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用于椎间盘(IVD)再生的仿生蛋白聚糖

Biomimetic Proteoglycans for Intervertebral Disc (IVD) Regeneration.

作者信息

Chopra Neha, Melrose James, Gu Zi, Diwan Ashish D

机构信息

Spine Service & Spine Labs, St George & Sutherland School of Clinical Medicine, Faculty of Health and Medicine, University of New South Wales, Kogarah, NSW 2217, Australia.

Graduate School of Biomedical Engineering, University of New South Wales, Sydney, NSW 2052, Australia.

出版信息

Biomimetics (Basel). 2024 Nov 22;9(12):722. doi: 10.3390/biomimetics9120722.

Abstract

Intervertebral disc degeneration, which leads to low back pain, is the most prevalent musculoskeletal condition worldwide, significantly impairing quality of life and imposing substantial socioeconomic burdens on affected individuals. A major impediment to the development of any prospective cell-driven recovery of functional properties in degenerate IVDs is the diminishing IVD cell numbers and viability with ageing which cannot sustain such a recovery process. However, if IVD proteoglycan levels, a major functional component, can be replenished through an orthobiological process which does not rely on cellular or nutritional input, then this may be an effective strategy for the re-attainment of IVD mechanical properties. Furthermore, biomimetic proteoglycans (PGs) represent an established polymer that strengthens osteoarthritis cartilage and improves its biomechanical properties, actively promoting biological repair processes. Biomimetic PGs have superior water imbibing properties compared to native aggrecan and are more resistant to proteolytic degradation, increasing their biological half-life in cartilaginous tissues. Methods have also now been developed to chemically edit the structure of biomimetic proteoglycans, allowing for the incorporation of bioactive peptide modules and equipping biomimetic proteoglycans as delivery vehicles for drugs and growth factors, further improving their biotherapeutic credentials. This article aims to provide a comprehensive overview of prospective orthobiological strategies that leverage engineered proteoglycans, paving the way for novel therapeutic interventions in IVD degeneration and ultimately enhancing patient outcomes.

摘要

椎间盘退变会导致腰痛,是全球最常见的肌肉骨骼疾病,严重损害生活质量,并给患者带来巨大的社会经济负担。在退变的椎间盘内,随着年龄增长,椎间盘细胞数量减少且活力下降,无法维持任何由细胞驱动的功能特性恢复过程,这是实现椎间盘功能特性前瞻性恢复的主要障碍。然而,如果作为主要功能成分的椎间盘蛋白聚糖水平能够通过一种不依赖细胞或营养输入的生物修复过程得到补充,那么这可能是恢复椎间盘力学性能的有效策略。此外,仿生蛋白聚糖是一种已被证实的聚合物,可增强骨关节炎软骨并改善其生物力学性能,积极促进生物修复过程。与天然聚集蛋白聚糖相比,仿生蛋白聚糖具有更强的吸水性能,且更耐蛋白水解降解,从而延长了它们在软骨组织中的生物半衰期。目前还开发了化学编辑仿生蛋白聚糖结构的方法,使生物活性肽模块得以掺入,并将仿生蛋白聚糖用作药物和生长因子的递送载体,进一步提升了它们的生物治疗资质。本文旨在全面概述利用工程化蛋白聚糖的前瞻性生物修复策略,为椎间盘退变的新型治疗干预铺平道路,并最终改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e22/11673487/7b543263b6a8/biomimetics-09-00722-g001.jpg

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