Tualang honey improves human corneal epithelial progenitor
cell migration and cellular resistance to oxidative stress in vitro
PLoS One, 2014 May 6;9(5):e96800
Stem cells with enhanced resistance to oxidative stress
after in vitro expansion have been shown to have improved engraftment and
regenerative capacities. Such cells can be generated by preconditioning them
with exposure to an antioxidant.
In this study we evaluated the effects of
Tualang honey (TH), an antioxidant-containing honey, on human corneal
epithelial progenitor (HCEP) cells in culture. Cytotoxicity, gene expression,
migration, and cellular resistance to oxidative stress were evaluated.
Immunofluorescence staining revealed that HCEP cells were holoclonal and
expressed epithelial stem cell marker p63 without corneal cytokeratin 3. Cell
viability remained unchanged after cells were cultured with 0.004, 0.04, and
0.4% TH in the medium, but it was significantly reduced when the concentration
was increased to 3.33%. Cell migration, tested using scratch migration assay,
was significantly enhanced when cells were cultured with TH at 0.04% and 0.4%.
We also found that TH has hydrogen peroxide (H2O2) scavenging ability, although
a trace level of H2O2 was detected in the honey in its native form.
Preconditioning HCEP cells with 0.4% TH for 48 h showed better survival
following H2O2-induced oxidative stress at 50 µM than untreated group, with a
significantly lower number of dead cells (15.3±0.4%) were observed compared to
the untreated population (20.5±0.9%, p < 0.01).
Both TH and ascorbic acid
improved HCEP viability following induction of 100 µM H2O2, but the benefit was
greater with TH treatment than with ascorbic acid. However, no significant
advantage was demonstrated using 5-hydroxymethyl-2-furancarboxaldehyde, a
compound that was found abundant in TH using GC/MS analysis. This suggests that
the cellular anti-oxidative capacity in HCEP cells was augmented by native TH
and was attributed to its antioxidant properties.
In conclusion, TH possesses
antioxidant properties and can improve cell migration and cellular resistance
to oxidative stress in HCEP cells in vitro.
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