[The effect of CD137-CD137 ligand interaction on the expression of nuclear factor of activated T cells c1 in apolipoprotein E-deficient mice atherosclerotic plaque model]

Zhonghua Xin Xue Guan Bing Za Zhi. 2012 Sep;40(9):775-9.
[Article in Chinese]

Abstract

Objective: To investigate the effects of CD137-CD137L interaction on the nuclear factor of activated T cells c1 (NFATc1) in apolipoprotein E knockout (ApoE(-/-)) mice.

Methods: Atherosclerotic plaque model was produced by rapid perivascular carotid collar placement in ApoE(-/-) mice. In vivo, the expression of NFATc1 in mice plaque and lymphocytes was detected by immunohistochemical and flow cytometry, respectively. In vitro, the NFATc1 mRNA and protein expressions in cultured lymphocytes of ApoE(-/-) mice were measured by RT-PCR and flow cytometry, respectively.

Results: In vivo, after stimulating CD137-CD137L signal pathway, the expression of NFATc1 was significantly upregulated in the atherosclerotic plaques and lymphocytes. In vitro, the mRNA and protein expressions of NFATc1 in cultured leukocytes of ApoE(-/-) mice were also significantly increased, the maximal effect appeared post 20 µg/ml anti-CD137 mAb-stimulation and reached maximum at 24 h at any concentrations. Anti-CD137L mAb significantly downregulated the mRNA and protein expressions of NFATc1 in lymphocytes of ApoE(-/-) mice, maximal effect appeared at 20 µg/ml anti-CD137L mAb and reached minimum at 24 h.

Conclusion: CD137-CD137L interactions can modulate the expression of NFATc1 in this ApoE(-/-) mice atherosclerotic plaque model.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • 4-1BB Ligand / metabolism*
  • Animals
  • Apolipoproteins E / genetics*
  • Disease Models, Animal
  • Mice
  • Mice, Knockout
  • NFATC Transcription Factors / metabolism*
  • Plaque, Atherosclerotic / metabolism*
  • RNA, Messenger / genetics
  • Tumor Necrosis Factor Receptor Superfamily, Member 9 / metabolism*

Substances

  • 4-1BB Ligand
  • Apolipoproteins E
  • NFATC Transcription Factors
  • RNA, Messenger
  • Tumor Necrosis Factor Receptor Superfamily, Member 9