RESUMEN
The high degree of clinical routine in percutaneous transluminal coronary angioplasty (PTCA) with and without stenting has not changed the fact that a large number of coronary heart disease patients are still affected by post-operative complications such as restenosis and thrombosis. Because re-endothelialization is the crucial aspect of wound healing after cardiovascular implant surgery, there is a need for modern biomaterials to aid endothelial cells in their adhesion and functional recovery post-stenting. This study systematically examines the potential of numerous chemical polymer modifications with regard to endothelialization. Poly(ε-caprolactone) (PCL) and its chemically activated forms are investigated in detail, as well as the impact of polymer surface morphology and precoating with matrix protein. Human umbilical vein endothelial cells (HUVECs) are used to characterize endothelial cell responses in terms of in vitro viability and adhesion. As a potential component in drug eluting implants, VEGF is applied as stimulus to boost endothelial cell proliferation on the polymer. In conclusion, plasma chemical activation of PCL combined with VEGF stimulation best enhances in vitro endothelialization. Examining the impact of morphological, chemical and biological modifications of PCL, this study makes an important new contribution towards the existing body of work on polymer endothelialization.
Asunto(s)
Endotelio Vascular/efectos de los fármacos , Poliésteres/química , Factor A de Crecimiento Endotelial Vascular/farmacología , Materiales Biocompatibles , Endotelio Vascular/citología , Células Endoteliales de la Vena Umbilical Humana , Humanos , Microscopía Electrónica , Propiedades de SuperficieRESUMEN
It has been suggested that deletions of mitochondrial DNA (mtDNA) are important players with regard to the ageing process. Since the early 1990s, the 4977 bp deletion has been studied in various tissues, especially in postmitotic tissues with high energy demand. Unfortunately, some of these studies included less than 10 subjects, so the aim of our study was to quantify reliably the deletion amount in nine different regions of human brain, heart and skeletal muscle in a cohort of 92 individuals. The basal ganglia contain the highest deletion amounts with values up to 2.93% and differences in deletion levels between early adolescence and older ages were up to three orders of magnitude. Values in frontal lobe were on average an order of magnitude lower, but lowest in cerebellar tissue where the amount was on average only 5 x 10(-3) of the basal ganglia. The deletion started to accumulate in iliopsoas muscle early in the fourth decade of life with values between 0.00019% and 0.0035% and was highest in a 102-year-old woman with 0.14%. In comparison to skeletal muscle, the overall abundance in heart muscle of the left ventricle was only one-third. The best linear logarithmic correlation between amount of the deletion and age was found in substantia nigra with r=0.87 (p<0.0005) followed by anterior wall of the left ventricle (r=0.82; p<0.0005). With regard to mitochondrial DNA damage, we propose to use the 4977 bp deletion as an ideal biomarker to discriminate between physiological ageing and accelerated ageing. The biological meaning of mitochondrial deletions in the process of ageing is under discussion, but there is experimental evidence that large-scale deletions impair the oxidative phosphorylation in single cells and sensitize these cells to undergo apoptosis.
Asunto(s)
Química Encefálica , ADN Mitocondrial/genética , Músculo Esquelético/química , Miocardio/química , Eliminación de Secuencia , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Envejecimiento/genética , Niño , Preescolar , Marcadores Genéticos , Humanos , Lactante , Persona de Mediana Edad , Mitocondrias Cardíacas/genética , Mitocondrias Musculares/genética , Reacción en Cadena de la Polimerasa/métodosRESUMEN
BACKGROUND: How different immune cell compartments contribute to a successful immune response is central to fully understanding the mechanisms behind normal processes such as tissue repair and the pathology of inflammatory diseases. However, the ability to observe and characterize such interactions, in real-time, within a living vertebrate has proved elusive. Recently, the zebrafish has been exploited to model aspects of human disease and to study specific immune cell compartments using fluorescent reporter transgenic lines. A number of blood-specific lines have provided a means to exploit the exquisite optical clarity that this vertebrate system offers and provide a level of insight into dynamic inflammatory processes previously unavailable. RESULTS: We used regulatory regions of the zebrafish lysozyme C (lysC) gene to drive enhanced green fluorescent protein (EGFP) and DsRED2 expression in a manner that completely recapitulated the endogenous expression profile of lysC. Labeled cells were shown by co-expression studies and FACS analysis to represent a subset of macrophages and likely also granulocytes. Functional assays within transgenic larvae proved that these marked cells possess hallmark traits of myelomonocytic cells, including the ability to migrate to inflammatory sources and phagocytose bacteria. CONCLUSION: These reporter lines will have utility in dissecting the genetic determinants of commitment to the myeloid lineage and in further defining how lysozyme-expressing cells participate during inflammation.
Asunto(s)
Animales Modificados Genéticamente/genética , Regulación del Desarrollo de la Expresión Génica , Muramidasa/genética , Células Mieloides/citología , Regiones Promotoras Genéticas/genética , Proteínas de Pez Cebra/genética , Pez Cebra/genética , Animales , Animales Modificados Genéticamente/metabolismo , Linaje de la Célula , Clonación Molecular , Embrión no Mamífero , Genes Reporteros , Proteínas Fluorescentes Verdes/genética , Proteínas Fluorescentes Verdes/metabolismo , Inmunohistoquímica , Hibridación in Situ , Muramidasa/metabolismo , Pez Cebra/embriología , Pez Cebra/metabolismo , Proteínas de Pez Cebra/metabolismoRESUMEN
As it has been demonstrated that bioactive substances can be delivered locally using coated surgical suture materials, the authors developed a vascular endothelial growth factor (VEGF)-releasing suture material that should promote vascularization and potentially wound healing. In this context, the study focused on the characterization of the developed suture material and the verification of its biological activity, as well as establishing a coating process that allows reproducible and stable coating of a commercially available polydioxanone suture material with poly(l-lactide) (PLLA) and 0.1µg and 1.0µg VEGF. The in vitro VEGF release kinetics was studied using a Sandwich ELISA. The biological activity of the released VEGF was investigated in vitro using human umbilical vein endothelial cells. The potential of the VEGF-releasing suture material was also studied in vivo 5days after implantation in the hind limb of Wistar rats, when the histological findings were analyzed. The essential results, enhanced cell viability in vitro as well as significantly increased vascularization in vivo, were achieved using PLLA/1.0µg VEGF-coated suture material. Furthermore, ELISA measurements revealed a high reproducibility of the VEGF release behavior. Based on the results achieved regarding the dose-effect relationship of VEGF, the stability during its processing and the release behavior, it can be predicted that a bioactive suture material would be successful in later in vivo studies. Therefore, this knowledge could be the basis for future studies, where bioactive substances with different modes of action are combined for targeted, overall enhancement of wound healing.
Asunto(s)
Inductores de la Angiogénesis/administración & dosificación , Vasos Sanguíneos/crecimiento & desarrollo , Implantes de Medicamentos/administración & dosificación , Células Endoteliales/fisiología , Neovascularización Fisiológica/fisiología , Suturas , Factor A de Crecimiento Endotelial Vascular/administración & dosificación , Inductores de la Angiogénesis/química , Animales , Vasos Sanguíneos/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Células Cultivadas , Difusión , Implantes de Medicamentos/química , Células Endoteliales/citología , Células Endoteliales/efectos de los fármacos , Humanos , Técnicas In Vitro , Masculino , Ratas , Ratas Wistar , Resultado del Tratamiento , Factor A de Crecimiento Endotelial Vascular/químicaRESUMEN
Contrast sensitivity (CS) is often used to assess spatial and temporal vision in animals. Conventional behavioral psychophysical techniques are both time and labor intensive, whereas measurement of CS functions by means of the pattern electroretinogram (PERG) is considerably more rapid and efficient. Are the two methods comparable, however? To answer this question, contrast-sensitivity functions were obtained using both the PERG and behavioral psychophysics in the same subjects, which were White Carneaux pigeons. The stimuli, in both methods, were phase-reversing, contrast-modulated sweeps of sinusoidal gratings. The PERG-CS functions were recorded via corneal electrodes and the behavioral data were collected using a modified staircase method that used moderate food deprivation and food reward. The results indicated that the PERG-CS functions had comparable bandwidth and peak spatial frequency to the behavioral CS functions. The PERG-CS functions, however, were lower on average than the behavioral curves by about 54%. The visual acuity of the two methods, as estimated from the high-frequency cutoff of the CS functions, differed by 37%. Both of these values are roughly consistent with the square root of 2 advantage of binocular viewing (behavioral method) over monocular viewing (PERG method). In addition, the peak spatial frequency showed a decrease of 0.125 c/deg with the PERG method and bandwidth was reduced by approximately 0.5 octave. These findings suggest that the PERG is an acceptable alternative to behavioral measurement of CS functions, especially in animal psychophysics, if one takes into account the underestimation of CS by the PERG method and the small changes in peak spatial frequency and bandwidth.