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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340713PMC
http://dx.doi.org/10.3980/j.issn.2222-3959.2011.02.06DOI Listing

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