69 results match your criteria: "P.O. Royal Brisbane Hospital[Affiliation]"

Stimulation of melanogenesis in a human melanoma cell line by bistratene A.

Biochem Pharmacol

May 1998

Queensland Cancer Fund Research Unit, Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Australia.

The polyether toxin, bistratene A, induced morphological and functional differentiation of a human melanoma cell line (MM96E). The cells became blocked at the G2/M transition and elaborated a number of processes. Tyrosinase activity and melanin content were substantially increased.

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Approaches to determine the specific role of the delta isoform of protein kinase C.

J Biochem Biophys Methods

December 1997

Cancer Unit, Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Australia.

Two dimensional gel electrophoresis of proteins from HL-60 human leukaemia cells treated with bistratene A, a specific activator of protein kinase C (PKC) delta, was performed in conjunction with sequencing in order to identify components of the signal transduction pathway of this isoform of PKC. Stathmin (oncoprotein 18) was identified in this way and the phosphorylation of this protein after treatment with bistratene A, was confirmed by Western blotting of 2D gels. Since stathmin has phosphorylation sites for mitogen activated protein (MAP) kinases, cyclin dependent kinases and calcium/calmodulin dependent protein kinases, it is assumed that one of these enzymes, acting downstream from PKC delta, is responsible for the phosphorylation.

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The sex-linked anemic (sla) mouse carries an anemia that results from an inherited defect of intestinal iron absorption and provides an ideal model with which to investigate this poorly understood yet clinically important process. We have precisely mapped the sla locus within the central region of the X chromosome in relation to a panel of microsatellite markers. Analysis of over 500 progeny from an intraspecific intercross and a smaller intraspecific backcross segregating sla established the following locus order in the sla region: DXMit45-sla- (DXMit16, DXMit96)-DXMit41-DXMit169-DXMit170- DXMit148-(DXMit18, DXMit171)-DXMit84-DXMit64.

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Deletion of Plasmodium berghei-specific CD4+ T cells adoptively transferred into recipient mice after challenge with homologous parasite.

Proc Natl Acad Sci U S A

February 1998

Malaria and Arbovirus Unit, The Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Brisbane 4029, Australia.

The immune response to malaria parasites includes T cell responses that reduce parasites by effector T cell responses and by providing help for antibody responses. Some parasites are more sensitive to antibody and others are more sensitive to cell-mediated immunity. We demonstrate that cultured CD4(+) T cells that produce interferon gamma and interleukin 2, but not interleukin 4, in response to stimulation with the rodent parasite Plasmodium berghei can reduce but not eliminate parasites in vivo after adoptive transfer.

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The transmembrane 4 superfamily (TM4SF) comprises an assemblage of surface antigens from mammalian cells and from the human blood flukes. Member proteins of the TM4SF are characterized by the presence of four hydrophobic domains, which are presumed to be membrane-spanning, and specific conserved motifs. The Sm23 group of TM4SF, which includes Sm23, Sj23, and Sh23 from blood flukes, shows potential as immunodiagnostic and vaccine target antigens for use in controlling human schistosomiasis.

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Hyperphosphorylation of the N-terminal domain of Cdc25 regulates activity toward cyclin B1/Cdc2 but not cyclin A/Cdk2.

J Biol Chem

November 1997

Queensland Cancer Fund Research Laboratories and Joint Oncology Program, Queensland Institute of Medical Research, P. O. Royal Brisbane Hospital, Queensland, Australia 4029.

Cdc25 regulates entry into mitosis by regulating the activation of cyclin B/cdc2. In humans, at least two cdc25 isoforms have roles in controlling the G2/M transition. Here we show, using bacterially expressed recombinant proteins, that two cdc25B splice variants, cdc25B2 and cdc25B3, are capable of activating cyclin A/cdk2 and cyclin B/cdc2, but that mitotic hyperphosphorylation of these proteins increases their activity toward only cyclin B1/cdc2.

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Resistance to radiation-induced apoptosis in Burkitt's lymphoma cells is associated with defective ceramide signaling.

Cancer Res

August 1997

Queensland Cancer Fund Research Unit, Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Herston, Australia.

Increased sensitivity to ionizing radiation has been shown to be due to defects in double-strand break repair and mutations in the proteins that detect DNA damage. However, it is now recognized that the cellular radiation response is complex and that radioresistance/radiosensitivity may also be regulated at different levels in the radiation signal transduction pathway. Here, we describe a direct relationship between resistance to radiation-induced apoptosis and defective ceramide signaling.

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From November 1990 to November 1992, immature mosquitoes were sampled from the shoreline and from emergent beds of the submerged aquatic plant Hydrilla verticillata at the Ross River reservoir, northern Australia. Aerial mapping of Hydrilla beds was done in conjunction with sampling to estimate total immature mosquito numbers. Larvae of 7 species were found.

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Response of Culex quinquefasciatus to visual stimuli.

J Am Mosq Control Assoc

June 1997

Queensland Institute of Medical Research, P. O. Royal Brisbane Hospital, Australia.

The vision of Culex quinquefasciatus was studied in the laboratory. The attractiveness of colors (black, white, brown, yellow, blue, a skin tone) was evaluated with respect to the collection of Cx. quinquefasciatus in natural light, in the dark, and in ultraviolet light.

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The recently cloned gene (ATM) mutated in the human genetic disorder ataxia-telangiectasia (A-T) is involved in DNA damage response at different cell cycle checkpoints and also appears to have a wider role in signal transduction. Antibodies prepared against peptides from the predicted protein sequence detected a approximately 350 kDa protein corresponding to the open reading frame, which was absent in 13/23 A-T homozygotes. Subcellular fractionation, immunoelectronmicroscopy and immunofluorescence showed that the ATM protein is present in the nucleus and cytoplasmic vesicles.

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Specific cleavage of the large subunit of replication factor C in apoptosis is mediated by CPP32-like protease.

Biochem Biophys Res Commun

April 1997

Queensland Institute of Medical Research, University of Queensland, P.O. Royal Brisbane Hospital, Australia.

Recent evidence suggests that the growing family of cysteine proteases related to the interleukin-1beta-converting enzyme (ICE) is of central importance in mediating apoptosis. Proteolytic cleavage of a small group of cellular substrates by these enzymes in association with the onset of apoptosis has been reported. In the present study, we searched a protein data base for potential death substrates possessing the CPP32 cleavage site, DEVD, and identified several candidates including RFC140, the large subunit of replication factor C, which we subsequently demonstrated to be specifically cleaved in a variety of cell types undergoing apoptosis in response to different cytotoxic agents, whereas no degradation is observed in a cell line resistant to etoposide-induced apoptosis.

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Defective signaling through the B cell antigen receptor in Epstein-Barr virus-transformed ataxia-telangiectasia cells.

J Biol Chem

April 1997

Queensland Cancer Fund Research Unit, Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Herston, Brisbane 4029, Australia.

A characteristic series of immunological abnormalities are observed in the human genetic disorder ataxia-telangiectasia (A-T). The recent cloning of a gene mutated in this syndrome provides additional evidence for a defect in intracellular signaling in A-T. We have investigated the possibility that signaling through the B cell antigen receptor is one manifestation of the A-T defect.

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Risk factors for childhood melanoma in Queensland, Australia.

Int J Cancer

January 1997

Epidemiology and Population Health Unit, Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Herston, Australia.

The causes of cutaneous melanoma among children under 15 years are largely unknown. We report the findings of an epidemiological study of childhood melanoma in Queensland, Australia, which has the highest incidence rates in the world. All 61 cases of melanoma in children less than 15 years notified to the Queensland Cancer Registry 1987-1994 were eligible to participate in a population-based, case-control study.

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Heteronuclear ribonucleoproteins C1 and C2, components of the spliceosome, are specific targets of interleukin 1beta-converting enzyme-like proteases in apoptosis.

J Biol Chem

November 1996

Queensland Cancer Fund Research Unit, Queensland Institute of Medical Research, P. O. Royal Brisbane Hospital, Herston, Brisbane, Queensland 4029, Australia.

Apoptosis induced by a variety of agents results in the proteolytic cleavage of a number of cellular substrates by enzymes related to interleukin 1beta-converting enzyme (ICE). A small number of substrates for these enzymes have been identified to date, including enzymes involved in DNA repair processes: poly(ADP-ribose) polymerase and DNA-dependent protein kinase. We describe here for the first time the specific cleavage of the heteronuclear ribonucleoproteins (hnRNPs) C1 and C2 in apoptotic cells induced to undergo apoptosis by a variety of stimuli, including ionizing radiation, etoposide, and ceramide.

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Previous studies have established that a relationship exists between apoptosis and cell surface (ecto-) peptidase activity. Thus dose-dependent increases were found both in ectopeptidase activities and in the proportion of cells undergoing apoptosis in HeLa cell monolayers after exposure to UV and other perturbants causing arrest of DNA synthesis (indirectly or directly as a result of DNA damage). The nature of the correlation made no distinction as to whether an increase in peptidase activity was causal of, or consequential to apoptosis, nor whether the increase was a general response by all cells.

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Aedes albopictus and other Aedes (Stegomyia) species in Fiji.

J Am Mosq Control Assoc

June 1995

Mosquito Control Laboratory, Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Australia.

During an assessment of the dengue situation in Fiji in early 1992, a house-to-house survey of container-breeding Aedes was made. Discarded tires and water drums were identified as key breeding sites for the 4 potential dengue vectors: Aedes aegypti, Aedes albopictus, Aedes pseudoscutellaris, and Aedes polynesiensis. Aedes albopictus were detected on Viti Levu, Vanua Levu, and on Taveuni.

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Quantitative sampling of immature Aedes aegypti in metal drums using sweep net and dipping methods.

J Am Mosq Control Assoc

September 1994

Tropical Health Program, Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Australia.

The behavior of aquatic stages of Aedes aegypti was evaluated in 200-liter metal drums to develop improved surveillance. When known numbers of larvae recovered with a rectangular net and with a standard dipper were compared, all stages except 1st instar were most numerous in the top 1/3 of the drum. Water temperature was the only significant variable affecting the vertical distribution of 4th-instar larvae; light intensity and pH were nonsignificant factors.

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Comparison of sampling efficacy of sweeping and dipping for Aedes aegypti larvae in tires.

J Am Mosq Control Assoc

September 1993

Queensland Institute of Medical Research, P. O. Royal Brisbane Hospital, Australia.

A sweep net with a flexible plastic frame was compared to a dipper for sampling efficacy for Aedes aegypti larvae in different-sized tires. When known numbers of mosquito larvae were introduced into tires, from 2 to 6.8 times more larvae were recovered by sweeping than by dipping.

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