10 research outputs found
Glucagon-Like Peptide-1 Protects Human Islets against Cytokine-Mediated β-Cell Dysfunction and Death: A Proteomic Study of the Pathways Involved
Glucagon-like peptide-1 (GLP-1) has been shown to protect pancreatic β-cells against cytokine-induced dysfunction and destruction. The mechanisms through which GLP-1 exerts its effects are complex and still poorly understood. The aim of this study was to analyze the protein expression profiles of human islets of Langerhans treated with cytokines (IL-1β and IFN-γ) in the presence or absence of GLP-1 by 2D difference gel electrophoresis and subsequent protein interaction network analysis to understand the molecular pathways involved in GLP-1-mediated β-cell protection. Co-incubation of cytokine-treated human islets with GLP-1 resulted in a marked protection of β-cells against cytokine-induced apoptosis and significantly attenuated cytokine-mediated inhibition of glucose-stimulated insulin secretion. The cytoprotective effects of GLP-1 coincided with substantial alterations in the protein expression profile of cytokine-treated human islets, illustrating a counteracting effect on proteins from different functional classes such as actin cytoskeleton, chaperones, metabolic proteins, and islet regenerating proteins. In summary, GLP-1 alters in an integrated manner protein networks in cytokine-exposed human islets while protecting them against cytokine-mediated cell death and dysfunction. These data illustrate the beneficial effects of GLP-1 on human islets under immune attack, leading to a better understanding of the underlying mechanisms involved, a prerequisite for improving therapies for diabetic patients.status: publishe
The Czech and Irish Protocols to the Lisbon Treaty: negotiation and argumentation of small states
This bachelor thesis focuses on negotiation strategies used by "small states" that are defined in the theoretical part of the thesis. In the form of a case study, the thesis analyses Irish and Czech approach to negotiations on the exemptions from the Treaty of Lisbon, that were put forward by political representation of both countries. The so- called small states use, due to their limited economic and personal resources, specifically aimed activities in order to gain favorable negotiating positions within the European Union. Both Ireland and Czech Republic are, according to the typology used, classified as "small states". During the ratification process of the Treaty of Lisbon, the European Union encountered obstacles caused by the result of the first Irish referendum and by the stance of Czech President Václav Klaus, regarding the completion of the ratification process. These obstacles led to the formulation of specific demands that were presented to the European Union. This thesis examines the strategies that were used in this stage of the ratification process to achieve legal guarantees for Ireland and Czech Republic. These strategies are analyses using official documents and public statements of national and European political elites. In its conclusive part the thesis states the applied..
Role of the Saturated Nonesterified Fatty Acid Palmitate in Beta Cell Dysfunction
Sustained elevated levels of saturated free fatty acids,
such as
palmitate, contribute to beta cell dysfunction, a phenomenon aggravated
by high glucose levels. The aim of this study was to investigate the
mechanisms of palmitate-induced beta cell dysfunction and death, combined
or not with high glucose. Protein profiling of INS-1E cells, exposed
to 0.5 mmol/L palmitate and combined or not with 25 mmol/L glucose,
for 24 h was done by 2D-DIGE, both on full cell lysate and on an enriched
endoplasmic reticulum (ER) fraction. Eighty-three differentially expressed
proteins (<i>P</i> < 0.05) were identified by MALDI-TOF/TOF
mass spectrometry and proteomic results were confirmed by functional
assays. 2D-DIGE analysis of whole cell lysates and ER enriched samples
revealed a high number of proteins compared to previous reports. Palmitate
induced beta cell dysfunction and death via ER stress, hampered insulin
maturation, generation of harmful metabolites during triglycerides
synthesis and altered intracellular trafficking. In combination with
high glucose, palmitate induced increased shunting of excess glucose,
increased mitochondrial reactive oxygen species production and an
elevation in many transcription-related proteins. This study contributes
to a better understanding and revealed novel mechanisms of palmitate-induced
beta cell dysfunction and death and may provide new targets for drug
discovery
Role of the Saturated Nonesterified Fatty Acid Palmitate in Beta Cell Dysfunction
Sustained elevated levels of saturated free fatty acids,
such as
palmitate, contribute to beta cell dysfunction, a phenomenon aggravated
by high glucose levels. The aim of this study was to investigate the
mechanisms of palmitate-induced beta cell dysfunction and death, combined
or not with high glucose. Protein profiling of INS-1E cells, exposed
to 0.5 mmol/L palmitate and combined or not with 25 mmol/L glucose,
for 24 h was done by 2D-DIGE, both on full cell lysate and on an enriched
endoplasmic reticulum (ER) fraction. Eighty-three differentially expressed
proteins (<i>P</i> < 0.05) were identified by MALDI-TOF/TOF
mass spectrometry and proteomic results were confirmed by functional
assays. 2D-DIGE analysis of whole cell lysates and ER enriched samples
revealed a high number of proteins compared to previous reports. Palmitate
induced beta cell dysfunction and death via ER stress, hampered insulin
maturation, generation of harmful metabolites during triglycerides
synthesis and altered intracellular trafficking. In combination with
high glucose, palmitate induced increased shunting of excess glucose,
increased mitochondrial reactive oxygen species production and an
elevation in many transcription-related proteins. This study contributes
to a better understanding and revealed novel mechanisms of palmitate-induced
beta cell dysfunction and death and may provide new targets for drug
discovery
Role of the Saturated Nonesterified Fatty Acid Palmitate in Beta Cell Dysfunction
Sustained elevated levels of saturated free fatty acids,
such as
palmitate, contribute to beta cell dysfunction, a phenomenon aggravated
by high glucose levels. The aim of this study was to investigate the
mechanisms of palmitate-induced beta cell dysfunction and death, combined
or not with high glucose. Protein profiling of INS-1E cells, exposed
to 0.5 mmol/L palmitate and combined or not with 25 mmol/L glucose,
for 24 h was done by 2D-DIGE, both on full cell lysate and on an enriched
endoplasmic reticulum (ER) fraction. Eighty-three differentially expressed
proteins (<i>P</i> < 0.05) were identified by MALDI-TOF/TOF
mass spectrometry and proteomic results were confirmed by functional
assays. 2D-DIGE analysis of whole cell lysates and ER enriched samples
revealed a high number of proteins compared to previous reports. Palmitate
induced beta cell dysfunction and death via ER stress, hampered insulin
maturation, generation of harmful metabolites during triglycerides
synthesis and altered intracellular trafficking. In combination with
high glucose, palmitate induced increased shunting of excess glucose,
increased mitochondrial reactive oxygen species production and an
elevation in many transcription-related proteins. This study contributes
to a better understanding and revealed novel mechanisms of palmitate-induced
beta cell dysfunction and death and may provide new targets for drug
discovery
Role of the Saturated Nonesterified Fatty Acid Palmitate in Beta Cell Dysfunction
Sustained elevated levels of saturated free fatty acids,
such as
palmitate, contribute to beta cell dysfunction, a phenomenon aggravated
by high glucose levels. The aim of this study was to investigate the
mechanisms of palmitate-induced beta cell dysfunction and death, combined
or not with high glucose. Protein profiling of INS-1E cells, exposed
to 0.5 mmol/L palmitate and combined or not with 25 mmol/L glucose,
for 24 h was done by 2D-DIGE, both on full cell lysate and on an enriched
endoplasmic reticulum (ER) fraction. Eighty-three differentially expressed
proteins (<i>P</i> < 0.05) were identified by MALDI-TOF/TOF
mass spectrometry and proteomic results were confirmed by functional
assays. 2D-DIGE analysis of whole cell lysates and ER enriched samples
revealed a high number of proteins compared to previous reports. Palmitate
induced beta cell dysfunction and death via ER stress, hampered insulin
maturation, generation of harmful metabolites during triglycerides
synthesis and altered intracellular trafficking. In combination with
high glucose, palmitate induced increased shunting of excess glucose,
increased mitochondrial reactive oxygen species production and an
elevation in many transcription-related proteins. This study contributes
to a better understanding and revealed novel mechanisms of palmitate-induced
beta cell dysfunction and death and may provide new targets for drug
discovery
Role of the Saturated Nonesterified Fatty Acid Palmitate in Beta Cell Dysfunction
Sustained elevated levels of saturated free fatty acids,
such as
palmitate, contribute to beta cell dysfunction, a phenomenon aggravated
by high glucose levels. The aim of this study was to investigate the
mechanisms of palmitate-induced beta cell dysfunction and death, combined
or not with high glucose. Protein profiling of INS-1E cells, exposed
to 0.5 mmol/L palmitate and combined or not with 25 mmol/L glucose,
for 24 h was done by 2D-DIGE, both on full cell lysate and on an enriched
endoplasmic reticulum (ER) fraction. Eighty-three differentially expressed
proteins (<i>P</i> < 0.05) were identified by MALDI-TOF/TOF
mass spectrometry and proteomic results were confirmed by functional
assays. 2D-DIGE analysis of whole cell lysates and ER enriched samples
revealed a high number of proteins compared to previous reports. Palmitate
induced beta cell dysfunction and death via ER stress, hampered insulin
maturation, generation of harmful metabolites during triglycerides
synthesis and altered intracellular trafficking. In combination with
high glucose, palmitate induced increased shunting of excess glucose,
increased mitochondrial reactive oxygen species production and an
elevation in many transcription-related proteins. This study contributes
to a better understanding and revealed novel mechanisms of palmitate-induced
beta cell dysfunction and death and may provide new targets for drug
discovery
Oleate-induced beta cell dysfunction and apoptosis: a proteomic approach to glucolipotoxicity by an unsaturated fatty acid.
High levels of fatty acids contribute to loss of functional beta cell mass in type 2 diabetes, in particular in combination with high glucose levels. The aim of this study was to elucidate the role of the unsaturated free fatty acid oleate in glucolipotoxicity and to unravel the molecular pathways involved. INS-1E cells were exposed to 0.5 mM oleate, combined or not with 25 mM glucose, for 24 h. Protein profiling of INS-1E cells was done by 2D-DIGE, covering pH ranges 4-7 and 6-9 (n = 4). Identification of differentially expressed proteins (P < 0.05) was based on MALDI-TOF analysis using Peptide Mass Fingerprint (PMF) and fragmentation (MS/MS) of the most intense peaks of PMF and proteomic results were confirmed by functional assays. Oleate impaired glucose-stimulated insulin secretion and decreased insulin content. 2D-DIGE analysis revealed 53 and 54 differentially expressed proteins for oleate and the combination of oleate and high glucose, respectively. Exposure to oleate down-regulated chaperones, hampered insulin processing and ubiquitin-related proteasomal degradation, and induced perturbations in vesicle transport and budding. In combination with high glucose, shunting of excess amounts of glucose toward reactive oxygen species production worsened beta cell death. The present findings provide new insights in oleate-induced beta cell dysfunction and identify target proteins for preservation of functional beta cell mass in type 2 diabetes.Journal ArticleResearch Support, Non-U.S. Gov'tSCOPUS: ar.jinfo:eu-repo/semantics/publishe