of neuropeptides acting on the cardiovascular, digestive, respiratory, reproductive and nervous systems. In this report we show that one of the members of the R15 neuropeptide family, the alpha 2 peptide is conserved in lower mammals. We have identified R15 alpha 2 immunoreactive neurons in the neurosecretory cell groups of the hypothalamus and in the brainstem of the hedgehog (Erinaceus europaeus). The majority of labeled cells were localized to the anterior periventricular part of the paraventricular nucleus and the accessory neurosecretory cell groups in the lateral hypothalamus as well as to the dorsal part of the nucleus tractus solitarii. In the paraventricular nucleus, R15 alpha 2 immunoreactive neurons also exhibit immunoreactivity for oxytocin, corticotropin releasing factor, vasoactive intestinal polypeptide and for the FMRFamide-related peptide which we found to be conserved in the hedgehog brain as well. No complete colocalization of R15 alpha 2 with any of the neuroactive substances tested, is observed. The highest degree of coexistence occurs with FMRFamide-related peptide, followed by vasoactive intestinal polypeptide, oxytocin and corticotropin releasing factor.