Stanley Caveney

Control of gap junction formation in early mouse embryos

Intercellular communication via gap junctions begins in the eight-cell stage in early mouse embryos. We have studied the timing of this event in relation to compaction, and have begun to explore some of the possible control mechanisms underlying it. Gap junction formation was inferred by measuring ionic coupling as well as by observing the intercellular transfer of fluorescent dye. Embryos were obtained early on Day 3 of pregnancy by flushing the oviducts of HA/ICR mice that had been mated with CB6F1/J males. Gap junctions were detected only in those embryos which had achieved the fully compacted state. Inhibition of protein synthesis by cycloheximide treatment beginning as early as the late four-cell stage failed to block compaction or the acquisition of gap junctions, demonstrating that the necessary proteinaceous components are present in advance of these events. In order to test the possibility that gap junctions could be induced to form prematurely, fully compacted, communication-competent eight-cell embryos were aggregated with two- or four-cell embryos. Even after 10 hr of aggregation, no interembryonic gap junctions could be detected. Fully compacted eight-cell embryos when aggregated with each other, however, became ionically coupled within 3-5 hr. The number of interembryonic junctional channels was judged to be effectively small, since the aggregated embryos exhibited obvious ionic coupling but very weak dye coupling. In contrast to gap junction formation within embryos, junction formation between embryos was blocked by cycloheximide. These results demonstrate that gap junction formation in early mouse embryos is under precise temporal control, involving the assembly or mobilisation of preexisting components. This stockpile of components is either unavailable or insufficient to allow the formation of additional gap junctions between aggregated communication-competent embryos without new protein synthesis.

New observations on the secondary chemistry of world Ephedra (Ephedraceae)

For several millennia, stem extracts of Ephedra (Ephedraceae, Gnetales) have been used as folk medicines in both the Old and New World. Some species were used in treatments of questionable efficacy for venereal disease in North America during the last century. Many Eurasian species produce phenylethylamine alkaloids, mostly ephedrine and pseudoephedrine, that interact with adrenergic receptors in the mammalian sympathetic nervous system. Asian Ephedra have been used recently in the clandestine manufacture of a street drug, methamphetamine. Although ephedrine alkaloids are not detectable in New World species of Ephedra, together with Asian species they contain other nitrogen-containing secondary metabolites with known neuropharmacological activity. Many mesic and particularly xeric species worldwide accumulate substantial amounts of quinoline-2-carboxylic acids, or kynurenates, in their aerial parts. Many species of Ephedra accumulate cyclopropyl amino acid analogues of glutamate and proline in their stems and roots, and particularly in the seed endosperm. Mesic species synthesize substantial amounts of three L-2-(carboxycyclopropyl)glycine stereomers rarely seen in nature. A cyclopropyl analogue of proline with known antimicrobial activity, cis-3,4-methanoproline, is found in large amounts in the stems and seeds of many Ephedra species. The ability to synthesize cyclopropyl amino acids may be an ancestral feature in the taxon. The natural function in the taxon of these three groups of secondary compounds remains to be established.

Genetic analysis of the xenobiotic resistance-associated ABC gene subfamilies of the Lepidoptera.

Some ATP‐binding cassette (ABC) transporters of subfamilies B, C and G confer resistance to xenobiotics including insecticides. We identified genes of these subfamilies expressed by the lepidopterans Trichoplusia ni and Bombyx mori. The B. mori genome includes eight, six and 13 ABC‐B, ‐C and ‐G genes, respectively, which encode P‐glycoprotein, multidrug resistance protein, MRP, and breast cancer resistance protein, BCRP, homologues. Among the ABC‐C and ‐G subfamilies, gene duplication contributes to protein diversity. We have identified three ABC‐B and two ABC‐C T. ni genes. Analyses of the T. ni MRP (TrnMRP) revealed unique features, including the potential for TrnMRP4 hyperglycosylation and the alternative splicing of TrnMRP1. Taken together, these attributes of moth multidrug resistance‐associated ABCs may confer distinct functional capacities to xenobiotic efflux.

Superposition optics and the time of flight in onitine dung beetles

Abstract Dung beetles fly to fresh dung, with vision essential for flight navigation. The daily period of flight varies among different species: some beetles fly only in sunlight, others only when ambient light levels change rapidly during dusk or dawn and others in the constant dark of night. Measurements of the optical properties of the lenses, eye geometry and photoreceptor dimensions were used in a computer ray-tracing model to determine the optical performance of the superposition eyes of nine species of onitine dung beetles. Eye sensitivity to light is determined mainly by body size, by the refractive-index parameters and size of the crystalline cones, and by the photoreceptor dimensions. Based on the optics of the ommatidial lenses and absorption of light in the retina, the most sensitive eyes, found in the crepuscular-nocturnal beetles, are 85 times or nearly two log units more sensitive than the eyes of the diurnal beetles. Three possible criteria are considered to determine the best position for the retina: maximum amount of light absorbed in the target rhabdom; maximum amount of light falling on the target rhabdom (best focus); and maximum resolution. The structure and physiological optics of the superposition compound eyes of an onitine dung beetle are matched to the range of light intensities at which it flies.

Elevation of ionic conductance between insect epidermal cells by β-ecdysone in vitro

Abstract Electrophysiological methods reveal that the cell-to-cell movement of inorganic ions in the epidermis of the beetle larva is facilitated by exposing the tissue to β-ecdysone in vitro . After exposure to 2 × 10 −6 M β-ecdysone for 24 hr, the resistivity of the intercellular pathway drops by 30%, from 389 Ωcm to 264 Ωcm. This response does not occur when α-ecdysone is used for extended incubation periods. As the resistivity of the epidermal cytoplasm in the absence (64 Ωcm) and presence of β-ecdysone (65 Ωcm) is constant, the hormone must exert its effect at the cell junctions. A simple geometrical model for the epidermal monolayer allows one to calculate that the ionic permeability of the junctional membrane increases by 66% in cells exposed to β-ecdysone for 24 hr in vitro .

Intercellular communication in a positional field: Movement of small ions between insect epidermal cells☆

Abstract The epidermal cells of the developing insect form a two-dimensional isodiffusion network of low resistance to the intercellular movement of at least one small inorganic ion. The spatial gradient in positional information found within the epidermis of each body segment could not be correlated with any quantitative regional or directional differences in intercellular ionic conductance. The lumped resistivity of the intercellular pathway during all stages of development analyzed (450 Ωcm) is only four times greater than the assumed resistivity of cytoplasm alone (100 Ω cm). The specific resistance of junctional membrane is at least three orders of magnitude less than the specific resistance of nonjunctional membrane. Little reduction in ionic conductance could be detected across the cells that form the intersegmental membrane, separating the positional fields of adjacent segments, in the pupa and adult. It is unlikely that a restricted spatial distribution of low-resistance pathways plays a role in the maintenance of the boundaries of neighboring developmental fields. No anteroposterior gradient in bioelectric potential was detected within the segment.

Ancestry of neuronal monoamine transporters in the Metazoa

SUMMARY Selective Na+-dependent re-uptake of biogenic monoamines at mammalian nerve synapses is accomplished by three types of solute-linked carrier family 6 (SLC6) membrane transporter with high affinity for serotonin (SERTs), dopamine (DATs) and norepinephrine (NETs). An additional SLC6 monoamine transporter (OAT), is responsible for the selective uptake of the phenolamines octopamine and tyramine by insect neurons. We have characterized a similar high-affinity phenoloamine transporter expressed in the CNS of the earthworm Lumbricus terrestris. Phylogenetic analysis of its protein sequence clusters it with both arthropod phenolamine and chordate catecholamine transporters. To clarify the relationships among metazoan monoamine transporters we identified representatives in the major branches of metazoan evolution by polymerase chain reaction (PCR)-amplifying conserved cDNA fragments from isolated nervous tissue and by analyzing available genomic data. Analysis of conserved motifs in the sequence data suggest that the presumed common ancestor of modern-day Bilateria expressed at least three functionally distinct monoamine transporters in its nervous system: a SERT currently found throughout bilaterian phyla, a DAT now restricted in distribution to protostome invertebrates and echinoderms and a third monoamine transporter (MAT), widely represented in contemporary Bilateria, that is selective for catecholamines and/or phenolamines. Chordate DATs, NETs, epinephrine transporters (ETs) and arthropod and annelid OATs all belong to the MAT clade. Contemporary invertebrate and chordate DATs belong to different SLC6 clades. Furthermore, the genes for dopamine and norepinephrine transporters of vertebrates are paralogous, apparently having arisen through duplication of an invertebrate MAT gene after the loss of an invertebrate-type DAT gene in a basal protochordate.

Lipophorin inhibits the adhesion of cockroach (Periplaneta americana) haemocytes in vitro

Abstract Lipophorin and lipophorin-deficient plasma, purified by KBr density ultracentrifugation, were tested for their ability to inhibit the adhesion of cockroach (Periplaneta americana) haemocytes in vitro. Haemocytes resuspended in purified lipophorin, either in the absence or presence of Ca2+, remained non-adherent and retained a discoid morphology in vitro for at least 30 min. In contrast, haemocytes incubated either with or without Ca2+ for 30 min in lipophorin-deficient plasma, bovine serum albumin, or saline alone adhered and flattened onto glass coverslips. This finding is important since to date it has been difficult to maintain insect haemocytes in a non-adhesive state in vitro.

Drugs that block calmodulin activity inhibit cell-to-cell coupling in the epidermis oftenebrio molitor

SummaryIn many cell systems, the permeability of membrane junctions is modulated by the cytoplasmic level of free Ca++. To examine whether the calcium-dependent regulatory protein calmodulin is involved in this process, the ability of anticalmodulin drugs to influence the cell-to-cell passage of injected current and an organic tracer was tested using standard intracellular glass microelectrode techniques. Several antipsychotics and local anesthetics were found to block junctional communication in the epidermis of the beetleTenebrio molitor. Treatment of the epidermis with chlorpromazine (0.25 mM) raised intercellular resistance two- to threefold within 20 to 25 min; cell-to-cell passage of electrical current was abolished within 41±5 min. Loss of electrotonic coupling was accompanied by a block in the cell-to-cell movement of the organic tracer carboxyfluorescein. The reaction is fully reversible, with normal electrotonic coupling being restored within 2 to 4 hr. Other antipsychotics and local anesthetics had similar effects on cell coupling. The order of potency found was: trifluoperazine>thioridazine> d-butaclamol>chlorprothixine=chlorpromazine> l-butaclamol> dibucaine>tetracaine. The relative uncoupling potencies of these drugs correlate well with their known ability to inhibit calmodulin-dependent phosphodiesterase activity. Other anesthetic compounds, procaine and pentobarbital, did not block cell-to-cell communication. Altering the extracellular Ca++ concentration did not affect the rate of uncoupling by antipsychotics, while chelation of extracellular Ca++ with EGTA raised electrotonic coupling. The effect of three metabolic inhibitors on coupling was also examined. Iodoacetate uncoupled the epidermal cells while DNP and cyanide did not. These results are discussed in terms of possible mechanisms by which calmodulin may control junctional communication in this tissue.

Patterns of daily flight activity in onitine dung beetles (Scarabaeinae: Onitini)

Different species of African dung beetles emerge from the soil at characteristic times of the day to fly and colonize the freshly-deposited dung of mammalian herbivores. Onitine dung beetles in their natural habitat displayed one of five distinctive daily flight behaviours: dusk crepuscular (Onitis alexis Klug, O. caffer Boheman, O. fulgidus Klug, O. tortuosus Houston, O. vanderkelleni Lansberge, O. westermanni Lansberge); dusk/dawn crepuscular (O. pecuarius Lansberge and O. viridulus Boheman); dusk/dawn crepuscular and nocturnal (O. aygulus (Fabricius), O. mendax Gillet, O. uncinatus Klug); late afternoon-dusk and dawn-early morning [Heteronitis castelnaui (Harold)]; or diurnal flight activity [O. belial (Fabricius), O. ion (Olivier)]. These diagnostic daily flight behaviours span a light intensity range of over 6 orders of magnitude and have been retained in selected species introduced into Australia. Ambient light intensity appears to be the primary determinant of the daily flight period in onitine dung beetles. Because the dung of mobile herbivores is rapidly exploited by onitine species for feeding and breeding purposes, different flight behaviours result in a spatial and temporal partitioning of species in the local dung beetle community. The timing of flight may contribute to, or lead to avoidance of, competition between species which may ultimately affect colonization success. Many onitines show a strong preference for dung of specific herbivores, which may further reduce interspecific competition. All crepuscular-nocturnal species examined raised their thoracic temperatures endothermically to between 35°C and 40°C before the onset of flight. In O. aygulus the thoracic temperature excess was as large as 19.3°C. The thermal threshold below which the frequency of flight onsets drops off rapidly is about 12°C for O. aygulus and 17°C for O. alexis and O. pecuarius. Radiant loss of body heat during cool nights and dawns may explain why smaller species (<0.4 g body weight), in particular, are adapted behaviourally so that they fly only during the day or early dusk.