echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Immunology News > ARD: In vitro mass spectrometry analysis reveals bone marrow pro-inflammatory features in the synovial fluid of psoriatic arthritis

    ARD: In vitro mass spectrometry analysis reveals bone marrow pro-inflammatory features in the synovial fluid of psoriatic arthritis

    • Last Update: 2022-01-07
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Purpose : Many immune cell groups are involved in the pathogenesis of psoriatic arthritis (PsA) .
    It is currently known that PsA is related to CD8+ T cells (especially those that produce IL-17 ); the role of myeloid cell population has not been explored to the same extent .
    In this study, mass spectrometry flow cytometry (CyTOF) combined with transcriptomics analysis was used to generate matched high-dimensional data sets of PsA synovial fluid (SF) and blood leukocytes, with the purpose of identifying cells in vitro in unstimulated lymphoid and bone marrow cells Factor generation .

    Purpose : Many immune cell groups are involved in the pathogenesis of psoriatic arthritis immunity (PsA) .


    It is currently known that PsA is related to CD8+ T cells (especially those that produce IL-17 ); the role of myeloid cell population has not been explored to the same extent .
    In this study, mass spectrometry flow cytometry (CyTOF) combined with transcriptomics analysis was used to generate matched high-dimensional data sets of PsA synovial fluid (SF) and blood leukocytes, with the purpose of identifying cells in vitro in unstimulated lymphoid and bone marrow cells Factor generation .

    Method : Fix fresh SF and matched blood or incubate with protein transport inhibitor for 6 hours
    .


    The samples were stained with two CyTOF panels: a phenotypic panel and an intracellular panel, including antibodies against T cells and myeloid cells secreted proteins


    Method : Fix fresh SF and matched blood or incubate with protein transport inhibitor for 6 hours


    Results : The study observed that the myeloid compartment of PsA SF has undergone significant changes relative to blood, and the intermediate monocytes, macrophages and dendritic cell populations have expanded


    Conclusion: Using multi-omics analysis, the graduate student has become a comprehensive cell atlas of PsA SF and blood to reveal the key bone marrow pro-inflammatory modules of PsA that are potentially pathogenic and therapeutically important


    Source:

    Yager N, Cole S, Lledo Lara A , et al .


    Ex vivo mass cytometry analysis reveals a profound myeloid proinflammatory signature in psoriatic arthritis synovial fluid.
    Annals of the Rheumatic Diseases2021; 80: 1559-1567.


    Yager N, Cole S, Lledo Lara A , et al .
    Ex vivo mass cytometry analysis reveals a profound myeloid proinflammatory signature in psoriatic arthritis synovial fluid.
    Annals of the Rheumatic Diseases  2021; 80: 1559-1567.
    , et al Annals of the Rheumatic Diseases  80: Leave a message here
    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.