Background Aloe vera has been used as a family medicine for promoting wound
healing, but it is not known which component of the plant is effective for
this purpose.
Objectives To isolate and characterize the component effective in wound hea
ling.
Methods Chromatography, electrophoresis and spectroscopic methods were used
. The cell-proliferation activity of each component isolated was measured b
y a [H-3]thymidine uptake assay. The cell-proliferation activity of the eff
ective component was tested on a three-dimensional raft culture (cell cultu
re technique by which artificial epidermis is made from keratinocytes). The
effect of the active component on cell migration and wound healing was obs
erved on a monolayer of human keratinocytes and in hairless mice.
Results A glycoprotein fraction was isolated and named G1G1M1DI2. It showed
a single band on sodium dodecyl sulphate-polyacrylamide gel electrophoresi
s, with an apparent molecular weight of about 5.5 kDa. It exhibited signifi
cant [H-3]thymidine uptake in squamous cell carcinoma cells. The effect of
G1G1M1DI2 on cell migration was confirmed by accelerated wound healing on a
monolayer of human keratinocytes. When this fraction was tested on a raft
culture, it stimulated the formation of epidermal tissue. Furthermore, prol
iferation markers (epidermal growth factor receptor, fibronectin receptor,
fibronectin, keratin 5/14 and keratin 1/10) were markedly expressed at the
immunohistochemical level. The glycoprotein fraction enhanced wound healing
in hairless mice by day 8 after injury, with significant cell proliferatio
n.
Conclusions It is considered that this glycoprotein fraction is involved in
the wound-healing effect of aloe vera via cell proliferation and migration
.