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体内机械载荷影响大鼠椎间盘内区域性聚集蛋白聚糖降解模式。

Region-dependent aggrecan degradation patterns in the rat intervertebral disc are affected by mechanical loading in vivo.

机构信息

School of Engineering, University of Vermont, Burlington, VT 05405, USA.

出版信息

Spine (Phila Pa 1976). 2011 Feb 1;36(3):203-9. doi: 10.1097/BRS.0b013e3181cec247.

Abstract

STUDY DESIGN

Immunoblotting study to evaluate aggrecan degradation patterns in rat intervertebral discs (IVDs) subjected to mechanical overload.

OBJECTIVE

To evaluate the effects of in vivo dynamic compression overloading on aggrecan degradation products associated with matrix metalloproteinase (MMP) and aggrecanase activity in different regions of the IVD.

SUMMARY OF BACKGROUND DATA

Aggrecan cleavage at the MMP and aggrecanase sites is an important event in human IVD aging, with distinct cleavage patterns in the anulus and nucleus regions.No such information is available on regional variations in rat IVDs, nor on how such cleavage is affected by mechanical loading.

METHODS

Sprague-Dawley rats were instrumented with an Ilizarov-type device and subjected to dynamic compression (1 MPa and 1 Hz for 8 hours per day for 8 weeks). Control, sham, and overloaded IVDs were separated by disc region and analyzed for aggrecan degradation products using immunoblotting techniques, with antibodies specific for the aggrecanase and MMP cleavage sites in the interglobular domain of aggrecan.

RESULTS

Control IVDs exhibited strong regional variation in aggrecan degradation patterns with minimal degradation products being present in the nucleus pulposus, degradation products associated with aggrecanase cleavage predominating in the inner anulus fibrosus (AF), and degradation products associated with MMP cleavage predominating in the outer AF. Dynamic compression overloading increased the amount of aggrecan degradation products associated with MMP cleavage not only in the AF but also in the nucleus pulposus. Degradation profiles of sham IVDs were similar to control.

CONCLUSION

Aggrecan G1 regions resulting from proteolysis were found to have a strong regionally specific pattern in the rat IVD, which was altered under excessive loading. The shift from aggrecanase to MMP-induced degradation products with dynamic compression overloading suggests that protein degradation and loss can precede major structural disruption in the IVD, and that MMP-induced aggrecan degradation may be a marker of mechanically induced disc degeneration.

摘要

研究设计

评估机械性超负荷对大鼠椎间盘中聚集蛋白聚糖降解模式的免疫印迹研究。

目的

评估体内动态压缩超负荷对不同椎间盘区域基质金属蛋白酶(MMP)和聚集蛋白聚糖酶活性相关聚集蛋白聚糖降解产物的影响。

背景资料概要

聚集蛋白聚糖在 MMP 和聚集蛋白聚糖酶位点的裂解是人类椎间盘老化的一个重要事件,在纤维环和核区域有明显的裂解模式。在大鼠椎间盘中,没有关于区域变化的此类信息,也没有关于机械加载如何影响这种裂解的信息。

方法

用伊里扎洛夫式装置对斯普拉格-道利大鼠进行仪器操作,并进行动态压缩(每天 8 小时,1 MPa 和 1 Hz)8 周。通过免疫印迹技术,用针对聚集蛋白聚糖球间域中聚集蛋白聚糖酶和 MMP 裂解位点的抗体,将对照、假手术和超负荷的椎间盘按椎间盘区域分离,分析聚集蛋白聚糖降解产物。

结果

对照椎间盘的聚集蛋白聚糖降解模式存在明显的区域差异,核髓质中存在最小的降解产物,内纤维环(AF)中主要存在与聚集蛋白聚糖酶裂解相关的降解产物,外纤维环(AF)中主要存在与 MMP 裂解相关的降解产物。动态压缩超负荷不仅增加了与 MMP 裂解相关的聚集蛋白聚糖降解产物的数量,而且增加了在核髓质中的数量。假手术椎间盘的降解谱与对照相似。

结论

在大鼠椎间盘中,发现聚集蛋白聚糖 G1 区域的蛋白水解产生了强烈的区域特异性模式,这种模式在超负荷下发生了改变。动态压缩超负荷导致从聚集蛋白聚糖酶到 MMP 诱导的降解产物的转变表明,蛋白降解和丢失可能先于椎间盘的主要结构破坏,并且 MMP 诱导的聚集蛋白聚糖降解可能是机械诱导的椎间盘退变的标志物。

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