The polyamidoamine-mediated inhibition of bcl-2 by small hairpin RNA to induce apoptosis in human lens epithelial cells

Mol Vis. 2012:18:74-80. Epub 2012 Jan 12.

Abstract

Purpose: To investigate whether apoptosis of human lens epithelial cells (HLECs) can be induced with the polyamidoamine (PAMAM)-mediated inhibition of bcl-2 (b-cell lymphoma 2) by small hairpin RNA (shRNA).

Methods: HLECs (SRA01/04) were transfected with the fifth generation of PAMAM (PAMAM G5) by bcl-2 shRNA. At 24, 48, and 72 h after transfection, the transfection rate was measured by flow cytometry. The transfection rates mediated by PAMAM and liposome were compared. The bcl-2 mRNA level was detected by real-time PCR. Whole cell protein was extracted and the bcl-2 protein level was detected by western blotting. The percentage of HLECs undergoing apoptosis was measured by Annexin V-FITC/PI staining. The nuclear morphology of HLECs was observed by staining with Hoechst 33258. The expression of cytochrome c and the activity of cleaved caspase-3 were analyzed by western blotting.

Results: At 24, 48, and 72 h after transfection, the rate of transfection of bcl-2 shRNA mediated by PAMAM was higher than in the liposome-mediated group (p<0.05). The mRNA and protein levels of bcl-2 were greatly downregulated. The percentage of HLECs undergoing apoptosis was greatly improved. Hoechst staining showed that bcl-2 shRNA transfected cells had a lower growth status with nuclear fragmentation. The expression of cytochrome c and the activity of cleaved caspase-3 was greatly improved (p<0.05).

Conclusions: PAMAM-mediated bcl-2 shRNA can downregulate the expression of bcl-2 and induce the apoptosis of HLECs by engaging the mitochondrial pathway, including catalytic activation of the caspases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Annexin A5 / analysis
  • Apoptosis / genetics
  • Blotting, Western
  • Caspase 3 / biosynthesis
  • Cell Line
  • Cytochromes c / biosynthesis
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism*
  • Flow Cytometry
  • Gene Expression Regulation
  • Gene Silencing
  • Humans
  • Lens, Crystalline / cytology
  • Lens, Crystalline / metabolism*
  • Liposomes / chemistry
  • Polyamines / chemistry*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • RNA, Messenger / biosynthesis*
  • RNA, Small Interfering / genetics*
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction
  • Transfection / methods

Substances

  • Annexin A5
  • Liposomes
  • Poly(amidoamine)
  • Polyamines
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger
  • RNA, Small Interfering
  • Cytochromes c
  • Caspase 3