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蛋白聚糖表位在关节软骨修复组织中的表达

Expression of proteoglycan epitopes in articular cartilage repair tissue.

作者信息

Lin P P, Buckwalter J A, Olmstead M, Caterson B

机构信息

Division of Orthopaedic Surgery, University of North Carolina Hospitals, Chapel Hill, USA.

出版信息

Iowa Orthop J. 1998;18:12-8.

Abstract

To determine if expression of specific proteoglycan epitopes distinguishes articular cartilage repair tissue from normal articular cartilage, we used seven monoclonal antibodies to examine normal articular cartilage and cartilage repair tissue from osteochondral defects 3.2 mm in diameter and 4.0 mm deep in the medial femoral condyles of 27 New Zealand white rabbits and seven cynomolgus monkeys. Following creation of the osteochondral defects, one limb of each animal was treated with cast immobilization while the other limb was treated with passive motion for two weeks. Rabbit knees were examined at eight (13 animals, 26 knees) and 36 weeks (14 animals, 28 knees) and monkey knees at eight weeks (seven animals, 14 knees) following surgery. Staining for six of the antibodies did not differ between repair cartilage and normal articular cartilage, but an antibody that recognizes atypical glycosaminoglycan structures in developing tissues (MAb 7D4) consistently distinguished repair cartilage from normal cartilage in rabbits and monkeys. Repair tissue consisting of hyaline toluidine blue-staining matrix containing chondrocytic cells uniformly showed strong 7D4 staining. In contrast, normal articular cartilage and fibrous repair tissue showed inconsistent weak 7D4 staining. At eight weeks following surgery, rabbit cartilage repair tissue stained more intensely for 7D4 than monkey cartilage repair tissue; in rabbits, cartilage repair tissue stained more intensely for 7D4 at eight weeks than at 36 weeks following surgery. Repair tissue staining for 7D4 did not differ between osteochondral defects treated with passive motion and those treated with immobilization in rabbits and monkeys. These results indicate that expression of a high level of proteoglycan epitope 7D4 distinguishes hyaline articular cartilage repair tissue from normal articular cartilage and fibrous cartilage repair tissue in the early stages of osteochondral healing, and that as hyaline articular cartilage repair tissue matures expression of 7D4 decreases. The ability to characterize repair cartilage proteoglycans with monoclonal antibodies may aid in the evaluation of the quality and maturity of cartilage repair tissue and thereby facilitate improvements in procedures for resurfacing joints.

摘要

为了确定特定蛋白聚糖表位的表达是否能区分关节软骨修复组织与正常关节软骨,我们使用了七种单克隆抗体来检测27只新西兰白兔和七只食蟹猴股骨内侧髁直径3.2毫米、深4.0毫米的骨软骨缺损处的正常关节软骨和软骨修复组织。在制造骨软骨缺损后,每只动物的一个肢体进行石膏固定治疗,而另一个肢体进行被动活动治疗,持续两周。在术后八周(13只动物,26个膝关节)和36周(14只动物,28个膝关节)检查兔膝关节,在术后八周(7只动物,14个膝关节)检查猴膝关节。六种抗体的染色在修复软骨和正常关节软骨之间没有差异,但一种识别发育组织中不典型糖胺聚糖结构的抗体(单克隆抗体7D4)在兔和猴中始终能区分修复软骨与正常软骨。由含软骨细胞的透明甲苯胺蓝染色基质组成的修复组织均匀显示强烈的7D4染色。相比之下,正常关节软骨和纤维性修复组织显示出不一致的弱阳性7D4染色。术后八周,兔软骨修复组织的7D4染色比猴软骨修复组织更强烈;在兔中,软骨修复组织在术后八周的7D4染色比术后36周更强烈。在兔和猴中,被动活动治疗的骨软骨缺损与固定治疗的骨软骨缺损的7D4修复组织染色没有差异。这些结果表明,高水平的蛋白聚糖表位7D4的表达在骨软骨愈合早期可区分透明关节软骨修复组织与正常关节软骨及纤维软骨修复组织,并且随着透明关节软骨修复组织成熟,7D4的表达降低。用单克隆抗体表征修复软骨蛋白聚糖的能力可能有助于评估软骨修复组织的质量和成熟度,从而促进关节表面置换手术的改进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4111/2378177/48acc59eea43/iowaorthj00001-0037-a.jpg

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