Browsing by Author "Mirkov, Ivana (23973384600)"
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Publication Lipopolysaccharide induces tumor necrosis factor receptor-1 independent relocation of lymphocytes from the red pulp of the mouse spleen(2018) ;Lalić, Ivana M. (56010928700) ;Bichele, Rudolf (55601114800) ;Repar, Anja (57201194098) ;Despotović, Sanja Z. (56010801100) ;Petričević, Saša (25226498300) ;Laan, Martti (7004351466) ;Peterson, Pärt (7402598650) ;Westermann, Jürgen (7006238755) ;Milićević, Živana (7003463353) ;Mirkov, Ivana (23973384600)Milićević, Novica M. (56268200000)It is well known that bacterial lipopolysaccharide (LPS) induces migration of several cellular populations within the spleen. However, there are no data about the impact of LPS on B and T lymphocytes present in the red pulp. Therefore, we used an experimental model in which we tested the effects of intravenously injected LPS on the molecular, cellular and structural changes of the spleen, with special reference to the red pulp lymphocytes. We discovered that LPS induced a massive relocation of B and T lymphocytes from the splenic red pulp, which was independent of the tumor necrosis factor receptor-1 signaling axis. Early after LPS treatment, quantitative real-time PCR analysis revealed the elevated levels of mRNA encoding numerous chemokines and proinflammatory cytokines (XCL1, CXCL9, CXCL10, CCL3, CCL4, CCL5, CCL17, CCL20, CCL22, TNFα and LTα) which affect the navigation and activities of B and T lymphocytes in the lymphoid tissues. An extreme increase in mRNA levels for CCL20 was detected in the white pulp of the LPS-treated mice. The CCL20-expressing cells were localized in the PALS. Some smaller CCL20-expressing cells were evenly dispersed in the B cell zone. Thus, our study provides new knowledge of how microbial products could be involved in shaping the structure of lymphatic organs. © 2018 Elsevier GmbH - Some of the metrics are blocked by yourconsent settings
Publication Lipopolysaccharide induces tumor necrosis factor receptor-1 independent relocation of lymphocytes from the red pulp of the mouse spleen(2018) ;Lalić, Ivana M. (56010928700) ;Bichele, Rudolf (55601114800) ;Repar, Anja (57201194098) ;Despotović, Sanja Z. (56010801100) ;Petričević, Saša (25226498300) ;Laan, Martti (7004351466) ;Peterson, Pärt (7402598650) ;Westermann, Jürgen (7006238755) ;Milićević, Živana (7003463353) ;Mirkov, Ivana (23973384600)Milićević, Novica M. (56268200000)It is well known that bacterial lipopolysaccharide (LPS) induces migration of several cellular populations within the spleen. However, there are no data about the impact of LPS on B and T lymphocytes present in the red pulp. Therefore, we used an experimental model in which we tested the effects of intravenously injected LPS on the molecular, cellular and structural changes of the spleen, with special reference to the red pulp lymphocytes. We discovered that LPS induced a massive relocation of B and T lymphocytes from the splenic red pulp, which was independent of the tumor necrosis factor receptor-1 signaling axis. Early after LPS treatment, quantitative real-time PCR analysis revealed the elevated levels of mRNA encoding numerous chemokines and proinflammatory cytokines (XCL1, CXCL9, CXCL10, CCL3, CCL4, CCL5, CCL17, CCL20, CCL22, TNFα and LTα) which affect the navigation and activities of B and T lymphocytes in the lymphoid tissues. An extreme increase in mRNA levels for CCL20 was detected in the white pulp of the LPS-treated mice. The CCL20-expressing cells were localized in the PALS. Some smaller CCL20-expressing cells were evenly dispersed in the B cell zone. Thus, our study provides new knowledge of how microbial products could be involved in shaping the structure of lymphatic organs. © 2018 Elsevier GmbH - Some of the metrics are blocked by yourconsent settings
Publication Melanoma tumor inhibition by tetrachlorido(O,O′-dibutyl- ethylenediamine-N,N′-di-3-propionate)platinum(iv) complex: In vitro and in vivo investigations(2012) ;Maksimović-Ivanić, Danijela (6507584634) ;Mijatović, Sanja (6508347659) ;Mirkov, Ivana (23973384600) ;Stošić-Grujičić, Stanislava (7004253020) ;Miljković, Djordje (7006524033) ;Sabo, Tibor J. (7004201321) ;Trajković, Vladimir (7004516866)Kaluerović, Goran N. (7801430570)Tetrachlorido(O,O′-dibutyl-ethylenediamine-N,N′-di-3- propionate)platinum(iv) complex, [PtCl4(n-Bu2eddp)], was previously found to be effective against fibrosarcoma and glioma cell lines. Here we presented that [PtCl4(n-Bu2eddp)] strongly reduced the growth of B16 melanoma cells in vitro. Inhibition of cell viability was accompanied with induction of both necrotic and apoptotic cell death. In addition, [PtCl4(n-Bu2eddp)] concealed the expansion of tumors induced in syngeneic C57Bl/6 mice without visible signs of nephrotoxicity. © The Royal Society of Chemistry 2012.
