ABSTRACT
Wnt proteins influence many aspects of embryonic development, and their activity is regulated by several secreted antagonists, including the Xenopus Dickkopf-1 (xDkk-1) protein. xDkk-1 inhibits Wnt activities in Xenopus embryos and may play a role in induction of head structures. Here, we characterize a family of human Dkk-related genes composed of Dkk-1, Dkk-2, Dkk-3, and Dkk-4, together with a unique Dkk-3 related protein termed Soggy (Sgy). hDkks 1-4 contain two distinct cysteine-rich domains in which the positions of 10 cysteine residues are highly conserved between family members. Sgy is a novel secreted protein related to Dkk-3 but which lacks the cysteine-rich domains. Members of the Dkk-related family display unique patterns of mRNA expression in human and mouse tissues, and are secreted when expressed in 293T cells. Furthermore, secreted hDkk-2 and hDkk-4 undergo proteolytic processing which results in cleavage of the second cysteine-rich domain from the full-length protein. Members of the human Dkk-related family differ not only in their structures and expression patterns, but also in their abilities to inhibit Wnt signaling. hDkk-1 and hDkk-4, but not hDkk-2, hDkk-3 or Sgy, suppress Wnt-induced secondary axis induction in Xenopus embryos. hDkk-1 and hDkk-4 do not block axis induction triggered either by Xenopus Dishevelled (Xdsh) or Xenopus Frizzled-8 (Xfz8), both of which function to transduce signals from Wnt ligands. Thus, hDkks 1 and 4 may inhibit Wnt activity by a mechanism upstream of Frizzled. Our findings highlight the structural and functional heterogeneity of human Dkk-related proteins.
Subject(s)
Multigene Family , Proteins/genetics , Amino Acid Sequence , Animals , Base Sequence , Cell Line , DNA Primers , Female , Humans , Intercellular Signaling Peptides and Proteins , Mice , Molecular Sequence Data , Protein Processing, Post-Translational , Proteins/metabolism , RNA, Messenger/genetics , Sequence Homology, Amino Acid , Xenopus/embryology , Xenopus ProteinsABSTRACT
Members of the epidermal growth factor family of receptors have long been implicated in the pathogenesis of various tumors, and more recently, apparent roles in the developing heart and nervous system have been described. Numerous ligands that activate these receptors have been isolated. We report here on the cloning and initial characterization of a second ligand for the erbB family of receptors. This factor, which we have termed Don-1 (divergent of neuregulin 1), has structural similarity with the neuregulins. We have isolated four splice variants, two each from human and mouse, and have shown that they are capable of inducing tyrosine phosphorylation of erbB3, erbB4, and erbB2. In contrast to those of neuregulin, high levels of expression of Don-1 are restricted to the cerebellum and dentate gyrus in the adult brain and to fetal tissues.
Subject(s)
Cerebellum/physiology , Glycoproteins/physiology , Hippocampus/physiology , Nerve Growth Factors/genetics , Amino Acid Sequence , Animals , Cell Division , Chromosome Mapping , Chromosomes, Human, Pair 5 , Cloning, Molecular , Gene Expression , Genetic Linkage , Humans , In Situ Hybridization , Ligands , Membrane Proteins/genetics , Mice , Mice, Inbred C57BL , Molecular Sequence Data , Neuregulins , Phosphotyrosine/metabolism , Receptors, Growth Factor/physiology , Sequence Alignment , Sequence Homology, Amino Acid , Tissue DistributionABSTRACT
Recently we identified three novel Schwann cell mitogens named GGF (glial growth factor)-I (34 kDa), GGF-II (59 kDa), and GGF-III (45 kDa), and provided evidence that they are three distinct but structurally related members of a larger family of factors, which includes heregulin, neu differentiation factor, and acetylcholine receptor-inducing activity (ARIA). We report here the characterization of the mitogenic and trophic activities for all three forms of GGF on rat Schwann cells and several other cell types. GGF-I, GGF-II, and GGF-III are potent mitogens for rat Schwann cells in vitro at nanomolar concentrations, whereas at lower concentrations they promote Schwann cell survival, in the absence of cAMP elevating agents. Forskolin, an adenylate cyclase activator, potently synergizes with the GGFs by an indirect mechanism, possibly involving transcriptional activation of GGF receptor(s). In addition, the GGFs stimulate DNA synthesis in rat glioma C6 cells, and in SK-BR-3 cells, which overexpress the p185 neu/erbB2. Fibroblasts obtained from different sources are weakly stimulated by GGFs, whereas PC12 cells are unable to respond under a variety of experimental conditions. These observations are consistent with the proposal that GGF-I, GGF-II, and GGF-III are a set of potent glial cell mitogens and putative ligands of members of the EGF receptor family, namely p185 neu/erbB2, p160/erbB3, and p180/erbB4, which may play important roles in the development, regeneration, and tumor biology of the peripheral nervous system.
Subject(s)
Mitogens/pharmacology , Nerve Tissue Proteins/pharmacology , Neuroglia/drug effects , Animals , Cell Division/drug effects , Cell Line , Colforsin/pharmacology , Cricetinae , Cyclic AMP/physiology , DNA/biosynthesis , Enzyme-Linked Immunosorbent Assay , Glia Maturation Factor , Mice , Nerve Tissue Proteins/isolation & purification , PC12 Cells , Rats , Schwann Cells/drug effects , Schwann Cells/metabolism , Sciatic Nerve/cytology , Sciatic Nerve/drug effects , Tumor Cells, CulturedABSTRACT
ARIA is a member of a family of polypeptide growth and differentiation factors that also includes glial growth factor (GGF), neu differentiation factor, and heregulin. ARIA mRNA is expressed in all cholinergic neurons of the central nervous systems of rats and chicks, including spinal cord motor neurons. In vitro, ARIA elevates the rate of acetylcholine receptor incorporation into the plasma membrane of primary cultures of chick myotubes. To study whether ARIA may regulate the synthesis of junctional synaptic acetylcholine receptors in chick embryos, we have developed riboprobes and polyclonal antibody reagents that recognize isoforms of ARIA that include an amino-terminal immunoglobulin C2 domain and examined the expression and distribution of ARIA in motor neurons and at the neuromuscular junction. We detected significant ARIA mRNA expression in motor neurons as early as embryonic day 5, around the time that motor axons are making initial synaptic contacts with their target muscle cells. In older embryos and postnatal animals, we found ARIA protein concentrated in the synaptic cleft at neuromuscular junctions, consistent with transport down motor axons and release at nerve terminals. At high resolution using immunoelectron microscopy, we detected ARIA immunoreactivity exclusively in the synaptic basal lamina in a pattern consistent with binding to synapse specific components on the presynaptic side of the basal lamina. These results support a role for ARIA as a trophic factor released by motor neuron terminals that may regulate the formation of mature neuromuscular synapses.
Subject(s)
Avian Proteins , Basement Membrane/metabolism , Nerve Tissue Proteins/analysis , Neuromuscular Junction/metabolism , Synapses/metabolism , Amino Acid Sequence , Animals , Chick Embryo , Microscopy, Electron , Molecular Sequence Data , Motor Neurons/metabolism , Neuregulin-1 , Neuromuscular Junction/embryology , Neuromuscular Junction/ultrastructure , RNA, Messenger/analysis , Rats , Spinal Cord/embryology , Spinal Cord/metabolism , Synapses/ultrastructureABSTRACT
Skeletal muscle ACh receptors (AChRs) accumulate at neuromuscular junctions (nmjs) at least partly because of the selective induction of AChR subunit genes in subsynaptic myotube nuclei by the motor nerve terminal. Additionally, mammalian AChRs undergo a postnatal change in subunit composition from embryonic (alpha 2 beta gamma delta) to adult (alpha 2 beta epsilon delta) forms, a switch that also depends on innervation. ARIA, a protein purified from chicken brains based on its ability to induce AChR synthesis in primary chick muscle cells, is a strong candidate for being the molecule responsible for these early developmental events. ARIA mRNA has been detected in embryonic motor neurons during synapse formation, and the gene continues to be expressed postnatally. In this report, we provide evidence that ARIA-like immunoreactivity is concentrated in rat motor nerve terminals from early postnatal ages, and that it can be detected in motor neurons in E18 embryos. ARIA is also detectable in axons within colchicine-treated sciatic nerves, suggesting that the protein in the nerve terminal has been transported from the cell body. ARIA mRNA is present in, but not restricted to, cholinergic neurons. Likewise, we report here that ARIA-like immunoreactivity is present in some noncholinergic central synapses. We also present evidence that isoforms of ARIA are differentially distributed among functionally distinct classes of neurons.
Subject(s)
Avian Proteins , Nerve Endings/metabolism , Nerve Tissue Proteins/metabolism , Neuromuscular Junction/metabolism , Synapses/metabolism , Animals , Animals, Newborn , Axons/metabolism , Embryo, Mammalian/metabolism , Embryonic and Fetal Development , Enzyme-Linked Immunosorbent Assay , Female , Motor Neurons/metabolism , Neuregulin-1 , Rats , Rats, Inbred Strains , Receptors, Cholinergic/metabolism , Tissue DistributionABSTRACT
Glial growth factors (GGFs) were purified from bovine pituitaries using an in vitro rat Schwann cell mitogenesis assay. In addition to an approximately 34-kDa species termed GGF-I, similar in molecular mass to a previously identified molecule (Lemke, G. E., and Brockes, J. P. (1984) J. Neuroscience 4, 75-83), two species named GGF-II and GGF-III were characterized with apparent molecular masses of approximately 59 and approximately 45 kDa, respectively. Highly purified preparations of all species share a similar dose-dependent stimulation of Schwann cell DNA synthesis at nanomolar concentrations. Forskolin synergizes with all three GGFs, shifting their dose dependence 3-8-fold into the sub-nanomolar range. The GGFs, which contain N-linked carbohydrate groups not essential for their in vitro mitogenic effects, are three distinct members of a novel family of glial cell mitogens.
Subject(s)
Nerve Tissue Proteins/isolation & purification , Pituitary Gland/chemistry , Schwann Cells/drug effects , Animals , Cattle , Cells, Cultured , Chromatography, Affinity , Chromatography, Gel , Chromatography, High Pressure Liquid , Chromatography, Liquid , DNA Replication/drug effects , Durapatite , Electrophoresis, Polyacrylamide Gel , Glia Maturation Factor , Growth Inhibitors/isolation & purification , Growth Inhibitors/pharmacology , Hydroxyapatites , Molecular Weight , Nerve Tissue Proteins/pharmacology , Rats , Schwann Cells/cytology , Schwann Cells/metabolism , Sciatic Nerve/cytologyABSTRACT
Glial growth factors, proteins that are mitogenic for Schwann cells, and several ligands for the p185erbB2 receptor, are products of the same gene. Alternative splicing of the messenger RNA generates an array of putative membrane-attached, intracellular and secreted signalling proteins, at least some of which are expressed in the developing spinal cord and brain. These factors are probably important in the development and regeneration of the nervous system.
Subject(s)
Brain/physiology , Nerve Tissue Proteins/metabolism , Oncogene Proteins, Viral/metabolism , Schwann Cells/metabolism , Spinal Cord/physiology , Alternative Splicing , Amino Acid Sequence , Animals , Base Sequence , Cattle , Cells, Cultured , Cloning, Molecular , Glia Maturation Factor , In Situ Hybridization , Mice , Molecular Sequence Data , Organ Specificity , Phosphorylation , RNA, Messenger/metabolism , Receptor, ErbB-2Subject(s)
Axons/physiology , Growth Substances/pharmacology , Schwann Cells/drug effects , Animals , Colforsin/pharmacology , Cyclic AMP/metabolism , Fibroblast Growth Factors/pharmacology , Glia Maturation Factor , Growth Inhibitors/pharmacology , Nerve Tissue Proteins/pharmacology , Platelet-Derived Growth Factor/pharmacology , Schwann Cells/metabolism , Schwann Cells/physiologyABSTRACT
Brief treatment of iron-saturated hen ovotransferrin with dithiothreitol selectively cleaves the disulphide bridge between residues 478 and 671, which is in the C-terminal domain of the protein. The reduced alkylated protein is less stable than the native protein, and its iron-binding properties are different. A fluorescent derivative was prepared by coupling N-iodoacetyl-N'-(5-sulpho-1-naphthyl)ethylenediamine to the thiol groups.