Temnocephalan symbionts of the freshwater crayfish Cherax quadricarinatus from northern Australia

Four species of turbellarian temnocephalan symbionts (Platyhelminthes: Temnocephalida) are reported for the first time from the external surfaces of Cherax quadricarinatus, a freshwater crayfish from northern Australia. Three of these species — Temnocephala rouxii Merton, 1913, Notodactylus handschini (Baer, 1945), and Diceratocephala boschmai Baer, 1953 — are known previously from related crayfish in New Guinea. The newly discovered fourth species, Decadidymus gulosus n. gen., n. sp., has an unusual combination of characters linking it with both the Temnocephalidae and the Scutariellidae. Together the four species possess an array of characters that challenges current concepts of families in the order. D. boschmai has an almost completely ciliated epidermis, a feature otherwise unknown in the order.     

Epidermis and sensory receptors of Temnocephala minor (Plathelminthes, Rhabdocoela, Temnocephalida): an electron microscopic study

 The epidermis, rhabditic glands and receptors of the commensal flatworm Temnocephala minor are described using electron microscopic techniques. The epidermis is syncytial and non-ciliated at the anterior body end; it bears folds, microvilli and other structures which differ according to the body side. The nuclei are located intraepithelially and distally from the basal membrane. Long cilia occur at the posterior end anteriorly from the sucker. All receptor structures described belong to a single morphological type and stand in groups arising from epidermal pits. On the tentacles these groups are regularly distributed. Each receptor has a single cilium and a long rootlet. More than 15 000 receptors of this type have been estimated to occur on the surface of a single medium-sized specimen of T. minor. Although the total number of receptor structures appears very high, the number of different receptor types is extremely low in comparison to other taxa of flatworms. Accepted: 8 July 1997     

Quantitative flow cytometric analysis of expression of tumor necrosis factor receptor types I and II on mononuclear cells

Abstract

Background: Tumor necrosis factor (TNF)-α is an inflammatory cytokine, the biological effects of which are mediated by the interaction with specific membrane-bound receptors. To assess TNF-α receptor (TNFR) expression, it is important to estimate both the number of cells that carry these receptors and the number of receptors per cell, because the cell fate depends on the balance between TNFRI and TNFRII signaling. Objective: The aim of the present study was to develop an optimized protocol to estimate the level of expression of membrane-bound TNFRI and TNFRII, using QuantiBRITE PE calibration beads. Materials and methods: The percentage of cells that expressed membrane-bound TNFRI and TNFRII and the mean number of receptors per cell were determined by flow cytometry using PE-labeled antibodies against TNFR. To create a calibration curve and convert cell fluorescence intensity values to absolute numbers of receptors, we used QuantiBRITE PE beads. Results: CD19⁺ B lymphocytes had the least percentage of cells expressing TNFRI and the greatest number of receptor molecules per cell, whereas CD3⁺ T lymphocytes had the greatest percentage of cells expressing TNFRII and the lowest density of these receptors. We also established that stimulation of peripheral blood mononuclear cells (PBMCs) with the lipopolysaccharide (LPS) significantly increased the number of TNFRI and TNFRII on CD14⁺ monocytes. Conclusion: Application of the protocol-identified differences in the percentage of cells that expressed TNFRs, as well as the absolute number of receptors per cell, among different subpopulations of PBMCs, and between PBMCs cultured with and without LPS.     

Ciliary receptors associated with the mouth and pharynx of Acoela (Acoelomorpha): a comparative ultrastructural study

The ultrastructure and distribution of receptor cells near the mouth and (where present) the pharynx of Hofstenia miamia, Proporus bermudensis, Conaperta thela, and Convoluta convoluta (Acoela) were investigated by transmission electron microscopy and confocal laser scanning microscopy of specimens stained with a fluorescence marker for actin. Five types of monociliary receptors were identified: (1) non‐collared receptors with a single long and narrow ciliary rootlet; (2) non‐collared receptors with a wide main ciliary rootlet and a smaller posterior rootlet; (3) non‐collared receptors with a single wide and hollow ciliary rootlet with a granulated core; (4) Collar (?) receptors with obliquely radial filament bundles in the cell apex and with a single hollow ciliary rootlet composed of numerous strand‐like elements; and (5) Collar receptors lacking a striated rootlet but with a granular body (swallow's nest rootlet). While H. miamia bears the first two receptor types, P. bermudensis has receptors of type 1, 3 and 5, and Cona. thela and Conv. convoluta have receptors of type 3, 4 and 5. The density of receptors is generally highest at the anterior body tip, regardless of where the mouth is located. Most receptor types occur scattered over the whole body but type 2 receptors of H. miamia are restricted to the pharynx and mouth region. The lack of a common receptor type specific for the mouth and pharynx of the investigated species points to an independent origin of the pharynges in Hofsteniidae and in Proporidae and of the mouth tube in Convolutidae. Moreover, the homology of the so‐called collar receptors in Acoela with typical collar receptors in other invertebrates is questioned.     

Two ciliate sense receptors in the larva of Austramphilina elongata Johnston, 1931 (Amphilinidea)

Summary The ultrastructure of a uniciliate and a quadruciliate receptor in the anterior end of the larva of Austramphilina elongata is described on the basis of serial sections. The uniciliate receptor has numerous branched and interconnected microvilli at its surface, several rings forming the electron dense collar, and cross-striated rootlets diverging from the basal body of the cilium. The quadruciliate receptor has four short club-shaped sensory cilia and a single electron-dense collar.Abbreviations used in figures ec electron-dense collar - ep epidermis - m microvilli - nt neurotubules - pe process of electron-dense collar - r rootlet of cilium - sc sensory cilium - sd septate desmosome     

Epidermale Collar-Receptoren der Nematoplanidae und Polystyliphoridae (Plathelminthes,Unguiphora)

Zusammenfassung Für die Nematoplanidae und die Polystyliphoridae (Proseriata) wird ein besonderer Collar-Receptor-Typus beschrieben, der vom Grundmuster der entsprechenden Receptoren der übrigen Proseriata und der Rhabdocoela in zwei Punkten abweicht: (1) Die Receptoren ziehen zwischen Epidermiszellen zur Körperoberfläche. (2) Im distalen Bereich der Receptoren ist im Cytoplasma eine elektronendichte Manschette differenziert. — Zusammen mit anderen Organisationsmerkmalen wird die Manschette dieses Receptor-Typus als Synapomorphie der Nematoplanidae und Polystyliphoridae, des monophyletischen Taxon Unguiphora Sopott-Ehlers, 1984, bewertet.

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Epidermal collar receptors of the nematoplanidae and the polystyliphoridae (Plathelminthes, Unguiphora)

Summary In the Nematoplanidae and the Polystyliphoridae (Proseriata) a special collar receptor type is found, which differs in two points from the basic pattern of these receptors in the other Proseriata and in the Rhabdocoela: (1) The receptors run between epidermal cells to the surface. (2) In the distal region of the receptor cells an electron-dense cuff is developed. The cuff of these receptors, together with some other features of organisation, is considered to be a synapomorphy of the Nematoplanidae and the Polystyliphoridae, which together form the monophyletic taxon Unguiphora Sopott-Ehlers, 1984.

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Abkürzungen in den Abbildungen ar Ringwurzel - cop männliches Begattungsorgan - epc Epidermiszelle - ge Germar - kc Kinocilium - mv Mikrovilli - ph Pharynx - pro Prostatoidorgan - sc Stereocilien (modifizierte Mikrovilli) - sd septierte Desmosomen - te Testes - vi Vitellarien     

Some aspects of the gross and fine structure of the amphibian papilla in the labyrinth of the newt, Triturus cristatus

Each receptor cell in the sensory macula bears a number of stereocilia and one peripherally located kinocilium; in the two halves of the macula, the kinocilia lie on opposite sides of their associated stereocilia. The morphological axes of the receptor cells are approximately parallel to the long axis of the papilla. The gelatinous cupula overlying the macula extends almost to the opposite wall of the papilla. These structural features are discussed in connection with both the proposed function of the papilla as a vibration detector and the possible evolutionary relationships with other acousticolateralis receptors.     

Sensory Spots of Echinoderes capitatus (Zelinka, 1928) (Kinorhyncha,Cyclorhagida)

The sensory spots of Echinoderes capitatus from the Gulf of Trieste were examined by transmission and scanning electron microscopy. Their arrangement is bilaterally symmetrical and is species-specific. At the cuticle surface the sensory spot appears as a rounded to ovoid area of small cuticular papillae in which two pores open. The sensory organ consists of two different sensory cells, the monociliary receptor and the collar receptor, and one sheath cell. The course of the axons and their connections to the nervous system are described. A survey of collar receptors among invertebrates is given. A comparison of the sensory spots within Kinorhyncha and a comparison with the flosculi of Priapulida and the N-flosculi of Loricifera is made. A possible homology of these three structures is discussed.     

Head sensory organs of Halobiotus stenostomus (Eutardigrada, Hypsibiidae)

The structure and arrangement of sensory organs in the tardigrade Halobiotus stenostomus (Richters 1908) have been studied using transmission and scanning electron microscopy techniques. The sensory organs found on the head of H. stenostomus are as follows: the circumoral sensory field, cephalic papillae, anterolateral and posterolateral sensory fields, and suboral sensory region. Four types of ciliated receptor structures are described in the sensory fields. The lateral sensory fields contain two types of receptor endings, dense and lucent, which differ in the presence or absence of a collar and in the structure of the outer dendrite segment. Two more types of receptor endings, ultrastructurally differing from the lateral sensory field receptors, are located in the suboral sensory region. Receptors with an asymmetric collar have been found, and a receptor ending without a collar is described for the first time in tardigrades. Unlike in other species studied, the sensory organs of H. stenostomus lack the lymph cavity surrounding the outer receptor segment. Similarity and differences in the ultrastructure of receptors between H. stenostomus and other species of Eutardigrada and Heterotardigrada are discussed.     

The IGF-I Receptor in Mitogenesis and Transformation of Mouse Embryo Cells: Role of Receptor Number

The type 1 receptor for insulin-like growth factors (IGF-IR) plays an important role in the growth and transformation of several types of cells. We have investigated the role of IGF-IR number in IGF-I-mediated mitogenesis and transformation of mouse embryo fibroblasts. We have used R⁻cells (3T3-like cells originating from mouse embryos with a targeted disruption of the IGF-IR genes) transfected with a plasmid expressing the human IGF-IR cDNA to generate clones with receptor numbers ranging from zero to 10⁶receptors per cell. In this model, between 15,000 and 22,000 receptors per cell are sufficient to render mouse embryo cells competent to grow in serum-free medium supplemented solely with IGF-I. For growth in soft agar, 30,000 receptors per cell seem to be the minimum requirement. These experiments indicate that a small increment in the number of receptors per cell, well within the physiological range, can modulate the mitogenic and transforming activities of the IGF-IR in 3T3-like cells.     

Quantification of receptor targeting aptamer binding characteristics using single-molecule spectroscopy

This experimental design presents a single molecule approach based on fluorescence correlation spectroscopy (FCS) for the quantification of outer membrane proteins which are receptors to an aptamer specifically designed to target the surface receptors of live Salmonella typhimurium. By using correlation analysis, we also show that it is possible to determine the associated binding kinetics of these aptamers on live single cells. Aptamers are specific oligonucleotides designed to recognize conserved sequences that bind to receptors with high affinity, and therefore can be integrated into selective biosensor platforms. In our experiments, aptamers were constructed to bind to outer membrane proteins of S. typhimurium and were assessed for specificity against Escherichia coli. By fluorescently labeling aptamer probes and applying FCS, we were able to study the diffusion dynamics of bound and unbound aptamers and compare them to determine the dissociation constants and receptor densities of the bacteria for each aptamer at single molecule sensitivity. The dissociation constants for these aptamer probes calculated from autocorrelation data were 0.1285 and 0.3772 nM and the respective receptor densities were 42.27 receptors per µm² and 49.82 receptors per µm². This study provides ample evidence that the number of surface receptors is sufficient for binding and that both aptamers have a high‐binding affinity and can therefore be used in detection processes. The methods developed here are unique and can be generalized to examine surface binding kinetics and receptor quantification in live bacteria at single molecule sensitivity levels. The impact of this study is broad because our approach can provide a methodology for biosensor construction and calculation of live single cell receptor‐ligand kinetics in a variety of environmental and biological applications. Bioeng. 2011; 108:1222–1227. © 2010 Wiley Periodicals, Inc.     

Dispersal of Trichogramma galloi in corn for the control of Diatraea saccharalis

Dispersal of natural enemies is an important part of a biological pest-control programme. In augmentative biological control programmes, studies of dispersal are essential to determine the optimal number of release points per hectare. This study evaluated the kind of infestation that is most suitable for conducting these studies, and the dispersal of Trichogramma galloi in corn on eggs of Diatraea saccharalis. Corn plants with eggs laid directly by D. saccharalis moths showed higher rates of parasitism by T. galloi. The dispersal radii of T. galloi were 11.8 and 12.1 m in V6 (collar of sixth leaf visible) and V8 (collar of eighth leaf visible), respectively, and the dispersal areas were 176 and 187 m² for the two corn phenological stages. Using these data, we determined that 58 and 54 release points are required per hectare to effect a homogeneous coverage of the release area by parasitoids on the corn phenological stages V6 and V8, respectively.     

Modeling of Neuropeptide Receptors Y1, Y4, Y5, and Docking Studies with Neuropeptide Antagonist Analogues: Implications for Selectivity

Abstract

Neuropeptide Y (NPY), receptors belong to the G-protein coupled receptor superfamily. NPY mediates several physiological responses, such as blood pressure, food intake, sedation. These actions of NPY are mediated by six receptor subtypes denoted as Y₁-Y₅ and y₆. Modeling of receptor subtypes and binding site identification is an important step in developing new therapeutic agents. We have attempted to model the three NPY receptor types, Y1, Y4, and Y5 using homology modeling and threading methods. The models are consistent with previously reported experimental evidence. To understand the interaction and selectivity of NPY analogues with different neuropeptide receptors, docking studies of two neuropeptide analogues (BVD10 and BVD15) with receptors Y1 and Y4 were carried out. Results of the docking studies indicated that the interaction of ligands BVD10 and BVD15 with Y1 and Y4 receptors are different. These results were evaluated for selectivity of peptide analogues BVD10 and BVD15 towards the receptors.     

Monociliary receptors in interstitial Proseriata and Neorhabdocoela (Turbellaria Neoophora)

Summary The ultrastructure of monociliary receptors in 10 species of the Proseriata and Neorhabdocoela is described, with particular reference to the epidermal dendritic part.Sensory cells with a single kinocilium situated at the level of the distal epidermis membrane are considered as mechano- or chemoreceptors.There exist sensory cells with a dendrite penetrating one epidermis cell and bearing an embedded kinocilium and a collar of 8 stereocilia or ridges with a fribrillose substructure. These collared receptors probably function as mechanoreceptors.In comparison with collared sensory cells in species of other turbellarian orders, the embedded receptors in the Proseriata and Neorhabdocoela are more advanced and possess synapomorphous characteristics. With the embedded receptors a new evidence is given for the close phylogenetic relationship between the Proseriata and Neorhabdocoela.The distribution of collared cells in the animal system and their phylogenetic implication for a choanoflagellate origin of the Metazoa are briefly discussed.List of abbreviations ar annular rootlet - bm basement membrane - cb crystalline body - cc collar cell - cw cell web - cwt cell web-thickening - d dendrite - kc kinocilium - lm longitudinal musculature - mv microvilli - n nerve - nt neurotubuli - pb parenchymal branches - r rootlet - rd ridges - rh rhabdite - rm ring musculature - sc stereocilia - sd septate desmosomes - tm transversal musculature - u ultrarhabdites - za zonula adhaerens     

Scanning electron microscope study of epidermal surface of six ectosymbiotic Temnocephala species (Platyhelminthes) from Argentina

The epidermis of six ectosymbiontic Temnocephala species (T. axenos, T. chilensis, T. digitata, T. microdactyla and T. pignalberiae from freshwater crustaceans and T. iheringi from a mollusc) from Argentina examined using scanning electron microscopy revealed characters indicating their relationships with other members of the Platyhelminthes and with the congeneric Australian and New Zealand species. In all species, the whole surface is covered with microvilli and no locomotory cilia were observed. Aggregates of monociliated receptors are on the tentacles of all species and on the ventral surfaces of three. Furthermore, T. axenos and T. chilensis show other ciliated structures interpreted as collar receptors, such as those described for some turbellarian groups (e.g. Proseriata and Rhabdocoela). Two species (T. digitata and T. iheringi) show structures that are probably related to the duo-gland adhesive system.     

Structural characterization and agonist binding to human α4β2 nicotinic receptors

The Cys-loop receptor super-family of neurotransmitter-gated ion channels mediates fast synaptic transmission throughout the human nervous system. These receptors exhibit widely varying pharmacologies, yet their structural characterization has relied heavily on their homology with the naturally abundant muscle-type Torpedo nicotinic acetylcholine receptor. Here we examine for the first time the structure of a human α4β2 neuronal nicotinic acetylcholine receptor. We show that human α4β2 nicotinic receptors adopt a secondary/tertiary fold similar to that of the Torpedo nicotinic receptor with a large proportion of both α-helix and β-sheet, but exhibit a substantially increased thermal stability. Both receptors bind agonist, but with different patterns of agonist recognition – particularly in the nature of the interactions between aromatic residues and the agonist quaternary amine functional group. By comparing α4β2 and Torpedo receptors, we begin to delineate their structural similarities and differences.     

NMDA受体通道的结构与功能

近来用分子克隆方法对N-甲基-门冬氨酸受体(NMDA受体)通道的分子结构进行了广泛的研究.这些研究清楚地显示了NMDA受体通道的分子多样性,为NMDA受体通道的在体功能多样性提供了基础.已获得的克隆为研究这些受体通道分布和生理作用提供了有价值的工具.     

Olfactory receptors in aquatic and terrestrial vertebrates

In species representing different levels of vertebrate evolution, olfactory receptor genes have been identified by molecular cloning techniques. Comparing the deduced amino-acid sequences revealed that the olfactory receptor gene family of Rana esculenta resembles that of Xenopus laevis, indicating that amphibians in general may comprise two classes of olfactory receptors. Whereas teleost fish, including the goldfish Carassius auratus, possess only class I receptors, the `living fossil' Latimeria chalumnae is endowed with both receptor classes; interestingly, most of the class II genes turned out to be pseudogenes. Exploring receptor genes in aquatic mammals led to the discovery of a large array of only class II receptor genes in the dolphin Stenella Coeruleoalba; however, all of these genes were found to be non-functional pseudogenes. These results support the notion that class I receptors may be specialized for detecting water-soluble odorants and class II receptors for recognizing volatile odorants. Comparing the structural features of both receptor classes from various species revealed that they differ mainly in their extracellular loop 3, which may contribute to ligand specificity. Comparing the number and diversity of olfactory receptor genes in different species provides insight into the origin and the evolution of this unique gene family. Accepted: 29 July 1998     

Thyroxine and propylthiouracil effects in vivo on alpha and beta adrenergic receptors in rat heart

Dihydroalprenolol and dihydroergocryptine were used to measure β and α adrenergic receptors respectively in heart ventricles from control, thyroxine (T₄)-treated and propylthiouracil (PTU)-treated rats. Ventricles from T₄-treated rats show an increase in the number of β receptors and a decrease in the number of α receptors. The β to α receptor ratio increases six fold. No change in binding affinity of the β receptor is observed but a decrease occurs in the affinity of the α receptor in ventricles from T₄-treated hearts. Ventricles from PTU-treated hearts show a small decrease in the number of β receptors but a large decrease in the number of α receptors. The binding affinity for both the α and β receptor is increased in the PTU-treated rats. The total number of α plus β receptors is increased in the T₄-treated rats and decreased in the PTU-treated rats.