Microfiber-Reinforced Composite Hydrogels Loaded with Rat Adipose-Derived Stem Cells and BMP-2 for the Treatment of Medication-Related Osteonecrosis of the Jaw in a Rat Model

自愈水凝胶 间充质干细胞 骨形态发生蛋白2 脂肪组织 材料科学 干细胞 生物医学工程 医学 化学 癌症研究 病理 细胞生物学 体外 内科学 生物 生物化学 高分子化学
作者
Haoran Ning,Xiaowei Wu,Qing Wu,Wanlu Yu,Huaiji Wang,Shang Zheng,Yunong Chen,Yongyong Li,Jiansheng Su
出处
期刊:ACS Biomaterials Science & Engineering [American Chemical Society]
卷期号:5 (5): 2430-2443 被引量:14
标识
DOI:10.1021/acsbiomaterials.8b01468
摘要

Severe adverse reactions of bisphosphonates and anti-resorptive or anti-angiogenic medications, termed medication-related osteonecrosis of the jaw (MRONJ), have been reported. MRONJ are difficult to completely cure and could cause great pain to patients. Recent studies have shown that mesenchymal stem cell (MSC) therapies are effective for treating MRONJ, but the method of intravenous injection is unstable and increases the risk of producing tumors. In the present study, low-acyl gellan gum (LAGG) hydrogels were modified with hemicellulose polysaccharide microfibers (PMs) to improve the performance of supporting three-dimensional (3D) cell growth. LAGG-PM composite hydrogels were found to be nontoxic to rat adipose-derived stem cells (rADSCs) in vitro. The hydrogels also promoted the secretion of angiogenic factors, induced osteoclastogenesis by conditioned medium, and supported osteogenic marker expression after the addition of human bone morphogenetic protein-2 (BMP-2). Due to its injectability, the LAGG-PM composite hydrogel incorporated with rADSCs and BMP-2 could be applied into the MRONJ lesion site, which promoted mucosal recovery, bone tissue reconstruction, and osteoclastogenesis. This study confirms the potential applications of LAGG-PM composite hydrogels as 3D cell culture platforms and delivery vehicles for the treatment of MRONJ in a rat model.

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