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  1. Article ; Online: AK2 deficiency: An awkward tale for B cells.

    Campos Codo, Ana / Moraes-Vieira, Pedro Manoel Mendes

    The Journal of allergy and clinical immunology

    2020  Volume 146, Issue 1, Page(s) 74–76

    MeSH term(s) B-Lymphocytes ; Humans ; Mitochondria ; Severe Combined Immunodeficiency
    Language English
    Publishing date 2020-07-06
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 121011-7
    ISSN 1097-6825 ; 1085-8725 ; 0091-6749
    ISSN (online) 1097-6825 ; 1085-8725
    ISSN 0091-6749
    DOI 10.1016/j.jaci.2020.04.060
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Effects of L-Dopa, SKF-38393, and quinpirole on exploratory, anxiety- and depressive-like behaviors in pubertal female and male mice.

    Moraes, Muiara Aparecida / Árabe, Laila Blanc / Resende, Bruna Lopes / Codo, Beatriz Campos / Reis, Ana Luiza de Araújo Lima / Souza, Bruno Rezende

    Behavioural brain research

    2023  Volume 459, Page(s) 114805

    Abstract: Adolescence is a phase of substantial changes in the brain, characterized by maturational remodeling of many systems. This remodeling allows functional plasticity to adapt to a changing environment. The dopaminergic system is under morphological and ... ...

    Abstract Adolescence is a phase of substantial changes in the brain, characterized by maturational remodeling of many systems. This remodeling allows functional plasticity to adapt to a changing environment. The dopaminergic system is under morphological and physiological changes during this phase. In the present study, we investigated if changes in the dopaminergic tone alter mice behavior in a receptor and sex-specific manner, specifically at the beginning of the puberty period. We administered L-Dopa, SKF-38393 (D1 dopamine receptor agonist), and Quinpirole (D2 dopamine receptor agonist) and tested male and female mice's motor, anxiety- and depressive-like behavior. While females displayed an impaired exploratory drive, males presented an intense depressive-like response. Our results provide insights into the function of dopaminergic development in adolescent behavior and highlight the importance of studies in this time window with male and female subjects.
    MeSH term(s) Humans ; Mice ; Male ; Female ; Animals ; Adolescent ; Quinpirole/pharmacology ; Levodopa/pharmacology ; 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine/pharmacology ; Dopamine Agonists/pharmacology ; Dopamine Agents/pharmacology ; Ergolines/pharmacology ; Receptors, Dopamine D1 ; Dopamine ; Anxiety/drug therapy
    Chemical Substances Quinpirole (20OP60125T) ; Levodopa (46627O600J) ; 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine (67287-49-4) ; Dopamine Agonists ; Dopamine Agents ; Ergolines ; Receptors, Dopamine D1 ; Dopamine (VTD58H1Z2X)
    Language English
    Publishing date 2023-12-12
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 449927-x
    ISSN 1872-7549 ; 0166-4328
    ISSN (online) 1872-7549
    ISSN 0166-4328
    DOI 10.1016/j.bbr.2023.114805
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  3. Article ; Online: Macrophage Polarization and Alveolar Bone Healing Outcome: Despite a Significant M2 Polarizing Effect, VIP and PACAP Treatments Present a Minor Impact in Alveolar Bone Healing in Homeostatic Conditions.

    Azevedo, Michelle de Campos Soriani / Fonseca, Angélica Cristina / Colavite, Priscila Maria / Melchiades, Jéssica Lima / Tabanez, André Petenuci / Codo, Ana Campos / de Medeiros, Alexandra Ivo / Trombone, Ana Paula Favaro / Garlet, Gustavo Pompermaier

    Frontiers in immunology

    2021  Volume 12, Page(s) 782566

    Abstract: Host inflammatory immune response comprises an essential element of the bone healing process, where M2 polarization allegedly contributes to a favorable healing outcome. In this context, immunoregulatory molecules that modulate host response, including ... ...

    Abstract Host inflammatory immune response comprises an essential element of the bone healing process, where M2 polarization allegedly contributes to a favorable healing outcome. In this context, immunoregulatory molecules that modulate host response, including macrophage polarization, are considered potential targets for improving bone healing. This study aims to evaluate the role of the immunoregulatory molecules VIP (Vasoactive intestinal peptide) and PACAP (Pituitary adenylate cyclase activating polypeptide), which was previously described to favor the development of the M2 phenotype, in the process of alveolar bone healing in C57Bl/6 (WT) mice. Experimental groups were submitted to tooth extraction and maintained under control conditions or treated with VIP or PACAP were evaluated by microtomographic (µCT), histomorphometric, immunohistochemical, and molecular analysis at 0, 3, 7, and 14 days to quantify tissue healing and host response indicators at the healing site. Gene expression analysis demonstrates the effectiveness of VIP or PACAP in modulating host response, evidenced by the early dominance of an M2-type response, which was paralleled by a significant increase in M2 (CD206
    MeSH term(s) Alveolar Process/drug effects ; Alveolar Process/immunology ; Alveolar Process/injuries ; Alveolar Process/surgery ; Animals ; Cell Differentiation/drug effects ; Cell Differentiation/immunology ; Disease Models, Animal ; Female ; Immunomodulation/drug effects ; Macrophage Activation/drug effects ; Male ; Mice ; Osteoblasts/physiology ; Osteogenesis/drug effects ; Osteogenesis/immunology ; Pituitary Adenylate Cyclase-Activating Polypeptide/administration & dosage ; Tooth Extraction/adverse effects ; Vasoactive Intestinal Peptide/administration & dosage ; Wound Healing/drug effects ; Wound Healing/immunology ; X-Ray Microtomography
    Chemical Substances Pituitary Adenylate Cyclase-Activating Polypeptide ; Vasoactive Intestinal Peptide (37221-79-7)
    Language English
    Publishing date 2021-12-21
    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.2021.782566
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  4. Article ; Online: Polymorphic KIR3DL3 expression modulates tissue-resident and innate-like T cells.

    Palmer, William H / Leaton, Laura Ann / Campos Codo, Ana / Crute, Bergren / Roest, James / Zhu, Shiying / Petersen, Jan / Tobin, Richard P / Hume, Patrick S / Stone, Matthew / van Bokhoven, Adrie / Gerich, Mark E / McCarter, Martin D / Zhu, Yuwen / Janssen, William J / Vivian, Julian P / Trowsdale, John / Getahun, Andrew / Rossjohn, Jamie /
    Cambier, John / Loh, Liyen / Norman, Paul J

    Science immunology

    2023  Volume 8, Issue 84, Page(s) eade5343

    Abstract: Most human killer cell immunoglobulin-like receptors (KIR) are expressed by natural killer (NK) cells and recognize HLA class I molecules as ligands. KIR3DL3 is a conserved but polymorphic inhibitory KIR recognizing a B7 family ligand, HHLA2, and is ... ...

    Abstract Most human killer cell immunoglobulin-like receptors (KIR) are expressed by natural killer (NK) cells and recognize HLA class I molecules as ligands. KIR3DL3 is a conserved but polymorphic inhibitory KIR recognizing a B7 family ligand, HHLA2, and is implicated for immune checkpoint targeting. The expression profile and biological function of KIR3DL3 have been somewhat elusive, so we searched extensively for KIR3DL3 transcripts, revealing highly enriched expression in γδ and CD8
    MeSH term(s) Humans ; CD8-Positive T-Lymphocytes ; Ligands ; Killer Cells, Natural ; Thymus Gland ; Receptors, Antigen, T-Cell, alpha-beta ; Immunoglobulins ; Receptors, KIR
    Chemical Substances Ligands ; Receptors, Antigen, T-Cell, alpha-beta ; HHLA2 protein, human ; Immunoglobulins ; KIR3DL3 protein, human ; Receptors, KIR
    Language English
    Publishing date 2023-06-30
    Publishing country United States
    Document type Journal Article
    ISSN 2470-9468
    ISSN (online) 2470-9468
    DOI 10.1126/sciimmunol.ade5343
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  5. Article ; Online: M-CSF- and L929-derived macrophages present distinct metabolic profiles with similar inflammatory outcomes.

    de Brito Monteiro, Lauar / Davanzo, Gustavo Gastão / de Aguiar, Cristhiane Fávero / Corrêa da Silva, Felipe / Andrade, Jessica Rodrigues de / Campos Codo, Ana / Silva Pereira, Jessica Aparecida da / Freitas, Leonardo Pimentel de / Moraes-Vieira, Pedro Manoel

    Immunobiology

    2020  Volume 225, Issue 3, Page(s) 151935

    Abstract: Macrophages are essential components of the immune system. Macrophages can be derived from the bone marrow of mice with either recombinant M-CSF or L929 supernatant. Recent literature considers recombinant M-CSF- and L929-derived macrophages as equals, ... ...

    Abstract Macrophages are essential components of the immune system. Macrophages can be derived from the bone marrow of mice with either recombinant M-CSF or L929 supernatant. Recent literature considers recombinant M-CSF- and L929-derived macrophages as equals, even though L929-derived macrophages are exposed to other substances secreted in the L929 supernatant, and not only M-CSF. Thus, we decided to perform a comparative analysis of both inflammatory and metabolic profiles of macrophages differentiated under the aforementioned conditions, which is relevant for standardization and interpretation of in vitro studies. We observed that, when treated with LPS, L929macs secrete lower levels of proinflammatory cytokines (TNF-α, IL-6, IL12) and present higher glycolysis and oxygen consumption when compared with M-CSFmacs. L929macs also have increased mitochondrial mass, with higher percentage of dysfunctional mitochondria. This sort of information can help direct further studies towards a more specific approach for macrophage generation.
    MeSH term(s) Animals ; Biomarkers ; Cell Line ; Cytokines/metabolism ; Energy Metabolism ; Inflammation Mediators/metabolism ; Macrophage Colony-Stimulating Factor/metabolism ; Macrophages/immunology ; Macrophages/metabolism ; Metabolome ; Metabolomics/methods ; Mice
    Chemical Substances Biomarkers ; Cytokines ; Inflammation Mediators ; Macrophage Colony-Stimulating Factor (81627-83-0)
    Language English
    Publishing date 2020-03-19
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 563292-4
    ISSN 1878-3279 ; 0171-2985
    ISSN (online) 1878-3279
    ISSN 0171-2985
    DOI 10.1016/j.imbio.2020.151935
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  6. Article ; Online: Inhibition of inflammasome activation by a clinical strain of Klebsiella pneumoniae impairs efferocytosis and leads to bacterial dissemination.

    Codo, Ana Campos / Saraiva, Amanda Correia / Dos Santos, Leonardo Lima / Visconde, Marina Francisco / Gales, Ana Cristina / Zamboni, Dario Simões / Medeiros, Alexandra Ivo

    Cell death & disease

    2018  Volume 9, Issue 12, Page(s) 1182

    Abstract: Klebsiella pneumoniae is a Gram-negative bacterium responsible for severe cases of nosocomial pneumonia. During the infectious process, both neutrophils and monocytes migrate to the site of infection, where they carry out their effector functions and can ...

    Abstract Klebsiella pneumoniae is a Gram-negative bacterium responsible for severe cases of nosocomial pneumonia. During the infectious process, both neutrophils and monocytes migrate to the site of infection, where they carry out their effector functions and can be affected by different patterns of cell death. Our data show that clinical strains of K. pneumoniae have dissimilar mechanisms for surviving within macrophages; these mechanisms include modulation of microbicidal mediators and cell death. The A28006 strain induced high IL-1β production and pyroptotic cell death in macrophages; by contrast, the A54970 strain induced high IL-10 production and low IL-1β production by macrophages. Pyroptotic cell death induced by the A28006 strain leads to a significant increase in bacterial sensitivity to hydrogen peroxide, and efferocytosis of the pyroptotic cells results in efficient bacterial clearance both in vitro and in vivo. In addition, the A54970 strain was able to inhibit inflammasome activation and pyroptotic cell death by inducing IL-10 production. Here, for the first time, we present a K. pneumoniae strain able to inhibit inflammasome activation, leading to bacterial survival and dissemination in the host. The understanding of possible escape mechanisms is essential in the search for alternative treatments against multidrug-resistant bacteria.
    MeSH term(s) Animals ; Bacteremia/genetics ; Bacteremia/immunology ; Bacteremia/microbiology ; Bacteremia/pathology ; Caspase 1/deficiency ; Caspase 1/genetics ; Caspase 1/immunology ; Caspases/deficiency ; Caspases/genetics ; Caspases/immunology ; Female ; Gene Expression ; Host-Pathogen Interactions/genetics ; Host-Pathogen Interactions/immunology ; Humans ; Inflammasomes/genetics ; Inflammasomes/immunology ; Interleukin-10/deficiency ; Interleukin-10/genetics ; Interleukin-10/immunology ; Klebsiella Infections/genetics ; Klebsiella Infections/immunology ; Klebsiella Infections/microbiology ; Klebsiella Infections/pathology ; Klebsiella pneumoniae/immunology ; Klebsiella pneumoniae/isolation & purification ; Klebsiella pneumoniae/pathogenicity ; Macrophages/immunology ; Macrophages/microbiology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Monocytes/immunology ; Monocytes/microbiology ; Neutrophils/immunology ; Neutrophils/microbiology ; Phagocytosis/genetics ; Pyroptosis/genetics ; Pyroptosis/immunology
    Chemical Substances IL10 protein, mouse ; Inflammasomes ; Interleukin-10 (130068-27-8) ; Casp11 protein, mouse (EC 3.4.22.-) ; Caspases (EC 3.4.22.-) ; Casp1 protein, mouse (EC 3.4.22.36) ; Caspase 1 (EC 3.4.22.36)
    Language English
    Publishing date 2018-12-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2541626-1
    ISSN 2041-4889 ; 2041-4889
    ISSN (online) 2041-4889
    ISSN 2041-4889
    DOI 10.1038/s41419-018-1214-5
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  7. Article ; Online: Impairment of motor but not anxiety-like behavior caused by the increase of dopamine during development is sustained in zebrafish larvae at later stages.

    de Souza Lima, Ana Carolina Monteiro / de Alvarenga, Kevin Augusto Farias / Codo, Beatriz Campos / Sacramento, Erika Kelmer / Rosa, Daniela Valadão Freitas / Souza, Renan Pedra / Romano-Silva, Marco Aurélio / Souza, Bruno Rezende

    International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

    2020  Volume 80, Issue 2, Page(s) 106–122

    Abstract: Many neuropsychiatric disorders are associated with both dopaminergic (DAergic) and developmental hypotheses. Since DAergic receptors are expressed in the developing brain, it is possible that alterations in dopamine (DA) signaling may impair brain ... ...

    Abstract Many neuropsychiatric disorders are associated with both dopaminergic (DAergic) and developmental hypotheses. Since DAergic receptors are expressed in the developing brain, it is possible that alterations in dopamine (DA) signaling may impair brain development and consequent behavior. In our previous study, using a zebrafish model, we showed that an increase of DA during the 3 to 5 days postfertilization (dpf) developmental window (an important window for GABAergic neuronal differentiation) affects the motor behavior of 5 dpf larvae. In this study, we set out to determine whether these behavioral alterations were sustained in larvae at older stages (7 and 14 dpf). To test this hypothesis, we chronically treated zebrafish larvae from 3 to 5 dpf with DA. After washing the drug, we recorded and analyzed the first 5 and 30 min of the motor behavior of 5, 7, and 14 dpf subjects. We analyzed mobile episodes, distance traveled, time mobile, distance traveled per mobile episode, time in movement per mobile episode, and distance traveled per time mobile. We showed, once again, that an increase of DA during the 3 to 5 dpf developmental window reduces the number of movement episodes initiated by 5 dpf larvae. We also detected a decrease of other motor behavior parameters in 5 dpf DA-treated larvae. We observed that these alterations are sustained in the 7 dpf larvae. However, we did not see these general locomotor alterations in the 14 dpf larvae. Moreover, we detected a decrease of distance traveled and an increase of time of locomotion per episode in the first 5 min of behavioral analyses in 14 dpf DA-treated larvae. To test if the alterations in the first 5 min were due to anxiety-like behavior, we used a light/dark preference paradigm. We recorded 5dpf, 7dpf, and 14dpf larvae for 5 min and analyzed time of freezing, preference for light or dark, number of entries to the dark, percentage of time in the light. We observed that 5dpf larvae treated with DA showed more freezing, less passages to the dark, and more time spent in the light as compared to their control counterparts. But 7dpf and 14dpf larvae did not show these alterations. Taken overall, therefore, our results suggest that DA does play a role in the development of zebrafish motor behavior, and, furthermore, that some behaviors are more sensitive than others to the effects of DAergic imbalances during development.
    MeSH term(s) Aging ; Animals ; Anxiety/chemically induced ; Anxiety/psychology ; Dopamine/pharmacology ; Larva/growth & development ; Light ; Locomotion/drug effects ; Motor Activity/drug effects ; Movement Disorders/psychology ; Zebrafish/growth & development
    Chemical Substances Dopamine (VTD58H1Z2X)
    Language English
    Publishing date 2020-02-12
    Publishing country United States
    Document type Journal Article
    ZDB-ID 605533-3
    ISSN 1873-474X ; 0736-5748
    ISSN (online) 1873-474X
    ISSN 0736-5748
    DOI 10.1002/jdn.10009
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  8. Article: Acid pH Increases SARS-CoV-2 Infection and the Risk of Death by COVID-19.

    Jimenez, Leandro / Campos Codo, Ana / Sampaio, Vanderson de Souza / Oliveira, Antonio E R / Ferreira, Lucas Kaoru Kobo / Davanzo, Gustavo Gastão / de Brito Monteiro, Lauar / Victor Virgilio-da-Silva, João / Borba, Mayla Gabriela Silva / Fabiano de Souza, Gabriela / Zini, Nathalia / de Andrade Gandolfi, Flora / Muraro, Stéfanie Primon / Luiz Proença-Modena, José / Val, Fernando Almeida / Cardoso Melo, Gisely / Monteiro, Wuelton Marcelo / Nogueira, Maurício Lacerda / Lacerda, Marcus Vinícius Guimarães /
    Moraes-Vieira, Pedro M / Nakaya, Helder I

    Frontiers in medicine

    2021  Volume 8, Page(s) 637885

    Abstract: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can infect a broad range of human tissues by using the host receptor angiotensin-converting enzyme 2 (ACE2). Individuals with comorbidities associated with severe COVID-19 display higher ... ...

    Abstract The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can infect a broad range of human tissues by using the host receptor angiotensin-converting enzyme 2 (ACE2). Individuals with comorbidities associated with severe COVID-19 display higher levels of
    Language English
    Publishing date 2021-08-20
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2021.637885
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  9. Article ; Online: Intestinal host defense outcome is dictated by PGE

    Dejani, Naiara Naiana / Orlando, Allan Botinhon / Niño, Victoria Eugenia / Penteado, Letícia de Aquino / Verdan, Felipe Fortino / Bazzano, Júlia Miranda Ribeiro / Codo, Ana Campos / Salina, Ana Carolina Guerta / Saraiva, Amanda Correia / Avelar, Matheus Rossi / Spolidorio, Luis Carlos / Serezani, C Henrique / Medeiros, Alexandra Ivo

    Proceedings of the National Academy of Sciences of the United States of America

    2018  Volume 115, Issue 36, Page(s) E8469–E8478

    Abstract: Inflammatory responses are terminated by the clearance of dead cells, a process termed efferocytosis. A consequence of efferocytosis is the synthesis of the antiinflammatory mediators TGF-β, ... ...

    Abstract Inflammatory responses are terminated by the clearance of dead cells, a process termed efferocytosis. A consequence of efferocytosis is the synthesis of the antiinflammatory mediators TGF-β, PGE
    MeSH term(s) Animals ; Citrobacter rodentium/immunology ; Colitis/immunology ; Colitis/microbiology ; Colitis/pathology ; Dendritic Cells/immunology ; Dendritic Cells/microbiology ; Dendritic Cells/pathology ; Dinoprostone/immunology ; Enterobacteriaceae Infections/immunology ; Enterobacteriaceae Infections/microbiology ; Enterobacteriaceae Infections/pathology ; Female ; Intestines/immunology ; Intestines/microbiology ; Macrophages/immunology ; Macrophages/microbiology ; Macrophages/pathology ; Mice ; Receptors, Prostaglandin E, EP4 Subtype/immunology
    Chemical Substances Ptger4 protein, mouse ; Receptors, Prostaglandin E, EP4 Subtype ; Dinoprostone (K7Q1JQR04M)
    Language English
    Publishing date 2018-08-20
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.1722016115
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  10. Article ; Online: Ghrelin effects on mitochondrial fitness modulates macrophage function.

    Corrêa da Silva, Felipe / Aguiar, Cristhiane / Pereira, Jéssica A S / de Brito Monteiro, Lauar / Davanzo, Gustavo Gastão / Codo, Ana Campos / Pimentel de Freitas, Leonardo / Berti, Aline Siqueira / Lopes Ferrucci, Danilo / Castelucci, Bianca Gazieri / Consonni, Sílvio Roberto / Carvalho, Hernandes F / Moraes-Vieira, Pedro M M

    Free radical biology & medicine

    2019  Volume 145, Page(s) 61–66

    Abstract: Over the past years, systemic derived cues that regulate cellular metabolism have been implicated in the regulation of immune responses. Ghrelin is an orexigenic hormone produced by enteroendocrine cells in the gastric mucosa with known immunoregulatory ... ...

    Abstract Over the past years, systemic derived cues that regulate cellular metabolism have been implicated in the regulation of immune responses. Ghrelin is an orexigenic hormone produced by enteroendocrine cells in the gastric mucosa with known immunoregulatory roles. The mechanism behind the function of ghrelin in immune cells, such as macrophages, is still poorly understood. Here, we explored the hypothesis that ghrelin leads to alterations in macrophage metabolism thus modulating macrophage function. We demonstrated that ghrelin exerts an immunomodulatory effect over LPS-activated peritoneal macrophages, as evidenced by inhibition of TNF-α and IL-1β secretion and increased IL-12 production. Concomitantly, ghrelin increased mitochondrial membrane potential and increased respiratory rate. In agreement, ghrelin prevented LPS-induced ultrastructural damage in the mitochondria. Ghrelin also blunted LPS-induced glycolysis. In LPS-activated macrophages, glucose deprivation did not affect ghrelin-induced IL-12 secretion, whereas the inhibition of pyruvate transport and mitochondria-derived ATP abolished ghrelin-induced IL-12 secretion, indicating a dependence on mitochondrial function. Ghrelin pre-treatment of metabolic activated macrophages inhibited the secretion of TNF-α and enhanced IL-12 levels. Moreover, ghrelin effects on IL-12, and not on TNF-α, are dependent on mitochondria elongation, since ghrelin did not enhance IL-12 secretion in metabolic activated mitofusin-2 deficient macrophages. Thus, ghrelin affects macrophage mitochondrial metabolism and the subsequent macrophage function.
    MeSH term(s) Adenosine Triphosphate/genetics ; Animals ; Gene Expression Regulation, Neoplastic/drug effects ; Ghrelin/chemistry ; Ghrelin/pharmacology ; Glycolysis/drug effects ; Inflammation/chemically induced ; Inflammation/drug therapy ; Inflammation/genetics ; Inflammation/pathology ; Interleukin-12/genetics ; Interleukin-1beta/genetics ; Lipopolysaccharides/toxicity ; Macrophages, Peritoneal/drug effects ; Macrophages, Peritoneal/pathology ; Membrane Potential, Mitochondrial/drug effects ; Mice ; Mitochondria/drug effects ; Mitochondria/ultrastructure ; Nitric Oxide/genetics ; Signal Transduction/genetics ; Tumor Necrosis Factor-alpha/genetics
    Chemical Substances Ghrelin ; IL1B protein, mouse ; Interleukin-1beta ; Lipopolysaccharides ; Tumor Necrosis Factor-alpha ; Interleukin-12 (187348-17-0) ; Nitric Oxide (31C4KY9ESH) ; Adenosine Triphosphate (8L70Q75FXE)
    Language English
    Publishing date 2019-09-14
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 807032-5
    ISSN 1873-4596 ; 0891-5849
    ISSN (online) 1873-4596
    ISSN 0891-5849
    DOI 10.1016/j.freeradbiomed.2019.09.012
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