Department of Orthopedic Surgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Am J Sports Med. 2018 Aug;46(10):2478-2485. doi: 10.1177/0363546518782975. Epub 2018 Jul 5.
Conversion to full-thickness tear in partial-thickness rotator cuff tears (PTRCTs) is based on the quality and thickness of the normal-looking untorn rotator cuff layer. However, whether the untorn tendon is a healthy tissue remains to be elucidated.
To compare the apoptotic gene expression of the untorn articular layer with the torn bursal layer in PTRCTs.
Controlled laboratory study.
Tendon tissues were harvested from 20 patients undergoing arthroscopic surgery for partial-thickness rotator cuff repair. As a control group, the tissues were harvested during intramedullary nail fixation in 10 proximal humeral fractures. In the experimental group, the samples were harvested from 2 sites: the torn bursal-sided tendon and the untorn articular-sided tendon. Hematoxylin and eosin (H&E) staining was conducted for basic histological evaluation, and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining was used to detect apoptosis of tissue cells. The expression of caspase 3, 8, and 9 was confirmed immunohistochemically. Western blot analysis was used to assay the caspase activities.
In H&E staining, the direction of collagen bundles in untorn tendon was disoriented when compared with those of control tendon. However, the shape of the nuclei was not different, although the nuclei of the untorn tendon showed apoptosis in the TUNEL staining similar to those of the torn tendon. The immunohistochemical staining of caspase 3, 8, and 9 was increased concomitantly in untorn and torn tendons. All of the caspase activities in the untorn articular layer and torn bursal layer were significantly higher than in controls ( P < .05). However, no significant differences were found between the two layers ( P > .05).
The study demonstrates that apoptotic gene expression is increased not only in the torn bursal layer but also in the untorn articular layer of PTRCTs.
The untorn articular layer of PTRCTs is abnormal, which triggers postoperative pain and further rotator cuff tears. Therefore, treatment of the abnormal untorn articular layer is essential in bursal-sided PTRCTs.
部分厚度肩袖撕裂(PTRCT)向全厚度撕裂的转变取决于外观正常未撕裂的肩袖层的质量和厚度。然而,未撕裂的肌腱是否为健康组织仍有待阐明。
比较 PTRCT 中未撕裂的关节层与撕裂的滑囊层的凋亡基因表达。
对照实验室研究。
从 20 名接受关节镜下肩袖部分修复术的患者中采集肌腱组织。作为对照组,在 10 例肱骨干骨折的髓内钉固定过程中采集组织。在实验组中,从撕裂的滑囊侧肌腱和未撕裂的关节侧肌腱的 2 个部位采集样本。进行苏木精和伊红(H&E)染色进行基本组织学评估,并进行末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记(TUNEL)染色以检测组织细胞凋亡。免疫组织化学法检测 caspase 3、8 和 9 的表达。采用 Western blot 分析测定半胱氨酸天冬氨酸蛋白酶活性。
在 H&E 染色中,与对照组相比,未撕裂肌腱的胶原束方向紊乱。然而,尽管未撕裂肌腱的细胞核在 TUNEL 染色中显示出与撕裂肌腱相似的凋亡,但细胞核的形状没有不同。未撕裂和撕裂肌腱的 caspase 3、8 和 9 的免疫组织化学染色均增加。未撕裂的关节层和撕裂的滑囊层中的所有半胱氨酸天冬氨酸蛋白酶活性均明显高于对照组(P <.05)。然而,两层之间没有发现显著差异(P >.05)。
该研究表明,不仅在撕裂的滑囊层,而且在 PTRCT 的未撕裂的关节层中,凋亡基因表达增加。
PTRCT 的未撕裂关节层异常,这会引发术后疼痛和进一步的肩袖撕裂。因此,在滑囊侧 PTRCT 中,治疗异常的未撕裂关节层至关重要。