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1.
J Trauma ; 47(6): 1045-50; discussion 1050-1, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10608531

ABSTRACT

BACKGROUND: Disruption of the indigenous gut microflora with overgrowth of gram-negative bacteria and Candida species is common in the critically ill patient. These organisms readily translocate in vitro, which may cause septic complications and organ failure. A synergistic effect between Escherichia coli and C. albicans in polymicrobial infections has been demonstrated. An interaction between these organisms at the mucosal barrier is unknown. METHODS: Ca(CO2) monolayers were grown to confluence in a two compartment culture system. E. coli and C. albicans or E. coli alone were added to the apical chambers. Secretory immunoglobulin A was added to half of the apical chambers as well. Cell cultures were incubated for a total of 240 minutes. Basal media were sampled at timed intervals for quantitative culture. Monolayer integrity was confirmed by serial measurement of transepithelial electrical resistance. RESULTS: Secretory immunoglobulin A decreased bacterial translocation across Ca(CO2) monolayers challenged with E. coli alone. Transepithelial passage of E. coli was significantly increased by coculture of bacteria with C. albicans. Augmentation of bacterial translocation by Candida occurred even in the presence of secretory immunoglobulin A. CONCLUSIONS: Candida colonization of the GI tract may impair mucosal barrier defense against gram-negative bacteria. The clinical role of gut antifungal prophylaxis in protecting against gut derived gram-negative sepsis is speculative.


Subject(s)
Bacterial Translocation/physiology , Candida albicans/physiology , Escherichia coli/physiology , Gastric Mucosa/immunology , Gastric Mucosa/microbiology , Immunoglobulin A, Secretory/immunology , Caco-2 Cells , Candidiasis/etiology , Candidiasis/prevention & control , Cell Culture Techniques/methods , Colony Count, Microbial , Critical Illness , Cross Infection/etiology , Cross Infection/prevention & control , Culture Media , Electric Impedance , Escherichia coli Infections/etiology , Escherichia coli Infections/prevention & control , Humans , Time Factors
2.
Int J Cancer ; 82(2): 268-73, 1999 Jul 19.
Article in English | MEDLINE | ID: mdl-10389762

ABSTRACT

Mitogen-activated protein kinases (MAPKs) play a major role in the mitogenic signal transduction pathway and are essential components of both growth and differentiation. Constitutive activation of the MAPK cascade is associated with the carcinogenesis and metastasis of human breast and renal cell carcinomas. The gelatinases B (MMP-9) and A (MMP-2) are 2 members of the matrix metalloproteinase (MMPs) family which are expressed in human cancers and thought to play a critical role in tumor cell invasion and metastasis. In a previous study, we have shown that EGF and amphiregulin upregulate MMP-9 in metastatic SKBR-3 cells but have no effect on MMP-2 secretion. We now investigated specific step(s) in EGF-induced signalling associated with regulation of cell proliferation and MMP-9 induction. EGF-induced signalling in SKBR-3 cells was blocked by relatively specific inhibitors either on ras (FPT inhibitor-1) or P13 kinase (Wortmannin) or by reduction in EGF-induced tyrosine kinase activity (RG 13022). Blocking these signalling pathways significantly inhibited of EGF-induced cell proliferation but only partially reduced in EGF-induced MMP-9 secretion. In contrast, when SKBR-3 cells were exposed to MEK inhibitor (PD 98059) or MAPK inhibitors (Apigenin or MAPK antisense phosphorothioate oligodeoxynucleotides), EGF-induced cell proliferation, MMP-9 induction and invasion through reconstituted basement membrane were significantly reduced. Our results suggest that interfering with MAPK activity may provide a novel means of controlling growth and invasiveness of tumors in which the signalling cascade is activated.


Subject(s)
Breast Neoplasms/enzymology , Breast/enzymology , Calcium-Calmodulin-Dependent Protein Kinases/physiology , Enzyme Precursors/biosynthesis , Gelatinases/biosynthesis , Gene Expression Regulation, Neoplastic , Intercellular Signaling Peptides and Proteins , MAP Kinase Kinase Kinase 1 , Metalloendopeptidases/biosynthesis , Neoplasm Proteins/biosynthesis , Amphiregulin , Breast Neoplasms/pathology , Cell Division/drug effects , Cells, Cultured , EGF Family of Proteins , Enzyme Induction/drug effects , Enzyme Inhibitors/pharmacology , Enzyme Precursors/genetics , Epidermal Growth Factor/pharmacology , Epithelial Cells/drug effects , Epithelial Cells/enzymology , Female , Fibroblasts/drug effects , Fibroblasts/enzymology , Gelatinases/genetics , Gene Expression Regulation, Neoplastic/drug effects , Glycoproteins/pharmacology , Growth Substances/pharmacology , Humans , Metalloendopeptidases/genetics , Neoplasm Invasiveness , Neoplasm Proteins/genetics , Neoplasm Proteins/physiology , Phosphatidylinositol 3-Kinases/metabolism , Phosphoinositide-3 Kinase Inhibitors , Protein Serine-Threonine Kinases/antagonists & inhibitors , Protein Serine-Threonine Kinases/metabolism , Protein-Tyrosine Kinases/antagonists & inhibitors , Protein-Tyrosine Kinases/metabolism , Proto-Oncogene Proteins p21(ras)/antagonists & inhibitors , Proto-Oncogene Proteins p21(ras)/metabolism , Signal Transduction/drug effects , Stromal Cells/drug effects , Stromal Cells/enzymology , Transfection , Tumor Cells, Cultured/drug effects , Tumor Cells, Cultured/enzymology
3.
J Trauma ; 46(3): 374-8; discussion 378-9, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10088836

ABSTRACT

BACKGROUND: Hyperoxia has been reported to be protective against gut-derived sepsis. Although secretory immunoglobulin A (IgA) is primarily responsible for humoral defense of mucosal surfaces, a potential synergistic effect with hyperoxia is unknown. An asanguineous cell monolayer system was used to study these aspects in vitro. METHODS: MDCK cells were grown as polarized monolayers in a two-chamber culture system. Apical chambers were inoculated with 10(8) Escherichia coli M14 with or without polyclonal IgA and incubated in a 21 or 95% O2 environment. Basal medium was sampled at 90 and 180 minutes for bacterial translocation. In a second experiment, MDCK cells were lysed at 90 minutes and intracellular bacteria were quantitated. RESULTS: Bacterial translocation was decreased versus normoxia by the treatment groups IgA without hyperoxia or IgA with hyperoxia at 90 minutes. Bacterial internalization at 90 minutes was reduced to the greatest extent by the combined effects of hyperoxia and IgA. Translocation data at 180 minutes confirmed the additional protective effect of hyperoxia with IgA. CONCLUSION: Hyperoxia exerts a significant protective effect on barrier function independent of enhanced leukocyte function. Hyperoxia has an added effect to the mucosal defense provided by IgA.


Subject(s)
Escherichia coli Infections/immunology , Immunity, Mucosal/immunology , Immunoglobulin A, Secretory/immunology , Oxygen/immunology , Sepsis/immunology , Aerobiosis/immunology , Animals , Bacterial Translocation/immunology , Cell Line/immunology , Electric Impedance , Escherichia coli Infections/microbiology , Escherichia coli Infections/prevention & control , Leukocytes/immunology , Rabbits , Sepsis/microbiology , Sepsis/prevention & control , Time Factors
4.
Pathol Oncol Res ; 5(1): 49-55, 1999.
Article in English | MEDLINE | ID: mdl-10079379

ABSTRACT

We determined the effects of low dose radiation (<200 cGy) on the cell-cell integrity of confluent monolayers of pulmonary microvascular endothelial cells (PMEC). We observed dose- and time-dependent reversible radiation induced injuries to PMEC monolayers characterized by retraction (loss of cell-cell contact) mediated by cytoskeletal F-actin reorganization. Radiation induced reorganization of F-actin microfilament stress fibers was observed > or =30 minutes post irradiation and correlated positively with loss of cell-cell integrity. Cells of irradiated monolayers recovered to form contact inhibited monolayers > or =24 hours post irradiation; concomitantly, the depolymerized microfilaments organized to their pre-irradiated state as microfilament stress fibers arrayed parallel to the boundaries of adjacent contact-inhibited cells. Previous studies by other investigators have measured slight but significant increases in mouse lung wet weight >1 day post thoracic or whole body radiation (> or =500 cGy). Little or no data is available concerning time intervals <1 day post irradiation, possibly because of the presumption that edema is mediated, at least in part, by endothelial cell death or irreversible loss of barrier permeability functions which may only arise 1 day post irradiation. However, our in vitro data suggest that loss of endothelial barrier function may occur rapidly and at low dose levels (< or =200 cGy). Therefore, we determined radiation effects on lung wet weight and observed significant increases in wet weight (standardized per dry weight or per mouse weight) in < or =5 hours post thoracic exposure to 50 200 cGy x-radiation. We suggest that a single fraction of radiation even at low dose levels used in radiotherapy, may induce pulmonary edema by a reversible loss of endothelial cell-cell integrity and permeability barrier function.


Subject(s)
Endothelium/radiation effects , Pulmonary Edema/etiology , Pulmonary Edema/pathology , Radiation Injuries, Experimental/pathology , Actin Cytoskeleton/metabolism , Actins/metabolism , Acute Disease , Animals , Cell Death , Cell Size/radiation effects , Cells, Cultured , Cytoskeleton/metabolism , Cytoskeleton/radiation effects , Dose-Response Relationship, Radiation , Endothelium/drug effects , Humans , Lipoxygenase Inhibitors/therapeutic use , Male , Masoprocol/pharmacology , Mice , Mice, Inbred C57BL , Permeability/radiation effects , Pulmonary Edema/prevention & control , Radiotherapy/adverse effects , Thorax/radiation effects , Whole-Body Irradiation/adverse effects
5.
Hypertension ; 31(1): 39-44, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9449388

ABSTRACT

Angiotensin-converting enzyme inhibitors block left ventricular hypertrophy in vivo. A component of this effect has been attributed to tissue accumulation of bradykinin. Little is known regarding the effect of bradykinin on cardiomyocytes. The objectives of the present study were to define the effects of bradykinin on isolated ventricular cardiomyocytes (from adult and neonatal rat hearts) and to determine the extent to which bradykinin blocks hypertrophy in vitro. Bradykinin was found to be a hypertrophic agonist, as defined by increased protein synthesis and atrial natriuretic peptide secretion and expression. Bradykinin (10 micromol/L) increased [3H]phenylalanine incorporation by 23+/-3% in adult and by 36+/-10% in neonatal cardiomyocytes. Constitutive atrial natriuretic peptide secretion by neonatal myocytes was increased 357+/-103%. All effects of bradykinin were abolished by the B2-kinin receptor antagonist Hoe 140. These increases were similar in magnitude to those observed with phenylephrine (20 micromol/L) and angiotensin II (1 micromol/L). However, in cardiomyocytes cocultured with endothelial cells, bradykinin did not increase protein synthesis. Angiotensin II increased [3H]phenylalanine incorporation by 24+/-3% in adult cardiomyocytes in monoculture and by 22+/-2% in adult rat cardiomyocytes cocultured with endothelial cells. Bradykinin abolished this angiotensin II-induced hypertrophy in myocytes cultured with endothelial cells but not in myocytes studied in the absence of endothelial cells. In conclusion, bradykinin has a direct hypertrophic effect on ventricular myocytes. The presence of endothelial cells is required for the antihypertrophic effects of bradykinin. The results suggest that the increase in local concentration of bradykinin associated with angiotensin-converting enzyme inhibition is an important mechanism by which hypertrophy can be blocked. Manifestation of this mechanism appears to require bradykinin-stimulated release of paracrine factor(s) from endothelial cells, which are also able to block the hypertrophic effects of Ang II.


Subject(s)
Bradykinin/pharmacology , Hypertrophy, Left Ventricular/chemically induced , Angiotensin II/pharmacology , Animals , Animals, Newborn , Bradykinin/analogs & derivatives , Bradykinin Receptor Antagonists , Cells, Cultured , Endothelium/cytology , Heart Ventricles/cytology , Heart Ventricles/drug effects , Hypertrophy, Left Ventricular/prevention & control , Male , Rats , Rats, Sprague-Dawley
6.
J Trauma ; 43(5): 759-63, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9390486

ABSTRACT

OBJECTIVE: To study the relative impact of previous hypoxic exposure and the addition of secretory immunoglobulin A (IgA) on bacterial translocation. DESIGN: In vitro randomized experimental study. MATERIALS AND METHODS: Transfected Madin-Darby canine kidney epithelial cells were grown as monolayers in a two-chamber tissue culture system. Stationary growth phase Escherichia coli M14 were inoculated in the apical chamber with medium or medium containing polymeric secretory IgA. Tissue culture dishes were then placed in a 21 or 5% O2 incubator environment for 90 minutes followed by a 21% O2 environment. Medium from the basal compartment was then obtained at timed intervals for bacterial culture. MEASUREMENT AND MAIN RESULTS: Bacterial translocation increased with time in co-culture. Previous hypoxic exposure augmented translocation across the monolayers. The addition of IgA blocked translocation under both normoxic and hypoxic conditions. CONCLUSION: Secretory IgA is important in mucosal defense under both normal and shock conditions.


Subject(s)
Bacterial Translocation/physiology , Escherichia coli/physiology , Hypoxia/physiopathology , Immunoglobulin A, Secretory/physiology , Animals , Bacterial Translocation/immunology , Cells, Cultured , Dogs , Escherichia coli/growth & development , Hypoxia/microbiology , Immunoglobulin A , Kidney/cytology , Kidney/microbiology
7.
J Surg Res ; 69(1): 178-82, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9202666

ABSTRACT

The importance of secretory immunoglobulin A (IgA) on intestinal barrier function has gained increasing acceptance. However, due to the complexity of the intestinal microenvironment, the relative role of secretory IgA (sIgA) in mucosal defense has been difficult to study in vivo. Polarized Madin-Darby canine kidney (MDCK) epithelial cells expressing the complementary DNA (cDNA) for the polymeric Ig receptor were grown as monolayers in an in vitro two-chamber cell culture system to study the impact of sIgA on bacterial translocation (BT). Polymeric sIgA or media alone was added to the apical chambers of cell monolayers followed by apical inoculation with bacteria. The basal compartment was sampled at timed intervals thereafter to determine BT. Bacterial passage across the MDCK epithelial cell monolayers occurred in a time and bacterial inoculum concentration gradient. Addition of sIgA led to significant reductions in BT across the epithelial cell monolayers. This is a useful model for further investigation on the role of sIgA in intestinal barrier function.


Subject(s)
Bacterial Translocation , Immune System/physiopathology , Immunoglobulin A, Secretory/pharmacology , Kidney/immunology , Kidney/microbiology , Animals , Bacterial Adhesion/drug effects , Bacterial Translocation/drug effects , Cell Line , Dogs , Escherichia coli/drug effects , Escherichia coli/physiology , Kidney/cytology , Mucous Membrane/cytology , Mucous Membrane/immunology , Mucous Membrane/microbiology
9.
Biochem Cell Biol ; 74(6): 799-810, 1996.
Article in English | MEDLINE | ID: mdl-9164649

ABSTRACT

Experimental and clinical evidence reveals that the growth of solid tumors is dependent on angiogenesis. Proteolytic enzymes such as plasminogen activators and matrix metalloproteinases have been implicated in this neovascularization. The role of lysosomal proteases in this process has yet to be explored. Increased expression of the lysosomal cysteine protease cathepsin B has been observed in many etiologically different tumors, including human brain, prostate, breast, and gastrointestinal cancers. Immunohistochemical and in situ histochemical studies have demonstrated expression of cathepsin B in neovessels induced during malignant progression of human glioblastoma and prostate carcinomas. In these two tumor types, neovessels stain strongly for cathepsin B compared with the normal microvasculature. As an initial point to elucidate whether cathepsin B is an important component of the angiogenic response in tumours, we analyzed expression of cathepsin B in endothelial cells during neovessel formation. We present evidence for strong immunostaining of cathepsin B in rat brain microvascular endothelial cells as they form capillary tubes in vitro. This finding is discussed within the general framework of the role of proteolytic enzymes in tumor invasion and angiogenesis.


Subject(s)
Cathepsin B/physiology , Neoplasms/blood supply , Neovascularization, Pathologic , Animals , Cathepsin B/analysis , Endothelium, Vascular/chemistry , Humans , Neoplasm Invasiveness
10.
Circ Res ; 77(1): 43-53, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7788881

ABSTRACT

Fibronectin (FN) plays an important role in endothelial cell adhesion, spreading, and motility. Within FN, a number of functional domains have been identified, including the 33/66-kD carboxyl-terminal heparin-binding fragments, which support the adhesion of vascular endothelial cells. A number of synthetic peptides representing amino acid sequences within the 33/66-kD fragments have been shown to promote the adhesion, spreading, and migration of a variety of cell types. Our working hypothesis is that one or more of these sequences may also mediate vascular endothelial cell adhesion, spreading, and migration to the 33/66-kD fragments. In support of this hypothesis, we have demonstrated that endothelial cells from various sources adhered in a concentration-dependent manner to surfaces coated with FN, the 33/66-kD fragments, and synthetic peptides derived from the 33/66-kD fragments of FN. FN and the 33/66-kD fragments also promoted endothelial cell spreading and migration. Although each of the six synthetic peptides tested supported endothelial cell adhesion, only one of these peptides within the carboxyl-terminal heparin-binding domain (FN-C/H-V) promoted endothelial cell spreading and migration. Cell spreading on FN-C/H-V, as well as on FN and the 33/66-kD fragments, was associated with the formation of a well-developed actin cytoskeleton and the formation of focal contacts. FN-C/H-V (but not scrambled FN-C/H-V) inhibited cell spreading on FN and the 33/66-kD fragments in a concentration-dependent manner. FN-C/H-V had a modest effect on the adhesion of a clonal population of rat heart endothelial cells (RHE-1A) to the 33/66-kD fragments of FN and no effect on RHE-1A cell adhesion to FN. These findings suggest that peptide FN-C/H-V is unique among this group of peptides derived from the 33/66-kD heparin-binding fragments of FN in its ability to promote the adhesion, spreading, and migration of vascular endothelial cells and further suggest that the sequence defined by this peptide plays an important role in vascular endothelial cell interactions with the 33/66-kD fragments of FN.


Subject(s)
Cell Adhesion , Cell Movement , Endothelium/cytology , Fibronectins/metabolism , Peptide Fragments/metabolism , Amino Acid Sequence , Animals , Aorta , Cattle , Cells, Cultured , Cytological Techniques , Cytoskeleton/metabolism , Endothelium/metabolism , Endothelium, Vascular/cytology , Endothelium, Vascular/metabolism , Fibronectins/physiology , Heparin/metabolism , Humans , Microscopy, Interference , Molecular Sequence Data , Peptide Fragments/chemical synthesis , Rats , Umbilical Veins
11.
J Cell Sci ; 108 ( Pt 7): 2629-44, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7593304

ABSTRACT

Previous work demonstrated that 12(S)-HETE [12(S)-hydroxyeicosatetraenic acid], a lipoxygenase metabolite of arachidonic acid, stimulates the surface expression of integrin alpha v beta 3 on mouse lung vascular endothelial cells (CD clone 3) in a post-transcriptional and protein kinase C (PKC)-dependent fashion. In this study we examined the effect of 12(S)-HETE on the expression of integrin receptors alpha v beta 3 and alpha 5 beta 1 in a different clone of a mouse endothelial cell population derived from lung microvasculature (designated CD clone 4). The results indicated that 12(S)-HETE transcriptionally activates the gene expression of integrin alpha v as assessed by quantitative reverse transcription/polymerase chain reaction/Southern hybridization, RNase protection assay, solution hybridization, and northern blotting. The induction of alpha v mRNA occurred within 1 hour, peaked at approximately 4 hours (2- to 4-fold increase), persisted for up to 16 hours, and thereafter gradually declined. The PKC activator phorbol 12-myristate 13-acetate (PMA) induced the alpha v mRNA, in a similar way. 12(S)-HETE treatment did not, in contrast, alter the mRNA levels of integrin subunit alpha 5 or beta 1. The induction of alpha v mRNA appeared to be protein synthesis-independent, since cycloheximide did not alter the 12(S)-HETE effect. 12(S)-HETE also did not appear to alter the mRNA half-life of alpha v. On the other hand, 12(S)-HETE-induced increase in alpha v mRNA levels was PKC-dependent, since pretreatment of CD clone 4 cells with calphostin C significantly inhibited 12(S)-HETE-increased alpha v mRNA. Nuclear runoff experiments revealed that the increase in alpha v mRNA results from an enhanced gene transcription. Facilitated alpha v gene transcription resulted in an increased surface expression of alpha v beta 3 protein, which resulted in an increased cell adhesion to vitronectin. The above observations, in conjunction with our previous experimental data, suggest that 12(S)-HETE may employ diverse mechanisms to stimulate the integrin alpha v beta 3 expression in vascular endothelial cells, which could play important roles in tumor cell adhesion, angiogenesis, hemostasis, and many other vascular events.


Subject(s)
Antigens, CD/biosynthesis , Endothelium, Vascular/metabolism , Hydroxyeicosatetraenoic Acids/pharmacology , Protein Kinase C/metabolism , Transcriptional Activation/drug effects , 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid , Animals , Antibodies , Antigens, CD/analysis , Base Sequence , Blotting, Northern , Blotting, Southern , Cell Nucleus/metabolism , Clone Cells , DNA Primers , Endothelium, Vascular/cytology , Endothelium, Vascular/drug effects , Flow Cytometry , Fluorescent Antibody Technique , Integrin alphaV , Mice , Molecular Sequence Data , Polymerase Chain Reaction , Pulmonary Circulation , RNA, Messenger/analysis , RNA, Messenger/biosynthesis , Tetradecanoylphorbol Acetate/pharmacology
12.
Biochem Biophys Res Commun ; 211(2): 462-8, 1995 Jun 15.
Article in English | MEDLINE | ID: mdl-7540838

ABSTRACT

12(S)-HETE [12(S)-hydroxyeicosatetraenoic acid] is a lipoxygenase metabolite of arachidonic acid. Treatment of murine-lung-derived microvascular endothelial cells (CD clone 4) with exogenous 12(S)-HETE promoted wound healing of injured endothelial cell monolayers. 12(S)-HETE, in a time- and dose-dependent manner, enhanced the growth of CD clone 4 cells. Thymidine incorporation assays demonstrated that 12(S)-HETE increased the DNA synthesis by > 4 fold. In addition, normal endothelial cell growth stimulated by serum could be dose-dependently inhibited by a select 12-lipoxygenase inhibitor (BHPP), suggesting that 12(S)-HETE is a physiological mitogenic factor for microvascular endothelial cells.


Subject(s)
Endothelium, Vascular/cytology , Hydroxyeicosatetraenoic Acids/pharmacology , Microcirculation , Mitogens/pharmacology , Neovascularization, Pathologic , Wound Healing/drug effects , 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid , Animals , Biotin/analogs & derivatives , Biotin/pharmacology , Cell Division/drug effects , Cells, Cultured , Clone Cells , DNA/biosynthesis , DNA/drug effects , Endothelium, Vascular/drug effects , Kinetics , Mice , Phalloidine/analogs & derivatives , Phalloidine/pharmacology , Pulmonary Circulation , Thymidine/metabolism
13.
J Cardiovasc Pharmacol ; 25(4): 611-8, 1995 Apr.
Article in English | MEDLINE | ID: mdl-7596130

ABSTRACT

Angiopeptin (AP: BIM23014C), a cyclic analogue of the peptide hormone somatostatin, inhibits intimal hyperplasia after balloon angioplasty. This inhibition has been attributed to a direct inhibitory effect on smooth muscle cell (SMC) proliferation. However, the SMC that proliferate in the intima and contribute to intimal hyperplasia arrive there by migrating from the injured media, suggesting that SMC migration may also play an important role in this process. Indeed, in the experiments we describe, AP inhibited the migration of rat aortic SMC cells (RA-SMC) in response to type I collagen, the predominant form of collagen in the vessel media, and did so dose dependently. RA-SMC migration was inhibited 70% in the presence of AP 100 nM. RA-SMC adhesion to type I collagen in these conditions was not inhibited, suggesting that AP does not interfere with RA-SMC recognition of type I collagen; instead, it blocks subsequent signaling events that are necessary for RA-SMC migration in response to type I collagen. AP inhibited the forskolin-stimulated accumulation of cyclic AMP by RA-SMC (35% at 30 nM). In addition, pertussis toxin (PT), which blocks Gi-mediated inhibition of adenylyl cyclase, blocked the inhibitory effect of AP on cyclic AMP (cAMP) accumulation and also blocked the inhibitory effect of AP on RA-SMC migration. These findings suggest that the inhibitory effect of AP on intimal hyperplasia is due at least in part to its effects on SMC migration and that these effects are mediated by a Gi-dependent pathway and may involve inhibition of adenylyl cyclase and cAMP accumulation.


Subject(s)
Adenylyl Cyclase Inhibitors , Antineoplastic Agents/pharmacology , Cyclic AMP/metabolism , GTP-Binding Proteins/physiology , Muscle, Smooth, Vascular/cytology , Oligopeptides/pharmacology , Somatostatin/analogs & derivatives , Adenylate Cyclase Toxin , Animals , Cell Adhesion/drug effects , Cell Division/drug effects , Cell Movement/drug effects , Cells, Cultured , Colforsin/pharmacology , Hyperplasia/pathology , Muscle, Smooth, Vascular/drug effects , Muscle, Smooth, Vascular/metabolism , Peptides, Cyclic , Pertussis Toxin , Rats , Somatostatin/pharmacology , Virulence Factors, Bordetella/pharmacology
14.
Int J Cancer ; 60(3): 418-25, 1995 Jan 27.
Article in English | MEDLINE | ID: mdl-7530235

ABSTRACT

We have investigated the regulatory role of PGI2 and its stable analogs, i.e., iloprost and cicaprost, on 12(S)-HETE- and TPA-enhanced tumor cell integrin expression and adhesion. Walker 256 carcinosarcoma cells express alpha IIb beta 3 integrin receptors, which mediate their adhesion to endothelium, subendothelial matrix and fibronectin. Adhesion is enhanced by treatment with exogenous 12(S)-HETE but not 12(R)-HETE or other lipoxygenase-derived hydroxy fatty acids, as well as by TPA. Both 12(S)-HETE and TPA enhanced alpha IIb beta 3 expression on W256 cells. PGI2 iloprost and cicaprost inhibited both 12(S)-HETE- and TPA-enhanced adhesion to endothelium and subendothelial matrix as well as alpha IIb beta 3 expression on W256 cells. The mechanism responsible for the effect of PGI2 was explored. Prostacyclin treatment of W256 cells resulted in an enhanced production of cAMP in a time- and dose-dependent manner. Pre-treatment of tumor cells with increasing concentrations of adenosine resulted in a dose-dependent decrease in the PGI2 effect on TPA or 12(S)-HETE-enhanced adhesion, suggesting that the PGI2 effect is mediated through PKA. Dibutyryl cAMP also blocked the 12(S)-HETE- or TPA-enhanced adhesion, and adenosine pre-treatment did not result in an inhibition of the dibutyryl cAMP effect. Collectively, our results suggest that the cyclooxygenase metabolite PGI2 can antagonize the lipoxygenase metabolite 12(S)-HETE- and TPA-enhanced alpha IIb beta 3 expression and tumor cell adhesion via activation of adenylate cyclase and elevation of intracellular levels of cAMP.


Subject(s)
Antineoplastic Agents , Cell Adhesion/drug effects , Epoprostenol/analogs & derivatives , Epoprostenol/pharmacology , Hydroxyeicosatetraenoic Acids/antagonists & inhibitors , Iloprost/pharmacology , Tetradecanoylphorbol Acetate/antagonists & inhibitors , 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid , Adenylyl Cyclases/metabolism , Animals , Cyclic AMP/physiology , In Vitro Techniques , Integrins/metabolism , Rats , Rats, Sprague-Dawley , Tumor Cells, Cultured
15.
Biochim Biophys Acta ; 1223(1): 141-7, 1994 Aug 11.
Article in English | MEDLINE | ID: mdl-8061046

ABSTRACT

Angiotensin II (AII) was found to stimulate TGF-beta 1 gene expression in rat heart endothelial cells in a dose- and time-dependent manner. The maximal induction of TGF-beta 1 mRNA was achieved by 6 h after the addition of AII. This induction was blocked by losartan, an AT1 receptor antagonist and by calphostin C, a protein kinase C inhibitor. Addition of actinomycin D and cycloheximide abolished the induction. TGF-beta 1 promoter activities were stimulated 5-fold by AII. TGF-beta 1 secreted by the rat heart endothelial cells in response to AII was in a latent form and could be activated by mild heat treatment. These results suggest that AII stimulates TGF-beta 1 production by a protein kinase C-dependent pathway which is dependent upon de novo RNA synthesis and protein synthesis. Since endothelial cells line the blood vessels and sense the rise in AII associated with hypertension, the release of TGF-beta 1 by these cells may provide the initial trigger leading to cardiac fibrosis in angiotensin-renin-dependent hypertension.


Subject(s)
Angiotensin II/pharmacology , Endothelium, Vascular/drug effects , Heart/drug effects , Transforming Growth Factor beta/biosynthesis , Angiotensin II/antagonists & inhibitors , Animals , Cells, Cultured , Endothelium, Vascular/metabolism , Myocardium/metabolism , RNA, Messenger/analysis , Rats , Transforming Growth Factor beta/genetics
16.
Lab Invest ; 70(3): 314-23, 1994 Mar.
Article in English | MEDLINE | ID: mdl-8145526

ABSTRACT

BACKGROUND: We have previously demonstrated that the metastatic potential of tumor cells can be increased by treatment with exogenous 12(S)hydroxyeicosatetraenoic acid [12(S)-HETE], a lipoxygenase metabolite of arachidonic acid. However, the biosynthesis of the authentic lipid mediator by tumor cells, and especially the correlation of its biosynthesis to tumor cell metastatic capacity have not been characterized. In addition, a role for other mono HETEs in influencing tumor cell metastatic behavior has been suggested, but conclusive evidence is lacking. In this study, we analyzed the biosynthesis of mono HETEs from arachidonic acid in tumor cells of different metastatic ability and correlated biosynthesis to metastatic potential. EXPERIMENTAL DESIGN: The biosynthesis of mono HETEs by low and high metastatic subpopulations of B16 amelanotic melanoma (B16a) cells was analyzed by high performance liquid chromatography (HPLC). The identity of biosynthetic 12-HETE was confirmed by gas chromatography/mass spectrometry (GC/MS) and its stereochemical structure assigned by chiral phase HPLC. The effect of a lipoxygenase inhibitor on the biosynthesis of mono HETEs and its effect on metastatic behavior was examined. RESULTS: HPLC analysis revealed that low (LM180) and high (HM340) metastatic B16a cells exhibited different profiles and efficiencies for conversion of arachidonic acid to mono HETEs. LM180 cells produced equal quantities of 12-HETE and 5-HETE. In contrast, HM340 cells synthesized predominantly 12-HETE and small amounts of 15-, 11- and 5-HETEs. At equal concentrations of substrate, four times more 12-HETE was synthesized by HM340 cells than by LM180 cells. The identity of biosynthetic 12-HETE was confirmed by gas chromatography/mass spectrometry and chiral phase HPLC demonstrated that it was the S enantiomer. The biosynthesis of 12(S)-HETE, but not other HETEs, was significantly inhibited by a lipoxygenase inhibitor, N-benzyl-N-hydroxy-5-phenylpentanamide. N-benzyl-N-hydroxy-5-phenylpentanamide, in a dose-dependent manner, decreased the adhesion of HM340 cells to murine pulmonary microvessel endothelium in vitro and lung colony formation in vivo. Furthermore, re-introduction of 12(S)-HETE, but not other mono HETEs, to HM340 cells pretreated with N-benzyl-N-hydroxy-5-phenylpentanamide, increased their adhesion to endothelium. CONCLUSIONS: Biosynthesis of 12(S)-HETE by tumor cells is a determinant of their metastatic potential and inhibition of 12(S)-HETE biosynthesis in tumor cells may be a crucial target for intervening in metastasis.


Subject(s)
Hydroxyeicosatetraenoic Acids/biosynthesis , Melanoma, Amelanotic/pathology , Skin Neoplasms/pathology , 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid , Animals , Arachidonic Acids/metabolism , Cell Adhesion , Chromatography, High Pressure Liquid , Gas Chromatography-Mass Spectrometry , Humans , Hydroxamic Acids/pharmacology , Hydroxyeicosatetraenoic Acids/chemistry , Lipoxygenase Inhibitors/pharmacology , Lung Neoplasms/secondary , Male , Melanoma, Amelanotic/metabolism , Melanoma, Amelanotic/secondary , Mice , Mice, Inbred C57BL , Molecular Conformation , Pentanoic Acids/pharmacology , Radioimmunoassay , Skin Neoplasms/metabolism , Tumor Cells, Cultured
17.
Cancer Res ; 54(4): 1119-29, 1994 Feb 15.
Article in English | MEDLINE | ID: mdl-8313370

ABSTRACT

Tumor cell interaction with endothelial cells is a crucial step leading to organ-selective metastasis. Adhesion of murine B16 amelanotic melanoma cells (B16a) to murine microvascular endothelial cells (CD3) was enhanced, in a dose- and time-dependent manner, by pretreating CD3 cells with 12(S)-hydroperoxyeicosatetraenoic acid [i.e., 12(S)-HETE], a 12-lipoxygenase metabolite of arachidonic acid. The metabolic precursor of 12(S)-HETE, 12-HPETE (12-hydroperoxyeicosatetraenoic acid) also enhanced B16a cell adhesion to CD3 monolayers, whereas other lipoxygenase products, i.e., 5(S), 11(S), and 15(S)-HETEs were ineffective. 12(S)-HETE-enhanced tumor cell adhesion was blocked by treating endothelial cells with antibodies against the alpha v beta 3 complex or against individual subunits but not with antibodies against alpha 5 beta 1. In contrast, neither of these two integrins appeared to be involved in tumor cell adhesion to unstimulated endothelium. Flow cytometric analysis, immunofluorescent labeling, and image analysis indicated that 12(S)-HETE induced a time- and dose-dependent increase in the surface expression of alpha v beta 3 but not alpha 5 beta 1 on CD3 cells. The increased surface expression of alpha v beta 3 on endothelial cells did not result from an increased transcription or translation of alpha v beta 3 message as confirmed by quantitative reverse transcription-polymerase chain reaction, Northern blotting, and quantitative Western blotting. Instead, subcellular fractionation studies revealed an increased translocation of alpha v beta 3 integrins from the cytosolic pool to the membrane fractions. Pretreatment of endothelial cells with several cytoskeleton-disrupting agents (i.e., cycloheximide or acrylamide to disrupt intermediate filament vimentin, cytochalasin D to disrupt microfilaments, colchicine or Nocodazole to disrupt microtubules) abolished the 12(S)-HETE-enhanced alpha v beta 3 surface expression as well as tumor cell adhesion to endothelial cells. Also, pretreatment of CD3 cells with protein kinase C inhibitor calphostin C, but not with protein kinase A inhibitor H8, blocked 12(S)-HETE-enhanced alpha v beta 3 surface expression and tumor cell adhesion. Collectively, these results suggest that eicosanoid 12(S)-HETE modulates tumor cell interaction with endothelium via protein kinase C- and cytoskeleton-dependent up-regulation of the surface expression of alpha v beta 3 integrin.


Subject(s)
Cytoskeleton/physiology , Endothelium, Vascular/drug effects , Hydroxyeicosatetraenoic Acids/pharmacology , Integrins/physiology , Neoplasms, Experimental/pathology , Protein Kinase C/physiology , 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid , Animals , Base Sequence , Biological Transport , Cell Adhesion/drug effects , Mice , Microcirculation/drug effects , Molecular Sequence Data , Transcription, Genetic , Tumor Cells, Cultured , Up-Regulation
18.
Cancer Res ; 54(2): 565-74, 1994 Jan 15.
Article in English | MEDLINE | ID: mdl-8275495

ABSTRACT

Our previous work demonstrated that the 12-lipoxygenase metabolite of arachidonic acid, 12(S)-hydroxyeicosatetraenoic acid [12(S)-HETE] induced a nondestructive and reversible retraction of cultured endothelial cells. In the current study we tested the hypothesis that tumor cells produce 12(S)-HETE during their interactions with endothelial cells which in turn induces endothelial cell retraction. Coincubation of Lewis lung carcinoma cells or elutriated B16 amelanotic melanoma (B16a) cells but not 3T3 fibroblasts with microvascular endothelial cells (CD3) resulted in a time- and concentration-dependent retraction of the CD3 monolayers as revealed by quantitative binding assays and phase contrast microscopy. Lewis lung carcinoma cell-induced endothelial cell retraction was blocked by specific lipoxygenase inhibitors but not by cyclooxygenase inhibitors, suggesting the involvement of a lipoxygenase metabolite(s). Radioimmunoassay and high-performance liquid chromatography analysis of tumor cell extracts identified 12(S)-HETE as the major lipoxygenase metabolite of arachidonic acid and tumor cell generation of 12(S)-HETE was specifically blocked by a select 12-lipoxygenase inhibitor N-benzyl-N-hydroxy-5-phenyl-pentamide. The identity and stereochemistry of tumor cell-derived 12-HETE was substantiated by gas chromatography-mass spectrometry analysis and chiral phase high-performance liquid chromatography, respectively. Lewis lung carcinoma cell adhesion to CD3 monolayers was accompanied by an enhanced 12(S)-HETE biosynthesis by tumor cells, which paralleled the tumor cell-induced endothelial cell retraction in a cell number-dependent manner. Pretreatment of tumor cells with N-benzyl-N-hydroxy-5-phenylpentamide inhibited both increased 12(S)-HETE biosynthesis and tumor cell-induced endothelial cell retraction. Highly metastatic variants of elutriated B16a cells which had been shown to produce large quantities of 12(S)-HETE induced significant CD3 cell retraction, while low metastatic subpopulations of B16a cells which synthesized no or little 12(S)-HETE did not induce endothelial cell retraction. These results suggest that 12(S)-HETE synthesis during tumor cell-endothelial cell interactions may represent a key contributory factor in cancer metastasis.


Subject(s)
Endothelium, Vascular/physiology , Hydroxyeicosatetraenoic Acids/physiology , 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid , Amides/pharmacology , Animals , Benzylamines/pharmacology , Carcinoma/blood supply , Carcinoma/metabolism , Cell Adhesion , Hydroxyeicosatetraenoic Acids/chemistry , Hydroxyeicosatetraenoic Acids/metabolism , Lipoxygenase Inhibitors/pharmacology , Lung Neoplasms/blood supply , Lung Neoplasms/metabolism , Melanoma, Experimental/blood supply , Melanoma, Experimental/metabolism , Mice , Mice, Inbred C57BL , Neoplasm Invasiveness , Tumor Cells, Cultured
19.
Exp Cell Res ; 210(1): 1-9, 1994 Jan.
Article in English | MEDLINE | ID: mdl-8269984

ABSTRACT

Platelets have been hypothesized to contribute to tumor cell metastasis, but the underlying mechanism(s) remain unknown. We demonstrate here that one mechanism whereby platelets may facilitate metastasis is by potentiating tumor cell-induced endothelial cell retraction, a prerequisite for the extravasation of most tumor cell types. The integrity of cultured microvascular endothelial cell (CD3 cells) monolayers was perturbed by 12[S]-hydroxyeicosatetraenoic acid (12(S)-HETE), a lipoxygenase metabolite of arachidonic acid, as well as by tumor cells (i.e., Lewis lung carcinoma cells or 3LL). 3LL cells induced a concentration- and time-dependent retraction of the CD3 monolayers, as assessed by quantitative binding assays as well as by phase-contrast microscopy. In contrast, normal murine fibroblasts (3T3) did not induce endothelial cell retraction. 3LL cell-induced endothelial cell retraction was potentiated, in a dose- and time-dependent manner, by homologous murine platelets while platelets alone did not induce endothelial cell retraction. Platelet-enhanced, tumor cell-induced endothelial cell retraction was inhibited by treating either tumor cells or platelets with the lipoxygenase inhibitors nordihydroguaiaretic acid or N-benzyl-N-hydroxy-5-phenylpentanamide (BHPP) as well as by PGI2 or its analogs iloprost and ZK96.480 (cicaprost), but not by the cyclooxygenase inhibitor aspirin (ASA). Tumor cells, upon adhesion to endothelium, initiated 12(S)-HETE biosynthesis, which was inhibited by pretreating tumor cells with BHPP but not with ASA. Additionally, 12(S)-HETE biosynthesis during tumor cell-endothelial cell adhesion was significantly enhanced by the addition of homologous platelets. Collectively, these results suggest that tumor cell-platelet-endothelial cell interactions lead to enhanced biosynthesis of 12(S)-HETE by tumor cells and/or platelets, which in turn induces endothelial cell retraction, thus facilitating tumor cell extravasation and metastasis.


Subject(s)
Blood Platelets/physiology , Endothelium, Vascular/cytology , Hydroxyeicosatetraenoic Acids/pharmacology , Neoplasm Metastasis , 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid , Animals , Biotin/analogs & derivatives , Biotin/pharmacology , Cell Adhesion/drug effects , Cells, Cultured , Collagen/metabolism , Endothelium, Vascular/drug effects , Hydroxyeicosatetraenoic Acids/metabolism , In Vitro Techniques , Lipoxygenase Inhibitors , Mice , Mice, Inbred C57BL , Phalloidine/analogs & derivatives , Phalloidine/pharmacology
20.
Tissue Cell ; 25(6): 833-46, 1993 Dec.
Article in English | MEDLINE | ID: mdl-8140579

ABSTRACT

Organ-derived endothelia have been shown to exhibit distinct patterns of morphology and growth responsiveness in vitro. This report describes the development, cloning and establishment of long-term serial cultures of rat vascular endothelial cells derived from cerebrocortical resistance vessels (small arteries and arterioles). Modification of our previous published technique for establishing resistance vessel-derived smooth muscle cells (RV-SMC) resulted in enhanced levels of endothelial outgrowth from collagenase-treated microvessel fragments. Although primary culture growth consisted predominantly of SMC, subsequent subcultivation of these cultures revealed the presence of distinct endothelial cell clusters within the SMC monolayer. Serial cloning of these isolates resulted in a homogeneous population of cells with the characteristic endothelial cobblestone growth pattern and positive immunofluorescence for factor VIII-related antigen. Previously established RV-SMC frozen stocks provided an additional source for obtaining resistance vessel endothelial cells. This was made possible by the slow proliferation rate of early-passage RV-SMC and their inability to withstand freezing procedures. Endothelial cells from both preparations were identical and designated resistance vessel derived endothelial cells RV-EC. Upon long-term cultivation (> P15), confluent RV-EC cultures expressed spontaneous multicellular cord development that stained positive for factor VIII-related antigen. Cell growth studies demonstrated that RV-EC were capable of significant growth when maintained in serum-free conditions. Growth kinetics using serum-free conditioned medium demonstrated mitogenic activity indicating the presence of an autocrine growth factor. Increase growth responsiveness was also noted in RV-EC when treated with a variety of peptide growth factors. These results indicate that resistance vessel endothelium can be successfully isolated and maintained in long-term serial cultures. Furthermore, the availability of cultured EC and SMC from this unique microvascular site will enable examination of cerebrovascular endothelial-smooth muscle cell interactions in vitro and may help to elucidate the mechanisms of altered vascular function in disease states.


Subject(s)
Arterioles/cytology , Capillary Resistance/physiology , Cerebral Arteries/cytology , Endothelium, Vascular/cytology , Animals , Arterioles/drug effects , Capillary Resistance/drug effects , Cell Division/physiology , Cells, Cultured , Cerebral Arteries/drug effects , Clone Cells/physiology , Culture Media, Conditioned , Endothelium, Vascular/drug effects , Fluorescent Antibody Technique , Growth Substances/pharmacology , Male , Microscopy, Phase-Contrast , Mitogens/biosynthesis , Rats , Rats, Sprague-Dawley
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