2016•PubMedRequires access

Preparation and characterization of a de-cellularized rabbit aorta as a promising scaffold in vascular tissue engineering.

Lei Song, P Duan, Qiang Zhou

Open publisher page 5 citations

Abstract

Development of scaffold is essential for promoting and supporting healing process. This study aims to establish a decellularized rabbit aorta for clinical vascular tissue engineering therapy. We successfully prepared decellularized small-diameter aortic scaffolds and investigated several properties of this engineered vascular tissue scaffolds, including cell adhesion, hydrophilicity, cytotoxicity, biocompatibility. Results showed that decellularized aortas have a porous structure with few cell remnants as examined by histochemistry and scanning electron microscopy. Both vascular smooth muscle cells (VSMCs) and endothelial cells (ECs) cultured on decellularized aortas were adhered and proliferated well. Cell adhesion rates of rat VSMCs and ECs reached to 64.32±2.03% and 52.77±1.19%, respectively. VSMCs were able to migrate into outer surface of scaffolds. Hydrophilisity reached its maximal rate at 519±23% in 12 h. Importantly, no overt cytotoxicity was observed when grown in extraction solution of aortic scaffolds. Lastly, we also engrafted cell-scaffolds subcutaneously into nude mice in vivo. Implanted scaffold structure and proliferation of seeded cells were well maintained up to 8 weeks. In conclusion, we successfully prepared a decellularized rabbit aorta that not only largely maintains its extra-cellular structure, but also shows little toxicity. It may constitute a potential tool as a small diameter scaffold in vascular tissue engineering.

About this research paper

What this paper is about

Development of scaffold is essential for promoting and supporting healing process. This study aims to establish a decellularized rabbit aorta for clinical vascular tissue engineering therapy. We successfully prepared decellularized small-diameter aortic scaffolds and investigated several properties of this engineered vascular tissue scaffolds, including cell adhesion, hydrophilicity, cytotoxicity, biocompatibility. Results showed that decellularized aortas have a porous structure with few cell remnants as examined by histochemistry and scanning electron microscopy. Both vascular smooth muscle cells (VSMCs) and endothelial cells (ECs) cultured on decellularized aortas were adhered and proliferated well. Cell adhesion rates of rat VSMCs and ECs reached to 64.32±2.03% and 52.77±1.19%, respectively. VSMCs were able to migrate into outer surface of scaffolds. Hydrophilisity reached its maximal rate at 519±23% in 12 h. Importantly, no overt cytotoxicity was observed when grown in extraction solution of aortic scaffolds. Lastly, we also engrafted cell-scaffolds subcutaneously into nude mice in vivo. Implanted scaffold structure and proliferation of seeded cells were well maintained up to 8 weeks. In conclusion, we successfully prepared a decellularized rabbit aorta that not only largely maintains its extra-cellular structure, but also shows little toxicity. It may constitute a potential tool as a small diameter scaffold in vascular tissue engineering.

Why it matters

OpenAlex reports 5 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Development of scaffold is essential for promoting and supporting healing process. This study aims to establish a decellularized rabbit aorta for clinical vascular tissue engineering therapy. We successfully prepared decellularized small-diameter aortic scaffolds and investigated several properties of this engineered vascular tissue scaffolds, including cell adhesion, hydrophilicity, cytotoxicity, biocompatibility. Results showed that decellularized aortas have a porous structure with few cell remnants as examined by histochemistry and scanning electron microscopy. Both vascular smooth muscle cells (VSMCs) and endothelial cells (ECs) cultured on decellularized aortas were adhered and proliferated well. Cell adhesion rates of rat VSMCs and ECs reached to 64.32±2.03% and 52.77±1.19%, respectively. VSMCs were able to migrate into outer surface of scaffolds. Hydrophilisity reached its maximal rate at 519±23% in 12 h. Importantly, no overt cytotoxicity was observed when grown in extraction solution of aortic scaffolds. Lastly, we also engrafted cell-scaffolds subcutaneously into nude mice in vivo. Implanted scaffold structure and proliferation of seeded cells were well maintained up to 8 weeks. In conclusion, we successfully prepared a decellularized rabbit aorta that not only largely maintains its extra-cellular structure, but also shows little toxicity. It may constitute a potential tool as a small diameter scaffold in vascular tissue engineering.

Key concepts: Decellularization, Tissue engineering, Scaffold, Biocompatibility, Chemistry, Vascular tissue, In vivo, Biomedical engineering

Related papers

Back to paper searchBrowse research topicsOriginal source
Preparation and characterization of a de-cellularized rabbit aorta as a promising scaffold in vascular tissue engineering. — Research Paper | ScholarLens