在椎间盘修复中平衡生物学和生物力学性能:可注射细胞递送生物材料的系统综述。

IF 3.2 3区 医学 Q3 CELL & TISSUE ENGINEERING European cells & materials Pub Date : 2020-11-18 DOI:10.22203/eCM.v040a15
C J Panebianco, J H Meyers, J Gansau, W W Hom, J C Iatridis
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引用次数: 15

摘要

椎间盘源性背痛是一种常见的疾病,没有批准的椎间盘修复治疗。使用可注射生物材料载体的细胞递送有望恢复椎间盘高度和生物力学功能,同时为递送的细胞提供修复退化组织的功能龛。本系统综述通过描述注射IVD细胞递送生物材料领域的现状和确定有前景的策略主题来推进注射IVD细胞递送生物材料领域。采用系统评价和Meta分析首选报告项目(PRISMA)指南筛选文献,183篇稿件符合纳入标准。从每项研究中提取细胞和生物材料输入,以及生物学和生物力学结果。大多数已确定的研究针对髓核(NP)修复。在细胞类型或生物材料载体方面尚无共识,但最常见的策略是使用天然生物材料组成的互穿网络/共聚(IPN/CoP)生物材料进行间充质干细胞(MSC)递送。所有的研究报告了生物学结果,大约一半的研究报告了生物力学结果。由于IVD是一个承重组织,研究报告压缩和剪切模量进行了分析,发现了两个主要主题。首先,观察到生物力学和生物性能之间的竞争平衡或“跷跷板”效应。模量越高的配方细胞性能越差,反之亦然。其次,一些低模量的生物材料具有良好的生物学性能,并且在整个培养过程中成熟,细胞外基质合成和生物力学模量增强。研究结果为开发下一代生物材料提供了一个机会,这种材料可以提供高初始生物力学能力,以稳定和修复受损的ivd,并促进细胞功能的长期愈合。
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Balancing biological and biomechanical performance in intervertebral disc repair: a systematic review of injectable cell delivery biomaterials.

Discogenic back pain is a common condition without approved intervertebral disc (IVD) repair therapies. Cell delivery using injectable biomaterial carriers offers promise to restore disc height and biomechanical function, while providing a functional niche for delivered cells to repair degenerated tissues. This systematic review advances the injectable IVD cell delivery biomaterials field by characterising its current state and identifying themes of promising strategies. Preferred Reporting Items for Systematic Reviews and Meta- Analyses (PRISMA) guidelines were used to screen the literature and 183 manuscripts met the inclusion criteria. Cellular and biomaterial inputs, and biological and biomechanical outcomes were extracted from each study. Most identified studies targeted nucleus pulposus (NP) repair. No consensus exists on cell type or biomaterial carrier, yet most common strategies used mesenchymal stem cell (MSC) delivery with interpenetrating network/co-polymeric (IPN/CoP) biomaterials composed of natural biomaterials. All studies reported biological outcomes with about half the studies reporting biomechanical outcomes. Since the IVD is a load-bearing tissue, studies reporting compressive and shear moduli were analysed and two major themes were found. First, a competitive balance, or 'seesaw' effect, between biomechanical and biological performance was observed. Formulations with higher moduli had inferior cellular performance, and vice versa. Second, several low-modulus biomaterials had favourable biological performance and matured throughout culture duration with enhanced extracellular matrix synthesis and biomechanical moduli. Findings identify an opportunity to develop next-generation biomaterials that provide high initial biomechanical competence to stabilise and repair damaged IVDs with a capacity to promote cell function for long-term healing.

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来源期刊
European cells & materials
European cells & materials 生物-材料科学:生物材料
CiteScore
6.00
自引率
6.50%
发文量
55
审稿时长
1.5 months
期刊介绍: eCM provides an interdisciplinary forum for publication of preclinical research in the musculoskeletal field (Trauma, Maxillofacial (including dental), Spine and Orthopaedics). The clinical relevance of the work must be briefly mentioned within the abstract, and in more detail in the paper. Poor abstracts which do not concisely cover the paper contents will not be sent for review. Incremental steps in research will not be entertained by eCM journal.Cross-disciplinary papers that go across our scope areas are welcomed.
期刊最新文献
Notochordal cell-derived matrix inhibits MAPK signaling in the degenerative disc environment Relationship between microscale shear modulus, composition, and structure in porcine, canine, and human temporomandibular-joint cartilage: relevance to disease and degeneration Treatment of volumetric muscle loss in female rats with biomimetic sponges Creating tissue with intervertebral disc-like characteristics using gdf5 functionalized silk scaffolds and human mesenchymal stromal cells Development of a 3D-printed bioabsorbable composite scaffold with mechanical properties suitable for treating large, load-bearingarticular cartilage defects.
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