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Defective responsiveness of CD5+ B1 cells to lipopolysaccharide in cytokine production

  • Naoki Koide
  • , Akiko Morikawa
  • , Hiroyasu Ito
  • , Tsuyoshi Sugiyama
  • , Ferdaus Hassan
  • , Shamima Islam
  • , Gantsetseg Tumurkhuu
  • , Isamu Mori
  • , Tomoaki Yoshida
  • , Takashi Yokochi

    Research output: Contribution to journal › Article › peer-review

    Abstract

    Previously, we found that mouse TH2.52 cells possess the characteristic of CD5+ B1 cells and proliferate in response to lipopolysaccharide (LPS). The effect of LPS on cytokine production by TH2.52 B1 cells was studied. TH2.52 cells constitutively produced a small amount of tumor necrosis factor (TNF)-α and interleukin (IL)-6, and TNF-α and IL-6 production was markedly enhanced by LPS stimulation. Although interferon (IFN)-γ caused the production of various cytokines, such as IL-2, IL-4, IL-6 and TNF-α in TH2.52 cells, LPS did not cause the production of such cytokines. LPS did not induce IFN-β production in TH2.52 cells and TH2.52 cells lacked the expression of several molecules participating in the MyD88-independent pathway in LPS signaling. Defective responsiveness of TH2.52 B1 cells to LPS in cytokine production might be responsible for the failure of IFN-β production due to the lack of molecules participating in the MyD88-independent pathway.

    Original languageEnglish
    Pages (from-to)346-351
    Number of pages6
    JournalJournal of Endotoxin Research
    Volume12
    Issue number6
    DOIs
    Publication statusPublished - 12-2006

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    All Science Journal Classification (ASJC) codes

    • Microbiology
    • Immunology
    • Molecular Biology
    • Cell Biology
    • Infectious Diseases

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