Alkali activated materials could be suitable alternative to construction materials based on ordinary Portland cement (OPC). Therefore, it is advisable to pursue these binders further on. Aim of this thesis is to clarify the effect of lignosulfonate-based plasticizer and polycarboxylate-based superplasticizer on the behaviour and nature of alkali activated materials. For the purposes of studying the efficiency of plasticizing additives, the change of workability of alkali activated blast furnace slag in dependence on time, effect of additives on mechanical properties as well as, with usage of isothermal calorimetry, their impact on kinetics of solidification and hardening had been observed. The stability of the plasticizing admixtures in a high alkaline environment such as water glass and sodium hydroxide had been studied using infrared spectrometry. As a last step, X-ray photoelectron spectroscopy (XPS) had been used while clarifying the chemical changes in the structure of plasticizing additives after adsorption to blast furnace slag.

Les maladies cardiovasculaires sont souvent causées par des arythmies qui proviennent d'une obstruction du système de conduction cardiaque. L'intervenant clé de ce système est le nœud sinu-atrial (SA), qui est responsable de l’initiation de chaque battement cardiaque. L’activation électrique à intervalles réguliers, assurant que le rythme cardiaque est un rythme normal. Le dysfonctionnement du nœud SA entraînerait des instabilités électriques dans le cœur. Une maladie cardiaque acquise, comme la cardiopathie rhumatismale, ou un bloc de conduction ne sont que quelques-uns des nombreux cas qui nécessitent un stimulateur cardiaque électronique pour surveiller la fréquence cardiaque et générer une impulsion lorsqu'elle bat anormalement. Bien que le stimulateur cardiaque électrique soit considéré comme une thérapie fiable, il n'est pas sans limites. Ces limites comprennent les complications chirurgicales, l'infection au plomb ainsi que la durée de vie limitée de la batterie, qui doit être remplacée à intervalles de quelques années, ce qui alourdit le fardeau hospitalier. Plusieurs approches ont été adoptées pour développer une méthode thérapeutique plus adéquate. Une stratégie qui sera étudiée implique l'utilisation d'une greffe de cellules de stimulateur cardiaque, créant fondamentalement un stimulateur biologique. Les approches de thérapie cellulaire utilisent des cellules souches embryonnaires pour évoluer vers les lignées de cellules cardiaques, y compris les cellules stimulatrices cardiaques. Ces cellules de stimulation sont caractérisées par une dépolarisation spontanée qui crée les impulsions rythmiques dans le cœur et contrôle la fréquence cardiaque. Un élément important des cellules du stimulateur cardiaque qui donne lieu à la dépolarisation spontanée sont les canaux « hyperpolarization-activated and cyclic nucleotide-gated » qui sont activés pendant l’hyperpolarisation et conduisent le courant sous le nom de « funny current ». Ce courant augmente la perméabilité intérieure de la cellule aux courants de sodium et de potassium conduisant à la dépolarisation de la cellule. D'autre part, le taux de conduction est déterminé par la connexine 30.2 et la connexine 45, qui sont des protéines transmembranaires qui s’assemblent pour former des jonctions lacunaires. L'expression de HCN et l'expression de la connexine ont toutes deux étés liés au facteur T-box 3 (Tbx3) dans le développement des myocytes auriculaires. Une approche praticable pour moduler l'expression des gènes et par conséquent l'expression des protéines est l'utilisation du conditionnement chimique. Le Phorbol 12- myristate 13-acétate (PMA) est un activateur de Protéine Kinase C (PKC) lié à l'expression de Tbx3, et par conséquent à l'expression de HCN et de connexine, et entraînant une modification de l'activité spontanée. Les cellules souches embryonnaires de souris sont des cellules qui sont isolées de la masse cellulaire interne des embryons. Ces cellules ont la capacité de se différencier en tous les types de cellules somatiques. En combinant les facteurs de croissance, ces cellules peuvent se différencier en cardiomyocytes. Nous émettons l'hypothèse que le conditionnement chronique de cardiomyocytes de souris avec PMA entraîne une régulation à la hausse de l'expression de Tbx3 et par conséquent une régulation à la hausse de l'expression de HCN et de l'expression de connexine, favorisant ainsi le développement des cellules stimulatrices cardiaques dans la population des cardiomyocytes. Afin de vérifier notre hypothèse, nous avons acheté des cellules de la lignée cellulaire E14TG2A de souris. Ces cellules ont été cultivées dans des pétris et différenciées en cardiomyocytes à l'aide d'un protocole en trois étapes (voir la section Méthodes). Les cardiomyocytes sont ensuite exposés à la PMA à des concentrations variables (0.1 µM vs 1 µM) pendant 1h (exposition aiguë) ou 24 h (exposition chronique). Les résultats variaient d'un groupe expérimental à l'autre par rapport au groupe témoin. Dans toutes les conditions expérimentales, il semble y avoir une augmentation initiale de l'activité spontanée, mais elle s'inverse rapidement à la marque des 24 heures, où le rythme diminue. Différentes concentrations jouent un rôle dose-dépendant dans l'effet inhibiteur de longue durée sur la stimulation des cellules. / Cardiovascular diseases are often caused by arrhythmias that originate from an obstruction within the cardiac conduction system. The key player within that system is the sinoatrial (SA) node, which is responsible for initiation the electrical impulses at a regular interval, insuring the heartbeat at a normal pace. Dysfunction of the SA node would lead to electrical instabilities in the heart. An acquired heart disease, such as rheumatic heart disease, or a conduction block are just some of many cases that would require an electronic pacemaker to monitor the heart rate and generate an impulse when it beats abnormally. Although the electric pacemaker is considered as a reliable therapy, it is not without limitations. These limitations include surgery complication, lead infection as well as limited battery lifespan, which requires replacement every few years thus adding to the hospital burden. Several approaches have been taken to develop a more adequate therapeutic method. A strategy that will be investigated involves using a graft of pacemaker cells, fundamentally creating a biological pacemaker. Cell therapy approaches use embryonic stem cells to evolve into the cardiac cell lines, including pacemaker cells. These pacing cells are characterized by spontaneous depolarization that create the rhythmic impulses in the heart and control the heart rate. An important element of the pacemaker cells that give rise to the spontaneous depolarization are the hyperpolarization- activated and cyclic nucleotide-gated (HCN) channels that are activated during hyperpolarization and conduct the funny current by increasing the cell’s inward permeability to sodium-potassium currents. On the other hand, the conduction rate is determined by connexin 30.2 and connexin 45, which are transmembrane proteins that assemble to form gap junctions. Both HCN expression and connexin expression has been linked to T-box factor 3 (Tbx3) in the development of atrial myocytes. A practicable approach to modulate gene expression and consequently protein expression is using chemical conditioning. Phorbol 12-myristate 13-acetate (PMA) is a Protein Kinase C (PKC) activator that has linked to Tbx3 expression, and consequently HCN and connexin expression, and lead to a modification in spontaneous activity. Mouse embryonic stem cells (ESCs) are cells that are isolated from the inner cell mass of early embryos. These cells can differentiate into all somatic cell types. Given the proper combination of growth factors, these cells can differentiate into cardiomyocytes. We hypothesize that chronic conditioning of mice cardiomyocytes with PMA lead to an upregulation of Tbx3 expression and consequently an upregulation of HCN expression and connexin expression, therefore promoting the development of pacemaker cells within the cardiomyocyte population. In order to test our hypothesis, we purchased cells from the mouse E14TG2A cell line. These cells were cultured in glass bottom petri dishes and differentiated into cardiomyocytes using a three-step protocol (shown in Methods section). The cardiomyocytes are then exposed to PMA in varying concentration (0.1 µM vs 1 µM) for either 1h (acute exposure) or 24 h (chronic exposure). The results varied between the experimental groups compared to the control. In all experimental conditions there seems to be an initial increase in spontaneous activity, but this is quickly reversed at the 24 h mark, where pacing decreased. Different concentration plays a dose-dependent role in long-lasting inhibitory effect on the pacing of the cells

Myeloid‐derived suppressor cells (MDSC s) and microRNA s (miRNA s) contribute to attenuating immune responses during chronic viral infection; however, the precise mechanisms underlying their suppressive activities remain incompletely understood. We have recently shown marked expansion of MDSC s that promote regulatory T (Treg) cell development in patients with chronic hepatitis C virus (HCV ) infection. Here we further investigated whether the HCV ‐induced expansion of MDSC s and Treg cells is regulated by an miRNA ‐mediated mechanism. The RNA array analysis revealed that six miRNA s were up‐regulated and six miRNA s were down‐regulated significantly in myeloid cells during HCV infection. Real‐time RT ‐PCR confirmed the down‐regulation of miR‐124 in MDSC s from HCV patients. Bioinformatic analysis suggested that miR‐124 may be involved in the regulation of signal transducer and activator of transcription 3 (STAT ‐3), which was overexpressed in MDSC s from HCV patients. Notably, silencing of STAT ‐3 significantly increased the miR‐124 expression, whereas reconstituting miR‐124 decreased the levels of STAT ‐3, as well as interleukin‐10 and transforming growth factor‐β , which were overexpressed in MDCS s, and reduced the frequencies of Foxp3+ Treg cells that were developed during chronic HCV infection. These results suggest that reciprocal regulation of miR‐124 and STAT ‐3 in MDSC s promotes Treg cell development, thus uncovering a novel mechanism for the expansion of MDSC and Treg cells during HCV infection.

京都大学 / 0048 / 新制・課程博士 / 博士(理学) / 甲第19261号 / 理博第4116号 / 新制||理||1592(附属図書館) / 32263 / 京都大学大学院理学研究科化学専攻 / (主査)教授 杉山 弘, 教授 三木 邦夫, 教授 藤井 紀子 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM

京都大学 / 新制・課程博士 / 博士(医学) / 甲第24487号 / 医博第4929号 / 新制||医||1063(附属図書館) / 京都大学大学院医学研究科医学専攻 / (主査)教授 竹内 理, 教授 上野 英樹, 教授 髙折 晃史 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM

Indiana University-Purdue University Indianapolis (IUPUI) / SIMPL is a transcriptional co-activator that alters the activity of transcription factor, NF-κB. In response to pathogens, cytokines such as Interleukin-1 (IL-1) and Tumor Necrosis Factor (TNF) signal through the IL-1 and TNF-α receptors, respectively, which are found on various cell types. Activation of these receptors can result in the nuclear localization of NF-κB where it enables the transcription of several different genes key in the innate immune response. Endogenous co-localization of the SIMPL protein with NF-κB in response to these same cytokine signals has yet to be demonstrated. Polyclonal antibody generated against a truncated version of the SIMPL protein was purified from the sera obtained from immunized rabbits using affinity chromatography. The antibody was found to have a high specificity for both the native and denatured form of the protein as demonstrated by the lack of nonspecific bands observed in immunoprecipitations and Western blotting. The antibody was utilized in immunofluorescence experiments on mouse endothelial cells that were either unstimulated or were stimulated (IL-1 or TNF-α). In the absence of cytokine, SIMPL was localized in both the cytoplasm and the nucleus as opposed to NF-κB which was almost exclusively localized in the cytoplasm. In the presence of IL-1, the concentration of SIMPL in the nucleus was increased, and in the presence of TNF-α, the concentration of SIMPL in the nucleus was even greater. Results of this study identified future routes for SIMPL antibody isolation as well as to demonstrate that endogenous SIMPL protein nuclear localization may not be solely dependent upon TNF-α signaling.

Objective: Regulatory T cells (Tregs) contribute to HIV-1 disease progression by impairing antiviral immunity; however, the precise mechanisms responsible for the development of Tregs in the setting of HIV-1 infection are incompletely understood. Design: In this study, we provide evidence that HIV-induced expansion of monocytic myeloid-derived suppressor cells (M-MDSCs) promote the differentiation of Foxp3+ Tregs. Methods: We measured MDSC induction and cytokine expression by flow cytometry and analyzed their functions by coculturing experiments. Results: We observed a dramatic increase in M-MDSC frequencies in the peripheral blood of HIV-1 seropositive (HIV-1+) individuals, even in those on antiretroviral therapy with undetectable viremia, when compared with healthy participants. We also observed increases in M-MDSCs after incubating healthy peripheral mononuclear cells (PBMCs) with HIV-1 proteins (gp120 or Tat) or Toll-like receptor 4 ligand lipopolysaccharides in vitro, an effect that could be abrogated in the presence of the phosphorylated signal transducer and activator of transcription 3 inhibitor, STA-21. Functional analyses indicated that M-MDSCs from HIV-1+ individuals express higher levels of IL-10, tumor growth factor-β, IL-4 receptor α, p47phex, programmed death-ligand 1, and phosphorylated signal transducer and activator of transcription 3 – all of which are known mediators of myelopoiesis and immunosuppression. Importantly, incubation of healthy CD4+ T cells with MDSCs derived from HIV-1+ individuals significantly increased differentiation of Foxp3+ Tregs. In addition, depletion of MDSCs from PBMCs of HIV-1+ individuals led to a significant reduction of Foxp3+ Tregs and increase of IFNγ production by CD4+ T effector cells. Conclusions: These results suggest that HIV-induced MDSCs promote Treg cell development and inhibit T cell function – a hallmark of many chronic infectious diseases.

<p> Proper gene expression programs cellular activities, while aberrant manipulation of transcription factors often leads to devastating consequences, such as cancer or cell death. The transcription factor family activator protein-1 (AP-1) plays an important role in many cellular activities including cell transformation, proliferation and survival (Shaulian and Karin 2002). However, little has been done to obtain a global view of the role of individual AP-1 members and how they cooperate in many cellular activities. We have discovered that blocking the AP-1 pathway by a c-Jun dominant negative mutant, TAM67, induced cell death in RSV-transformed primary chicken embryo fibroblasts (CEF), suggesting that AP-1 activity is vital for cell survival upon v-Src transformation. In addition, accumulation of cytoplasmic vesicles was observed in the cytoplasm of a proportion of RSV-transformed CEF expressing TAM67. Oil-red staining of these vesicles indicated the presence of lipid droplets in these cells, suggesting that the inhibition of AP-1 promotes the adipogenic conversion of v-Src transformed CEF. To understand the role of individual members of the AP-1 family, a retroviral-based shRNA expressing system was designed to stably downregulate individual AP-1 members. This retroviral-based RNAi system provided sustained gene downregulation of AP-1 family members. Reduction of the c-Jun protein level by shRNA induced senescence in normal CEF, while it modestly downregulated AP-1 activity in RSV -transformed CEF indicating that c-Jun is not the main component of the AP-1 complex in RSV-transformed CEF. Inhibition of JunD expression induced apoptosis and was deleterious to both normal and RSV-transformed CEF, suggesting that JunD is crucial for the survival of CEF. Transient express10n reporter-assays also showed that loss-of-function of JunD by shRNA dramatically repressed AP-1 activity. Hence JunD is the main component of the AP-1 complex that regulates the survival of CEF. Furthermore, we determined that loss of JunD expression resulted in an elevated level of tumour suppressor p53. Co-inhibition of p53 and JunD restored the transforming ability of v-Src transformed CEF, as indicated by foci formation in soft agar assays. Hence, repression of p53 induction was able to bypass the death signal released as a result of AP-1 inhibition in v-Src transformed CEF. Downregulation of Fra-2 (Fos-related antigen 2) level by shRNA did not affect the proliferation of normal CEF. However, RSV -transformed CEFs expressing fra -2 shRNA were transformation-defective with the presence of multiple vesicles in cytoplasm. Oil-red staining of these vesicles indicated the presence of lipid droplets, which resembles the effect of T AM67 in RSV -transformed CEF indicating that Fra-2 blocks differentiation. These findings help us to understand the role of individual members of the AP-1 transcription factor family in normal and RSV -transformed CEF. Importantly, global gene profiling of v-Src transformed CEF expressing shRNA for individual AP-1 members will improve our knowledge of the transformation process. Functional characterization of the cascade will rely on the use of retroviral-based shRNA expressing system as described above. </p> / Thesis / Doctor of Philosophy (PhD)

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