Tuncel Mehmet, Halici Mehmet, Canoz Ozlem, Yildirim Turk Cemil, Oner Mithat, Ozturk Figen, Kabak Sevki
Orthopaedics and Traumatology Department, Medical Faculty, Erciyes University, Kayseri 38039, Turkey.
Knee. 2005 Apr;12(2):113-9. doi: 10.1016/j.knee.2004.04.003.
The purpose of this study was to investigate the effects of exogenous local Insulin like growth factor-I (IGF-I) on the repair of full-thickness articular cartilage defects in immature rabbits.
Thirty-six skeletally immature New Zealand rabbits between 6 and 8 weeks old were used. A single defect, 3.5-mm-wide by 4-mm-deep full-thickness articular cartilage defect in the medial femoral condyle, was created. The defect was either filled with a collagen sponge or with a collagen sponge impregnated with 5 mug of recombinant IGF-I. The animals were sacrificed at 4, 8 or 12 weeks, and the repair tissue was examined macroscopically and histologically. Repair tissue was also examined immunohistochemically for the presence of type-I collagen, type-II collagen and PCNA at all weeks.
Newly formed tissue in all of the defects in the IGF-I group had the gross, histological and histochemical appearance of a smooth, intact hyaline articular cartilage. The average total scores on the histological grading scale were significantly better (p<0.05) for the defects treated with recombinant IGF-I at all time points. Immunostaining with an antibody against type-II collagen showed the diffuse presence of the repair cartilage in the IGF-I treated defects. The control groups demonstrated minimum staining with type-II collagen antibody.
These findings suggest that repair of full-thickness immature cartilage defects can be enhanced by recombinant IGF-I.
本研究旨在探讨外源性局部胰岛素样生长因子-I(IGF-I)对未成熟兔全层关节软骨缺损修复的影响。
选用36只6至8周龄骨骼未成熟的新西兰兔。在内侧股骨髁制造一个单一缺损,为宽3.5毫米、深4毫米的全层关节软骨缺损。缺损处要么填充胶原海绵,要么填充浸渍有5微克重组IGF-I的胶原海绵。在4周、8周或12周处死动物,并对修复组织进行大体和组织学检查。在所有时间点,还对修复组织进行免疫组织化学检查,以检测I型胶原、II型胶原和增殖细胞核抗原(PCNA)的存在情况。
IGF-I组所有缺损处新形成的组织在大体、组织学和组织化学上均呈现出光滑、完整的透明关节软骨外观。在所有时间点,用重组IGF-I治疗的缺损在组织学分级量表上的平均总分明显更好(p<0.05)。用抗II型胶原抗体进行免疫染色显示,在IGF-I治疗的缺损处有弥漫性的修复软骨存在。对照组用II型胶原抗体染色最少。
这些发现表明重组IGF-I可增强未成熟全层软骨缺损的修复。