Bone tissue engineering has emerged
as an effective alternative treatment to the problem of bone defect.
To repair a bone defect, antibiosis and osteogenesis are two essential
aspects of the repair process. By searching the literature and performing
exploratory experiments, we found that β defensin 2 (BD2), with
bifunctional properties of antibiosis and osteogenesis, was a feasible
alternative for traditional growth factors. The antimicrobial ability
of BD2 against Staphylococcus aureus and Escherichia coli was studied
by the spread plate and live/dead staining methods (low effective
concentration of 20 ng/mL). BD2 was also demonstrated to enhance osteogenesis,
with higher messenger RNA (mRNA) and protein expression of the osteogenic
markers collagen I (Col1), runt-related transcription factor 2 (Runx2),
osteopontin (Opn), and osteocalcin (Ocn) in vitro (1.5–2.5-fold
increase compared with the control group in the most effective concentration
group), which was consistent with the alkaline phosphatase (ALP) and
alizarin red S (ARS) staining results. We implanted poly(sebacoyl
diglyceride) (PSeD) combined with BD2 and rat bone tissue-derived
mesenchymal stem cells (rBMSCs) under the back skin of rats and found
that the inflammatory response was significantly lower with this combination
than with the PSeD/rBMSCs scaffold without BD2 and the pure PSeD group
and was similar to the control group. Importantly, when assessed in
a critical-sized in vivo rat 8 m diameter calvaria defect model, a
scaffold we developed combining bifunctional BD2 with porous organic
polymer displayed an osteogenic effect that was 160–200% greater
than the control group. The in vivo study results revealed a significant
osteogenic response and antimicrobial effect and were consistent with
the in vitro results. In summary, BD2 displayed a great potential
of simultaneously promoting bone regeneration and preventing infection
and could provide a viable alternative to traditional growth factors
applied in bone defect repair.
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