RESUMEN
We report the identification of a fourth member of the VPS10 domain containing receptor family, SorCS2, highly expressed in the developing and mature murine central nervous system. During early central nervous system development its main site of expression is the floor plate. In addition, high transcript levels were detected transiently in a variety of brain regions including the dopaminergic midbrain nuclei and the dorsal thalamus. Outside the nervous system expression is detected in lung and heart and transiently in a variety of mesodermally derived tissues.
Asunto(s)
Proteínas Fúngicas/biosíntesis , Proteínas del Tejido Nervioso/biosíntesis , Proteínas del Tejido Nervioso/genética , Receptores de Superficie Celular/biosíntesis , Receptores de Superficie Celular/genética , Proteínas de Saccharomyces cerevisiae , Proteínas de Transporte Vesicular , Secuencia de Aminoácidos , Animales , Northern Blotting , Sistema Nervioso Central/embriología , Sistema Nervioso Central/metabolismo , Clonación Molecular , ADN Complementario/metabolismo , Corazón/embriología , Hibridación in Situ , Pulmón/embriología , Mesencéfalo/embriología , Ratones , Datos de Secuencia Molecular , Neuronas/metabolismo , Estructura Terciaria de Proteína , Distribución TisularRESUMEN
The expression of the sorCS1 protein in the central nervous system of adult mice was studied by immunohistochemistry. A detailed mapping revealed a distribution of sorCS1 immunoreactivity in a widespread population of neurons throughout the brain. Two different types of cellular localization were observed. Many neurons exhibited a punctate cytoplasmic staining which extended into the dendrites, in other neurons sorCS1 immunoreactivity was associated with the plasma membrane. This suggests variable functions for sorCS1 in the neurons of the brain.
Asunto(s)
Encéfalo/citología , Dendritas/química , Glicoproteínas de Membrana , Proteínas de Transporte de Membrana , Neuronas/química , Receptores de Superficie Celular/análisis , Proteínas de Saccharomyces cerevisiae , Proteínas de Transporte Vesicular , Animales , Western Blotting , Membrana Celular/química , Citoplasma/química , Proteínas Fúngicas/química , Inmunohistoquímica , Ratones , Ratones Endogámicos C57BL , Neuronas/ultraestructura , Estructura Terciaria de Proteína , Conejos , Receptores de Superficie Celular/química , Receptores de Superficie Celular/inmunologíaRESUMEN
A novel receptor, SorCS, was isolated from murine brain. It shows homology to the mosaic receptor SorLA and the neurotensin receptor sortilin based on a common VPS10 domain which is the hallmark of this new receptor family. In the N-terminus of SorCS two putative cleavage sites for the convertase furin mark the beginning of the VPS10 domain, followed by a module of imperfect leucine-rich repeats and a transmembrane domain. The short intracellular C-terminus contains consensus signals for rapid internalization. The identified putative binding motifs for SH2 and SH3 domains are unique in the family of VPS10 domain receptors. SorCS is predominantly expressed in brain, but also in heart, liver, and kidney. SorCS transcripts detected by in situ hybridization in the murine central nervous system point to a neuronal expression.
Asunto(s)
Proteínas de Transporte de Membrana , Proteínas del Tejido Nervioso/genética , Receptores de Superficie Celular/genética , Receptores de LDL , Proteínas de Saccharomyces cerevisiae , Proteínas de Transporte Vesicular , Proteínas Adaptadoras del Transporte Vesicular , Secuencia de Aminoácidos , Animales , Encéfalo/metabolismo , Clonación Molecular , Proteínas Fúngicas/química , Hibridación in Situ , Glicoproteínas de Membrana/química , Ratones , Datos de Secuencia Molecular , Proteínas del Tejido Nervioso/química , ARN Mensajero/metabolismo , Receptores de Superficie Celular/química , Alineación de Secuencia , Homología de Secuencia de AminoácidoRESUMEN
The single transmembrane receptor SorLA is the mammalian orthologue of the head activator-binding protein, HAB, from hydra. The human neuronal precursor cell line NT2 and the neuroendocrine cell line BON produce head activator (HA) and respond to HA by entry into mitosis and cell proliferation. They express SorLA, and bind HA with nanomolar affinity. HA coupled to Sepharose is able to precipitate SorLA specifically proving that SorLA binds HA. Using antisera directed against extra- and intracellular epitopes we find SorLA as membrane receptor and as soluble protein released from cells into the culture medium. Cell lines differ strongly in processing of SorLA, with NT2 cells expressing SorLA mainly as membrane receptor, whereas release predominates in BON cells. Soluble SorLA lacks the intracellular domain and is shed from the transmembrane protein by a metalloprotease. Release from cells and brain slices is stimulated by HA and by phorbol ester, and it is blocked by a metalloprotease inhibitor and by lowering the temperature to 20 degrees C. Blockade of SorLA shedding and treatment of cells with SorLA antisense oligonucleotides lead to a decrease in the rate of cell proliferation. From this we conclude that SorLA is necessary to mediate the mitogenic effect of endogenous HA. HA enhances the translocation of SorLA from internal membranes to the cell surface and its internalization. In addition, HA stimulates SorLA synthesis hinting at an autocatalytic feedback loop in which the ligand activates production, processing, and translocation of its receptor.
Asunto(s)
Proteínas de Transporte de Membrana , Proteínas del Tejido Nervioso/metabolismo , Neuropéptidos/metabolismo , Receptores de LDL/metabolismo , Animales , Encéfalo/metabolismo , Encéfalo/patología , Línea Celular , Membrana Celular/metabolismo , Furina , Humanos , Proteínas Relacionadas con Receptor de LDL , Ligandos , Metaloendopeptidasas/metabolismo , Ratones , Proteínas del Tejido Nervioso/biosíntesis , Proteínas del Tejido Nervioso/genética , Procesamiento Proteico-Postraduccional , Ácido Pirrolidona Carboxílico/análogos & derivados , Receptores de LDL/biosíntesis , Receptores de LDL/genética , Solubilidad , Subtilisinas/metabolismoRESUMEN
The neuropeptide head activator stimulates cell proliferation of neuronal precursor and neuroendocrine cells. The mitogenic signaling cascade requires Ca(2+) influx for which, as we show in this paper, the growth-factor-regulated Ca(2+)-permeable cation channel, GRC, is responsible. GRC is a member of the transient receptor potential channel family. In uninduced cells only low amounts of GRC are present on the plasma membrane but, upon stimulation with head activator, GRC translocates from an intracellular compartment to the cell surface. Head activator functions as an inducer of GRC translocation in neuronal and neuroendocrine cells, which express GRC endogenously, and also in COS-7 cells after transfection with GRC. Head activator is no direct ligand for GRC, but its action requires the presence of a receptor coupled to a pertussis-toxin inhibitable G-protein. Heterologously expressed GRC becomes activated by head activator, which results in opening of the channel and Ca(2+) influx. SK&F 96365, an inhibitor specific for TRP-like channels, blocks Ca(2+) entry and, consequently, translocation of GRC is prevented. Head activator-induced GRC activation and translocation are also inhibited by wortmannin and KN-93, blockers of the phosphatidylinositol 3-kinase and of the Ca(2+)/calmodulin-dependent kinase, respectively, which implies a role for both kinases in head-activator signaling to GRC.