Browsing by Subject "Cytokine"
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Publication Der Einfluss verschiedener Ölemulsionen und der IL-6-Typ-Zytokine CNTF und LIF auf die Differenzierung von 3T3-L1-Präadipozyten zu Fettzellen(2009) Stäbler, Antje; Graeve, LutzType 2 diabetes is a disease of civilization spreading all over the world like an epidemic. Among other things it is characterized by increased glucose and triglyceride levels of the blood. Thus the differentiation of preadipocytes into adipocytes that are specialized in storing large fat depots is essential for the removal of excess nutrients from the circulation. This process can be simulated through the differentiation of 3T3-L1 cells by treatment with insulin, IBMX, and dexamethasone. In this study a compensative effect of olive oil as well as soy bean oil on the differentiation of 3T3-L1 cells was found. The differentiation triggered by insulin, IBMX, and dexamethasone was somewhat inhibited by incubating the cells with one of the two oils, whereas both olive and soy bean oil had a certain potential to act as differentiating agents them-selves when insulin, IBMX, and dexamethasone were not added. This points to benefits of certain oils contained in food compared to thiazolidinediones that are used as antidiabetics and lead to weight gain in the long term. Furthermore the inhibitory effect of the proinflammatory cytokine TNFα on the differentiation process could be compensated to some degree by either oil. The transcription factor PPARγ was used to measure the state of differentiation. Caveolin1 is involved in both buildup and degradation of intracellular fat stores and was induced by oil incubation in differentiated as well as in undifferentiated 3T3-L1 cells. Moreover the signal transduction of the IL-6-related cytokine CNTF in 3T3-L1 cells and its influence on the differentiation process of these cells was investigated. In recent years CNTF was spotlighted because of its leptin-like properties that persist even in leptin resistant states. In this study an increasing sensitivity to CNTF during the differentiation of 3T3-L1 cells was shown. Furthermore the positive effects of the cytokine on fatty acid metabolism and adipocyte development were verified. CNTF favored the emergence of many small adipocytes compared to fewer, but larger adi-pocytes under different conditions. Thereby the functionality of the cells is influenced in a positive way and the protection from the development of insulin resistance is increased. The effect of LIF - another IL-6-related cytokine - was not similar to that of CNTF but was more comparable to the effect of the oils.Publication Posttranslationale Modifikationen der IL-6-Typ-Zytokin-Rezeptoren gp130 und LIFR und ihr Einfluss auf die Assoziation mit Detergenz-resistenten Membranmikrodomänen (DRM)(2008) Ziegler, Inna; Graeve, LutzPost-translational modification of proteins is an important event in the regulation of cellular functions. Glycosylation or palmitoylation, but also ligand binding can affect the localization of proteins in membrane microdomains and thus affect signal transduction. The aim of this study was to analyze how posttranslational modifications of LIFR and the common signal transducer gp130 impact the translocation to detergent resistant membranes (DRMs, lipid rafts). Palmitoylation of cysteine residues within the transmembrane domain of a protein is considered to be one process that assists in the localization of proteins to DRMs. Gp130 has two cysteine residues C711 and C725 in its transmembrane domain. My studies indicate that these cysteine residues have no significant influence on lipid raft association of gp130. Contrary to our expectations, after isolation of DRMs with Brij 58 and Triton X-100 an increase of raft association of the C->A-mutants was detected. Partial DRM association of LIFR was confirmed by using Brij 58 and Triton X-100 protocols. Furthermore, two different N-glycosylation types of that receptor could be detected. The mannose-rich (precursor) species is preferentially found in non-DRMs and is degraded by Endo-Glycosidase Hf. The hybrid-type (mature) tends towards an association with DRMs. My results indicate that only the mature-type of LIFR was phosphorylated after LIF binding to the receptor complex in 3T3-L1 and HepG2 cells. Combined with other data from our workgroup these findings suggest that only the mature-type of LIFR is expressed at the plasma membrane surface and involved in signal transduction. After stimulation with LIF an increase of LIFR tyrosine phosphorylation was observed in DRMs in HepG2 cells. However, phosphorylation of gp130 was detected only in non-DRMs fractions after stimulation with LIF. The inconsistency of these results can be explained with methodical problems. Furthermore, the translocation of phosphorylated receptors described above could not confirmed in 3T3-L1 cells. In this cell line, the activation of gp130 and LIFR occurs in detergent-resistant membranes. These findings indicate differences between cell lines with respect to receptor activation and translocation within the plasma membrane on the one hand and demonstrate a differential sensitivity of raft subdomains to extraction by different detergents on the other hand.