Epigallocatechin Gallate-Modified Gelatin Sponges Treated by Vacuum Heating as a Novel Scaffold for Bone Tissue Engineering.
Yoshitomo HondaYoshihiro TakedaPeiqi LiAnqi HuangSatoshi SasayamaEiki HaraNaoya UemuraMamoru UedaMasanori HashimotoKenji AritaNaoyuki MatsumotoYoshiya HashimotoShunsuke BabaTomonari TanakaPublished in: Molecules (Basel, Switzerland) (2018)
Chemical modification of gelatin using epigallocatechin gallate (EGCG) promotes bone formation in vivo. However, further improvements are required to increase the mechanical strength and bone-forming ability of fabricated EGCG-modified gelatin sponges (EGCG-GS) for practical applications in regenerative therapy. In the present study, we investigated whether vacuum heating-induced dehydrothermal cross-linking of EGCG-GS enhances bone formation in critical-sized rat calvarial defects. The bone-forming ability of vacuum-heated EGCG-GS (vhEGCG-GS) and other sponges was evaluated by micro-computed tomography and histological staining. The degradation of sponges was assessed using protein assays, and cell morphology and proliferation were verified by scanning electron microscopy and immunostaining using osteoblastic UMR106 cells in vitro. Four weeks after the implantation of sponges, greater bone formation was detected for vhEGCG-GS than for EGCG-GS or vacuum-heated gelatin sponges (dehydrothermal cross-linked sponges without EGCG). In vitro experiments revealed that the relatively low degradability of vhEGCG-GS supports cell attachment, proliferation, and cell-cell communication on the matrix. These findings suggest that vacuum heating enhanced the bone forming ability of EGCG-GS, possibly via the dehydrothermal cross-linking of EGCG-GS, which provides a scaffold for cells, and by maintaining the pharmacological effect of EGCG.
Keyphrases
- tissue engineering
- bone regeneration
- single cell
- cell therapy
- computed tomography
- bone mineral density
- induced apoptosis
- electron microscopy
- soft tissue
- stem cells
- hyaluronic acid
- high throughput
- oxidative stress
- cell cycle arrest
- magnetic resonance imaging
- small molecule
- cell death
- positron emission tomography
- atomic force microscopy
- mass spectrometry
- gestational age
- cell proliferation
- drug induced
- contrast enhanced
- high resolution
- preterm birth
- angiotensin ii
- protein protein
- flow cytometry