Aim: To study the effect of troglitazone on primary culture human pterygium fibroblasts (HPF).
Methods: Cell viability loss and apoptosis were quantified by cell counting kit-8, AnnexinV-FITC/PI double staining, caspases activity test and western blotting. Flow cytometry was used to detect mitochondrial membrane potential.
Results: Peroxisome proliferator-activated receptor γ (PPAR-γ) was positively expressed in pterygium specimens (n=5). Troglitazone showed dose-dependent inhibition of cell survival, induced phospholipids redistribution, activated caspase-3, -9, and altered mitochondrial potential. Western blot assay demonstrated the increase of Bax/Bcl-2 protein ratio.
Conclusion: Troglitazone induced apoptosis of HPF through a mitochondrial-dependent pathway.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340713 | PMC |
http://dx.doi.org/10.3980/j.issn.2222-3959.2011.02.06 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!