Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 9 de 9
Filter
Add more filters










Database
Language
Publication year range
1.
Arthritis Res Ther ; 12(2): R37, 2010.
Article in English | MEDLINE | ID: mdl-20196869

ABSTRACT

INTRODUCTION: Urokinase-type plasminogen activator (u-PA) has been implicated in fibrinolysis, cell migration, latent cytokine activation, cell activation, T-cell activation, and tissue remodeling, all of which are involved in the development of rheumatoid arthritis. Previously, u-PA has been reported to play a protective role in monoarticular arthritis models involving mBSA as the antigen, but a deleterious role in the systemic polyarticular collagen-induced arthritis (CIA) model. The aim of the current study is to determine how u-PA might be acting in systemic arthritis models. METHODS: The CIA model and bone marrow chimeras were used to determine the cellular source of u-PA required for the arthritis development. Gene expression of inflammatory and destructive mediators was measured in joint tissue by quantitiative PCR and protein levels by ELISA. The requirement for u-PA in the type II collagen mAb-induced arthritis (CAIA) and K/BxN serum transfer arthritis models was determined using u-PA(-/-) mice. Neutrophilia was induced in the peritoneal cavity using either ovalbumin/anti-ovalbumin or the complement component C5a. RESULTS: u-PA from a bone marrow-derived cell was required for the full development of CIA. The disease in u-PA(-/-) mice reconstituted with bone marrow from C57BL/6 mice was indistinguishable from that in C57BL/6 mice, in terms of clinical score, histologic features, and protein and gene expression of key mediators. u-PA(-/-) mice were resistant to both CAIA and K/BxN serum transfer arthritis development. u-PA(-/-) mice developed a reduced neutrophilia and chemokine production in the peritoneal cavity following ovalbumin/anti-ovalbumin injection; in contrast, the peritoneal neutrophilia in response to C5a was u-PA independent. CONCLUSIONS: u-PA is required for the full development of systemic arthritis models involving immune complex formation and deposition. The cellular source of u-PA required for CIA is bone marrow derived and likely to be of myeloid origin. For immune complex-mediated peritonitis, and perhaps some other inflammatory responses, it is suggested that the u-PA involvement may be upstream of C5a signaling.


Subject(s)
Arthritis, Experimental/genetics , Arthritis, Rheumatoid/genetics , Gene Expression , Immune Complex Diseases/genetics , Urokinase-Type Plasminogen Activator/genetics , Animals , Arthritis, Experimental/metabolism , Arthritis, Experimental/pathology , Arthritis, Rheumatoid/immunology , Arthritis, Rheumatoid/metabolism , Bone Marrow Cells/metabolism , Bone Marrow Cells/pathology , Collagen/immunology , Collagen/pharmacology , Cytokines/metabolism , Female , Hindlimb , Immune Complex Diseases/immunology , Immune Complex Diseases/metabolism , Immunohistochemistry , Joints/metabolism , Joints/pathology , Male , Matrix Metalloproteinase 9/metabolism , Mice , Mice, Inbred C57BL , Mice, Knockout , Neutrophils/immunology , Ovalbumin/pharmacology , Peritonitis/genetics , Peritonitis/immunology , Peritonitis/metabolism , Urokinase-Type Plasminogen Activator/deficiency
2.
J Leukoc Biol ; 85(5): 766-78, 2009 May.
Article in English | MEDLINE | ID: mdl-19181863

ABSTRACT

Information about the development and function of human macrophage lineage populations, such as osteoclasts, is limited because of the lack of defined in vitro systems for their large-scale generation. Two M-CSF-containing cytokine cocktails were found under serum-free conditions to expand dramatically and to differentiate over time human CD34(+) hemopoietic stem cells into nonadherent and adherent macrophage populations. These populations exhibited increasing degrees of maturity over a 3-week period characterized by morphology, surface marker expression (CD11b, CD86, CD64, CD14, and c-Fms), phagocytic function, and gene-expression profiling using quantitative PCR and microarray analysis (principal component analysis, k-means clustering, and gene ontology classification). As assessed by the last criterion, the adherent population obtained at 3 weeks from the one protocol tested had high similarity to the well-studied peripheral blood monocyte-derived macrophages. The one population tested could be induced to differentiate into osteoclasts in the presence of M-CSF and receptor activator of NF-kappaB ligand, as judged by morphology, gene expression, and bone-resorbing ability. In addition to the large numbers of macrophage lineage cells able to be produced, this replicating system may be suitable for the molecular analysis of macrophage lineage commitment and progression and for gene targeting and delivery.


Subject(s)
Cell Differentiation , Hematopoietic Stem Cells/physiology , Macrophages/physiology , Antigens, CD34/metabolism , Biomarkers , Cell Culture Techniques , Cells, Cultured , Cluster Analysis , Culture Media, Serum-Free , Flow Cytometry , Gene Expression Profiling , Hematopoietic Stem Cells/cytology , Hematopoietic Stem Cells/metabolism , Humans , Macrophage Colony-Stimulating Factor/pharmacology , Macrophages/cytology , Macrophages/metabolism , Oligonucleotide Array Sequence Analysis , Osteoclasts/cytology , Osteoclasts/metabolism , Phagocytosis
3.
Thromb Haemost ; 95(4): 659-67, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16601837

ABSTRACT

There are two plasminogen activators (PAs), urokinase type-PA (u-PA) and tissue type-PA (t-PA). While u-PA is considered to be involved in cellular migration and tissue remodeling and t-PA in fibrinolysis, this distinction is not always clear-cut. With the use of u-PA and t-PA gene deficient mice (u-PA-/- and t-PA-/- mice, respectively) we have assessed the role of each PA in acute peritonitis. The cellular infiltrate in both thioglycolate- and antigen-induced peritoneal exudates was unaffected in u-PA-/- mice; in contrast, in t-PA-/- mice, the macrophage numbers, particularly of the Mac-1(hi) population, in the peritoneal cavity by day 4 were significantly reduced compared to wild-type mice. However, examination of the peritoneal wall revealed in fact increased numbers of macrophages adhering on/in the cavity lining at all time points studied; in addition, increased fibrin(ogen) staining was observed for these mice. The reduced macrophage numbers in the peritoneal cavities of t-PA-/- mice could be increased by administration of plasmin or t-PA prior to harvesting the thioglycolate-elicited exudates. These results suggest that t-PA and not u-PA is the PA controlling fibrinolysis in murine peritonitis. In its absence macrophages adhere to the accumulated fibrin(ogen) on/in the cavity wall lining, most likely via Mac-1 binding, thus affecting migration into and/or out of the peritoneal cavity. They also highlight the need to examine both the peritoneal cavity and wall in order to monitor accurately the extent of a peritoneal inflammatory reaction. Peritoneal inflammation in t-PA-/- mice represents a useful model to study the progression of intra-abdominal adhesions during surgery and clinical peritonitis.


Subject(s)
Fibrinogen/metabolism , Gene Deletion , Macrophages/metabolism , Peritoneum/metabolism , Tissue Plasminogen Activator/physiology , Urokinase-Type Plasminogen Activator/physiology , Animals , Inflammation , Methylation , Mice , Mice, Inbred C57BL , Mice, Transgenic , Peritonitis/pathology , Tissue Plasminogen Activator/genetics , Urokinase-Type Plasminogen Activator/genetics
4.
Diabetes ; 55(3): 691-8, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16505232

ABSTRACT

Activation of protein kinase C (PKC) in vascular tissue is associated with endothelial dysfunction and insulin resistance. However, the effect of vascular PKC activation on insulin-stimulated endothelial nitric oxide (NO) synthase (eNOS) regulation has not been characterized in obesity-associated insulin resistance. Diacylglycerol (DAG) concentration and PKC activity were increased in the aorta of Zucker fatty compared with Zucker lean rats. Insulin-stimulated increases in Akt phosphorylation and cGMP concentration (a measure of NO bioavailability) after euglycemic-hyperinsulinemic clamp were blunted in the aorta of fatty compared with lean rats but were partly normalized after 2 weeks of treatment with the PKCbeta inhibitor ruboxistaurin (LY333531). In endothelial cell culture, overexpression of PKCbeta1 and -beta2, but not PKCalpha, -delta, or -zeta, decreased insulin-stimulated Akt phosphorylation and eNOS expression. Overexpression of PKCbeta1 and -beta2, but not PKCalpha or -delta, also decreased Akt phosphorylation stimulated by vascular endothelial growth factor (VEGF). In microvessels isolated from transgenic mice overexpressing PKCbeta2 only in vascular cells, Akt phosphorylation stimulated by insulin was decreased compared with wild-type mice. Thus, activation of PKCbeta in endothelial cells and vascular tissue inhibits Akt activation by insulin and VEGF, inhibits Akt-dependent eNOS regulation by insulin, and causes endothelial dysfunction in obesity-associated insulin resistance.


Subject(s)
Blood Vessels/enzymology , Insulin Resistance , Nitric Oxide Synthase Type III/antagonists & inhibitors , Obesity/metabolism , Protein Kinase C/physiology , Proto-Oncogene Proteins c-akt/physiology , Animals , Atherosclerosis/etiology , Cattle , Cells, Cultured , Cyclic GMP/biosynthesis , Diglycerides/blood , Enzyme Activation , Male , Mice , Mice, Transgenic , Nitric Oxide Synthase Type III/physiology , Obesity/complications , Phosphorylation , Protein Kinase C beta , Rats , Rats, Zucker , Vascular Endothelial Growth Factor A/pharmacology
5.
Arterioscler Thromb Vasc Biol ; 26(4): 787-93, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16469952

ABSTRACT

OBJECTIVE: This study characterized the role of insulin receptors and resistance on vascular endothelial growth factor (VEGF) expression and myocardial vascularization in physiological conditions and after ischemia. METHODS AND RESULTS: Cardiac microvascular density was reduced by 30% in insulin-resistant Zucker fatty rats versus lean controls. This was associated with a parallel 40% inhibition of insulin-stimulated activation of both Akt and VEGF expression in the myocardium and cardiomyocytes. In contrast, the activation of Erk1/2 by insulin remained unchanged. In cultured cardiomyocytes, insulin or insulin-like growth factor (IGF)-1 increased VEGF mRNA and protein expression by 2-fold. Inhibition of PI3K/Akt, especially Akt2-mediated cascades but not the Ras/MEK/Erk pathway, using chemical inhibitors, dominant negative adenoviral constructs, or siRNA approaches suppressed VEGF mRNA expression by insulin. Ventricular tissues from muscle insulin receptor knockout (MIRKO) mice, which lack insulin receptors in the myocardium, have significant reductions in insulin but not IGF-1 signaling, VEGF expression, and vascular density before and after ischemia versus controls. CONCLUSIONS: Insulin regulates VEGF gene expression and vascularization in the myocardium specifically via insulin receptors and the activation of PI3K/Akt pathway. Selective inhibition of this pathway may lead to the decreases in VEGF expression and capillary density in the myocardium of patients with insulin resistance.


Subject(s)
Insulin Resistance , Myocardial Ischemia/metabolism , Neovascularization, Pathologic/metabolism , Receptor, Insulin/physiology , Vascular Endothelial Growth Factor A/biosynthesis , Androstadienes/pharmacology , Animals , Cells, Cultured , Coronary Vessels/metabolism , Coronary Vessels/pathology , Coronary Vessels/physiopathology , Flavonoids/pharmacology , Humans , Insulin/pharmacology , Male , Mice , Myocardial Ischemia/physiopathology , Myocytes, Cardiac/metabolism , Myocytes, Cardiac/pathology , Neovascularization, Pathologic/physiopathology , Phosphatidylinositol 3-Kinases/physiology , Phosphoinositide-3 Kinase Inhibitors , Protein Kinase Inhibitors/pharmacology , Proto-Oncogene Proteins c-akt/antagonists & inhibitors , Proto-Oncogene Proteins c-akt/physiology , Rats , Rats, Zucker , Signal Transduction , Wortmannin
6.
J Biol Chem ; 280(16): 15719-26, 2005 Apr 22.
Article in English | MEDLINE | ID: mdl-15699040

ABSTRACT

Protein kinase C (PKC) and angiotensin II (AngII) can regulate cardiac function in pathological conditions such as in diabetes or ischemic heart disease. We have reported that expression of connective tissue growth factor (CTGF) is increased in the myocardium of diabetic mice. Now we showed that the increase in CTGF expression in cardiac tissues of streptozotocin-induced diabetic rats was reversed by captopril and islet cell transplantation. Infusion of AngII in rats increased CTGF mRNA expression by 15-fold, which was completely inhibited by co-infusion with AT1 receptor antagonist, candesartan. Similarly, incubation of cultured cardiomyocytes with AngII increased CTGF mRNA expression by 2-fold, which was blocked by candesartan and a general PKC inhibitor, GF109203X. The role of PKC isoform-dependent action was further studied using adenoviral vector-mediated gene transfer of dominant negative (dn) PKC or wild type PKC isoforms. Expression of dnPKCalpha, -epsilon, and -zeta isoforms suppressed AngII-induced CTGF expression in cardiomyocytes. In contrast, expression of dominant negative PKCdelta significantly increased AngII-induced CTGF expression, whereas expression of wild type PKCdelta inhibited this induction. This inhibitory effect was further confirmed in the myocardium of transgenic mice with cardiomyocyte-specific overexpression of PKCdelta (deltaTg mice). Thus, AngII can regulate CTGF expression in cardiomyocytes through a PKC activation-mediated pathway in an isoform-selective manner both in physiological and diabetic states and may contribute to the development of cardiac fibrosis in diabetic cardiomyopathy.


Subject(s)
Angiotensin II/metabolism , Immediate-Early Proteins/genetics , Intercellular Signaling Peptides and Proteins/genetics , Myocardium/metabolism , Protein Kinase C/metabolism , Animals , Cells, Cultured , Connective Tissue Growth Factor , Diabetes Mellitus , Gene Expression Regulation/physiology , Immediate-Early Proteins/biosynthesis , Intercellular Signaling Peptides and Proteins/biosynthesis , Isoenzymes/metabolism , Mice , Myocytes, Cardiac/metabolism , Rats
8.
Diabetes ; 51(9): 2709-18, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12196463

ABSTRACT

Protein kinase C (PKC) beta isoform activity is increased in myocardium of diabetic rodents and heart failure patients. Transgenic mice overexpressing PKCbeta2 (PKCbeta2Tg) in the myocardium exhibit cardiomyopathy and cardiac fibrosis. In this study, we characterized the expression of connective tissue growth factor (CTGF) and transforming growth factor beta (TGFbeta) with the development of fibrosis in heart from PKCbeta2Tg mice at 4-16 weeks of age. Heart-to-body weight ratios of transgenic mice increased at 8 and 12 weeks, indicating hypertrophy, and ratios did not differ at 16 weeks. Collagen VI and fibronectin mRNA expression increased in PKCbeta2Tg hearts at 4-12 weeks. Histological examination revealed myocyte hypertrophy and fibrosis in 4- to 16-week PKCbeta2Tg hearts. CTGF expression increased in PKCbeta2Tg hearts at all ages, whereas TGFbeta increased only at 8 and 12 weeks. In 8-week diabetic mouse heart, CTGF and TGFbeta expression increased two- and fourfold, respectively. Similarly, CTGF expression increased in rat hearts at 2-8 weeks of diabetes. This is the first report of increased CTGF expression in myocardium of diabetic rodents suggesting that cardiac injury associated with PKCbeta2 activation, diabetes, or heart failure is marked by increased CTGF expression. CTGF could act independently or together with other cytokines to induce cardiac fibrosis and dysfunction.


Subject(s)
Cardiomyopathies/metabolism , Diabetes Mellitus, Experimental/enzymology , Growth Substances/metabolism , Immediate-Early Proteins/metabolism , Intercellular Signaling Peptides and Proteins , Isoenzymes/metabolism , Myocardium/metabolism , Protein Kinase C/metabolism , Animals , Cardiomyopathies/pathology , Connective Tissue Growth Factor , Enzyme Activation , Extracellular Matrix/metabolism , Fibrosis , Heart Ventricles , Immunologic Techniques , Male , Mice , Mice, Transgenic , Myocardium/pathology , Protein Kinase C beta , Rats , Staining and Labeling , Transforming Growth Factor beta/metabolism
9.
Circulation ; 105(3): 373-9, 2002 Jan 22.
Article in English | MEDLINE | ID: mdl-11804995

ABSTRACT

BACKGROUND: Inadequate angiogenic response to ischemia in the myocardium of diabetic patients could result in poor collateral formation. Yet, excessive neovascularization in the retina causes proliferative diabetic retinopathy. Since vascular endothelial growth factor (VEGF) is the major angiogenic factor expressed in response to hypoxia, we have characterized expression of VEGF and its receptors in retina, renal glomeruli, aorta, and myocardium in insulin-resistant and diabetic states. Methods and Results- The expression of mRNA and protein for VEGF and its receptors, VEGF-R1 and VEGF-R2, in the myocardium was decreased significantly by 40% to 70% in both diabetic and insulin-resistant nondiabetic rats. Twofold reductions in VEGF and VEGF-R2 were observed in ventricles from diabetic patients compared with nondiabetic donors. In contrast, expression of VEGF and its receptors were increased 2-fold in retina and glomeruli from diabetic or insulin-resistant rats. Insulin treatment of diabetic rats normalized changes in both cardiac and microvascular tissues. Insulin increased VEGF mRNA expression in cultured rat neonatal cardiac myocytes. CONCLUSIONS: The results documented for the first time that differential regulation of VEGF and its receptors exist between microvascular and cardiac tissues, which can be regulated by insulin. These results provide a potential explanation for concomitant capillary leakage and neovascularization in the retina and inadequate collateral formation in the myocardium of insulin-resistant and diabetic patients.


Subject(s)
Diabetes Mellitus/metabolism , Endothelial Growth Factors/metabolism , Insulin Resistance , Lymphokines/metabolism , Myocardium/metabolism , Receptor Protein-Tyrosine Kinases/metabolism , Receptors, Growth Factor/metabolism , Animals , Cells, Cultured , Collateral Circulation , Coronary Circulation , Diabetes Mellitus/blood , Endothelial Growth Factors/genetics , Female , Gene Expression Regulation/drug effects , Humans , Insulin/pharmacology , Kidney Glomerulus/metabolism , Lymphokines/genetics , Male , Middle Aged , Neovascularization, Pathologic , Obesity , RNA, Messenger/biosynthesis , Rats , Rats, Sprague-Dawley , Rats, Zucker , Receptor Protein-Tyrosine Kinases/genetics , Receptors, Growth Factor/genetics , Receptors, Vascular Endothelial Growth Factor , Retina/metabolism , Transcription, Genetic/drug effects , Vascular Endothelial Growth Factor A , Vascular Endothelial Growth Factors
SELECTION OF CITATIONS
SEARCH DETAIL
...