Han Soo-Hong, Kim Hyung Kyung, Ahn Jong-Ho, Lee Dong Hyeon, Baek Minjung, Ye Geunhee, Lee Joong-Myung, Min Kyunghoon, Oh Chihoon, Lee Soonchul
Department of Orthopaedic Surgery, CHA Bundang Medical Center, CHA University School of Medicine.
Department of Pathology, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine.
J Vis Exp. 2018 Jun 9(136):57634. doi: 10.3791/57634.
Tendinopathy, a painful condition that develops in response to tendon degeneration, is on the rise in the developed world due to increasing physical activity and longer life expectancy. Despite its increasing prevalence, the underlying pathogenesis still remains unclear, and treatment is generally symptomatic. Recently, numerous therapeutic options, including growth factors, stem cells, and gene therapy, were investigated in hopes of enhancing the healing potency of the degenerative tendon. However, the majority of these research studies were conducted only on animal models or healthy human tenocytes. Despite some studies using pathological tenocytes, to the best of our knowledge there is currently no protocol describing how to obtain human degenerative tenocytes. The aim of this study is to describe a standard protocol for acquiring human degenerative tenocytes. Initially, the tendon tissue was harvested from a patient with lateral epicondylitis during surgery. Then biopsy samples were taken from the extensor carpi radialis brevis tendon corresponding to structural changes observed at the time of surgery. All of the harvested tendons appeared to be dull, gray, friable, and edematous, which made them visually distinct from the healthy ones. Tenocytes were cultured and used for experiments. Meanwhile, half of the harvested tissues were analyzed histologically, and it was shown that they shared the same key features of tendinopathy (angiofibroblastic dysplasia or hyperplasia). A secondary analysis by immunocytochemistry confirmed that the cultured cells were tenocytes with the majority of the cells having positive stains for mohawk and tenomodulin proteins. The qualities of the degenerative nature of tenocytes were then determined by comparing the cells with the healthy control using a proliferation assay or qRT-PCR. The degenerative tenocyte displayed a higher proliferation rate and similar gene expression patterns of tendinopathy that matched previous reports. Overall, this new protocol might provide a useful tool for future studies of tendinopathy.
肌腱病是一种因肌腱退变而引发的疼痛病症,在发达国家,由于体育活动增加和预期寿命延长,其发病率呈上升趋势。尽管其患病率不断上升,但其潜在发病机制仍不清楚,治疗通常只是对症治疗。最近,人们研究了多种治疗方法,包括生长因子、干细胞和基因治疗,以期提高退变肌腱的愈合能力。然而,这些研究大多仅在动物模型或健康人肌腱细胞上进行。尽管有一些研究使用了病理肌腱细胞,但据我们所知,目前尚无关于如何获取人退变肌腱细胞的方案。本研究的目的是描述一种获取人退变肌腱细胞的标准方案。最初,在手术过程中从一名患有外侧上髁炎的患者身上采集肌腱组织。然后从桡侧腕短伸肌腱取活检样本,对应手术时观察到的结构变化。所有采集的肌腱看起来都暗淡、呈灰色、易碎且水肿,在视觉上与健康肌腱明显不同。对肌腱细胞进行培养并用于实验。与此同时,对采集的一半组织进行组织学分析,结果表明它们具有肌腱病的相同关键特征(血管纤维母细胞发育异常或增生)。通过免疫细胞化学进行的二次分析证实,培养的细胞是肌腱细胞,大多数细胞对莫霍克蛋白和肌腱调节蛋白呈阳性染色。然后通过增殖试验或qRT-PCR将这些细胞与健康对照进行比较,确定肌腱细胞退变的性质。退变的肌腱细胞显示出更高的增殖率和与先前报道相符的肌腱病相似基因表达模式。总体而言,这一新方案可能为未来肌腱病的研究提供一个有用的工具。