Effect of immunosuppression on the human mesangial cell cycle

Xiaoshuang Zhou, Biruh Workeneh, Zhaoyong Hu, Rongshan Li

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

The present study investigated the effects of immunosuppressive agents [tacrolimus (Tac), cyclosporine A (CsA), mycophenolic acid (MMF) and methylprednisone (MP)] on the proliferation, cell cycle progression and apoptotic rate of human mesangial cells. Cultured human mesangial cells were treated with several concentrations of the immunosuppressive agents for 24, 48 or 72 h. Cell cycle progression, proliferation and apoptosis were analyzed using an MTT assay and flow cytometry. Tac and CsA significantly inhibited the proliferation of human mesangial cells in a dose- and time-dependent manner. Cell cycle analysis revealed that Tac and CsA arrested mesangial cells in the G0/G1 phase, preventing them from entering S phase. Similarly, MP inhibited human mesangial cell growth by causing cell cycle arrest in G0/G1 phase. MMF also inhibited mesangial cell proliferation, but accomplished this by preventing progression from S phase to the G2/M phase. The combination of MP and MMF synergistically inhibited mesangial cell proliferation. Tac, CsA, MP and MMF inhibited proliferation of human mesangial cells by blocking progression of the cell cycle. In conclusion, these agents, sequentially or in combination, may be used to effectively treat mesangial proliferative glomerular disease.

Original languageEnglish (US)
Pages (from-to)910-916
Number of pages7
JournalMolecular medicine reports
Volume11
Issue number2
DOIs
StatePublished - Feb 1 2015
Externally publishedYes

Keywords

  • Calcineurin-inhibitors
  • Cell cycle
  • Mesangial cell
  • Methylprednisolone
  • Mycophenolic acid

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Genetics
  • Oncology
  • Cancer Research

Fingerprint

Dive into the research topics of 'Effect of immunosuppression on the human mesangial cell cycle'. Together they form a unique fingerprint.

Cite this