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阻断聚集蛋白聚糖酶对聚集蛋白聚糖球状间结构域的切割可消除软骨侵蚀并促进软骨修复。

Blocking aggrecanase cleavage in the aggrecan interglobular domain abrogates cartilage erosion and promotes cartilage repair.

作者信息

Little Christopher B, Meeker Clare T, Golub Suzanne B, Lawlor Kate E, Farmer Pamela J, Smith Susan M, Fosang Amanda J

机构信息

Arthritis Research Group, University of Melbourne Department of Paediatrics and Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.

出版信息

J Clin Invest. 2007 Jun;117(6):1627-36. doi: 10.1172/JCI30765. Epub 2007 May 17.

Abstract

Aggrecan loss from cartilage in arthritis is mediated by aggrecanases. Aggrecanases cleave aggrecan preferentially in the chondroitin sulfate-2 (CS-2) domain and secondarily at the E(373) downward arrow(374)A bond in the interglobular domain (IGD). However, IGD cleavage may be more deleterious for cartilage biomechanics because it releases the entire CS-containing portion of aggrecan. Recent studies identifying aggrecanase-2 (ADAMTS-5) as the predominant aggrecanase in mouse cartilage have not distinguished aggrecanolysis in the IGD from aggrecanolysis in the CS-2 domain. We generated aggrecan knockin mice with a mutation that rendered only the IGD resistant to aggrecanases in order to assess the contribution of this specific cleavage to cartilage pathology. The knockin mice were viable and fertile. Aggrecanase cleavage in the aggrecan IGD was not detected in knockin mouse cartilage in situ nor following digestion with ADAMTS-5 or treatment of cartilage explant cultures with IL-1 alpha. Blocking cleavage in the IGD not only diminished aggrecan loss and cartilage erosion in surgically induced osteoarthritis and a model of inflammatory arthritis, but appeared to stimulate cartilage repair following acute inflammation. We conclude that blocking aggrecanolysis in the aggrecan IGD alone protects against cartilage erosion and may potentiate cartilage repair.

摘要

关节炎中软骨蛋白聚糖的丢失是由蛋白聚糖酶介导的。蛋白聚糖酶优先在硫酸软骨素 -2(CS -2)结构域切割蛋白聚糖,其次在球状间结构域(IGD)的E(373)↓(374)A键处切割。然而,IGD切割可能对软骨生物力学更具损害性,因为它会释放蛋白聚糖中整个含CS的部分。最近的研究将蛋白聚糖酶 -2(ADAMTS -5)鉴定为小鼠软骨中的主要蛋白聚糖酶,但尚未区分IGD中的蛋白聚糖分解与CS -2结构域中的蛋白聚糖分解。我们构建了一种蛋白聚糖敲入小鼠,其突变使得只有IGD对蛋白聚糖酶具有抗性,以便评估这种特定切割对软骨病理学的作用。敲入小鼠存活且可育。在敲入小鼠软骨原位,在用ADAMTS -5消化后或用IL -1α处理软骨外植体培养物后,均未检测到蛋白聚糖IGD中的蛋白聚糖酶切割。阻断IGD中的切割不仅减少了手术诱导的骨关节炎和炎性关节炎模型中蛋白聚糖的丢失和软骨侵蚀,而且似乎还刺激了急性炎症后的软骨修复。我们得出结论,单独阻断蛋白聚糖IGD中的蛋白聚糖分解可防止软骨侵蚀,并可能增强软骨修复。

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