Inhibitory effect of mabuterol on proliferation of rat ASMCs induced by PDGF-BB via regulating [Ca2+]i and mitochondrial fission/fusion

Chem Biol Interact. 2019 Jul 1:307:63-72. doi: 10.1016/j.cbi.2019.04.023. Epub 2019 Apr 19.

Abstract

This study is aimed to investigate whether Mabuterol (Mab) inhibits proliferation of airway smooth muscle cells (ASMCs) induced by platelet-derived growth factor BB (PDGF-BB) and how far it is related to mitochondrial fission/fusion and intracellular calcium if it comes into play. To explore the mechanism of Mab's antagonizing the proliferation, Mdivi-1, DRP1 inhibitor, which has an inhibitory effect on mitochondrial fission, is used to compare with Mab. Cell viability was measured by either MTT or CCK-8. The inhibitory effect of Mab on S phase of ASM cell cycle induced by PDGF-BB was analyzed by flow cytometry (FCM). Fluo-3/AM, Ca2+ fluorescent probe, was used to detect Ca2+ fluorescence intensity by inverted microscope and flow cytometry. The gene expression of Drp-1 and Mfn-2 was observed with Real time PCR and the proteins of Drp-1, Mfn-2, PCNA and cyclin D1 were assessed by Western Blot. Mab and Mdivi-1 both suppressed the proliferation induced by PDGF-BB. The results from inverted microscope and flow cytometry showed that Mab inhibited [Ca2+]i in rat ASMCs induced by PDGF-BB. Cell cycle concept map illustrated that Mab significantly controlled the S phase of ASM cell cycle induced by PDGF-BB. As a consequence, Real time PCR and Western blot revealed the fact that Mab decreased the expression of Drp-1 mRNA and protein, and promoted the expression of Mfn-2 mRNA and protein. These findings suggested that Mab placed restrictions on the proliferation of rat ASMCs induced by PDGF-BB and the mechanism might be associated with the intracellular calcium inhibited and the mitochondrial fission/fusion regulated by Mab.

Keywords: ASMCs; Cell proliferation; Intracellular calcium; Mab; Mitochondrial fusion and fission.

MeSH terms

  • Animals
  • Becaplermin / pharmacology*
  • Calcium / metabolism*
  • Cell Cycle Checkpoints / drug effects
  • Cell Proliferation / drug effects*
  • Cells, Cultured
  • Clenbuterol / analogs & derivatives*
  • Clenbuterol / pharmacology
  • Cyclin D1 / genetics
  • Cyclin D1 / metabolism
  • Down-Regulation / drug effects
  • Female
  • Male
  • Membrane Potential, Mitochondrial / drug effects
  • Mitochondrial Dynamics / drug effects*
  • Muscle, Smooth, Vascular / cytology
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / metabolism
  • Quinazolinones / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species / metabolism

Substances

  • 3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinone
  • Quinazolinones
  • Reactive Oxygen Species
  • Cyclin D1
  • Becaplermin
  • mabuterol
  • Calcium
  • Clenbuterol