CKBM stimulates MAPKs but inhibits LPS-induced IFN-γ in lymphocytes

Anthony S.L. Chan, Eric C.H. Yip, Lisa Y. Yung, Haihong Pang, Sharon C.W. Luk, Shiu F. Pang, Yung H. Wong*

*Corresponding author for this work

Research output: Contribution to journalJournal Articlepeer-review

Abstract

CKBM is an herbal formula composed of five Chinese medicinal herbs (Panax ginseng, Schisandra chinensis, Fructus crataegi, Ziziphus jujuba and Glycine max) supplemented with processed Saccharomyces cerevisiae. It has been demonstrated that CKBM is capable of triggering the release of IL-6 and TNFα from human peripheral blood mononuclear cells. In this report, T-lymphocytic Sup-T1 cells and B-lymphocytic Ramos cells were utilized as cellular models to investigate how CKBM regulates intracellular signaling as well as the production of cytokines. CKBM stimulated the three major subgroups of mitogen-activated protein kinase (i.e. ERK, JNK and p38) in Sup-T1 cells, but only triggered the activation of ERK and p38 in Ramos cells. The induction of mitogen-activated protein kinases (MAPK) activations varied with the duration of treatment, as well as with the dosage of CKBM. In terms of cytokine production, treatment of CKBM alone did not trigger the release of IL-1β and IFNγ, but it suppressed the LPS-induced IFNγ production from both Sup-T1 cells and Ramos cells. In view of the therapeutic effects of traditional Chinese medicines in inflammatory and autoimmune disorders, the results suggest that CKBM may exhibit its immuno-modulatory effects by regulating intracellular signaling as well as cytokine production in different lymphocytic cell types.

Original languageEnglish
Pages (from-to)725-731
Number of pages7
JournalPhytotherapy Research
Volume20
Issue number9
DOIs
Publication statusPublished - Sept 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

Keywords

  • B-lymphocytes
  • Cytokines
  • IFNγ
  • Immuno-modulation
  • MAPK
  • T lymphocytes

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