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Inzidenz und Charakterisierung von GPIIb-IIIa-Antagonisten-abhängigen antithrombozytären AntikörpernNúñez Bresgen, Ana Linda. January 2008 (has links) (PDF)
Zugl.: Giessen, Universiẗat, Diss., 2008.
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Thrombozyteninhibition und Glykoprotein-IIb/IIIa- Rezeptorbesetzung bei intrakoronarer versus intravenöser Bolusgabe von Abciximab bei Patienten mit ST-Hebungs- InfarktKulle, Konrad 04 February 2015 (has links) (PDF)
Bei Patienten mit ST-Strecken-Elevations-Myokardinfarkt (STEMI) ist die direkte intrakoronare Bolusverabreichung des Glykoprotein-IIb/IIIa-Rezeptorantagonist Abciximab, im Gegensatz zur periphervenösen Bolusinjektion, mit einer Reduktion von Infarktgröße und mikrovaskulärer Obstruktion sowie mit einem höheren Anteil geretteten Myokards assoziiert, vermutlich ausgelöst durch eine höhere lokale
Arzneimittelkonzentration und der dadurch gesteigerten Hemmung der
Plättcheninhibition. Ziel der Arbeit war es herauszufinden, ob es Unterschiede gibt bezüglich der GP-IIb/IIIa Rezeptorbesetzung und der Thrombozyteninhibition im venösen Koronarblut, welches kurz nach intrakoronarer oder periphervenöser Abciximab-Bolusinjektion entnommen wurde.
Dafür wurden bei 16 Patienten mit akutem STEMI vor und unmittelbar nach der Gabe eines Abciximab-Bolus sowie nach 30 Minuten Blutproben aus dem Korornarsinus entnommen. Jeweils 8 Patienten erhielten entweder den Bolus intrakoronar oder peripher venös verabreicht. Sofort nach der Bolusapplikation war die Rezeptorbesetzung im venösem Koronarblut signifikant höher bei Patienten, die einen direkten intrakoronaren Bolus erhalten hatten, im Vergleich mit Patienten mit peripherer Bolusadministration (intrakorornarer Bolus: 93.5% [IQR 92.7–95.4], intravenöser Bolus: 74.0% [IQR 17.6–94.0], p = 0.04). Das Ausmaß der Plättcheninhibition war früh nach Bolusgabe ebenso deutlich höher bei intrakoronarer anstatt intravenöser Bolusapplikation. In der späten Blutentnahme 30 Minuten nach der Bolusapplikation konnten keine signifikanten Unterschiede zwischen beiden untersuchten Gruppen, weder bezüglich der GP-IIb/IIIa Rezeptorbesetzung noch der Thrombozytenaggregationshemmung, gefunden werden.
Zusammenfassend kann man sagen, dass die direkte intrakoronare Bolusapplikation akut in eine höhere lokale Inhibition der Thrombozytenfunktion und einem größeren Anteil an geblockten GP-IIb/IIIa Rezeptoren im Vergleich zur peripher venösen Bolusinjektion resultiert. Limitierend muss die geringe Fallzahl erwähnt werden. Die Ergebnisse sollten deshalb zurückhaltend interpretiert werden.
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Intéraction P-sélection/PSGL-1 : impact sur l'agrégation et l'activation plaquettaireThéorêt, Jean-François January 2006 (has links)
Thèse numérisée par la Direction des bibliothèques de l'Université de Montréal.
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Analýza projektů předložených na česko-slovenské hranici v rámci Iniciativy Společenství INTERREG IIIA / Analysis of projects presented on czechoslovak border in the framework of the INTERREG IIIA programmeNožičková, Jana January 2006 (has links)
Práce pojednává o realizaci Iniciativy Společenství INTERREG IIIA na česko-slovenské hranici. Je zde zachycen vývoj Iniciativy, legislativní ukotvení, organizační struktura a projektový cyklus. Teoretická část je věnována analýze kvantitativních charakteristik (počet předložených projektů, objem alokovaných prostředků) a kvalitativních charakteristik. Práce dále porovnává realizaci s programy na ostatních hranicích.
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Characterization of the IIIa protein of porcine adenovirus type 3Van Kessel, Jill Andrea 26 April 2006
The L1 region of the porcine adenovirus (PAdV)-3 genome encodes a protein of 622 amino acids named IIIa. Although it binds a neighboring group of nine (GON) hexons at the capsid level and cement the icosahedral shell that contains the viral DNA, little is known regarding its function with respect to viral life cycle. Moreover, the known location of IIIa protein in the capsid may help to express targeting ligands for altering the tropism of PAdV-3. The objective of this study was to characterize the IIIa protein of porcine adenovirus Type 3 (PAdV-3). <p> In order to characterize the IIIa protein, polyclonal antisera were raised in rabbits against different regions of IIIa. Anti-IIIa sera detected a specific protein of 70 kDa in PAdV-3 infected cells using Western blot assay. Immunofluorescence studies indicated that IIIa is predominantly localized in the nucleus of PAdV-3 infected cells. Analysis of PAdV-3 IIIa using antibodies specific for N- and C- terminal domains of the protein suggested that although the N-terminus and C-terminal domains of IIIa are immunogenic, they are not exposed on the surface of PAdV-3 virions. These results were further confirmed by our inability to isolate a chimeric PAdV-3 virion containing a heterologous protein fused to the N-terminus or C-terminus of IIIa. <p>Functional analysis suggested that IIIa may transactivate the major late promoter and down regulate the early region (E) 1A promoter. In order to locate the domains of IIIa responsible for different functions, in-frame deleted/truncated forms of IIIa were constructed. Analysis of the deleted/truncated forms of IIIa suggested that a) the sequences located between amino acids 273-410 and between amino acids 410-622b) affect the nuclear localization and transactivation function respectively.<p>Since protein- protein interactions are important for the biological functions of the protein, we determined the interaction of PAdV-3 IIIa with other viral proteins. IIIa was found to interact with DNA binding protein (DBP), E3 13.7 kDa protein, hexon, fiber, and pIX. These results suggest that PAdV3 IIIa may do more in the viral life cycle than merely act as cement between the hexons to maintain capsid stability and may actually be involved in regulating early to late gene transcription at appropriate stages during viral infection.
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Characterization of the IIIa protein of porcine adenovirus type 3Van Kessel, Jill Andrea 26 April 2006 (has links)
The L1 region of the porcine adenovirus (PAdV)-3 genome encodes a protein of 622 amino acids named IIIa. Although it binds a neighboring group of nine (GON) hexons at the capsid level and cement the icosahedral shell that contains the viral DNA, little is known regarding its function with respect to viral life cycle. Moreover, the known location of IIIa protein in the capsid may help to express targeting ligands for altering the tropism of PAdV-3. The objective of this study was to characterize the IIIa protein of porcine adenovirus Type 3 (PAdV-3). <p> In order to characterize the IIIa protein, polyclonal antisera were raised in rabbits against different regions of IIIa. Anti-IIIa sera detected a specific protein of 70 kDa in PAdV-3 infected cells using Western blot assay. Immunofluorescence studies indicated that IIIa is predominantly localized in the nucleus of PAdV-3 infected cells. Analysis of PAdV-3 IIIa using antibodies specific for N- and C- terminal domains of the protein suggested that although the N-terminus and C-terminal domains of IIIa are immunogenic, they are not exposed on the surface of PAdV-3 virions. These results were further confirmed by our inability to isolate a chimeric PAdV-3 virion containing a heterologous protein fused to the N-terminus or C-terminus of IIIa. <p>Functional analysis suggested that IIIa may transactivate the major late promoter and down regulate the early region (E) 1A promoter. In order to locate the domains of IIIa responsible for different functions, in-frame deleted/truncated forms of IIIa were constructed. Analysis of the deleted/truncated forms of IIIa suggested that a) the sequences located between amino acids 273-410 and between amino acids 410-622b) affect the nuclear localization and transactivation function respectively.<p>Since protein- protein interactions are important for the biological functions of the protein, we determined the interaction of PAdV-3 IIIa with other viral proteins. IIIa was found to interact with DNA binding protein (DBP), E3 13.7 kDa protein, hexon, fiber, and pIX. These results suggest that PAdV3 IIIa may do more in the viral life cycle than merely act as cement between the hexons to maintain capsid stability and may actually be involved in regulating early to late gene transcription at appropriate stages during viral infection.
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Application of proteomics to the study of protein translation in stored platelet unitsThon, Jonathan Noah 11 1900 (has links)
Platelet products have a short shelf life (5 to 7 days) owing in part to the deterioration of
the quality of platelets stored at 22°C. This creates significant inventory challenges, and blood banks may suffer shortages and high wastage as a result. Proteomics offers a global quantitative
approach to investigate changes occurring in stored blood products. These data sets can identify
processes leading to storage-associated losses of blood component quality such as the platelet
storage lesion (PSL). Changes to the platelet proteome between days 1 and 7 of storage were
analysed with 3 complementary proteomic approaches with final mass spectrometric (MS)
analysis: 2-dimensional (2D) gel electrophoresis/differential gel electrophoresis (DIGE), isobaric
tagging for relative and absolute quantification (iTRAQ), and isotope-coded affinity tagging
(ICAT). Although proteomics analyses identified many storage-associated protein changes, these
varied significantly by method suggesting that a combination of protein-centric (2D gel or
DIGE) and peptide-centric (iTRAQ or ICAT) approaches is necessary to acquire the most
informative data.
Validation of the proteomics results by western blotting, flow cytometry, quantitative real-time polymerase chain reaction (qRT PCR) and ³ٰ⁵S-methionine incorporation confirmed that
platelets are capable of synthesising biologically relevant proteins ex vivo throughout a 10-day
storage period with particularly long-lived mRNA (half-life of approximately 2.4 days), and has
provided the first evidence for one of the mechanisms of the PSL. The development of an ³ٰ⁵Smethionine
assay has since shown that stored human blood platelets incorporate ³ٰ⁵S-methionine at a rate that is proportional to time and substrate concentration, and is slower for freshly drawn platelets than those stored in pooled buffy coat derived units for 10 days. More interesting still are the observations that the overall ³ٰ⁵S-methionine incorporation rate was higher in pooled buffy coat platelet units versus freshly drawn platelets, that this rate increased upon agonist exposure in both, and that day 8 platelets showed significantly greater total protein translation than on days 2,3,7 and 10 of storage. This may be indicative of translational regulation of the platelet proteome during storage and upon activation. Translational control is a consequence of remarkable cellular specialisation and precise biochemical pathways which, in the case of platelets, may lead to storage-associated losses of blood component quality and must be understood if platelet storage times are to be extended.
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Application of proteomics to the study of protein translation in stored platelet unitsThon, Jonathan Noah 11 1900 (has links)
Platelet products have a short shelf life (5 to 7 days) owing in part to the deterioration of
the quality of platelets stored at 22°C. This creates significant inventory challenges, and blood banks may suffer shortages and high wastage as a result. Proteomics offers a global quantitative
approach to investigate changes occurring in stored blood products. These data sets can identify
processes leading to storage-associated losses of blood component quality such as the platelet
storage lesion (PSL). Changes to the platelet proteome between days 1 and 7 of storage were
analysed with 3 complementary proteomic approaches with final mass spectrometric (MS)
analysis: 2-dimensional (2D) gel electrophoresis/differential gel electrophoresis (DIGE), isobaric
tagging for relative and absolute quantification (iTRAQ), and isotope-coded affinity tagging
(ICAT). Although proteomics analyses identified many storage-associated protein changes, these
varied significantly by method suggesting that a combination of protein-centric (2D gel or
DIGE) and peptide-centric (iTRAQ or ICAT) approaches is necessary to acquire the most
informative data.
Validation of the proteomics results by western blotting, flow cytometry, quantitative real-time polymerase chain reaction (qRT PCR) and ³ٰ⁵S-methionine incorporation confirmed that
platelets are capable of synthesising biologically relevant proteins ex vivo throughout a 10-day
storage period with particularly long-lived mRNA (half-life of approximately 2.4 days), and has
provided the first evidence for one of the mechanisms of the PSL. The development of an ³ٰ⁵Smethionine
assay has since shown that stored human blood platelets incorporate ³ٰ⁵S-methionine at a rate that is proportional to time and substrate concentration, and is slower for freshly drawn platelets than those stored in pooled buffy coat derived units for 10 days. More interesting still are the observations that the overall ³ٰ⁵S-methionine incorporation rate was higher in pooled buffy coat platelet units versus freshly drawn platelets, that this rate increased upon agonist exposure in both, and that day 8 platelets showed significantly greater total protein translation than on days 2,3,7 and 10 of storage. This may be indicative of translational regulation of the platelet proteome during storage and upon activation. Translational control is a consequence of remarkable cellular specialisation and precise biochemical pathways which, in the case of platelets, may lead to storage-associated losses of blood component quality and must be understood if platelet storage times are to be extended.
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Application of proteomics to the study of protein translation in stored platelet unitsThon, Jonathan Noah 11 1900 (has links)
Platelet products have a short shelf life (5 to 7 days) owing in part to the deterioration of
the quality of platelets stored at 22°C. This creates significant inventory challenges, and blood banks may suffer shortages and high wastage as a result. Proteomics offers a global quantitative
approach to investigate changes occurring in stored blood products. These data sets can identify
processes leading to storage-associated losses of blood component quality such as the platelet
storage lesion (PSL). Changes to the platelet proteome between days 1 and 7 of storage were
analysed with 3 complementary proteomic approaches with final mass spectrometric (MS)
analysis: 2-dimensional (2D) gel electrophoresis/differential gel electrophoresis (DIGE), isobaric
tagging for relative and absolute quantification (iTRAQ), and isotope-coded affinity tagging
(ICAT). Although proteomics analyses identified many storage-associated protein changes, these
varied significantly by method suggesting that a combination of protein-centric (2D gel or
DIGE) and peptide-centric (iTRAQ or ICAT) approaches is necessary to acquire the most
informative data.
Validation of the proteomics results by western blotting, flow cytometry, quantitative real-time polymerase chain reaction (qRT PCR) and ³ٰ⁵S-methionine incorporation confirmed that
platelets are capable of synthesising biologically relevant proteins ex vivo throughout a 10-day
storage period with particularly long-lived mRNA (half-life of approximately 2.4 days), and has
provided the first evidence for one of the mechanisms of the PSL. The development of an ³ٰ⁵Smethionine
assay has since shown that stored human blood platelets incorporate ³ٰ⁵S-methionine at a rate that is proportional to time and substrate concentration, and is slower for freshly drawn platelets than those stored in pooled buffy coat derived units for 10 days. More interesting still are the observations that the overall ³ٰ⁵S-methionine incorporation rate was higher in pooled buffy coat platelet units versus freshly drawn platelets, that this rate increased upon agonist exposure in both, and that day 8 platelets showed significantly greater total protein translation than on days 2,3,7 and 10 of storage. This may be indicative of translational regulation of the platelet proteome during storage and upon activation. Translational control is a consequence of remarkable cellular specialisation and precise biochemical pathways which, in the case of platelets, may lead to storage-associated losses of blood component quality and must be understood if platelet storage times are to be extended. / Medicine, Faculty of / Biochemistry and Molecular Biology, Department of / Graduate
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Structural and functional studies of Xenopus laevis transcription factor IIIA zinc finger mutantsDel Rio, Samuel January 1992 (has links)
No description available.
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