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1.
Eur J Immunol ; 31(6): 1736-46, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11385618

ABSTRACT

The deleterious effects of ultraviolet B radiation (UVR) on cutaneous immunity are mediated in part by cytokines released from cutaneous cells following radiation exposure. On the one hand, TNF-alpha has been advocated as the primary mediator of failed contact hypersensitivity induction, and, on the other hand, IL-10 has been held responsible for tolerance. While keratinocytes exposed to UVR have been found to produce both TNF-alpha and IL-10, there is reason to question whether these major cellular constituents of the epidermis are the relevant source of immunomodulatory cytokines after UVR. Dermal mast cells also produce TNF-alpha and IL-10, and we have recently reported that mast cell-derived TNF-alpha is required for UVR-induced impairment of CH induction. In this study, we have examined whether mast cells are also a relevant source of IL-10 in UVR-dependent tolerance. We found that (a) UVR fails to induce tolerance in mast cell-deficient mice, and (b) that tolerance occurs if mast cells are triggered to degranulate after ligation of the IgE receptor. Both types of tolerance were neutralized with anti-IL-10 antibodies, are hapten specific, and are associated with regulatory lymphoid cells. We conclude that mast cells are required in UVR-induced tolerance and may be one of the major sources of IL-10 that mediates the tolerance induced by acute, low-dose UVR.


Subject(s)
Cell Degranulation , Immune Tolerance/immunology , Mast Cells/immunology , Picryl Chloride/immunology , Skin/radiation effects , Ultraviolet Rays , Adjuvants, Immunologic , Animals , Cell Degranulation/immunology , Cell Degranulation/radiation effects , Dermatitis, Contact/immunology , Histamine Release/immunology , Immunoglobulin E/immunology , Interleukin-10/genetics , Interleukin-10/immunology , Interleukin-10/metabolism , Mast Cells/radiation effects , Mice , Mice, Inbred C3H , Mice, Inbred C57BL , Oxazolone/administration & dosage , Oxazolone/immunology , Picryl Chloride/administration & dosage , Radiation Dosage , Skin/cytology , Skin/immunology
2.
J Trauma ; 47(5): 885-90, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10568717

ABSTRACT

BACKGROUND: Sequelae of traumatic brain injury include generation of oxygen-free radicals and fibrin deposition, which worsen the initial injury. Superoxide dismutases (SODs) scavenge and bind to the free-radical superoxide anion (O2-), potentially defending against oxidative stress. In the present study, we investigated the production of SOD within human cerebral microvascular endothelial (HCME) cells after exposure to alpha-thrombin, hypothesizing that manganese SOD (MnSOD) expression is increased. Our aims were to determine whether alterations in SOD are observed at the mRNA level, to examine whether a particular species is preferentially expressed, and to determine the requirement of the active site of alpha-thrombin. METHODS: HCME cells were characterized and grown to confluence. Control cells and cells exposed to 10 nmol/L alpha-thrombin were harvested for mRNA isolation using reverse transcriptase-polymerase chain reaction. Quantitation of mRNA production determined the levels of copper-zinc SOD and MnSOD. Active site blocked alpha-thrombin was used as a negative control and determined the specificity of the response. RESULTS: The cells in culture were identified as endothelial after fulfilling criteria, such as positive immunocytochemical staining for factor VIII/von Willebrand factor antigen and binding of Ulex europaeus agglutinin-1 lectin. Levels of MnSOD mRNA were elevated at all time points in response to alpha-thrombin, whereas the cytosolic form was undetectable. HCME cells that were exposed to active site-blocked alpha-thrombin produced mRNA levels of MnSOD that were increased above those of controls, but this increase was half that of mRNA levels of MnSOD produced by HCME cells that were exposed to alpha-thrombin. CONCLUSION: Our study showed for the first time that alpha-thrombin partially modulates SOD in HCME cells, causing a preferential increase in MnSOD. Further investigation into secondary brain injury will provide insights into the role of alpha-thrombin in the mechanism of free radical-induced alterations, potentially improving the outcome of patients with head injury.


Subject(s)
Cerebral Cortex/blood supply , Endothelium, Vascular/enzymology , Superoxide Dismutase/metabolism , Thrombin/physiology , Cells, Cultured , Fibrin/metabolism , Free Radicals , Humans , Microcirculation/enzymology , Reactive Oxygen Species/metabolism
3.
Coron Artery Dis ; 10(7): 437-42, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10562909

ABSTRACT

BACKGROUND: Determinants of predisposition to intracranial bleeding in response to the administration of thrombolytic drugs have not yet been well characterized. OBJECTIVE: To delineate factors involved, by characterizing susceptibility of human cerebral microvascular endothelium (HCME) to injury associated with inflammatory cytokines, levels of which are typically elevated in blood in patients who have suffered a myocardial infarction or stroke and been treated with thrombolytic drugs. METHODS: Elaboration of fibrinolytic system proteins by HCME exposed either to interleukin-1 beta or to tumor necrosis factor-alpha (TNF) in serum-free medium for 24 h was characterized. Cell-conditioned medium was assayed for tissue-type plasminogen activator (t-PA), urokinase-type plasminogen activator (u-PA), and plasminogen activator inhibitor type 1--(PAI-1) by enzyme-linked immunosorbent assay. To determine whether the induction of u-PA was mediated by oxygen-centered radicals, the following were added to media: superoxide dismutase (a scavenger of O2-.), catalase (a scavenger of O2-. and H2O2) and dimethylthiourea (a scavenger of OH.). RESULTS: Interleukin-1 beta had no effect upon elaboration of fibrinolytic system proteins by HCME. By contrast, TNF selectively increased elaboration of u-PA. Accumulation of t-PA and PAI-1 remained unchanged. Accumulation of u-PA was inhibited by cycloheximide, implying that there was a requirement for protein synthesis. Dimethylthiourea abolished the increase elaboration of u-PA induced by TNF completely, catalase did so partially, and SOD did not do so at all. CONCLUSION: The propensity of HCME to elaborate u-PA rather than PAI-1 appears to render cerebral microvasculature particularly vulnerable to proteolytic attack in settings in which inflammatory cytokines are elaborated locally or in which their concentrations in blood are elevated.


Subject(s)
Brain/blood supply , Brain/pathology , Endothelium, Vascular/metabolism , Endothelium, Vascular/pathology , Fibrinolytic Agents/metabolism , Brain/drug effects , Brain/metabolism , Brain Injuries/chemically induced , Brain Injuries/metabolism , Brain Injuries/physiopathology , Catalase/pharmacology , Cells, Cultured , Culture Media, Conditioned , Cycloheximide/pharmacology , Endothelium, Vascular/enzymology , Endothelium, Vascular/physiopathology , Enzyme-Linked Immunosorbent Assay , Fibrinolysis , Fibrinolytic Agents/adverse effects , Free Radical Scavengers/pharmacology , Free Radicals/metabolism , Humans , Interleukin-1/pharmacology , Microcirculation/enzymology , Microcirculation/metabolism , Microcirculation/pathology , Microcirculation/physiopathology , Reactive Oxygen Species/metabolism , Time Factors , Tumor Necrosis Factor-alpha/pharmacology
4.
Cell Immunol ; 175(2): 150-6, 1997 Feb 01.
Article in English | MEDLINE | ID: mdl-9023420

ABSTRACT

Cytotoxic T-cell (CTL) cultures were generated from five ovarian cancer patients (OvCTL) and from three breast cancer patients (BrCTL). All CTL lines were T-cell receptor (TcR) alphabeta+ and predominantly CD8+ (73 +/- 13%). These CTL lines preferentially recognized autologous tumor cells in an HLA class I-restricted, and in part HLA-A2-restricted, manner. In addition, the CTL lines recognized allogeneic HLA-A2+ ovarian and breast tumor cells. Specific recognition was determined by T-cell-mediated cytotoxicity as well as cytokine release. Coculture of irradiated autologous tumor cells with OvCTL induced secretion of IFN-gamma, GM-CSF and TNF-alpha, but not IL-4, indicating a T helper-1-type response. Similar results were obtained when OvCTL and BrCTL were stimulated with histologically matched HLA-A2+ tumor cells. Also, BrCTL stimulated with HLA-A2+ but not HLA-A2- ovarian tumor cells produced significant levels of GM-CSF and TNF-alpha. Finally, the Her2/neu peptide p654-662, earlier identified as a tumor antigen in both ovarian and breast cancer, induced cytotoxicity as well as the specific release of IFN-gamma and TNF-alpha but not IL-4 by OvCTL and BrCTL. Thus, tumor-specific recognition by CTL was verified by cytotoxicity and cytokine release. The secretion of Th1-like cytokines as opposed to Th2-like cytokines suggest that therapeutically OvCTL and BrCTL could potentially enhance the endogenous immune response to tumor.


Subject(s)
Breast Neoplasms/immunology , Cytokines/metabolism , Ovarian Neoplasms/immunology , T-Lymphocytes, Cytotoxic/immunology , T-Lymphocytes, Helper-Inducer/immunology , Antigens, Neoplasm/immunology , Coculture Techniques , Cytotoxicity Tests, Immunologic , Female , HLA-A2 Antigen/immunology , Humans , Immunophenotyping , Peptide Fragments/immunology , Receptor, ErbB-2/immunology , Tumor Cells, Cultured
5.
Circulation ; 94(4): 636-42, 1996 Aug 15.
Article in English | MEDLINE | ID: mdl-8772682

ABSTRACT

BACKGROUND: Intracranial bleeding is the most catastrophic potential complication of treatment with thrombolytic agents. To identify potential factors that may contribute to this problem, we characterized elaboration by human brain endothelial cells of plasminogen activator inhibitor-1 (PAI-1) and measured PAI-1 mRNA levels. METHODS AND RESULTS: When human cerebral microvascular endothelial cells (HCMEC), pial arterial endothelial cells, and middle meningeal arterial endothelial cells were exposed to 10 to 1000 ng/mL recombinant tissue-type plasminogen activator (RTPA), urokinase-type plasminogen activator (UPA), or streptokinase/ plasminogen (37 U streptokinase plus 2 mumol/L plasminogen) for 24 hours, they exhibited concentration-dependent decreases in elaboration of PAI-1 of 65 +/- 3%, 48 +/- 3%, and 59 +/- 8%. UPA and streptokinase/plasminogen elicited decreases of 33 +/- 8% and 35 +/- 4%, respectively, that were specific with respect to the protease agonists as to total protein synthesis and cell type; ie, neither human umbilical vein endothelial cells nor cerebral pericytes exhibited inhibition of PAI-1 elaboration. No decrease in HCMEC PAI-1 elaboration was induced by coagulation factor XB (10 nmol/L). A 2.7 +/- 0.5-fold increase was induced by alpha-thrombin (10 nmol/L). PAI-1 secretion from HCMEC decreased within 4 hours of exposure to 100 ng/mL RTPA. In HCMEC exposed to RTPA for 8 hours, PAI-1 mRNA decreased from 176 +/- 20 to 43 +/- 2.2 pg/microgram RNA. CONCLUSIONS: These results indicate that brain endothelial cells exposed to RTPA exhibit paradoxically diminished elaboration of PAI-1. This property may render brain vasculature vulnerable to attack by serine proteases, thereby predisposing to injury and initiating an underlying subsequent intracerebral hemorrhage in patients given plasminogen activators for treatment of coronary thrombosis.


Subject(s)
Cerebral Cortex/blood supply , Cerebral Hemorrhage/physiopathology , Cerebrovascular Circulation , Endothelium, Vascular/physiology , Plasminogen Activator Inhibitor 1/biosynthesis , Plasminogen Activators/pharmacology , Plasminogen/pharmacology , Streptokinase/pharmacology , Tissue Plasminogen Activator/pharmacology , Urokinase-Type Plasminogen Activator/pharmacology , Aprotinin/pharmacology , Cells, Cultured , Culture Techniques/methods , Cycloheximide/pharmacology , Disease Susceptibility , Endothelium, Vascular/cytology , Endothelium, Vascular/drug effects , Humans , Kinetics , Meningeal Arteries , Meninges/blood supply , Microcirculation , Pia Mater/blood supply , Plasminogen Activator Inhibitor 1/metabolism , RNA, Messenger/biosynthesis , Recombinant Proteins/pharmacology , Transcription, Genetic/drug effects , Umbilical Veins
7.
Arterioscler Thromb Vasc Biol ; 15(7): 903-11, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7600122

ABSTRACT

alpha-Thrombin regulation of endothelial cell (EC) fibrinolysis has been documented by using endothelia derived from a number of anatomic locations but not with those derived from the human cerebral vasculature. In the present study, the fibrinolytic properties of human cerebral microvascular ECs and their regulation by alpha-thrombin are delineated and contrasted with those of human umbilical vein and foreskin microvascular ECs. In cerebral ECs, alpha-thrombin elicited a unique dose-dependent increase in urokinase production and DNA synthesis. Maximal stimulation, observed with 10 nmol/L alpha-thrombin, resulted in a 30- to 50-fold increase in urokinase production and a concomitant fourfold increase in DNA synthesis; the increase in urokinase was reflected in higher steady-state levels of urokinase mRNA. The major urokinase product secreted is the single-chain form of the enzyme. No effect was observed with the addition of other proteases or catalytically inactive variants of alpha-thrombin. A thrombin receptor agonist peptide upregulated urokinase production but had no effect on DNA synthesis, suggesting that fibrinolysis is mediated by the thrombin receptor but that proliferation is regulated by a different pathway. These findings suggest the possibility that the cerebral microvasculature may be a specialized region of the vascular system in which urokinase-type plasminogen activator, not tissue-type plasminogen activator, is the key catalyst of fibrin lysis when the brain responds to thrombotic events and that alpha-thrombin may regulate repair of the cerebral microvascular system.


Subject(s)
Brain/blood supply , DNA/biosynthesis , Endothelium, Vascular/metabolism , Microcirculation/metabolism , Thrombin/pharmacology , Urokinase-Type Plasminogen Activator/biosynthesis , Blotting, Northern , Cells, Cultured , Endothelium, Vascular/drug effects , Humans , Immunoblotting , Male , Receptors, Thrombin/physiology , Umbilical Veins
8.
J Trauma ; 37(3): 347-57, 1994 Sep.
Article in English | MEDLINE | ID: mdl-8083892

ABSTRACT

The delivery of a blow to the head represents a transfer of energy, part of which manifests itself as a short-lived pressure change within the skull. An in vitro model was developed to test whether cerebral endothelial cell hemostatic function is altered with exposure to this type of pressure event. Human cerebral microvascular endothelium (HCME) cells were subjected to rapid (2-5 msec) changes in pressure (delta atmosphere = 1.2-10), the sublethal range defined (delta atmosphere < or = 6.5), and the nonthrombogenic status of sublethally percussed HCME cells assessed using the adherence of alpha-thrombin activated platelets as an indicator. The HCME cells had lost their normal capacity to suppress adherence of activated platelets when evaluated 1 hour or 24 hours after percussion. Adherence of activated platelets to percussed HCME cells was blocked by the addition of PGI2, an inhibitor of platelet adherence, when evaluated at 1 hour but not 24 hours after percussion, indicating that percussed HCME cells were undergoing further derangement of their nonthrombogenic mechanisms. Percussed HCME cells cultured for 24 hours in medium containing scavengers of oxygen free radicals recovered their capacity to block platelet adherence. We conclude that sublethal percussion immediately compromises the nonthrombogenic character of HCME cells and initiates the development of a persisting prothrombotic state in HCME cells. This derangement appears linked to increased production of reactive oxygen species by percussed HCME cells.


Subject(s)
Brain Injuries/physiopathology , Brain/blood supply , Endothelium, Vascular/physiopathology , Hemostasis , Platelet Adhesiveness , Endothelium, Vascular/cytology , Epoprostenol/pharmacology , Free Radical Scavengers , Humans , Platelet Adhesiveness/drug effects , Platelet Adhesiveness/physiology , Pressure , Reactive Oxygen Species/metabolism
11.
J Biol Chem ; 267(1): 597-601, 1992 Jan 05.
Article in English | MEDLINE | ID: mdl-1730619

ABSTRACT

Clinical and experimental data indicate that activated oxygen species interfere with vascular endothelial cell function. Here, the impact of extracellular oxidant injury on the fibrinolytic response of cultured human umbilical vein endothelial (HUVE) cells was investigated at the protein and mRNA levels. Xanthine (50 microM) and xanthine oxidase (100 milliunits), which produces the superoxide anion radical (O2-) and hydrogen peroxide (H2O2), was used to sublethally injure HUVE cells. Following a 15-min exposure, washed cells were incubated for up to 24 h in serum-free culture medium. Tissue-type plasminogen activator (t-PA) antigen, plasminogen activator inhibitor-1 (PAI-1) antigen, and PAI-1 activity were determined in 1.25 ml of conditioned medium and t-PA and PAI-1 mRNA in the cell extracts of 2 x 10(6) HUVE cells. Control cells secreted 3.9 +/- 1.3 ng/ml (mean +/- S.D., n = 12) within 24 h. Treatment with xanthine/xanthine oxidase for 15 min induced a 2.8 +/- 0.4-fold increase (n = 12, p less than 0.05) of t-PA antigen secretion after 24 h. The t-PA antigen was recovered predominantly in complex with PAI-1. The oxidant injury caused a 3.0 +/- 0.8-fold increase (n = 9, p less than 0.05) in t-PA mRNA within 2 h. Total protein synthesis was unaltered by xanthine/xanthine oxidase. The oxidant scavengers superoxide dismutase and catalase, in combination, abolished the effect of xanthine/xanthine oxidase on t-PA secretion and t-PA mRNA synthesis. Xanthine/xanthine oxidase treatment of HUVE cells did not affect the PAI-1 secretion in conditioned medium nor the PAI-1 mRNA levels in cell extracts. Thus extracellular oxidant injury induces t-PA but not PAI-1 synthesis in HUVE cells.


Subject(s)
Endothelium, Vascular/metabolism , Fibrinolysis , Oxygen/metabolism , Antigens/biosynthesis , Blotting, Northern , Blotting, Western , Cells, Cultured , Endothelium, Vascular/cytology , Free Radicals , Humans , Hydrogen Peroxide , Plasminogen Inactivators/metabolism , Precipitin Tests , RNA, Messenger/metabolism , Tissue Plasminogen Activator/metabolism , Umbilical Veins , Xanthine , Xanthine Oxidase/metabolism , Xanthines/metabolism
12.
Arterioscler Thromb ; 11(3): 594-601, 1991.
Article in English | MEDLINE | ID: mdl-1851431

ABSTRACT

This study was directed to the ability of oxygen free radicals to cause reversible vascular endothelial cell dysfunction. A well-characterized system for the production of the superoxide anion radical (O2(-).) and hydrogen peroxide (H2O2), employing xanthine and xanthine oxidase, was used to sublethally injure human umbilical vein endothelial (HUVE) cells in vitro. We examined the effects of a 15-minute incubation of HUVE cells with xanthine (50 microM) and xanthine oxidase (2.5-100 munits) on platelet adherence and prostacyclin (PGI2) release. All experiments were conducted in a serum-free N-(2-hydroxyethyl)piperazine-N'-(2-ethanesulfonic acid)-Tyrode buffer (pH 7.4) incubation system. Exposure of HUVE cells to sublethal concentrations of oxygen free radicals caused significant enhancement of platelet adherence (65 +/- 6.3%) to injured endothelium. A 12-fold increase in PGI2 release resulted after a 15-minute treatment with xanthine and xanthine oxidase. The addition of exogenous PGI2 (150 mM) to platelet-endothelial systems did not completely prevent the enhanced platelet adherence, suggesting that a lack of PGI2 was not completely responsible for the adherence of platelets to O2(-).-injured cells. When superoxide dismutase (SOD) and catalase, scavengers of O2(-). and H2O2, were added in combination to treated cells, platelet adherence decreased by 42-77% and PGI2 release approached that of control cultures. No decrease in either platelet adherence or PGI2 release occurred when chemically inactivated forms of SOD and catalase or bovine serum albumin were added to oxidant-treated cultures.


Subject(s)
Endothelium, Vascular/physiology , Epoprostenol/metabolism , Hydrogen Peroxide/pharmacology , Platelet Adhesiveness , Superoxides/pharmacology , Catalase/pharmacology , Cells, Cultured , Endothelium, Vascular/cytology , Endothelium, Vascular/drug effects , Epoprostenol/pharmacology , Free Radicals , Humans , Superoxide Dismutase/pharmacology , Umbilical Veins , Xanthine , Xanthine Oxidase/metabolism , Xanthines/metabolism
13.
J Public Health Dent ; 51(3): 186-8, 1991.
Article in English | MEDLINE | ID: mdl-1920272
14.
J Biol Chem ; 265(33): 20443-8, 1990 Nov 25.
Article in English | MEDLINE | ID: mdl-2122975

ABSTRACT

The effect of anoxia and reoxygenation on the synthesis and secretion of tissue-type plasminogen activator (t-PA) and plasminogen activator inhibitor-1 (PAI-1) was studied in primary cultures of human umbilical vein endothelial cells. Sublethal anoxia, determined by trypan blue dye exclusion and lactate dehydrogenase release, was produced by cell culture under a 95% N2, 5% CO2 atmosphere for 2-24 h and was followed by reoxygenation with 95% air, 5% CO2 for 24 or 48 h. Anoxia did not alter the levels of mRNA for t-PA or PAI-1 in the cells or the secretion of t-PA or PAI-1 into the medium. At 24 h, t-PA secreted into conditioned medium was 7.0 +/- 1.4 ng/2 x 10(6) cells (n = 9) and PAI-1 was 300 +/- 13 IU/2 x 10(6) cells (n = 9), whereas the content of t-PA mRNA was 2.2 pg/micrograms of RNA and PAI-1 mRNA was 180 pg/micrograms of RNA. During reoxygenation, however, t-PA antigen and PAI-1 activity as well as mRNA for PAI-1 decreased proportionally to the duration of anoxia, to reach 27 +/- 1.0, 49 +/- 2.0, and 47 +/- 14% of control values, respectively, within 24 h of anoxia. t-PA mRNA also decreased significantly during reoxygenation following anoxia, but the extent could not be accurately quantitated. Addition, during anoxia, of a 200 micrograms/ml concentration of the superoxide anion radical scavenger superoxide dismutase or of a 5 mM concentration of the iron chelator deferoxamine mesylate prevented the subsequent decrease of t-PA antigen during reoxygenation; addition of these compounds during reoxygenation had no effect. Superoxide dismutase, but not deferoxamine mesylate, when added during anoxia prevented the subsequent decrease in PAI-1 activity. These studies suggest that the marked alteration of endothelial cell fibrinolysis during anoxia followed by reoxygenation is most likely mediated by a mechanism dependent on oxygen radicals. Impaired endothelial cell fibrinolysis may contribute to the pathophysiology of ischemia/reperfusion injury.


Subject(s)
Endothelium, Vascular/metabolism , Plasminogen Inactivators/metabolism , Tissue Plasminogen Activator/biosynthesis , Aerobiosis , Anaerobiosis , Cells, Cultured , Deferoxamine/pharmacology , Free Radical Scavengers , Free Radicals , Humans , Hypoxia/metabolism , Kinetics , Superoxide Dismutase/pharmacology
16.
J Am Dent Assoc ; 119(2): 234, 1989 Aug.
Article in English | MEDLINE | ID: mdl-2535638
17.
Environ Res ; 44(1): 103-16, 1987 Oct.
Article in English | MEDLINE | ID: mdl-3115771

ABSTRACT

Cell injury and inflammation caused by asbestos are critical to the pathogenesis of pulmonary fibrosis (asbestosis). Our goal in studies here was to investigate the possible modulation of asbestos-related cell death using antioxidants in both target and effector cells of asbestosis. After exposure to crocidolite asbestos at a range of concentrations (2.5-25 micrograms/cm2 dish), the viability of a normal rat lung fibroblast line (RL-82) and freshly isolated alveolar macrophages (AM) was determined by exclusion of trypan blue and nigrosin, respectively. In comparison to fibroblasts, AM were more resistant to the cytotoxic effects of asbestos. Cytotoxic concentrations of asbestos then were added to both cell types in combination with the antioxidants, superoxide dismutase (SOD), a scavenger of superoxide (O2-.), and catalase, an enzyme scavenging H2O2. Dimethylthiourea (DMTU), a scavenger of the hydroxyl radical (OH.) and deferoxamine, an iron chelator, also were evaluated in similar studies. Results showed significant dosage-dependent reduction (P less than 0.001) of asbestos-associated cell death with all agents. In contrast, asbestos-induced toxicity was not ameliorated after addition of chemically inactivated SOD and catalase or bovine serum albumin. Results above suggest asbestos-induced cell damage is mediated by active oxygen species. In this regard, the iron associated with the fiber and/or its interaction with cell membranes might be critical in driving a modified Haber-Weiss (Fenton-type) reaction resulting in production of OH(.).


Subject(s)
Antioxidants/pharmacology , Asbestos/antagonists & inhibitors , Cell Survival/drug effects , Lung/drug effects , Macrophages/drug effects , Animals , Catalase/metabolism , Deferoxamine/pharmacology , Free Radicals , Macrophages/cytology , Pulmonary Alveoli/cytology , Rats , Superoxide Dismutase/metabolism , Thiourea/analogs & derivatives , Thiourea/pharmacology
18.
Cancer Res ; 46(9): 4650-5, 1986 Sep.
Article in English | MEDLINE | ID: mdl-3731118

ABSTRACT

A glycoprotein which stimulates bone resorption in vitro has been purified at least 375-fold from human cancer ascites fluid. Purification was accomplished utilizing fractionation with ammonium sulfate, anion exchange chromatography, high-performance size exclusion chromatography, adsorptive chromatography on hydroxylapatite, and high-performance anion exchange chromatography. The homogeneous bone-resorptive protein possesses an apparent molecular weight of 52,000 as calculated from electrophoresis in sodium dodecyl sulfate:polyacrylamide gels. On polyacrylamide gels at pH 8.9 in the absence of sodium dodecyl sulfate, the bone-resorptive protein migrates with the mobility of an alpha 2-globulin. The amino acid composition of this protein is marked by the absence of methionine and by a relatively high content of nonpolar amino acids. The protein possesses a single amino- and a single carboxyl-terminal amino acid, alanine, and leucine, respectively. The carbohydrate moiety, comprising 20% of the total weight, consists of neutral hexoses, galactosamine and glucosamine, and sialic acids. With respect to its biological activity, the ascites glycoprotein is one-fourth as potent as parathyroid hormone, on a molar basis, in its ability to stimulate calcium release from bone explants in vitro. Calcium release is significantly decreased on heating at 60 degrees C but is not inhibited by indomethacin.


Subject(s)
Ascitic Fluid/physiopathology , Biological Products/isolation & purification , Bone Resorption , Breast Neoplasms/analysis , Cytokines , Glycoproteins/isolation & purification , Neoplasm Proteins/isolation & purification , Adult , Female , Glycoproteins/physiology , Humans , Molecular Weight
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