LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 3 of total 3

Search options

  1. Article ; Online: High Salt Induces a Delayed Activation of Human Neutrophils.

    Mazzitelli, Ignacio / Bleichmar, Lucía / Melucci, Claudia / Gerber, Pehuén Pereyra / Toscanini, Agustina / Cuestas, María Luján / Diaz, Fernando Erra / Geffner, Jorge

    Frontiers in immunology

    2022  Volume 13, Page(s) 831844

    Abstract: High salt (NaCl) concentrations are found in a number of tissues under physiological and pathological conditions. Here, we analyzed the effects induced by high salt on the function of human neutrophils. The culture of neutrophils in medium supplemented ... ...

    Abstract High salt (NaCl) concentrations are found in a number of tissues under physiological and pathological conditions. Here, we analyzed the effects induced by high salt on the function of human neutrophils. The culture of neutrophils in medium supplemented with high salt (50 mM NaCl) for short periods (30-120 min) inhibited the ability of conventional agonists to induce the production of IL-8 and the activation of respiratory burst. By contrast, exposure to high salt for longer periods (6-18 h) resulted in the activation of neutrophils revealed by the production of high levels of IL-8, the activation of the respiratory burst, and a marked synergistic effect on the production of TNF-α induced by LPS. Increasing osmolarity of the culture medium by the addition of sorbitol or mannitol (100 mM) was shown to be completely unable to stimulate neutrophil responses, suggesting that high sodium but not an increased osmolarity mediates the activation on neutrophils responses. A similar biphasic effect was observed when the function of monocytes was analyzed. Short term exposure to high salt suppressed IL-8 and TNF-α production induced by LPS while culture for longer periods triggered the production of IL-8 but not TNF-α in the absence of LPS stimulation. Contradictory results have been published regarding how high salt modulates neutrophil function. Our results suggest that the modulation of neutrophil function by high salt is strongly dependent on the exposure time.
    MeSH term(s) Humans ; Interleukin-8/pharmacology ; Lipopolysaccharides/pharmacology ; Neutrophils/pathology ; Sodium Chloride/pharmacology ; Tumor Necrosis Factor-alpha/pharmacology
    Chemical Substances Interleukin-8 ; Lipopolysaccharides ; Tumor Necrosis Factor-alpha ; Sodium Chloride (451W47IQ8X)
    Language English
    Publishing date 2022-06-03
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2022.831844
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Concomitant inhibition of PPARγ and mTORC1 induces the differentiation of human monocytes into highly immunogenic dendritic cells.

    Erra Diaz, Fernando / Mazzitelli, Ignacio / Bleichmar, Lucía / Melucci, Claudia / Thibodeau, Asa / Dalotto Moreno, Tomás / Marches, Radu / Rabinovich, Gabriel A / Ucar, Duygu / Geffner, Jorge

    Cell reports

    2023  Volume 42, Issue 3, Page(s) 112156

    Abstract: Monocytes can differentiate into macrophages (Mo-Macs) or dendritic cells (Mo-DCs). The cytokine granulocyte-macrophage colony-stimulating factor (GM-CSF) induces the differentiation of monocytes into Mo-Macs, while the combination of GM-CSF/interleukin ( ...

    Abstract Monocytes can differentiate into macrophages (Mo-Macs) or dendritic cells (Mo-DCs). The cytokine granulocyte-macrophage colony-stimulating factor (GM-CSF) induces the differentiation of monocytes into Mo-Macs, while the combination of GM-CSF/interleukin (IL)-4 is widely used to generate Mo-DCs for clinical applications and to study human DC biology. Here, we report that pharmacological inhibition of the nuclear receptor peroxisome proliferator-activated receptor gamma (PPARγ) in the presence of GM-CSF and the absence of IL-4 induces monocyte differentiation into Mo-DCs. Remarkably, we find that simultaneous inhibition of PPARγ and the nutrient sensor mammalian target of rapamycin complex 1 (mTORC1) induces the differentiation of Mo-DCs with stronger phenotypic stability, superior immunogenicity, and a transcriptional profile characterized by a strong type I interferon (IFN) signature, a lower expression of a large set of tolerogenic genes, and the differential expression of several transcription factors compared with GM-CSF/IL-4 Mo-DCs. Our findings uncover a pathway that tailors Mo-DC differentiation with potential implications in the fields of DC vaccination and cancer immunotherapy.
    MeSH term(s) Humans ; Monocytes/metabolism ; Granulocyte-Macrophage Colony-Stimulating Factor/pharmacology ; Granulocyte-Macrophage Colony-Stimulating Factor/metabolism ; PPAR gamma/metabolism ; Interleukin-4/pharmacology ; Interleukin-4/metabolism ; Dendritic Cells/metabolism ; Cell Differentiation/physiology ; Cells, Cultured
    Chemical Substances Granulocyte-Macrophage Colony-Stimulating Factor (83869-56-1) ; PPAR gamma ; Interleukin-4 (207137-56-2)
    Language English
    Publishing date 2023-02-26
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2023.112156
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Immunoglobulin G Immune Complexes May Contribute to Neutrophil Activation in the Course of Severe Coronavirus Disease 2019.

    Mazzitelli, Ignacio / Bleichmar, Lucia / Ludueña, María Guillermina / Pisarevsky, Andrea / Labato, Mariana / Chiaradia, Verónica / Finocchieto, Paola / Paulin, Francisco / Hormanstorfer, Macarena / Baretto, María Constanza / Adanza, Santiago Piombi / Parodi, María Noel / Ragusa, Martín / Melucci, Claudia / Díaz, Fernando Erra / Paletta, Ana / Di Diego, Facundo / Ceballos, Ana / Geffner, Jorge

    The Journal of infectious diseases

    2021  Volume 224, Issue 4, Page(s) 575–585

    Abstract: Severe coronavirus disease 2019 (COVID-19) is associated with an overactive inflammatory response mediated by macrophages. Here, we analyzed the phenotype and function of neutrophils in patients with COVID-19. We found that neutrophils from patients with ...

    Abstract Severe coronavirus disease 2019 (COVID-19) is associated with an overactive inflammatory response mediated by macrophages. Here, we analyzed the phenotype and function of neutrophils in patients with COVID-19. We found that neutrophils from patients with severe COVID-19 express high levels of CD11b and CD66b, spontaneously produce CXCL8 and CCL2, and show a strong association with platelets. Production of CXCL8 correlated with plasma concentrations of lactate dehydrogenase and D-dimer. Whole blood assays revealed that neutrophils from patients with severe COVID-19 show a clear association with immunoglobulin G (IgG) immune complexes. Moreover, we found that sera from patients with severe disease contain high levels of immune complexes and activate neutrophils through a mechanism partially dependent on FcγRII (CD32). Interestingly, when integrated in immune complexes, anti-severe acute respiratory syndrome coronavirus 2 IgG antibodies from patients with severe COVID-19 displayed a higher proinflammatory profile compared with antibodies from patients with mild disease. Our study suggests that IgG immune complexes might promote the acquisition of an inflammatory signature by neutrophils, worsening the course of COVID-19.
    MeSH term(s) Adult ; Aged ; Antibodies, Viral/blood ; Antibodies, Viral/immunology ; Antigen-Antibody Complex/blood ; Antigen-Antibody Complex/immunology ; Antigens, CD/immunology ; CD11b Antigen/immunology ; COVID-19/immunology ; Cell Adhesion Molecules/immunology ; Female ; GPI-Linked Proteins/immunology ; Humans ; Immunoglobulin G/blood ; Immunoglobulin G/immunology ; Interleukin-8/immunology ; Male ; Middle Aged ; Neutrophil Activation/immunology ; Neutrophils/immunology ; Receptors, IgG/immunology ; SARS-CoV-2/immunology ; Young Adult
    Chemical Substances Antibodies, Viral ; Antigen-Antibody Complex ; Antigens, CD ; CD11b Antigen ; CEACAM8 protein, human ; CXCL8 protein, human ; Cell Adhesion Molecules ; GPI-Linked Proteins ; Immunoglobulin G ; Interleukin-8 ; Receptors, IgG
    Language English
    Publishing date 2021-08-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiab174
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top