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  • 1
    In: Medical Immunology (Russia), SPb RAACI, Vol. 24, No. 5 ( 2022-10-31), p. 1057-1064
    Abstract: Chronic psychosocial stress provokes anxious behavior and depressive disorders. The longitudinal stress-induced neuroendocrine signals may alter functioning of immune (central and peripheral) organs. Increased myelopoiesis is observed in bone marrow, being detrimental to lympho- and erythropoiesis, with increased emigration of monocytic bone marrow cells to the periphery and their acquisition of “inflammatory” phenotype. The subsequent migration of such monocytes to the brain with differentiation into the M1 type macrophages which form inflammatory signals, and their effect upon endothelial cells and microglia leads to increased production of cytokines, chemokines, and adhesion molecules, thus accelerating accumulation of bone marrow-derived monocytes migrating to the brain. The signals from bone marrow monocytes and activated microglia promote neuroinflammatory condition which leads to behavioral changes. Current data on the presence of non-resident bone marrow macrophages in the brain of depressed patients require studies of hematopoiesis in depression-like states. Pronounced plasticity is a characteristic feature of macrophages, i.e., their ability to acquire M1 or M2 phenotype depending on the microenvironment signals. M1 exhibit high pro-inflammatory activity and have neurodestructive properties, whereas M2 cells are characterized by low pro-inflammatory activity and pronounced regenerative potential, due to the production of multiple soluble mediators and cytokines, including neurotrophic and immunoregulatory factors, anti-inflammatory substances that provide neuroprotection, stimulate neurogenesis, synaptogenesis, growth and myelinization of axons, thus theoretically substantiating an opportunity of using the potential of M2 macrophages in the treatment of depression. In this work, we studied the effect of soluble factors of human macrophages, polarized into cells with M2 phenotype under the conditions of serum deprivation, upon bone marrow hematopoiesis and peripheral blood cells in a model of stress-induced depression. We have shown enhanced differentiation of hematopoietic stem cells into the granulocyte-macrophage (CFU-GM) lineage, along with increased monocyte population in peripheral blood in the depressive-like murine model. Development of a depressive-like state in the animals was associated with reduced amounts of both erythroid precursors in bone marrow and erythrocytes/hemoglobin in peripheral blood. Intranasal administration of soluble M2 macrophage factors (M2-SFs) for 7 days was accompanied by a corrective effect on the above parameters, being significant for peripheral blood monocytes. The data obtained suggest effectiveness of the M2-SFS anti-inflammatory effects in correcting changes in hematopoiesis caused by social stress in depressive-like animals.
    Type of Medium: Online Resource
    ISSN: 2313-741X , 1563-0625
    Language: Unknown
    Publisher: SPb RAACI
    Publication Date: 2022
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  • 2
    In: Medical Immunology (Russia), SPb RAACI, Vol. 12, No. 3 ( 2014-07-14), p. 191-
    Type of Medium: Online Resource
    ISSN: 2313-741X , 1563-0625
    URL: Issue
    Language: Unknown
    Publisher: SPb RAACI
    Publication Date: 2014
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  • 3
    Online Resource
    Online Resource
    Siberian State Medical University ; 2017
    In:  Bulletin of Siberian Medicine Vol. 16, No. 4 ( 2017-01-01), p. 155-164
    In: Bulletin of Siberian Medicine, Siberian State Medical University, Vol. 16, No. 4 ( 2017-01-01), p. 155-164
    Type of Medium: Online Resource
    ISSN: 1819-3684 , 1682-0363
    URL: Issue
    Language: Unknown
    Publisher: Siberian State Medical University
    Publication Date: 2017
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  • 4
    Online Resource
    Online Resource
    Russian Society of Immunology ; 2022
    In:  Russian Journal of Immunology Vol. 25, No. 4 ( 2022-10-07), p. 423-430
    In: Russian Journal of Immunology, Russian Society of Immunology, Vol. 25, No. 4 ( 2022-10-07), p. 423-430
    Abstract: An increased concentration of extracellular cell free DNA (cfDNA) is a distinctive characteristic of pathologies that mainly occur in acute inflammation (myocardial infarction, sepsis, stroke, trauma). The increase of cfDNA in chronic inflammatory processes, oncological, autoimmune diseases is less significant and is mainly due to aberrant cell death processes. One of such diseases is systemic lupus erythematosus (SLE). It has recently been shown that, in addition to increased cfDNA concentration, the degree of inflammation can reflect the N/L index (neutrophil to lymphocyte ratio), being a simple and informative marker of disease activity in patients with SLE. The aim of the study was to study the dynamics of the level of cfDNA and the N/L index in the model of LPS-induced inflammatory response as observed in intact mice, and their relation to the phenotypic heterogeneity of model SLE. We used female hybrid mice (C57Bl/6xDBA/2) F1 and female DBA/2 mice at the age of 6-8 weeks. LPS of E. coli strain 111: B4 (Sigma) was injected intraperitoneally once at doses of 10 ng, 1 g and 100 g per mouse in PBS. The control group was injected with the appropriate volume of buffer. The TNF-binding domain of the variola virus CRMB protein was used as an inhibitor of TNF, which was administered 30 min before the introduction of LPS. The dynamics of the response to LPS was assessed after 4, 8, 11, 24 hours by the N/L index and the level of cfDNA; at the zero point, the parameters were determined before the introduction of LPS. A day after a single injection of LPS at a dose of 1 g/mouse, a SLE model was induced on the same hybrid mice (double intravenous administration with an interval of 6 days of spleen cells of the DBA/2 line, 60-70 106 cells each). Three months later, with proteinuria of 3 mg/ mL or more, mice were assigned to the SLEnephritis+ group, with a protein of less than 3 mg/mL, to the SLEnephritis- group. Statistical processing of the results was carried out by nonparametric statistics using the MannWhitney test. Differences were considered statistically significant at p 0.05. It was found that the change in the N/L index, as well as the change in the level of cfDNA, depends on the dose of LPS administered. It was shown that the level of cfDNA reaches its maximum after 8 and 11 hours after the introduction of LPS is reliably reduced when using the inhibitor TNF. A retrospective analysis indicates that there is a definite relationship between the response of intact mice to LPS before induction of cGVHD, and their subsequent division into variants of SLEnephritis + and SLEnephritis - in the course of disease development.
    Type of Medium: Online Resource
    ISSN: 1028-7221
    Language: Unknown
    Publisher: Russian Society of Immunology
    Publication Date: 2022
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  • 5
    Online Resource
    Online Resource
    Russian Society of Immunology ; 2023
    In:  Russian Journal of Immunology Vol. 26, No. 4 ( 2023-09-22), p. 533-540
    In: Russian Journal of Immunology, Russian Society of Immunology, Vol. 26, No. 4 ( 2023-09-22), p. 533-540
    Abstract: Many studies have shown that the level of cell-free DNA (cfDNA) in blood of patients with oncological diseases, sepsis, systemic lupus erythematosus, and some rheumatic diseases significantly exceeds the value of similar index in healthy donors and is closely related to the clinical features of the disease. Systemic inflammatory response is among the most frequent pathophysiological processes along with markedly changed levels of cfDNA in blood plasma. The levels of cfDNA in blood plasma of patients with RA are shown to be closely associated with a shifted balance of helpers to the Th1-side. It is an adequate intensity index of inflammatory processes and effectiveness of therapy. At the same time, there only limited number of works concerning changes in cfDNA levels in pathological processes with predominance of Th2 lymphocytes. According to generally accepted concept, the pathogenesis of bronchial asthma is of distinct interest, being critically dependent on the production of specific antibodies controlled by activated Th2 lymphocytes. The aim of this work was to study the level of cfDNA in blood and compare its changes with intensity of NETs and inflammation in patients with asthma. The study included 20 patients with asthma, who underwent hospital treatment at the Department Allergology (Clinic of Immunopathology, RIFCI, Novosibirsk), and 10 conditionally healthy donors. We have shown that, upon admission to the clinic, the level of cfDNA in patients with asthma was significantly reduced against the control group of healthy donors. After a course of therapy, the average level of cfDNA in patients plasma was increased and did not differ statistically significantly from this index in controls. The data obtained for other parameters indicate that the patients with asthma did not reveal any signs of pronounced systemic inflammatory response. One should suggest that the observed changes in the level of cfDNA in blood plasma in bronchial asthma are not caused by chronic inflammatory process in lungs of these patients, but they are determined by some other pathophysiological mechanisms. It has been shown that the level of in vitro stimulated NETs in patients with asthma is higher than in healthy donors, thus being consistent with current opinions on the role of neutrophils in pathogenesis of asthma.
    Type of Medium: Online Resource
    ISSN: 2782-7291 , 1028-7221
    Language: Unknown
    Publisher: Russian Society of Immunology
    Publication Date: 2023
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  • 6
    Online Resource
    Online Resource
    SPb RAACI ; 2022
    In:  Medical Immunology (Russia) Vol. 24, No. 4 ( 2022-07-13), p. 853-860
    In: Medical Immunology (Russia), SPb RAACI, Vol. 24, No. 4 ( 2022-07-13), p. 853-860
    Abstract: Increased concentration of cell-free DNA (cfDNA) in the circulating blood of humans and animals is a sign of inflammatory conditions and a distinctive characteristic of various pathophysiological processes in the body. The aim of the present study was to investigate the possible role of tumor necrosis factor (TNFα) in changes of cfDNA contents in peripheral blood as a response to experimentally induced systemic inflammation. We used 40 female hybrid mice (C57Bl/6xDBA/2) F1 at the age of 6-8 weeks. The concentration of cfDNA and its individual fractions was determined using a PicoGreen fluorescent dye. The dynamics of inflammatory process was evaluated after 4, 8, 11 and 24 hours following LPS injection. A significant increase in the blood plasma cfDNA levels was shown under the action of E. coli lipopolysaccharide (LPS), along with simultaneous decreased levels of cfDNA, associated with cell surface. The ratio of cell surface-bound cfDNA to the total cfDNA contents was reduced in dose-dependent manner as early as 4 hours after LPS injection to the animals, thus allowing us to consider this ratio a characteristic sign of netosis of neutrophilic granulocytes during the development of acute inflammation. The described effects are significantly suppressed with co-injection of recombinant TNFα neutralizing protein along with LPS, whereas increased intake of neutrophils in the tissues is determined by some other factors which are not directly related to the production of this cytokine. Based on the obtained data, we proposed a following hypothesis: induction of netosis by inflammatory stimuli causes an increase in the concentration of cfDNA in blood plasma not only due to de novo emerging extracellular DNA by neutrophil netosis, but also by the release of distinct cfDNA fraction that was previously firmly bound to cell membranes in multiple body tissues under the action of proteases released during netosis.
    Type of Medium: Online Resource
    ISSN: 2313-741X , 1563-0625
    Language: Unknown
    Publisher: SPb RAACI
    Publication Date: 2022
    detail.hit.zdb_id: 3041761-2
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  • 7
    Online Resource
    Online Resource
    SPb RAACI ; 2014
    In:  Medical Immunology (Russia) Vol. 14, No. 1-2 ( 2014-07-19), p. 67-
    In: Medical Immunology (Russia), SPb RAACI, Vol. 14, No. 1-2 ( 2014-07-19), p. 67-
    Type of Medium: Online Resource
    ISSN: 2313-741X , 1563-0625
    URL: Issue
    Language: Unknown
    Publisher: SPb RAACI
    Publication Date: 2014
    detail.hit.zdb_id: 3041761-2
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  • 8
    Online Resource
    Online Resource
    SPb RAACI ; 2014
    In:  Medical Immunology (Russia) Vol. 13, No. 1 ( 2014-07-18), p. 29-
    In: Medical Immunology (Russia), SPb RAACI, Vol. 13, No. 1 ( 2014-07-18), p. 29-
    Type of Medium: Online Resource
    ISSN: 2313-741X , 1563-0625
    URL: Issue
    Language: Unknown
    Publisher: SPb RAACI
    Publication Date: 2014
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  • 9
    Online Resource
    Online Resource
    SPb RAACI ; 2021
    In:  Medical Immunology (Russia) Vol. 23, No. 4 ( 2021-10-19), p. 659-664
    In: Medical Immunology (Russia), SPb RAACI, Vol. 23, No. 4 ( 2021-10-19), p. 659-664
    Abstract: While conducting numerous studies, including researchers in our laboratory, it was found that Th1/Th2 balance plays an essential role in the regulation of reactions that determine the outcomes of immunopathological processes in both chronic and acute GVHD models. However, the question about activity of which element in the regulatory process during GVHD induction (for example, a receptor or an enzyme) affects the ratio of this balance depends remains open. It has been suggested that the degree of activation of the GPR84 receptor during GVHD induction can significantly affect the host Th1/Th2 balance. And, by assessing this parameter, the direction of development and the intensity of the pathological process can be determined. The aim of this work was to investigate the effect of ligands such as medium-chain fatty acid receptor GPR84 on the Th1/Th2 balance in an experimental model in an in vivo system. Female DBA/2 and hybrids (C57Bl/6 × DBA/2) F1 mouse strains were used in the experiments.The studied ligands of GPR84 were capric and lauric acids, as well as a synthetic ligand 6-OAU. Chronic GVHD in the semi-allogenic system was induced by injecting splenocytes from DBA/2 mice to B6D2F1 hybrid mice: 60-70 × 106 -cells iv twice with an interval of 6 days. The first administration of the GPR84 ligands was performed one hour after the donor cell transfer and then once a day for two weeks.The effect of the study drugs on the course of chronic GVHD was assessed three months after the onset of the experiment. It was shown that the administration of GPR84 ligands to to animals during the induction of chronic GVHD affects the activity of the receptor and the host Th1/Th2 ratio. In the group with the injection of 6-OAU, the number of animals which the immunopathological process developed according to the Th1-dependent variant increased by more than 1.5-fold, compared with the control group. This fact is consistent with the literature data obtained in the in vitro system. Apparently, the effect of a mixture of capric and lauric acids is mediated by some other mechanism, differed from the GPR84 activation. Therefore, further research is required to realize the promising possibility of adjusting immune responses by including certain fatty acids in the diet.  
    Type of Medium: Online Resource
    ISSN: 2313-741X , 1563-0625
    Language: Unknown
    Publisher: SPb RAACI
    Publication Date: 2021
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  • 10
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2010
    In:  Bulletin of Experimental Biology and Medicine Vol. 149, No. 1 ( 2010-7), p. 54-56
    In: Bulletin of Experimental Biology and Medicine, Springer Science and Business Media LLC, Vol. 149, No. 1 ( 2010-7), p. 54-56
    Type of Medium: Online Resource
    ISSN: 0007-4888 , 1573-8221
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2010
    detail.hit.zdb_id: 2037110-X
    SSG: 12
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