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刺激诱导的聚集蛋白聚糖分解对野生型和抗聚集蛋白聚糖酶突变型小鼠软骨纳米级形态和力学性能的影响。

Effects of stimulated aggrecanolysis on nanoscale morphological and mechanical properties of wild-type and aggrecanase-resistant mutant mice cartilages.

作者信息

Uddin Md Hemayet, Wang Huabin, Rogerson Fraser M, Lee Peter Vee-Sin, Zhang Xuehua

机构信息

Melbourne Central of Nanofabrication, Victorian Node of Australian National Fabrication Facility, 3149, Clayton, Victoria, Australia.

Chongqing Key Laboratory of Multi-Scale Manufacturing Technology, Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, 400714, Chongqing, China.

出版信息

Eur Phys J E Soft Matter. 2017 Aug;40(8):72. doi: 10.1140/epje/i2017-11561-1. Epub 2017 Aug 16.

Abstract

A key event in arthritis pathogenesis is the degradation of aggrecan, the major component in articular cartilage. In this work, we investigate the effects of stimulated aggrecanolysis on the morphological and nanomechanical properties of cartilage harvested from wild-type mice and aggrecanase-resistant mutant mice named "Jaffa". The cartilages were native or were subjected to stimulated aggrecanolysis by interleukin-1[Formula: see text] (IL-1[Formula: see text]) treatment. The nanoscale morphological and mechanical properties of the sectioned cartilages were measured by using a sharp probe by atomic force microscopy (AFM). The IL-1[Formula: see text] treatment resulted in a higher nanoroughess and stiffness of the cartilage from wild-type mice. However, the same treatment did not lead to any measurable change in the nanoroughness or stiffness of the cartilage from mutant mice Jaffa. This suggests that blocking aggrecanolysis by genetic modification has created the stability in the structures and mechanical properties of the cartilage at nanoscale. The present study provides insight into the mechanism of aggrecan degradation, which can complement the examination by biochemical and histological techniques.

摘要

关节炎发病机制中的一个关键事件是聚集蛋白聚糖(关节软骨的主要成分)的降解。在这项研究中,我们研究了刺激聚集蛋白聚糖分解对从野生型小鼠和名为“雅法”的抗聚集蛋白聚糖酶突变小鼠获取的软骨的形态和纳米力学性能的影响。这些软骨是天然的,或者通过白细胞介素-1β(IL-1β)处理进行刺激聚集蛋白聚糖分解。使用原子力显微镜(AFM)的尖锐探针测量切片软骨的纳米级形态和力学性能。IL-1β处理导致野生型小鼠软骨的纳米粗糙度和硬度更高。然而,相同的处理并未导致突变小鼠雅法的软骨在纳米粗糙度或硬度上出现任何可测量的变化。这表明通过基因改造阻断聚集蛋白聚糖分解在纳米尺度上创造了软骨结构和力学性能的稳定性。本研究为聚集蛋白聚糖降解机制提供了见解,可补充生化和组织学技术的检测。

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