Unglaub Frank, Wolf Maya Barbara, Thome Martin Andreas, Germann Guenter, Sauerbier Michael, Reiter Andreas
Department of Hand, Plastic and Reconstructive Surgery, Burn Center, BG Trauma Center Ludwigshafen, Plastic and Hand Surgery of the University of Heidelberg, Ludwigshafen, Germany.
Arthroscopy. 2008 Mar;24(3):299-304. doi: 10.1016/j.arthro.2007.09.006. Epub 2007 Nov 9.
The purpose of this study was to investigate apoptosis in degenerative disc lesions (Palmer type IIC) and differentiate between patients with ulna-plus and ulna-neutral variance.
Seventeen patients with degenerative tears (Palmer type IIC) in the articular disc of the triangular fibrocartilage were included in this study. The triangular fibrocartilage was debrided arthroscopically with a punch and the histologic sections were used to analyze necrosis and apoptosis. Apoptosis and necrosis was quantified by terminal deoxyribonucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL) assay. Apoptotic cells were visualized by poly(ADP-ribose) polymerase (PARP) p85 immunohistochemistry. The number of apoptotic and necrotic cells was then correlated with ulnar length.
PARP- and TUNEL-positive cells were found in each patient. In addition, patients with an ulna plus variance showed a significantly increased number of apoptotic cells in comparison to patients with an ulna neutral variance. The distribution of the apoptosis-positive cells did not show any accumulation in the inner part of the specimen, but were evenly distributed.
This study showed that patients with ulna plus present with significantly higher numbers of apoptotic cells in degenerative lesions in comparison to patients with ulna neutral. The apoptotic cells were evenly distributed throughout the entire specimen.
The results of this study revealed that increased length of the ulna is related to increased cell death. Therefore, techniques that decrease the ulna variance would appear to be appropriate and would improve the clinical situation by preventing further cell death.
本研究旨在调查退变椎间盘病变(帕尔默II C型)中的细胞凋亡情况,并区分尺骨正向变异和尺骨中立变异的患者。
本研究纳入了17例三角纤维软骨关节盘退变撕裂(帕尔默II C型)的患者。通过关节镜用咬骨钳清理三角纤维软骨,并使用组织学切片分析坏死和细胞凋亡情况。通过末端脱氧核苷酸转移酶(TdT)介导的dUTP缺口末端标记(TUNEL)法对细胞凋亡和坏死进行定量分析。通过聚(ADP - 核糖)聚合酶(PARP)p85免疫组织化学观察凋亡细胞。然后将凋亡和坏死细胞的数量与尺骨长度进行关联分析。
在每位患者中均发现了PARP和TUNEL阳性细胞。此外,与尺骨中立变异的患者相比,尺骨正向变异的患者凋亡细胞数量显著增加。凋亡阳性细胞的分布在标本内部未显示出任何聚集,而是均匀分布。
本研究表明,与尺骨中立的患者相比,尺骨正向的患者在退变病变中凋亡细胞数量显著更高。凋亡细胞在整个标本中均匀分布。
本研究结果显示,尺骨长度增加与细胞死亡增加有关。因此,减少尺骨变异的技术似乎是合适的,并且通过防止进一步的细胞死亡可以改善临床状况。