Chondrocyte apoptosis in the regenerated articular cartilage after allogenic chondrocyte transplantation in the rabbit knee

被引:7
作者
Lee, J. H.
Prakash, K. V. B.
Pengatteeri, Y. H.
Park, S. E.
Koh, H. S.
Han, C. W.
机构
[1] Dept Orthoped Surg, Seoul 134060, South Korea
[2] Histostem Res Ctr, Seoul, South Korea
来源
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME | 2007年 / 89B卷 / 07期
关键词
GROWTH-PLATE; DEFECTS; DEATH; CHONDROGENESIS; OSTEOARTHRITIS; CASPASE-3; REPAIR; MODEL; BCL-2; DNA;
D O I
10.1302/0301-620X.89B7.18983
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
We attempted to repair full-thickness defects in the articular cartilage of the trochlear groove of the femur in 30 rabbit knee joints using allogenic cultured chondrocytes embedded in a collagen gel. The repaired tissues were examined at 2, 4, 8, 12 and 24 weeks after operation using histological and histochemical methods. The articular defect filling index measurement was derived from safranin-O stained sections. Apoptotic cellular fractions were derived from analysis of apoptosis in situ using TUNEL staining, and was confirmed using caspase-3 staining along with quantification of the total cellularity. The mean articular defect filling index decreased with time. After 24 weeks it was 0.7 (SD 0.10), which was significantly lower than the measurements obtained earlier (p < 0.01). The highest mean percentage of apoptotic cells were observed at 12 weeks, although the total cellularity decreased with time. Because apoptotic cell death may play a role in delamination after chondrocyte transplantation, anti-apoptotic gene therapy may protect transplanted chondrocytes from apoptosis.
引用
收藏
页码:977 / 983
页数:7
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