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骨关节炎中的纤溶酶原激活物与受体

Plasminogen activator and receptor in osteoarthritis.

作者信息

Serni U, Fibbi G, Anichini E, Zamperini A, Pucci M, Mannoni A, Matucci A, Benucci M, Del Rosso A, Del Rosso M

机构信息

Institute of General Pathology, Florence University, Italy.

出版信息

J Rheumatol Suppl. 1995 Feb;43:120-2.

PMID:7752114
Abstract

Evidence indicates that breakdown of articular cartilage resulting in the loss of normal joint function is the distinctive feature of osteoarthritis. Degradation of cartilage extracellular matrix components involves the action of at least 2 classes of proteinases: serine proteinases and metalloproteinases. Receptors have been described on a wide range of cell lines for many such proteinases [urokinase-type plasminogen activator (u-PA), plasminogen/plasmin, collagenase], which subsequently activate each other on the solid phase of the cell surface, leading to cartilage destruction. We review the leading role of u-PA and its receptor (u-PAR) in cartilage degradation.

摘要

有证据表明,导致正常关节功能丧失的关节软骨破坏是骨关节炎的显著特征。软骨细胞外基质成分的降解涉及至少两类蛋白酶的作用:丝氨酸蛋白酶和金属蛋白酶。许多这类蛋白酶[尿激酶型纤溶酶原激活剂(u-PA)、纤溶酶原/纤溶酶、胶原酶]在多种细胞系上都有受体,这些受体随后在细胞表面的固相上相互激活,导致软骨破坏。我们综述了u-PA及其受体(u-PAR)在软骨降解中的主导作用。

相似文献

1
Plasminogen activator and receptor in osteoarthritis.骨关节炎中的纤溶酶原激活物与受体
J Rheumatol Suppl. 1995 Feb;43:120-2.
2
Antisense targeting of the urokinase receptor blocks urokinase-dependent proliferation, chemoinvasion, and chemotaxis of human synovial cells and chondrocytes in vitro.尿激酶受体的反义靶向作用可阻断体外培养的人滑膜细胞和软骨细胞的尿激酶依赖性增殖、化学侵袭和趋化性。
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The urokinase receptor and cell migration.尿激酶受体与细胞迁移
Semin Thromb Hemost. 1996;22(6):513-6. doi: 10.1055/s-2007-999053.
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Urokinase-dependent angiogenesis in vitro and diacylglycerol production are blocked by antisense oligonucleotides against the urokinase receptor.针对尿激酶受体的反义寡核苷酸可阻断体外尿激酶依赖性血管生成及二酰基甘油的产生。
Lab Invest. 1998 Sep;78(9):1109-19.
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Ethanol-induced up-regulation of the urokinase receptor in cultured human endothelial cells.乙醇诱导培养的人内皮细胞中尿激酶受体上调。
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7
[Expression of urokinase-type plasminogen activator (uPA) and uPA receptor (uPAR) plays a role in destruction of joint tissue in rapidly destructive coxarthropathy (RDC)].尿激酶型纤溶酶原激活剂(uPA)和uPA受体(uPAR)的表达在快速破坏性髋关节病(RDC)的关节组织破坏中起作用。
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Glucosamine sulfate suppresses the expressions of urokinase plasminogen activator and inhibitor and gelatinases during the early stage of osteoarthritis.硫酸氨基葡萄糖在骨关节炎早期抑制尿激酶型纤溶酶原激活剂、抑制剂和明胶酶的表达。
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Growth inhibition of vascular smooth muscle cells derived from urokinase receptor (u-PAR)-deficient mice in the presence of carcinoma cells.在癌细胞存在的情况下,源自尿激酶受体(u-PAR)缺陷小鼠的血管平滑肌细胞的生长抑制。
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Interaction of urokinase-type plasminogen activator with its receptor rapidly induces activation of glucose transporters.尿激酶型纤溶酶原激活剂与其受体的相互作用迅速诱导葡萄糖转运蛋白的激活。
Biochemistry. 1997 Mar 18;36(11):3076-83. doi: 10.1021/bi9619379.

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