Efficacy of Zhonglun'a-decoction-containing serum on fibroblast-like synoviocyte apoptosis in rats with collagen-induced arthritis via inhibiting Janus kinase/signal transducer and activator of transcription signaling pathway

J Tradit Chin Med. 2019 Apr;39(2):181-190.

Abstract

Objective: To investigate the efficacy of Zhonglun'a-decoction-containing serum (ZHONGL-CS) on the in vitro apoptosis of fibroblast-like synoviocytes (FLS) from rats with collagen-induced arthritis (CIA) by investigating the Janus kinase/signal transducer and activator of transcription (JAK/STAT) signaling pathway.

Methods: A CIA rat model was established using bovine type Ⅱ collagen. FLS were isolated, cultured and identified. A cell counting kit-8 was used to detect cell activity. The half maximal inhibitory concentration (IC50) was calculated. Experimental subjects were divided into control, CIA, ZHONGL-CS, JAK2 inhibitor AG490, and ZHONGLCS with AG490 groups. The in vitro cell cycle and apoptosis rate were detected in FLS by flow cytometry. Bcl-2-associated X protein (Bax), B-cell lymphoma 2 (Bcl-2), caspase-3, cyclin D1, phosphorylated JAK2, STAT1, and STAT3 protein expressions in FLS were examined by Western blotting. JAK2, STAT1 and STAT3 mRNA levels were examined by quantitative real-time polymerase chain reaction.

Results: Compared with the CIA group, FLS proliferation was inhibited, the FLS G0/G1 cell cycle was arrested, and the rate of FLS apoptosis was increased in the ZHONGL-CS group. In the ZHONGLCS group, the protein levels of Bcl-2 and cyclin D1 were reduced compared with the CIA group and the levels of Bax and caspase-3 in FLS were increased. In the ZHONGL-CS group, the expressions of JAK2, STAT1, and STAT3 mRNA and the levels of phosphorylated JAK2, STAT1, and STAT3 proteins were reduced.

Conclusion: ZHONGL-CS may induce FLS apoptosis in CIA rats. Activation of the JAK/STAT signaling pathway was inhibited in FLS in vitro.

Keywords: Arthritis, rheumatoid; Janus kinases; Synoviocytes; Apoptosis; Zhonglun'a-decoctioncontaining serum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Arthritis, Experimental / pathology*
  • Caspase 3 / metabolism
  • Cell Proliferation / drug effects
  • Cyclin D1 / metabolism
  • Drugs, Chinese Herbal / pharmacology*
  • Fibroblasts / pathology
  • Janus Kinases / metabolism*
  • Male
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • STAT Transcription Factors / metabolism*
  • Serum / chemistry*
  • Signal Transduction / drug effects*
  • Synoviocytes / drug effects
  • Synoviocytes / pathology*
  • bcl-2-Associated X Protein / metabolism

Substances

  • Drugs, Chinese Herbal
  • Proto-Oncogene Proteins c-bcl-2
  • STAT Transcription Factors
  • bcl-2-Associated X Protein
  • zhonglun
  • Cyclin D1
  • Janus Kinases
  • Caspase 3