Burrow construction and behavior of tilefish,Lopholatilus chamaeleonticeps,in Hudson Submarine Canyon

Synopsis During 22 daylight submersible dives in August 1979 numerous juvenile and adult tilefish, Lopholatilus chamaeleonticeps, were observed in and around vertical burrows in the clay substrate of portions of Hudson submarine canyon in depths from 110–230 m. The size and shape of the burrows varied considerably with the smallest juveniles occupying simple vertical shafts in the substrate. Larger fish were found in much larger burrows (up to 4–5 m in diameter and at least 2–3 m deep) that were funnel shaped in cross-section with the upper conical portions containing numerous smaller burrows of associated crabs. The range of burrow sizes observed suggests a regular sequence of burrow construction by tilefish and the associated crabs. Both juvenile and adult tilefish swam into the burrows head first and exited tail first. This behavior, which would preclude the possibility of ambushing prey, and evidence of predation by sharks and other tilefish, suggests that the burrow is a refuge from predators.Tilefish burrows appear to serve as a focus for biological activity. Species associated with the burrows included galatheid crabs, Cancer sp., Acanthocarpus alexandri, Homarus americanus, Heliocolenus dactylopterus and Conger oceanicus. Tilefish may play an important role in structuring outer continental shelf communities. They physically shape their environment and probably have significant biological interactions with the species that associate with their burrows.     

Macrophages activated as suspension cultures with lymphocyte mediators devoid of antigen become cytotoxic for tumor cells.

Normal peritoneal exudate cells (PEC) were activated as suspension cultures either in mediator-rich supernatants from o-chlorobenzoyl-bovine gamma-globulin (OCB-BGG) stimulated lymphocytes or in antigen-free Sephadex fractions from these supernants. After 24 hr incubation thration. The adherent cell fractions of PEC, recovered by trypsinization from monolayers and activated by this technique, were as cytotoxic as unfractionated PEC. Lymphocyte supernatants and antigen-free fractions of the supernatants induced comparable macrophage-mediated tumor cytotoxicity. Treatment of activated macrophages with trypsin did not alter their cytotoxic capacity.     

The first 10 years of the dialysis-transplantation program at The Hospital for Sick Children,Toronto. 1: Predialysis and dialysis.

Renal dialysis and transplantation have been used for many years for adults with kidney failure but only recently for children. In May 1967 a renal-dialysis-transplantation program was established at The Hospital for Sick Children, Toronto for patients aged 6 to 18 years living within 240 km of Toronto. In 1973, children aged 1 to 5 years began to be accepted into the program, and by August 1977, 90 children (mean age 11 years) from all parts of Canada had been admitted to the program. The creation of vascular access in very small patients is difficult; the most successful types of access have been central shunts (established above the knee or the elbow) and bovine grafts. Specially made dialysis equipment is necessary for young patients. Young children should only be accepted in a dialysis-transplantation program that has a medical staff expert in meeting the specific needs of such children.     

Electrical and adaptive properties of rod photoreceptors in bufo marinus. I. Effects of altered extracellular Ca(2+) levels

The effects of altering extracellular Ca(2+) levels on the electrical and adaptive properties of toad rods have been examined. The retina was continually superfused in control (1.6 mM Ca(2+)) or test ringer’s solutions, and rod electrical activity was recorded intracellularly. Low-calcium ringer’s (10(-9)M Ca(2+)) superfused for up to 6 min caused a substantial depolarization of the resting membrane potential, an increase in light-evoked response amplitudes, and a change in the waveform of the light-evoked responses. High Ca(2+) ringer’s (3.2 mM) hyperpolarized the cell membrane and decreased response amplitudes. However, under conditions of either low or high Ca(2+) superfusion for up to 6 min, in both dark-adapted and partially light-adapted states, receptor sensitivity was virtually unaffected; i.e., the V-log I curve for the receptor potential was always located on the intensity scale at a position predicted by the prevailing light level, not by Ca(2+) concentration. Thus, we speculate that cytosol Ca(2+) concentration is capable of regulating membrane potential levels and light-evoked response amplitudes, but not the major component of rod sensitivity. Low Ca(2+) ringer’s also shortened the period of receptor response saturation after a bright but nonbleaching light flash, hence accelerating the onset of both membrane potential and sensitivity recovery during dark adaptation.

Exposure of the retina to low Ca(2+) (10(-9)M) ringer’s for long periods (7-15 min) caused dark-adapted rods to lose responsiveness. Response amplitudes gradually decreased, and the rods became desensitized. These severe conditions of low Ca(2+) caused changes in the dark-adapted rod that mimic those observed in rods during light adaptation. We suggest that loss of receptor sensitivity during prolonged exposure to low Ca(2+) ringer’s results from a decrease of intracellular (intradisk) stores of Ca(2+); i.e., less Ca(2+) is thereby released per quantum catch.

     

ASF1 binds to a heterodimer of histones H3 and H4: a two-step mechanism for the assembly of the H3-H4 heterotetramer on DNA

The first step in the formation of the nucleosome is commonly assumed to be the deposition of a histone H3-H4 heterotetramer onto DNA. Antisilencing function 1 (ASF1) is a major histone H3-H4 chaperone that deposits histones H3 and H4 onto DNA. With a goal of understanding the mechanism of deposition of histones H3 and H4 onto DNA, we have determined the stoichiometry of the Asf1-H3-H4 complex. We have established that a single molecule of Asf1 binds to an H3-H4 heterodimer using gel filtration, amino acid, reversed-phase chromatography, and analytical ultracentrifugation analyses. We demonstrate that Asf1 blocks formation of the H3-H4 heterotetramer by a mechanism that likely involves occlusion of the H3-H3 dimerization interface.     

Protein kinase Cdelta activation induces apoptosis in response to cardiac ischemia and reperfusion damage: a mechanism involving BAD and the mitochondria

Heart attacks caused by occlusion of coronary arteries are often treated by mechanical or enzymatic removal of the occlusion and reperfusion of the ischemic heart. It is now recognized that reperfusion per se contributes to myocardial damage, and there is a great interest in identifying the molecular basis of this damage. We recently showed that inhibiting protein kinase Cdelta (PKCdelta) protects the heart from ischemia and reperfusion-induced damage. Here, we demonstrate that PKCdelta activity and mitochondrial translocation at the onset of reperfusion mediates apoptosis by facilitating the accumulation and dephosphorylation of the pro-apoptotic BAD (Bcl-2-associated death promoter), dephosphorylation of Akt, cytochrome c release, PARP (poly(ADP-ribose) polymerase) cleavage, and DNA laddering. Our data suggest that PKCdelta activation has a critical proapoptotic role in cardiac responses following ischemia and reperfusion.     

Allelic polymorphism of T-cell receptor constant domains is widespread in fishes

T-cell receptor chains contain membrane-proximal constant domains of the immunoglobulin superfamily that are relatively invariant in mammalian species. In contrast, recent studies in the bicolor damselfish have demonstrated surprising allelic polymorphism in the TCR alpha (A) and TCR beta (B) constant (C) domain genes. This report extends these initial observations beyond Perciformes to two other orders of teleost fishes. Studies in both the Atlantic cod and zebrafish show high levels of polymorphism in the TCRA constant genes. Levels of 13% and 15% amino acid nonidentity were found within cod and zebrafish, respectively. Evolutionary analysis of codon usage suggests that positive selection maintains the high number of TCRAC alleles in these fish populations. Additionally, investigation of a TCRB constant gene from the Beau Gregory, a sister species of the bicolor damselfish, shows no evidence of transpecies maintenance of constant region alleles. These data argue that the T-cell receptor constant domain is being employed by many vertebrates in a manner inconsistent with our current understanding, and may indicate unheralded complexity in signal transduction through the TCR/CD3 complex.Electronic Supplementary Material Supplementary material is available in the online version of this article at M.F. Criscitiello and N.E. Wermenstam contributed equally to this workNucleotide sequence data reported here are available in the GenBank database under the accession numbers AJ439464–AJ439499 and AY476721–AY476734.     

Using ANOVA to analyze microarray data

ANOVA provides a general approach to the analysis of single and multiple factor experiments on both one- and two-color microarray platforms. Mixed model ANOVA is important because in many microarray experiments there are multiple sources of variation that must be taken into consideration when constructing tests for differential expression of a gene. The genome is large, and the signals of expression change can be small, so we must rely on rigorous statistical methods to distinguish signal from noise. We apply statistical tests to ensure that we are not just making up stories based on seeing patterns where there may be none.     

Downstream dispersal of zebra mussels (<Emphasis Type="Italic">Dreissena polymorpha</Emphasis>) under different flow conditions in a coupled lake-stream ecosystem

Dispersal, establishment, and spread of aquatic invasive species such as the zebra mussel (Dreissena polymorpha) can be influenced by riverine velocities and volumetric flows in invaded lake-stream ecosystems. Zebra mussels, which have a planktonic larval form (veliger), disperse rapidly downstream from a source population. Concentrations, dispersal, and body conditions of zebra mussel veligers were studied under different volumetric flow, or discharge, conditions in a coupled lake-stream ecosystem in northern Texas, USA. Veliger densities in lotic environments were strongly related to population dynamics in upstream lentic source populations. A strong exponential decrease in veliger density was observed through a 28-km downstream study reach. Increased water releases from the source reservoir increased veliger flux and dispersal potential, concomitantly increasing veliger flux and decreasing transit time. However, passage through release gates in the dam and increased turbulence in the river during high-discharge events could negatively affect body condition of veligers, and veliger body condition generally decreased from the source population to the farthest downstream site and was lower for veligers during periods of high discharge. Thus increased discharge appears to reduce the proportion of viable veligers because of increased turbulence-induced mortality. Colonization of distant downstream reservoirs can occur if discharge and propagule pressure are sufficient or if interim habitats are suitable for establishment of in-stream populations.