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受润滑素启发:一种具有耐用润滑性和自噬激活抗氧化性的定制软骨盔甲,用于骨关节炎的靶向治疗。

Inspired by lubricin: a tailored cartilage-armor with durable lubricity and autophagy-activated antioxidation for targeted therapy of osteoarthritis.

机构信息

College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials Engineering, Med-X Center for Materials, Sichuan University, Chengdu 610065, P. R. China.

Experimental and Research Animal Institute, Sichuan University, Chengdu 610207, P. R. China.

出版信息

Mater Horiz. 2024 Oct 28;11(21):5352-5365. doi: 10.1039/d4mh00812j.

Abstract

Osteoarthritis (OA), which disables articular cartilage, affects millions of people. The self-healing capacity is inhibited by internal oxidative stress and external lubrication deficiency and enzymatic degradation. To overcome these challenges, a tailored cartilage-armor is designed to ameliorate the inflamed cartilage, which is implemented by a novel collagen type II (Col II)-binding peptide conjugated zwitterionic polymer (PSB--PColBP, PSP). By mimicking natural lubricin, PSP specifically targets the cartilage surface and forms an hydration armor. This engineered cartilage-armor can prevent enzymatic cartilage degradation (nearly 100% resistance to catabolic enzymes) and provide durable lubrication properties (COF < 0.013 for 500 cycles). An autophagy-activation process, absent in previous biomimetic lubricants, enhances the enzymatic activity of the tailored cartilage-armor, offering effective anti-oxidant properties to suppress oxidative stress. By inhibiting the PI3K-Akt/NF-κB signaling pathway, chondrocytes protected by the tailored armor can secrete a cartilage matrix even in inflammatory microenvironments. In OA rat models, osteophyte formation and the inflammatory response have been inhibited by the cartilage-armor, demonstrating a therapeutic effect comparable to most drug-loaded systems. This study underscores the potential of tailoring cartilage-armor with the cartilage targeting and autophagy-activating properties in integrating offensive-defensive mechanisms for cartilage remodeling. This represents an alternative strategy for clinical OA therapy.

摘要

骨关节炎(OA)会使关节软骨失能,影响数百万人。内部氧化应激和外部润滑不足以及酶降解抑制了自我修复能力。为了克服这些挑战,设计了一种定制的软骨装甲来改善发炎的软骨,这是通过一种新型的与 II 型胶原(Col II)结合的聚电解质聚合物(PSB-PColBP,PSP)来实现的。通过模拟天然润滑素,PSP 特异性地靶向软骨表面并形成水合装甲。这种工程软骨装甲可以防止酶促软骨降解(对分解酶的抵抗力接近 100%)并提供持久的润滑性能(500 个循环的 COF<0.013)。一个以前的仿生润滑剂中不存在的自噬激活过程增强了定制软骨装甲的酶促活性,提供了有效的抗氧化特性来抑制氧化应激。通过抑制 PI3K-Akt/NF-κB 信号通路,受定制装甲保护的软骨细胞即使在炎症微环境中也能分泌软骨基质。在 OA 大鼠模型中,软骨装甲抑制了骨赘形成和炎症反应,其治疗效果可与大多数载药系统相媲美。这项研究强调了通过与软骨靶向和自噬激活特性相结合来定制软骨装甲的潜力,以整合软骨重塑的进攻-防御机制。这代表了一种替代策略,用于临床 OA 治疗。

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