Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Purchase individual online access for 1 year to this journal.
Price: EUR 185.00Authors: Cherkouk, Charaf | Rebohle, Lars | Lenk, Jens | Keller, Adrian | Ou, Xin | Laube, Markus | Neuber, Christin | Haase-Kohn, Cathleen | Skorupa, Wolfgang | Pietzsch, Jens
Article Type: Research Article
Abstract: Gold surfaces functionalized with nickel-nitrilotriacetic acid (Ni2+ -NTA) as self-assembled monolayers (SAM) to immobilize histidine (His)-tagged biomolecules are broadly reported in the literature. However, the increasing demand of using microfluidic systems and biosensors takes more and more advantage on silicon technology which provides dedicated glass surfaces and substantially allows cost and resource savings. Here we present a novel method for the controlled oriented immobilization of His-tagged proteins on glass surfaces functionalized with a Ni2+ -NTA layer. Exemplarily, the protein pattern morphology after immobilization on the Ni2+ -NTA layer of His6 -tagged soluble receptor for advanced glycation endproducts (sRAGE) was investigated …and compared to non-oriented immobilization of sRAGE on amino SAM by using scanning electron microscopy (SEM). Moreover, we demonstrated interaction of immobilized sRAGE with three structurally different ligands, S100A12, S100A4, and glycated low density lipoproteins (glycLDL), by means of peak-force tapping atomic force microscopy (PF-AFM). We showed a clear discrimination of different protein-ligand orientations by differential height measurements. Show more
Keywords: His-tagged proteins, glycated low density lipoproteins, microfluidic systems and biosensors, S100 proteins, self-assembled monolayers, soluble receptor for advanced glycation endproducts
DOI: 10.3233/CH-151950
Citation: Clinical Hemorheology and Microcirculation, vol. 61, no. 3, pp. 523-539, 2015
Authors: Pabisiak, A. | Bromboszcz, J. | Kmiec, S. | Dendura, M. | Dabrowski, Z. | Smolenski, O.
Article Type: Research Article
Abstract: INTRODUCTION: The aim of cardiovascular disease treatment is to reduce the risk of thrombogenesis and improve tissue perfusion, depending inter alia on the rheological properties of the blood. The reduction in blood viscosity and erythrocyte aggregation, as well as increase of erythrocyte deformability was observed under the influence of physical training. AIM: To compare the blood count and rheological properties of blood samples before and after outpatient cardiac rehabilitation programme. MATERIAL AND METHODS: 35 men (average age: 57.2 ± 5.42), who after suffering myocardial infarction treated with percutaneous coronary intervention (PCI), took part in 24 physical …training sessions of moderate intensity (40–60% of heart rate reserve). The standard ergometer submaximal (up to 85% of predicted HRmax) exercise test and echocardiography was performed before and after training. Blood count, fibrinogen concentration as well as aggregation and elongation properties of erythrocytes were analyzed too. RESULTS: Patients significantly increased exercise capacity (p < 0.00001) and ejection fraction (p < 0.00001) after completion of the training cycle. There was noted a reduction in aggregation index AI (p < 0.01), an increase in the number of erythrocytes RBC (p < 0.05), while reducing their volume MCV (p < 0.05) and a decrease in hemoglobin content MCH (p < 0.05). The number of leukocytes WBC (p < 0.01) was decreased too. CONCLUSIONS: Beneficial changes in blood rheology and blood count have been found in patients after myocardial infarction who took part in the physical training sessions of moderate intensity. Show more
Keywords: Myocardial infarction, rehabilitation, physical training, blood count, blood rheology
DOI: 10.3233/CH-151954
Citation: Clinical Hemorheology and Microcirculation, vol. 61, no. 3, pp. 541-547, 2015
Authors: Jung, Christian | Drummer, Karl | Oelzner, Peter | Figulla, Hans R. | Boettcher, Joachim | Franz, Marcus | Betge, Stefan | Foerster, Martin | Wolf, Gunter | Pfeil, Alexander
Article Type: Research Article
Abstract: Systemic sclerosis (SSc) is a systemic, autoimmune connective tissue disease characterized by vasculopathy and microvascular changes. Fluorescence Optical Imaging (FOI) is a technique used to assess inflammation in patients with arthritis; in this study FOI is used to quantify inflammation in the hand. Endothelial Microparticle (EMP) can reflect damage or activation of the endothelium but also actively modulate processes of inflammation, coagulation and vascular function. The aim of the present study was to quantify EMP and FOI, to determine an association between these microparticles and inflammation and to endothelial function. METHODS: EMP were quantified in plasma samples of 25 …patients (24 female, 1 male, age: 41 ± 9 years) with SSc using flow cytometry. EMP was defined as CD31+/CD42− MP, and CD62+ MP. Perivascular inflammation was assessed using fluorescence optical imaging (FOI) of the hand. Macrovascular endothelial function was non-invasively estimated using the Endopat system. RESULTS: Plasma levels of CD31+/CD42− EMP and CD62+ EMP were lower in patients with SSc compared to controls (both p < 0.05). An impaired endothelial function with an increased hyperemia index was observed. A strong association could be demonstrated between CD62+ EMP and perivascular soft tissue inflammation as assessed by the FOI global score (Spearman, p = 0.002, r = 0.61). CONCLUSIONS: EMP indicate molecular vascular damage in SSc; in this study a strong association between EMP and perivascular inflammation as quantified by FOI is demonstrated. Consequently EMP, using FOI, may be a potential marker benefitting the diagnosis and therapy monitoring of patients with SSc with associated Raynaud‘s phenomenon. Show more
Keywords: Systemic sclerosis, endothelial microparticles, fluorescence optical imaging, microcirculation
DOI: 10.3233/CH-151956
Citation: Clinical Hemorheology and Microcirculation, vol. 61, no. 3, pp. 549-557, 2015
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
sales@iospress.com
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
info@iospress.nl
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office info@iospress.nl
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
china@iospress.cn
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
如果您在出版方面需要帮助或有任何建, 件至: editorial@iospress.nl