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可注射纳米羟磷灰石-壳聚糖-明胶微支架诱导膝关节软骨下骨病变再生。

Injectable nanohydroxyapatite-chitosan-gelatin micro-scaffolds induce regeneration of knee subchondral bone lesions.

机构信息

Arthritis clinic and research center, Peking University People's Hospital, Beijing, 100044, People's Republic of China.

Department of Orthopaedics, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, 030001, People's Republic of China.

出版信息

Sci Rep. 2017 Dec 1;7(1):16709. doi: 10.1038/s41598-017-17025-6.

Abstract

Subchondral bone has been identified as an attractive target for KOA. To determine whether a minimally invasive micro-scaffolds could be used to induce regeneration of knee subchondral bone lesions, and to examine the protective effect of subchondral bone regeneration on upper cartilage, a ready-to-use injectable treatment with nanohydroxyapatite-chitosan-gelatin micro-scaffolds (HaCGMs) is proposed. Human-infrapatellar-fat-pad-derived adipose stem cells (IPFP-ASCs) were used as a cellular model to examine the osteo-inductivity and biocompatibility of HaCGMs, which were feasibly obtained with potency for multi-potential differentiations. Furthermore, a subchondral bone lesion model was developed to mimic the necrotic region removing performed by surgeons before sequestrectomy. HaCGMs were injected into the model to induce regeneration of subchondral bone. HaCGMs exhibited desirable swelling ratios, porosity, stiffness, and bioactivity and allowed cellular infiltration. Eight weeks after treatment, assessment via X-ray imaging, micro-CT imaging, and histological analysis revealed that rabbits treated with HaCGMs had better subchondral bone regeneration than those not treated. Interestingly, rabbits in the HaCGM treatment group also exhibited improved reservation of upper cartilage compared to those in other groups, as shown by safranin O-fast green staining. Present study provides an in-depth demonstration of injectable HaCGM-based regenerative therapy, which may provide an attractive alternative strategy for treating KOA.

摘要

软骨下骨已被确定为治疗骨关节炎(KOA)的一个有吸引力的靶点。为了确定微创微支架是否可用于诱导膝关节软骨下骨病变的再生,并研究软骨下骨再生对上层软骨的保护作用,提出了一种即用型的纳米羟基磷灰石-壳聚糖-明胶微支架(HaCGM)注射治疗方法。人类髌下脂肪垫来源的脂肪间充质干细胞(IPFP-ASCs)被用作细胞模型,以研究 HaCGM 的成骨诱导性和生物相容性,HaCGM 可通过多向分化潜能来获得。此外,建立了软骨下骨病变模型来模拟外科医生在切除游离体前进行的坏死区域清除。将 HaCGM 注射到模型中以诱导软骨下骨再生。HaCGM 表现出理想的溶胀比、孔隙率、硬度和生物活性,并允许细胞浸润。治疗 8 周后,通过 X 射线成像、微 CT 成像和组织学分析评估显示,接受 HaCGM 治疗的兔子的软骨下骨再生情况优于未治疗的兔子。有趣的是,与其他组相比,HaCGM 治疗组的兔子的上层软骨保留情况也有所改善,这通过番红 O-快绿染色显示出来。本研究深入展示了基于可注射 HaCGM 的再生治疗方法,这可能为治疗 KOA 提供一种有吸引力的替代策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b395/5711958/dedab59c2de6/41598_2017_17025_Fig1_HTML.jpg

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