Laboratory of Translational Medicine, Department of Medicine, Surgery and Dentistry, University of Salerno, Via S. Allende, 84081 Baronissi, Italy.
Hematology and Transplant Center, University Hospital "San Giovanni di Dio e Ruggi D'Aragona", 84131 Salerno, Italy.
Cells. 2022 Aug 16;11(16):2545. doi: 10.3390/cells11162545.
The aim of this study was to investigate the effect of triiodothyronine (T3) on tendon specific markers and cytokines expression of stem cells extracted from human tendons. Indeed, thyroid hormones have been reported to be protective factors, maintaining tendons' homeostasis, whereas tendinopathy is believed to be related to a failed healing response. Healthy and tendinopathic human tendons were harvested to isolate tendon stem/progenitor cells (TSPCs). TSPCs obtained from pathological samples showed gene expression and morphological modifications at baseline in comparison with cells harvested from healthy tissues. When cells were maintained in a medium supplemented with T3 (10 M), only pathological populations showed a significant upregulation of tenogenic markers (, , , ). Immunostaining revealed that healthy cells constantly released type I collagen, typical of tendon matrix, whereas pathological ones overexpressed and secreted type III collagen, typical of scarred and impaired tissue. Pathological cells also overexpressed pro- and anti-inflammatory cytokines, suggesting an impaired balance in the presence of T3, without STAT3 activation. Moreover, DKK-1 was significantly high in the culture medium of pathological cell cultures and was reversed by T3. This study opens perspectives on the complex biochemical alteration of cells from pathological tendons, which may lead to the chronic disease context with an impaired extracellular matrix.
本研究旨在探讨三碘甲状腺原氨酸(T3)对人肌腱来源干细胞中肌腱特异性标志物和细胞因子表达的影响。甲状腺激素被认为是一种保护因素,维持肌腱的内稳态,而腱病被认为与修复反应失败有关。本研究从健康和腱病的人肌腱中提取肌腱干细胞/祖细胞(TSPCs)。与从健康组织中提取的细胞相比,来自病理样本的 TSPCs 在基线时表现出基因表达和形态学改变。当细胞在添加 T3(10 μM)的培养基中培养时,只有病理群体表现出明显的腱形成标志物上调(、、、)。免疫染色显示健康细胞持续释放 I 型胶原,这是肌腱基质的典型特征,而病理细胞过度表达和分泌 III 型胶原,这是疤痕和受损组织的典型特征。病理细胞还过度表达促炎和抗炎细胞因子,表明在存在 T3 的情况下,STAT3 没有被激活,平衡被破坏。此外,DKK-1 在病理细胞培养物的培养基中显著升高,而 T3 可逆转其升高。这项研究为病理肌腱细胞的复杂生化改变开辟了新的研究视角,这些改变可能导致慢性疾病,伴有细胞外基质受损。