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  1. Article ; Online: Target lysis by cholesterol extraction is a rate limiting step in the resolution of phagolysosomes.

    Barreda, Dante / Grinstein, Sergio / Freeman, Spencer A

    European journal of cell biology

    2023  Volume 103, Issue 1, Page(s) 151382

    Abstract: The ongoing phagocytic activity of macrophages necessitates an extraordinary capacity to digest and resolve incoming material. While the initial steps leading to the formation of a terminal phagolysosome are well studied, much less is known about the ... ...

    Abstract The ongoing phagocytic activity of macrophages necessitates an extraordinary capacity to digest and resolve incoming material. While the initial steps leading to the formation of a terminal phagolysosome are well studied, much less is known about the later stages of this process, namely the degradation and resolution of the phagolysosomal contents. We report that the degradation of targets such as splenocytes and erythrocytes by phagolysosomes occurs in a stepwise fashion, requiring lysis of their plasmalemmal bilayer as an essential initial step. This is achieved by the direct extraction of cholesterol facilitated by Niemann-Pick protein type C2 (NPC2), which in turn hands off cholesterol to NPC1 for export from the phagolysosome. The removal of cholesterol ulimately destabilizes and permeabilizes the membrane of the phagocytic target, allowing access of hydrolases to its internal compartments. In contrast, we found that saposins, which activate the hydrolysis of sphingolipids, are required for lysosomal tubulation, yet are dispensable for the resolution of targets by macrophages. The extraction of cholesterol by NPC2 is therefore envisaged as rate-limiting in the clearance of membrane-bound targets such as apoptotic cells. Selective cholesterol removal appears to be a primary mechanism that enables professional phagocytes to distinguish the target membrane from the phagolysosomal membrane and may be conserved in the resolution of autolysosomes.
    MeSH term(s) Glycoproteins/metabolism ; Membrane Glycoproteins/metabolism ; Carrier Proteins/metabolism ; Intracellular Signaling Peptides and Proteins/metabolism ; Vesicular Transport Proteins/metabolism ; Cholesterol/metabolism ; Phagosomes/metabolism ; Lysosomes/metabolism
    Chemical Substances Glycoproteins ; Membrane Glycoproteins ; Carrier Proteins ; Intracellular Signaling Peptides and Proteins ; Vesicular Transport Proteins ; Cholesterol (97C5T2UQ7J)
    Language English
    Publishing date 2023-12-27
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 391967-5
    ISSN 1618-1298 ; 0070-2463 ; 0171-9335
    ISSN (online) 1618-1298
    ISSN 0070-2463 ; 0171-9335
    DOI 10.1016/j.ejcb.2023.151382
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Two-pore channels regulate endomembrane tension to enable remodeling and resolution of phagolysosomes.

    Chadwick, Sarah R / Barreda, Dante / Wu, Jing Ze / Ye, Gang / Yusuf, Bushra / Ren, Dejian / Freeman, Spencer A

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

    2024  Volume 121, Issue 8, Page(s) e2309465121

    Abstract: Phagocytes promptly resolve ingested targets to replenish lysosomes and maintain their responsiveness. The resolution process requires that degradative hydrolases, solute transporters, and proteins involved in lipid traffic are delivered and made active ... ...

    Abstract Phagocytes promptly resolve ingested targets to replenish lysosomes and maintain their responsiveness. The resolution process requires that degradative hydrolases, solute transporters, and proteins involved in lipid traffic are delivered and made active in phagolysosomes. It also involves extensive membrane remodeling. We report that cation channels that localize to phagolysosomes were essential for resolution. Specifically, the conductance of Na
    MeSH term(s) Mice ; Animals ; Two-Pore Channels ; Phagosomes/metabolism ; Lysosomes/metabolism ; Hydrolases/metabolism ; Cholesterol/metabolism
    Chemical Substances Two-Pore Channels ; Hydrolases (EC 3.-) ; Cholesterol (97C5T2UQ7J)
    Language English
    Publishing date 2024-02-14
    Publishing country United States
    Document type Journal Article
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.2309465121
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: SARS-CoV-2 Spike Protein and Its Receptor Binding Domain Promote a Proinflammatory Activation Profile on Human Dendritic Cells.

    Barreda, Dante / Santiago, César / Rodríguez, Juan R / Rodríguez, José F / Casasnovas, José M / Mérida, Isabel / Ávila-Flores, Antonia

    Cells

    2021  Volume 10, Issue 12

    Abstract: Dendritic cells (DCs) are the most potent antigen-presenting cells, and their function is essential to configure adaptative immunity and avoid excessive inflammation. DCs are predicted to play a crucial role in the clinical evolution of the infection by ... ...

    Abstract Dendritic cells (DCs) are the most potent antigen-presenting cells, and their function is essential to configure adaptative immunity and avoid excessive inflammation. DCs are predicted to play a crucial role in the clinical evolution of the infection by the severe acute respiratory syndrome (SARS) coronavirus (CoV)-2. DCs interaction with the SARS-CoV-2 Spike protein, which mediates cell receptor binding and subsequent fusion of the viral particle with host cell, is a key step to induce effective immunity against this virus and in the S protein-based vaccination protocols. Here we evaluated human DCs in response to SARS-CoV-2 S protein, or to a fragment encompassing the receptor binding domain (RBD) challenge. Both proteins increased the expression of maturation markers, including MHC molecules and costimulatory receptors. DCs interaction with the SARS-CoV-2 S protein promotes activation of key signaling molecules involved in inflammation, including MAPK, AKT, STAT1, and NFκB, which correlates with the expression and secretion of distinctive proinflammatory cytokines. Differences in the expression of ACE2 along the differentiation of human monocytes to mature DCs and inter-donor were found. Our results show that SARS-CoV-2 S protein promotes inflammatory response and provides molecular links between individual variations and the degree of response against this virus.
    MeSH term(s) Angiotensin-Converting Enzyme 2/metabolism ; Cell Adhesion Molecules/metabolism ; Cell Differentiation ; Cytokines/biosynthesis ; Dendritic Cells/pathology ; Dendritic Cells/virology ; Extracellular Signal-Regulated MAP Kinases/metabolism ; Humans ; Inflammation/pathology ; Lectins, C-Type/metabolism ; Protein Domains ; Proto-Oncogene Proteins c-akt/metabolism ; Receptors, Cell Surface/metabolism ; Receptors, Virus/metabolism ; SARS-CoV-2/metabolism ; STAT Transcription Factors/metabolism ; Signal Transduction ; Spike Glycoprotein, Coronavirus/chemistry ; Spike Glycoprotein, Coronavirus/metabolism ; Tissue Donors
    Chemical Substances Cell Adhesion Molecules ; Cytokines ; DC-specific ICAM-3 grabbing nonintegrin ; Lectins, C-Type ; Receptors, Cell Surface ; Receptors, Virus ; STAT Transcription Factors ; Spike Glycoprotein, Coronavirus ; spike protein, SARS-CoV-2 ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1) ; Extracellular Signal-Regulated MAP Kinases (EC 2.7.11.24) ; ACE2 protein, human (EC 3.4.17.23) ; Angiotensin-Converting Enzyme 2 (EC 3.4.17.23)
    Language English
    Publishing date 2021-11-23
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2661518-6
    ISSN 2073-4409 ; 2073-4409
    ISSN (online) 2073-4409
    ISSN 2073-4409
    DOI 10.3390/cells10123279
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The Scribble Complex PDZ Proteins in Immune Cell Polarities.

    Barreda, Dante / Gutiérrez-González, Luis H / Martínez-Cordero, Erasmo / Cabello-Gutiérrez, Carlos / Chacón-Salinas, Rommel / Santos-Mendoza, Teresa

    Journal of immunology research

    2020  Volume 2020, Page(s) 5649790

    Abstract: hScrib and hDlg belong to the PDZ family of proteins. Since the identification of these highly phylogenetically conserved scaffolds, an increasing amount of experiments has elucidated the roles of hScrib and hDlg in a variety of cell functions. ... ...

    Abstract hScrib and hDlg belong to the PDZ family of proteins. Since the identification of these highly phylogenetically conserved scaffolds, an increasing amount of experiments has elucidated the roles of hScrib and hDlg in a variety of cell functions. Remarkably, their participation during the establishment of polarity in epithelial cells is well documented. Although the role of both proteins in the immune system is scantly known, it has become a growing field of investigation. Here, we summarize the interactions and functions of hScrib and hDlg1, which participate in diverse functions involving cell polarization in immune cells, and discuss their relevance in the immune cell biology. The fundamental role of hScrib and hDlg1 during the establishment of the immunological synapse, hence T cell activation, and the recently described role of hScrib in reactive oxygen species production in macrophages and of hDlg1 in cytokine production by dendritic cells highlight the importance of both proteins in immune cell biology. The expression of these proteins in other leukocytes can be anticipated and needs to be confirmed. Due to their multiple interaction domains, there is a wide range of possible interactions of hScrib and hDlg1 that remains to be explored in the immune system.
    MeSH term(s) Cell Polarity/immunology ; Cytokines/metabolism ; Dendritic Cells/immunology ; Dendritic Cells/metabolism ; Discs Large Homolog 1 Protein/metabolism ; Humans ; Immunity, Cellular ; Immunological Synapses/immunology ; Immunological Synapses/metabolism ; Lymphocyte Activation/immunology ; Macrophages/immunology ; Macrophages/metabolism ; Membrane Proteins/metabolism ; Reactive Oxygen Species ; T-Lymphocytes/immunology ; T-Lymphocytes/metabolism ; Tumor Suppressor Proteins/metabolism
    Chemical Substances Cytokines ; DLG1 protein, human ; Discs Large Homolog 1 Protein ; Membrane Proteins ; Reactive Oxygen Species ; SCRIB protein, human ; Tumor Suppressor Proteins
    Language English
    Publishing date 2020-04-30
    Publishing country Egypt
    Document type Journal Article ; Review
    ZDB-ID 2817541-4
    ISSN 2314-7156 ; 2314-8861
    ISSN (online) 2314-7156
    ISSN 2314-8861
    DOI 10.1155/2020/5649790
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Scrib and Dlg1 polarity proteins regulate Ag presentation in human dendritic cells.

    Barreda, Dante / Ramón-Luing, Lucero A / Duran-Luis, Olivia / Bobadilla, Karen / Chacón-Salinas, Rommel / Santos-Mendoza, Teresa

    Journal of leukocyte biology

    2020  Volume 108, Issue 3, Page(s) 883–893

    Abstract: We recently reported, for the first time, the expression and regulation of the PDZ polarity proteins Scrib and Dlg1 in human APCs, and also described the viral targeting of these proteins by NS1 of influenza A virus in human dendritic cells (DCs). Scrib ... ...

    Abstract We recently reported, for the first time, the expression and regulation of the PDZ polarity proteins Scrib and Dlg1 in human APCs, and also described the viral targeting of these proteins by NS1 of influenza A virus in human dendritic cells (DCs). Scrib plays an important role in reactive oxygen species (ROS) production in Mϕs and uropod formation and migration in T cells, while Dlg1 is important for T cell downstream activation after Ag recognition. Nevertheless, the functions of these proteins in human DCs remain unknown. Here, we knocked-down the expression of both Scrib and Dlg1 in human DCs and then evaluated the expression of co-stimulatory molecules and cytokine production during maturation. We demonstrated that Scrib is necessary for adequate CD86 expression, while Dlg1 is important for CD83 up-regulation and IL-6 production upon maturation, suggesting that Scrib and Dlg1 participate in separate pathways in DCs. Additionally, both proteins are required for adequate IL-12 production after maturation. Furthermore, we showed that the inefficient maturation of DCs induced by Scrib or Dlg1 depletion leads to impaired T cell activation. Our results revealed the previously unknown contribution of Scrib and Dlg1 in human DCs pivotal functions, which may be able to impact innate and adaptive immune response.
    MeSH term(s) Adaptive Immunity ; Antigen Presentation ; Antigens, CD/biosynthesis ; Antigens, CD/genetics ; B7-2 Antigen/biosynthesis ; B7-2 Antigen/genetics ; Cells, Cultured ; Cytokines/biosynthesis ; Cytokines/genetics ; Dendritic Cells/immunology ; Discs Large Homolog 1 Protein/antagonists & inhibitors ; Discs Large Homolog 1 Protein/genetics ; Discs Large Homolog 1 Protein/physiology ; Gene Knockdown Techniques ; Humans ; Immunity, Innate ; Immunoglobulins/biosynthesis ; Immunoglobulins/genetics ; Interleukin-12/metabolism ; Interleukin-6/biosynthesis ; Interleukin-6/genetics ; Membrane Glycoproteins/biosynthesis ; Membrane Glycoproteins/genetics ; Membrane Proteins/antagonists & inhibitors ; Membrane Proteins/genetics ; Membrane Proteins/physiology ; Post-Synaptic Density/physiology ; RNA Interference ; RNA, Small Interfering/genetics ; RNA, Small Interfering/pharmacology ; Tumor Suppressor Proteins/antagonists & inhibitors ; Tumor Suppressor Proteins/genetics ; Tumor Suppressor Proteins/physiology ; Up-Regulation ; CD83 Antigen
    Chemical Substances Antigens, CD ; B7-2 Antigen ; CD86 protein, human ; Cytokines ; DLG1 protein, human ; Discs Large Homolog 1 Protein ; IL6 protein, human ; Immunoglobulins ; Interleukin-6 ; Membrane Glycoproteins ; Membrane Proteins ; RNA, Small Interfering ; SCRIB protein, human ; Tumor Suppressor Proteins ; Interleukin-12 (187348-17-0)
    Language English
    Publishing date 2020-04-15
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 605722-6
    ISSN 1938-3673 ; 0741-5400
    ISSN (online) 1938-3673
    ISSN 0741-5400
    DOI 10.1002/JLB.4MA0320-544RR
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Extracellular vesicles from Mycobacterium tuberculosis-infected neutrophils induce maturation of monocyte-derived dendritic cells and activation of antigen-specific Th1 cells.

    Vázquez-Flores, Luis / Castañeda-Casimiro, Jessica / Vallejo-Castillo, Luis / Álvarez-Jiménez, Violeta D / Peregrino, Eliud S / García-Martínez, Mariano / Barreda, Dante / Rosales-García, Víctor Hugo / Segovia-García, C David / Santos-Mendoza, Teresa / Wong-Baeza, Carlos / Serafín-López, Jeanet / Chacón-Salinas, Rommel / Estrada-Parra, Sergio / Estrada-García, Iris / Wong-Baeza, Isabel

    Journal of leukocyte biology

    2023  Volume 113, Issue 6, Page(s) 588–603

    Abstract: Tuberculosis remains one of the leading public health problems in the world. The mechanisms that lead to the activation of the immune response against Mycobacterium tuberculosis have been extensively studied, with a focus on the role of cytokines as the ... ...

    Abstract Tuberculosis remains one of the leading public health problems in the world. The mechanisms that lead to the activation of the immune response against Mycobacterium tuberculosis have been extensively studied, with a focus on the role of cytokines as the main signals for immune cell communication. However, less is known about the role of other signals, such as extracellular vesicles, in the communication between immune cells, particularly during the activation of the adaptive immune response. In this study, we determined that extracellular vesicles released by human neutrophils infected with M. tuberculosis contained several host proteins that are ectosome markers. In addition, we demonstrated that extracellular vesicles released by human neutrophils infected with M. tuberculosis released after only 30 min of infection carried mycobacterial antigens and pathogen-associated molecular patterns, and we identified 15 mycobacterial proteins that were consistently found in high concentrations in extracellular vesicles released by human neutrophils infected with M. tuberculosis; these proteins contain epitopes for CD4 T-cell activation. We found that extracellular vesicles released by human neutrophils infected with M. tuberculosis increased the expression of the costimulatory molecule CD80 and of the coinhibitory molecule PD-L1 on immature monocyte-derived dendritic cells. We also found that immature and mature dendritic cells treated with extracellular vesicles released by human neutrophils infected with M. tuberculosis were able to induce IFN-γ production by autologous M. tuberculosis antigen-specific CD4 T cells, indicating that these extracellular vesicles acted as antigen carriers and transferred mycobacterial proteins to the antigen-presenting cells. Our results provide evidence that extracellular vesicles released by human neutrophils infected with M. tuberculosis participate in the activation of the adaptive immune response against M. tuberculosis.
    MeSH term(s) Humans ; Mycobacterium tuberculosis ; Th1 Cells ; Neutrophils ; Monocytes ; Tuberculosis ; Extracellular Vesicles ; Dendritic Cells
    Language English
    Publishing date 2023-05-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 605722-6
    ISSN 1938-3673 ; 0741-5400
    ISSN (online) 1938-3673
    ISSN 0741-5400
    DOI 10.1093/jleuko/qiad037
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Identification of conserved peptides containing B-cell epitopes of Babesia bovis AMA-1 and their potential as diagnostics candidates.

    Barreda, Dante / Hidalgo-Ruiz, Mario / Hernandez-Ortiz, Ruben / Ramos, Juan Alberto / Galindo-Velasco, Edelmira / Mosqueda, Juan

    Transboundary and emerging diseases

    2019  Volume 67 Suppl 2, Page(s) 60–68

    Abstract: The apical membrane antigen 1 (AMA-1) is a protein of the micronemes that is present in all organisms of the phylum Apicomplexa; it has been shown that AMA-1 plays an essential role for parasite invasion to target cells. It has been reported that AMA-1 ... ...

    Abstract The apical membrane antigen 1 (AMA-1) is a protein of the micronemes that is present in all organisms of the phylum Apicomplexa; it has been shown that AMA-1 plays an essential role for parasite invasion to target cells. It has been reported that AMA-1 is conserved among different isolates of Babesia; however, it is unknown whether the protein contains conserved B-cell epitopes and whether these epitopes are recognized by antibodies from cattle in endemic areas. In this research, using an in silico analysis, four peptides were designed containing exposed and conserved linear B-cell epitopes from the extracellular region of Babesia bovis AMA-1. The selected peptides were chemically synthesized, and then each peptide was emulsified and used to immunize two bovines per peptide. The antibodies produced against these peptides were able to recognize intra-erythrocytic parasites in an IFAT, except peptide 4, which was insoluble. The synthetic peptides were covalently fixed to the wells of an ELISA plate and incubated with sera from B. bovis naturally infected cattle. Peptides P2AMA and P3AMA were recognized by the sera of naturally infected cattle from different regions of Mexico. Statistical analysis showed that the ELISA test for peptides P2AMA and P3AMA had a concordance of 91.2% and 61.1% compared to the IFAT, a sensitivity of 94.56% and 71.74%, and a specificity of 76.19% and 14.2%, respectively. The presence of antibodies in bovine sera from endemic areas that bind to the identified peptides indicates that AMA-1 from B. bovis has conserved B-cell epitopes involved in the immune response under natural conditions. However, to propose their use as vaccine or diagnostics candidates, a further characterization of the humoral immune response elicited in cattle by these peptides is needed.
    MeSH term(s) Animals ; Antibodies, Protozoan/blood ; Antigens, Protozoan/immunology ; Babesia bovis/immunology ; Babesiosis/immunology ; Cattle ; Cattle Diseases/immunology ; Computer Simulation ; Enzyme-Linked Immunosorbent Assay/veterinary ; Epitopes, B-Lymphocyte/immunology ; Fluorescent Antibody Technique, Indirect/veterinary ; Immunity, Humoral ; Immunization/veterinary ; Membrane Proteins/immunology ; Mexico ; Peptides/immunology ; Protozoan Proteins/immunology ; Vaccination/veterinary
    Chemical Substances Antibodies, Protozoan ; Antigens, Protozoan ; Epitopes, B-Lymphocyte ; Membrane Proteins ; Peptides ; Protozoan Proteins
    Language English
    Publishing date 2019-06-24
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 2414822-2
    ISSN 1865-1682 ; 1865-1674
    ISSN (online) 1865-1682
    ISSN 1865-1674
    DOI 10.1111/tbed.13213
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: PDZ proteins are expressed and regulated in antigen-presenting cells and are targets of influenza A virus.

    Barreda, Dante / Sánchez-Galindo, Marisa / López-Flores, Jessica / Nava-Castro, Karen E / Bobadilla, Karen / Salgado-Aguayo, Alfonso / Santos-Mendoza, Teresa

    Journal of leukocyte biology

    2017  Volume 103, Issue 4, Page(s) 731–738

    Abstract: In this work, we identified the expression, regulation, and viral targeting of Scribble and Dlg1 in antigen-presenting cells. Scribble and Dlg1 belong to the family of PDZ (postsynaptic density (PSD95), disc large (Dlg), and zonula occludens (ZO-1)) ... ...

    Abstract In this work, we identified the expression, regulation, and viral targeting of Scribble and Dlg1 in antigen-presenting cells. Scribble and Dlg1 belong to the family of PDZ (postsynaptic density (PSD95), disc large (Dlg), and zonula occludens (ZO-1)) proteins involved in cell polarity. The relevance of PDZ proteins in cellular functions is reinforced by the fact that many viruses interfere with host PDZ-dependent interactions affecting cellular mechanisms thus favoring viral replication. The functions of Scribble and Dlg have been widely studied in polarized cells such as epithelial and neuron cells. However, within the cells of the immune system, their functions have been described only in T and B lymphocytes. Here we demonstrated that Scribble and Dlg1 are differentially expressed during antigen-presenting cell differentiation and dendritic cell maturation. While both Scribble and Dlg1 seem to participate in distinct dendritic cell functions, both are targeted by the viral protein NS1 of influenza A in a PDZ-dependent manner in dendritic cells. Our findings suggest that these proteins might be involved in the mechanisms of innate immunity and/or antigen processing and presentation that can be hijacked by viral pathogens.
    MeSH term(s) Adaptor Proteins, Signal Transducing/genetics ; Adaptor Proteins, Signal Transducing/metabolism ; Antigen-Presenting Cells/immunology ; Antigen-Presenting Cells/metabolism ; Antigen-Presenting Cells/virology ; Dendritic Cells/immunology ; Dendritic Cells/metabolism ; Dendritic Cells/virology ; Host-Pathogen Interactions ; Humans ; Influenza A virus/pathogenicity ; Influenza, Human/immunology ; Influenza, Human/metabolism ; Influenza, Human/virology ; Macrophages/immunology ; Macrophages/metabolism ; Macrophages/virology ; Membrane Proteins/genetics ; Membrane Proteins/metabolism ; Monocytes/immunology ; Monocytes/metabolism ; Monocytes/virology ; PDZ Domains ; Tumor Suppressor Proteins/genetics ; Tumor Suppressor Proteins/metabolism ; Viral Nonstructural Proteins/genetics ; Viral Nonstructural Proteins/metabolism
    Chemical Substances Adaptor Proteins, Signal Transducing ; DLG1 protein, human ; INS1 protein, influenza virus ; Membrane Proteins ; SCRIB protein, human ; Tumor Suppressor Proteins ; Viral Nonstructural Proteins
    Language English
    Publishing date 2017-12-27
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 605722-6
    ISSN 1938-3673 ; 0741-5400
    ISSN (online) 1938-3673
    ISSN 0741-5400
    DOI 10.1002/JLB.4AB0517-184R
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Insuficiencia cardíaca aguda en época de COVID-19

    Ángel Gaspar Obregón Santos / Juan Adolfo Prohias / Aylen Pérez Barreda / Elena Esther Vila García

    Revista Cubana de Cardiología y Cirugía Cardiovascular, Vol 26, Iss 2, Pp e995-e

    2020  Volume 995

    Abstract: ... Este nuevo virus afecta a múltiples órganos y entre ellos el corazón provocando en algunos casos daño cardiaco ...

    Abstract A finales del 2019, fue reportado en Wuhan, Hubei, China un grupo de enfermos afectados de una neumonía que por sus características se parecían a la neumonía viral. Rápidamente fue identificado el germen infeccioso como un coronavirus denominado SARS CoV2 y la enfermedad como COVID 19. Este nuevo virus afecta a múltiples órganos y entre ellos el corazón provocando en algunos casos daño cardiaco agudo y en ocasiones la muerte. Varios colegios de cardiología a nivel mundial se han pronunciado en consenso médico para orientar los puntos de vistas diagnósticos y terapéuticos en esta nueva enfermedad. El objetivo de este trabajo es hacer una revisión lo más exhaustiva posible para conocer la fisiopatología de la insuficiencia cardíaca aguda y el shock cardiogénico como su expresión más severa y las alteraciones que a nivel de todos los órganos provoca, elemento fundamental para intentar prevenir o tratar una vez que está establecido. Método. Hicimos una amplia revisión de la literatura en bases de datos importante como Medline, Pubmed, Scielo, Cochrane, National Institute for Health and Care Excellence (NICE) y otras, Además, se revisaron ensayos clínicos controlados y randomizados, revisión sistemática de ensayos clínicos controlados, metaanálisis y estudio de cohorte de alta calidad, así como también estudios observacionales y revisión sistemática de estudios observacionales, desde enero 2010 hasta marzo 2020. Resultados: después de un análisis para incluir y excluir trabajos de investigación se encontraron un total de 270 artículos relevantes. La mayoría de los artículos excluidos no contenían información contundente en cuanto a los criterios de insuficiencia cardíaca aguda, shock cardiogénico y su fisiopatología. Conclusiones. El conocimiento de las alteraciones que se producen en la insuficiencia cardiaca aguda y en el shock cardiogénico como su expresión más severa, permite conocer la repercusión que tiene en los diferentes sistemas de nuestro organismo, acción fundamental para intentar prevenir o tratar a tiempo este síndrome, y con ello disminuir su alta mortalidad.
    Keywords insuficiencia cardiaca ; shock cardiogénico ; daño de órgano ; Internal medicine ; RC31-1245 ; Diseases of the circulatory (Cardiovascular) system ; RC666-701 ; covid19
    Language Spanish
    Publishing date 2020-05-01T00:00:00Z
    Publisher ECIMED
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Insuficiencia cardíaca aguda en época de COVID-19

    Obregón Santos, Angel G. / Adolfo Prohias, Juan / Pérez Barreda, Aylen / Vila García, Elena Esther

    Revista Cubana de Cardiología y Cirugía Cardiovascular, ISSN 1561-2937, Vol. 26, Nº. 2, 2020 (Ejemplar dedicado a: Abr-Jun; e913)

    2020  

    Abstract: ... Este nuevo virus afecta a múltiples órganos y entre ellos el corazón provocando en algunos casos daño cardiaco ...

    Abstract A finales del 2019, fue reportado en Wuhan, Hubei, China un grupo de enfermos afectados de una neumonía que por sus características se parecían a la neumonía viral. Rápidamente fue identificado el germen infeccioso como un coronavirus denominado SARS CoV2 y la enfermedad como COVID 19. Este nuevo virus afecta a múltiples órganos y entre ellos el corazón provocando en algunos casos daño cardiaco agudo y en ocasiones la muerte. Varios colegios de cardiología a nivel mundial se han pronunciado en consenso médico para orientar los puntos de vistas diagnósticos y terapéuticos en esta nueva enfermedad. El objetivo de este trabajo es hacer una revisión lo más exhaustiva posible para conocer la fisiopatología de la insuficiencia cardíaca aguda y el shock cardiogénico como su expresión más severa y las alteraciones que a nivel de todos los órganos provoca, elemento fundamental para intentar prevenir o tratar una vez que está establecido. Método. Hicimos una amplia revisión de la literatura en bases de datos importante como Medline, Pubmed, Scielo, Cochrane, National Institute for Health and Care Excellence (NICE) y otras, Además, se revisaron ensayos clínicos controlados y randomizados, revisión sistemática de ensayos clínicos controlados, metaanálisis y estudio de cohorte de alta calidad, así como también estudios observacionales y revisión sistemática de estudios observacionales, desde enero 2010 hasta marzo 2020. Resultados: después de un análisis para incluir y excluir trabajos de investigación se encontraron un total de 270 artículos relevantes. La mayoría de los artículos excluidos no contenían información contundente en cuanto a los criterios de insuficiencia cardíaca aguda, shock cardiogénico y su fisiopatología. Conclusiones. El conocimiento de las alteraciones que se producen en la insuficiencia cardiaca aguda y en el shock cardiogénico como su expresión más severa, permite conocer la repercusión que tiene en los diferentes sistemas de nuestro organismo, acción fundamental para intentar prevenir o tratar a tiempo este síndrome, y con ello disminuir su alta mortalidad.
    Keywords cardiología ; insuficiencia cardiaca ; shock cardiogénico ; daño de órgano ; covid19
    Language Spanish
    Publishing country es
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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