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 journalArticlepeer-review

2 Citations (Scopus)

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
Externally publishedYes

All Science Journal Classification (ASJC) codes

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

Fingerprint

Dive into the research topics of 'Defective responsiveness of CD5<sup>+</sup> B1 cells to lipopolysaccharide in cytokine production'. Together they form a unique fingerprint.

Cite this