Jiang Jian, Jang Kwi-Hoon, Ahn Sung Yong, Jo Chris Hyunchul
Department of Translational Medicine, Seoul National University College of Medicine, Seoul, Korea.
Department of Orthopedic Surgery, SMG-SNU Boramae Medical Center, Seoul National University College of Medicine, Seoul, Korea.
Clin Orthop Surg. 2025 Feb;17(1):138-147. doi: 10.4055/cios24125. Epub 2024 Dec 9.
This study aimed to investigate changes in gene expression related to matrix synthesis in individuals with full-thickness rotator cuff tears (RCTs) and normal tendon tissues. The study also aimed to examine the differences in gene expression according to 4 distinct tear sizes.
A total of 12 patients with full-thickness RCTs were included in the study, all of whom underwent arthroscopic rotator cuff repair. The RCTs were stratified by size into small, medium, large, and massive. Tendon samples were harvested from the midpoint between the lateral end of the torn tendon and the musculotendinous junction. Subsequent analysis of the tissue samples revealed the mRNA expression levels of 11 collagen types, 6 proteoglycans, and 8 glycoproteins through real-time polymerase chain reaction techniques. For control purposes, supraspinatus tendon tissue was sourced from 3 patients who had proximal humerus fractures but did not present with RCTs.
Among the 11 collagens and 14 non-collagenous protein (NCP) genes examined in this study, and showed a significant increase, whereas and showed a tendency to decrease compared to those in the normal group. significantly increased by 8.92-fold ( < 0.001) compared to that in the normal group, whereas and showed a tendency to decrease. and increased significantly by 3.47-fold ( = 0.003) and 5.38-fold ( = 0.005), respectively, and the genes , , and were all significantly reduced compared to those in the normal group. In the NCPs, almost all the genes with increased expression levels had the highest level in small size RCTs, and gene expression decreased as the size increased. The 3 proteoglycans (, , and ) showed the highest levels of expression in small size RCTs compared to those in the normal group, and 5 glycoproteins (, , , , and ) also showed the highest expression in small size RCTs.
We confirmed that most of the detected extracellular matrix gene expression changes were related to the size of the full-thickness RCTs. In NCPs, gene expression was increased in small-size tears, and gene expression levels were significantly reduced when the size increased.
本研究旨在调查全层肩袖撕裂(RCT)患者和正常肌腱组织中与基质合成相关的基因表达变化。该研究还旨在根据4种不同的撕裂大小检查基因表达的差异。
本研究共纳入12例全层RCT患者,所有患者均接受关节镜下肩袖修复。RCT按大小分为小、中、大、巨大。从撕裂肌腱外侧端与肌-腱交界处的中点采集肌腱样本。随后通过实时聚合酶链反应技术对组织样本进行分析,揭示11种胶原蛋白、6种蛋白聚糖和8种糖蛋白的mRNA表达水平。为作对照,取自3例肱骨近端骨折但无RCT的患者的冈上肌腱组织。
在本研究检测的11种胶原蛋白和14种非胶原蛋白(NCP)基因中,[具体基因1]和[具体基因2]显示显著增加,而[具体基因3]和[具体基因4]与正常组相比呈下降趋势。[具体基因5]与正常组相比显著增加8.92倍(P<0.001),而[具体基因6]和[具体基因7]呈下降趋势。[具体基因8]和[具体基因9]分别显著增加3.47倍(P = 0.003)和5.38倍(P = 0.005),并且[具体基因10]、[具体基因11]和[具体基因12]与正常组相比均显著降低。在NCP中,几乎所有表达水平增加的基因在小尺寸RCT中水平最高,且基因表达随尺寸增加而降低。3种蛋白聚糖([具体蛋白聚糖1]、[具体蛋白聚糖2]和[具体蛋白聚糖3])与正常组相比在小尺寸RCT中显示最高表达水平,5种糖蛋白([具体糖蛋白1]、[具体糖蛋白2]、[具体糖蛋白3]、[具体糖蛋白4]和[具体糖蛋白5])在小尺寸RCT中也显示最高表达。
我们证实,大多数检测到的细胞外基质基因表达变化与全层RCT的大小有关。在NCP中,小尺寸撕裂中基因表达增加,尺寸增加时基因表达水平显著降低。