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  1. Article ; Online: LTβR overexpression promotes plasma cell accumulation.

    Kotov, Jessica A / Xu, Ying / Carey, Nicholas D / Cyster, Jason G

    PloS one

    2022  Volume 17, Issue 8, Page(s) e0270907

    Abstract: Multiple myeloma (MM), a malignancy of plasma cells (PCs), has diverse genetic underpinnings and in rare cases these include amplification of the lymphotoxin b receptor (Ltbr) locus. LTβR has well defined roles in supporting lymphoid tissue development ... ...

    Abstract Multiple myeloma (MM), a malignancy of plasma cells (PCs), has diverse genetic underpinnings and in rare cases these include amplification of the lymphotoxin b receptor (Ltbr) locus. LTβR has well defined roles in supporting lymphoid tissue development and function through actions in stromal and myeloid cells, but whether it is functional in PCs is unknown. Here we showed that Ltbr mRNA was upregulated in mouse PCs compared to follicular B cells, but deficiency in the receptor did not cause a reduction in PC responses to a T-dependent or T-independent immunogen. However, LTβR overexpression (OE) enhanced PC formation in vitro after LPS or anti-CD40 stimulation. In vivo, LTβR OE led to increased antigen-specific splenic and bone marrow (BM) plasma cells responses. LTβR OE PCs had increased expression of Nfkb2 and of the NF-kB target genes Bcl2 and Mcl1, factors involved in the formation of long-lived BM PCs. Our findings suggest a pathway by which Ltbr gene amplifications may contribute to MM development through increased NF-kB activity and induction of an anti-apoptotic transcriptional program.
    MeSH term(s) Animals ; B-Lymphocytes/metabolism ; Lymphotoxin beta Receptor/genetics ; Lymphotoxin beta Receptor/metabolism ; Mice ; NF-kappa B/genetics ; NF-kappa B/metabolism ; Plasma Cells/metabolism ; Spleen/metabolism
    Chemical Substances Ltbr protein, mouse ; Lymphotoxin beta Receptor ; NF-kappa B
    Language English
    Publishing date 2022-08-04
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0270907
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Cutting Edge: T Cell-Dependent Plasmablasts Form in the Absence of Single Differentiated CD4

    Kotov, Jessica A / Jenkins, Marc K

    Journal of immunology (Baltimore, Md. : 1950)

    2018  Volume 202, Issue 2, Page(s) 401–405

    Abstract: The T follicular helper (Tfh) cell subset of ... ...

    Abstract The T follicular helper (Tfh) cell subset of CD4
    MeSH term(s) Animals ; Antibody Affinity ; Antibody-Producing Cells/immunology ; Antigen Presentation ; CD4-Positive T-Lymphocytes/immunology ; CD40 Antigens/metabolism ; CD40 Ligand/metabolism ; Cell Communication ; Cell Differentiation ; Cells, Cultured ; Female ; Germinal Center/immunology ; Immunoglobulin Class Switching ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Plasma Cells/immunology ; Signal Transduction ; T-Lymphocyte Subsets/immunology
    Chemical Substances CD40 Antigens ; CD40 Ligand (147205-72-9)
    Language English
    Publishing date 2018-12-14
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 3056-9
    ISSN 1550-6606 ; 0022-1767 ; 1048-3233 ; 1047-7381
    ISSN (online) 1550-6606
    ISSN 0022-1767 ; 1048-3233 ; 1047-7381
    DOI 10.4049/jimmunol.1801349
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Many Th Cell Subsets Have Fas Ligand-Dependent Cytotoxic Potential.

    Kotov, Dmitri I / Kotov, Jessica A / Goldberg, Michael F / Jenkins, Marc K

    Journal of immunology (Baltimore, Md. : 1950)

    2018  Volume 200, Issue 6, Page(s) 2004–2012

    Abstract: ... ...

    Abstract CD4
    MeSH term(s) Animals ; CD4-Positive T-Lymphocytes/immunology ; Fas Ligand Protein/immunology ; Lymphocyte Activation/immunology ; Mice ; Mice, Inbred C57BL ; T-Lymphocytes, Cytotoxic/immunology ; Th1 Cells/immunology ; Th17 Cells/immunology ; fas Receptor/immunology
    Chemical Substances Fas Ligand Protein ; Fas protein, mouse ; fas Receptor
    Language English
    Publishing date 2018-02-07
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 3056-9
    ISSN 1550-6606 ; 0022-1767 ; 1048-3233 ; 1047-7381
    ISSN (online) 1550-6606
    ISSN 0022-1767 ; 1048-3233 ; 1047-7381
    DOI 10.4049/jimmunol.1700420
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: BCL6 corepressor contributes to Th17 cell formation by inhibiting Th17 fate suppressors.

    Kotov, Jessica A / Kotov, Dmitri I / Linehan, Jonathan L / Bardwell, Vivian J / Gearhart, Micah D / Jenkins, Marc K

    The Journal of experimental medicine

    2019  Volume 216, Issue 6, Page(s) 1450–1464

    Abstract: ... ...

    Abstract CD4
    MeSH term(s) Animals ; CRISPR-Cas Systems/genetics ; Cell Differentiation ; Cell Lineage ; Co-Repressor Proteins/metabolism ; Cytokines/metabolism ; F-Box Proteins/metabolism ; Female ; Gene Expression Regulation ; Jumonji Domain-Containing Histone Demethylases/metabolism ; Lymphocyte Subsets/metabolism ; Male ; Mice, Inbred C57BL ; Proto-Oncogene Proteins c-bcl-6/metabolism ; Receptors, Chemokine/metabolism ; Repressor Proteins/metabolism ; Signal Transduction ; Streptococcus pyogenes/physiology ; Th17 Cells/cytology ; Th17 Cells/metabolism
    Chemical Substances Bcl6 protein, mouse ; Bcor protein, mouse ; Co-Repressor Proteins ; Cytokines ; F-Box Proteins ; Proto-Oncogene Proteins c-bcl-6 ; Receptors, Chemokine ; Repressor Proteins ; Jumonji Domain-Containing Histone Demethylases (EC 1.14.11.-) ; Kdm2b protein, mouse (EC 1.14.11.27)
    Language English
    Publishing date 2019-05-03
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 218343-2
    ISSN 1540-9538 ; 0022-1007
    ISSN (online) 1540-9538
    ISSN 0022-1007
    DOI 10.1084/jem.20182376
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Polymicrobial Sepsis Chronic Immunoparalysis Is Defined by Diminished Ag-Specific T Cell-Dependent B Cell Responses.

    Sjaastad, Frances V / Condotta, Stephanie A / Kotov, Jessica A / Pape, Kathryn A / Dail, Cody / Danahy, Derek B / Kucaba, Tamara A / Tygrett, Lorraine T / Murphy, Katherine A / Cabrera-Perez, Javier / Waldschmidt, Thomas J / Badovinac, Vladimir P / Griffith, Thomas S

    Frontiers in immunology

    2018  Volume 9, Page(s) 2532

    Abstract: Immunosuppression is one hallmark of sepsis, decreasing the host response to the primary septic pathogens and/or secondary nosocomial infections. CD4 T cells and B cells are among the array of immune cells that experience reductions in number and ... ...

    Abstract Immunosuppression is one hallmark of sepsis, decreasing the host response to the primary septic pathogens and/or secondary nosocomial infections. CD4 T cells and B cells are among the array of immune cells that experience reductions in number and function during sepsis. "Help" from follicular helper (Tfh) CD4 T cells to B cells is needed for productive and protective humoral immunity, but there is a paucity of data defining the effect of sepsis on a primary CD4 T cell-dependent B cell response. Using the cecal ligation and puncture (CLP) mouse model of sepsis induction, we observed reduced antibody production in mice challenged with influenza A virus or TNP-KLH in alum early (2 days) and late (30 days) after CLP surgery compared to mice subjected to sham surgery. To better understand how these CD4 T cell-dependent B cell responses were altered by a septic event, we immunized mice with a Complete Freund's Adjuvant emulsion containing the MHC II-restricted peptide 2W1S
    MeSH term(s) Animals ; Antibodies/metabolism ; Antigens, Bacterial/immunology ; B-Lymphocytes/immunology ; Cecum/surgery ; Cell Differentiation ; Cells, Cultured ; Chronic Disease ; Coinfection/immunology ; Cytokines/metabolism ; Disease Models, Animal ; Female ; Immune Tolerance ; Influenza A virus/physiology ; Lymphocyte Activation ; Mice ; Mice, Inbred C57BL ; Orthomyxoviridae Infections/immunology ; Sepsis/immunology ; T-Lymphocytes, Helper-Inducer/immunology
    Chemical Substances Antibodies ; Antigens, Bacterial ; Cytokines
    Language English
    Publishing date 2018-10-31
    Publishing country Switzerland
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2018.02532
    Database MEDical Literature Analysis and Retrieval System OnLINE

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