8 results on '"Pennig J"'
Search Results
2. P1939Tumor necrosis factor receptor-associated factor 5 (TRAF-5) deficiency exacerbates diet-induced adipose tissue inflammation and aggravates metabolic syndrome in mice
- Author
-
Gissler, M C, primary, Anto Michel, N, additional, Pennig, J, additional, Scherrer, P, additional, Pfeiffer, K, additional, Haerdtner, C, additional, Von Elverfeldt, D, additional, Hoppe, N, additional, Stachon, P, additional, Machulsky, N, additional, Hilgendorf, I, additional, Bode, C, additional, Wolf, D, additional, Zirlik, A, additional, and Willecke, F, additional
- Published
- 2019
- Full Text
- View/download PDF
3. Deficiency of Endothelial CD40 Induces a Stable Plaque Phenotype and Limits Inflammatory Cell Recruitment to Atherosclerotic Lesions in Mice.
- Author
-
Gissler MC, Scherrer P, Anto-Michel N, Pennig J, Hoppe N, Füner L, Härdtner C, Stachon P, Li X, Mitre LS, Marchini T, Madl J, Wadle C, Hilgendorf I, von Zur Mühlen C, Bode C, Weber C, Lutgens E, Wolf D, Gerdes N, Zirlik A, and Willecke F
- Subjects
- Animals, Aorta immunology, Aorta pathology, Aortic Diseases genetics, Aortic Diseases immunology, Aortic Diseases pathology, Apoptosis, Atherosclerosis genetics, Atherosclerosis immunology, Atherosclerosis pathology, CD40 Antigens genetics, Cell Adhesion, Cells, Cultured, Coculture Techniques, Disease Models, Animal, Endothelial Cells immunology, Endothelial Cells pathology, Humans, Intercellular Adhesion Molecule-1 metabolism, Macrophages immunology, Male, Mice, Knockout, ApoE, Monocytes immunology, Plaque, Atherosclerotic, Signal Transduction, Vascular Cell Adhesion Molecule-1 metabolism, Mice, Aorta metabolism, Aortic Diseases metabolism, Atherosclerosis metabolism, CD40 Antigens deficiency, Chemotaxis, Leukocyte, Endothelial Cells metabolism, Macrophages metabolism, Monocytes metabolism
- Abstract
Objectives: The co-stimulatory CD40L-CD40 dyad exerts a critical role in atherosclerosis by modulating leukocyte accumulation into developing atherosclerotic plaques. The requirement for cell-type specific expression of both molecules, however, remains elusive. Here, we evaluate the contribution of CD40 expressed on endothelial cells (ECs) in a mouse model of atherosclerosis., Methods and Results: Atherosclerotic plaques of apolipoprotein E-deficient ( Apoe
-/- ) mice and humans displayed increased expression of CD40 on ECs compared with controls. To interrogate the role of CD40 on ECs in atherosclerosis, we induced EC-specific (BmxCreERT2 -driven) deficiency of CD40 in Apoe-/- mice. After feeding a chow diet for 25 weeks, EC-specific deletion of CD40 (iEC-CD40) ameliorated plaque lipid deposition and lesional macrophage accumulation but increased intimal smooth muscle cell and collagen content, while atherosclerotic lesion size did not change. Leukocyte adhesion to the vessel wall was impaired in iEC-CD40-deficient mice as demonstrated by intravital microscopy. In accord, expression of vascular cell adhesion molecule 1 (VCAM-1) and intercellular adhesion molecule 1 (ICAM-1) in the vascular endothelium declined after deletion of CD40. In vitro, antibody-mediated inhibition of human endothelial CD40 significantly abated monocyte adhesion on ECs., Conclusion: Endothelial deficiency of CD40 in mice promotes structural features associated with a stable plaque phenotype in humans and decreases leukocyte adhesion. These results suggest that endothelial-expressed CD40 contributes to inflammatory cell migration and consecutive plaque formation in atherogenesis., Competing Interests: L. F., P. S., L. S. M., J. M., C. W., I. H., C. v. z. M., C. B., and D. W. are members of the Collaborative Research Centre SFB1425 of the German Research Foundation., (Thieme. All rights reserved.)- Published
- 2021
- Full Text
- View/download PDF
4. Genetic Deficiency of TRAF5 Promotes Adipose Tissue Inflammation and Aggravates Diet-Induced Obesity in Mice.
- Author
-
Gissler MC, Anto-Michel N, Pennig J, Scherrer P, Li X, Marchini T, Pfeiffer K, Härdtner C, Abogunloko T, Mwinyella T, Sol Mitre L, Spiga L, Koentges C, Smolka C, von Elverfeldt D, Hoppe N, Stachon P, Dufner B, Heidt T, Piepenburg S, Hilgendorf I, Bjune JI, Dankel SN, Mellgren G, Seifert G, Eisenhardt SU, Bugger H, von Zur Muhlen C, Bode C, Zirlik A, Wolf D, and Willecke F
- Subjects
- Adipocytes immunology, Adipocytes pathology, Adipose Tissue immunology, Adipose Tissue pathology, Adiposity, Adult, Aged, Animals, Diet, High-Fat, Disease Models, Animal, Female, Humans, Lymphocytes immunology, Macrophages immunology, Macrophages metabolism, Male, Mice, Inbred C57BL, Mice, Knockout, Middle Aged, Obesity genetics, Obesity immunology, Obesity pathology, Panniculitis genetics, Panniculitis immunology, Panniculitis pathology, Signal Transduction, TNF Receptor-Associated Factor 5 genetics, Mice, Adipocytes metabolism, Adipose Tissue metabolism, Cytokines metabolism, Inflammation Mediators metabolism, Lymphocytes metabolism, Obesity metabolism, Panniculitis metabolism, TNF Receptor-Associated Factor 5 deficiency
- Abstract
Objective: The accumulation of inflammatory leukocytes is a prerequisite of adipose tissue inflammation during cardiometabolic disease. We previously reported that a genetic deficiency of the intracellular signaling adaptor TRAF5 (TNF [tumor necrosis factor] receptor-associated factor 5) accelerates atherosclerosis in mice by increasing inflammatory cell recruitment. Here, we tested the hypothesis that an impairment of TRAF5 signaling modulates adipose tissue inflammation and its metabolic complications in a model of diet-induced obesity in mice. Approach and Results: To induce diet-induced obesity and adipose tissue inflammation, wild-type or Traf5-/- mice consumed a high-fat diet for 18 weeks. Traf5-/- mice showed an increased weight gain, impaired insulin tolerance, and increased fasting blood glucose. Weight of livers and peripheral fat pads was increased in Traf5-/- mice, whereas lean tissue weight and growth were not affected. Flow cytometry of the stromal vascular fraction of visceral adipose tissue from Traf5-/- mice revealed an increase in cytotoxic T cells, CD11c+ macrophages, and increased gene expression of proinflammatory cytokines and chemokines. At the level of cell types, expression of TNF[alpha], MIP (macrophage inflammatory protein)-1[alpha], MCP (monocyte chemoattractant protein)-1, and RANTES (regulated on activation, normal T-cell expressed and secreted) was significantly upregulated in Traf5-deficient adipocytes but not in Traf5-deficient leukocytes from visceral adipose tissue. Finally, Traf5 expression was lower in adipocytes from obese patients and mice and recovered in adipose tissue of obese patients one year after bariatric surgery. Conclusions: We show that a genetic deficiency of TRAF5 in mice aggravates diet-induced obesity and its metabolic derangements by a proinflammatory response in adipocytes. Our data indicate that TRAF5 may promote anti-inflammatory and obesity-preventing signaling events in adipose tissue.
- Published
- 2021
- Full Text
- View/download PDF
5. Glucose lowering by SGLT2-inhibitor empagliflozin accelerates atherosclerosis regression in hyperglycemic STZ-diabetic mice.
- Author
-
Pennig J, Scherrer P, Gissler MC, Anto-Michel N, Hoppe N, Füner L, Härdtner C, Stachon P, Wolf D, Hilgendorf I, Mullick A, Bode C, Zirlik A, Goldberg IJ, and Willecke F
- Subjects
- Animals, Atherosclerosis blood, Blood Glucose analysis, Diabetes Mellitus, Experimental blood, Male, Mice, Mice, Inbred C57BL, Plaque, Atherosclerotic blood, Plaque, Atherosclerotic drug therapy, Plaque, Atherosclerotic etiology, Atherosclerosis drug therapy, Atherosclerosis etiology, Benzhydryl Compounds therapeutic use, Diabetes Mellitus, Experimental complications, Diabetes Mellitus, Experimental drug therapy, Glucosides therapeutic use, Sodium-Glucose Transporter 2 Inhibitors therapeutic use
- Abstract
Diabetes worsens atherosclerosis progression and leads to a defect in repair of arteries after cholesterol reduction, a process termed regression. Empagliflozin reduces blood glucose levels via inhibition of the sodium glucose cotransporter 2 (SGLT-2) in the kidney and has been shown to lead to a marked reduction in cardiovascular events in humans. To determine whether glucose lowering by empagliflozin accelerates atherosclerosis regression in a mouse model, male C57BL/6J mice were treated intraperitoneally with LDLR- and SRB1- antisense oligonucleotides and fed a high cholesterol diet for 16 weeks to induce severe hypercholesterolemia and atherosclerosis progression. At week 14 all mice were rendered diabetic by streptozotocin (STZ) injections. At week 16 a baseline group was sacrificed and displayed substantial atherosclerosis of the aortic root. In the remaining mice, plasma cholesterol was lowered by switching to chow diet and treatment with LDLR sense oligonucleotides to induce atherosclerosis regression. These mice then received either empagliflozin or vehicle for three weeks. Atherosclerotic plaques in the empagliflozin treated mice were significantly smaller, showed decreased lipid and CD68
+ macrophage content, as well as greater collagen content. Proliferation of plaque resident macrophages and leukocyte adhesion to the vascular wall were significantly decreased in empagliflozin-treated mice. In summary, plasma glucose lowering by empagliflozin improves plaque regression in diabetic mice.- Published
- 2019
- Full Text
- View/download PDF
6. Relation of endogenous digoxin-like immunoreacting activities to salt balance and renal function in man.
- Author
-
Kramer HJ, Heppe M, Pennig J, Kipnowski J, Klingmüller D, Düsing R, and Krück F
- Subjects
- Adult, Aged, Chromatography, Gel, Creatinine blood, Diet, Sodium-Restricted, Female, Humans, Kidney Failure, Chronic physiopathology, Male, Middle Aged, Radioimmunoassay, Sodium-Potassium-Exchanging ATPase antagonists & inhibitors, Digoxin blood, Kidney physiology, Sodium metabolism
- Abstract
We have previously shown that a natriuretic factor which is present in a small molecular weight fraction (IV) of serum and urine from salt loaded animals and healthy subjects, respectively, inhibits the Na-K-ATPase enzyme in vitro and also binds to a specific digoxin antibody. In the present study digoxin-like immunoreacting activity (DLIA) was therefore determined in the serum of healthy volunteers during low (35 nmol/day) and high (greater than 400 mmol/day) sodium intake and of patients with chronic renal failure and serum creatinine concentrations ranging from 127 to 757 mumol/l. DLIA was determined with a radioimmunoassay for digoxin in native serum and in the salt (III) and post-salt (IV) serum fractions eluted from a Sephadex G-25 column. DLIA in native serum of healthy subjects was less than 0.125 ng/ml. After gel filtration DLIA eluted exclusively in the small molecular weight salt (F III) and post-salt (F IV) fractions. Whereas DLIA increased in F III and decreased in F IV, total DLIA in F III + IV slightly increased from 0.37 +/- 0.03 to 0.49 +/- 0.05 ng/ml (p less than 0.01) with the change from low to high sodium intake. DLIA in native serum of uremic patients ranged from 0 to 1.70 ng/ml and was detectable consistently only in patients with serum creatinine concentrations above 250 mumol/l. DLIA in F III which averaged 0.22 +/- 0.04 ng/ml and total activity which ranged from 0.11 to 0.88 ng/ml closely correlated with the degree of renal impairment (p less than 0.001).(ABSTRACT TRUNCATED AT 250 WORDS)
- Published
- 1985
7. Digoxin-like immunoreacting substance(s) in the serum of patients with chronic uremia.
- Author
-
Kramer HJ, Pennig J, Klingmüller D, Kipnowski J, Glänzer K, and Düsing R
- Subjects
- Adult, Aged, Antigen-Antibody Reactions, Chromatography, Gel, Chronic Disease, Female, Humans, Male, Middle Aged, Digoxin blood, Uremia blood
- Abstract
In patients with chronic uremia we have previously demonstrated a significant inhibition of the Na-K-ATPase enzyme which represents the specific receptor protein for cardiac glycosides. Since an endogenous inhibitor of this enzyme was previously shown to react with a digoxin antibody, in the present study we determined digoxin-like immunoreacting activity(ies) (DLIA) by a radioimmunoassay in 15 nondialyzed patients with chronic renal failure. In native serum, DLIA ranged from 0 to 1.70 ng/ml and was unrelated to the degree of renal failure. After gel filtration of serum, DLIA exclusively eluted in the small molecular weight salt (FIII) and post-salt (FIV) fractions and averaged 0.22 +/- 0.04 and 0.20 +/- 0.05 ng/ml in fractions III and IV, respectively. Total activities ranged from 0.11 to 0.88 ng/ml with a mean of 0.42 +/- 0.06 ng/ml and closely correlated with the degree of renal impairment (p less than 0.001). The results confirm the presence of small molecular weight digoxin-like immunoreacting substance(s) in uremic serum. The variable activities in native serum and the lack of correlation between the degree of renal failure and DLIA in serum fraction IV previously shown to possess the Na-K-ATPase-inhibiting activity, however, indicate that DLIA may not reflect specifically the endogenous sodium pump inhibitor and that unspecific binding to this digoxin antibody of uremic toxins or other endogenous compounds, such as steroids other than aldosterone, may have occurred.
- Published
- 1985
- Full Text
- View/download PDF
8. [Autotransplantation of teeth as replacement of the 6-year molars].
- Author
-
Jewan J and Pennig J
- Subjects
- Adolescent, Adult, Female, Humans, Male, Molar, Third transplantation
- Published
- 1985
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.