Yao Chenglun, Zhou Xijie, Weng Weidong, Poonit Keshav, Sun Chao, Yan Hede
Department of Orthopedics (Division of Plastic and Hand Surgery), The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325027, P.R. China.
Exp Ther Med. 2021 Dec;22(6):1414. doi: 10.3892/etm.2021.10850. Epub 2021 Oct 8.
Transforming growth factor-beta 1 (TGF-β1) is a powerful activator of connective tissue synthesis that is strongly associated with the pathophysiology of traumatic neuroma. Previous studies have demonstrated that aligned nanofiber conduits made from silk fibroin and poly (L-lactic acid-co-ε-caprolactone; PLCL) could prevent traumatic neuromas. In the present study, the possible mechanisms of conduits in treating traumatic neuromas were investigated to provide theoretical basis for procedures. Aligned nanofiber conduits were used for nerve capping. Sciatic nerves of Sprague-Dawley rats were used to create an animal model. The present study contains two parts, each including four experimental groups. SB-431542/SRI-011381 hydrochloride was used to suppress/enhance TGF-β1/SMAD signaling. Part I discussed the connections between traumatic neuroma and the proliferation of alpha smooth muscle actin (α-SMA) and collagen; it also investigated the therapeutic effect of conduits. Part II hypothesized that conduits suppressed TGF-β1/SMAD signaling. Histological characteristics, quantitative analysis of α-SMA, collagens and signaling-related parameters were assessed and compared among groups one month postoperatively. Results from Part I demonstrated that aligned nanofiber conduits suppressed the expression of α-SMA and collagens; and results from Part II revealed the downregulation of pathway-related proteins, suggesting that the suppression was mediated by TGF-β1/SMAD signaling. Aligned nanofiber conduits may be effective nerve capping biomaterials. One of the mechanisms involves suppressing TGF-β1/SMAD signaling. Novel treatments using aligned nanofiber conduits could be developed to manage traumatic neuromas.
转化生长因子-β1(TGF-β1)是结缔组织合成的强大激活剂,与创伤性神经瘤的病理生理学密切相关。先前的研究表明,由丝素蛋白和聚(L-乳酸-共-ε-己内酯;PLCL)制成的排列纳米纤维导管可以预防创伤性神经瘤。在本研究中,研究了导管治疗创伤性神经瘤的可能机制,为手术提供理论依据。使用排列纳米纤维导管进行神经封端。采用Sprague-Dawley大鼠坐骨神经建立动物模型。本研究分为两部分,每部分包括四个实验组。使用SB-431542/盐酸SRI-011381抑制/增强TGF-β1/SMAD信号通路。第一部分讨论了创伤性神经瘤与α平滑肌肌动蛋白(α-SMA)和胶原蛋白增殖之间的联系;还研究了导管的治疗效果。第二部分假设导管抑制TGF-β1/SMAD信号通路。术后1个月对各组的组织学特征、α-SMA、胶原蛋白和信号相关参数进行评估和比较。第一部分结果表明,排列纳米纤维导管抑制α-SMA和胶原蛋白的表达;第二部分结果显示通路相关蛋白下调,提示这种抑制作用是由TGF-β1/SMAD信号通路介导的。排列纳米纤维导管可能是有效的神经封端生物材料。其中一个机制涉及抑制TGF-β1/SMAD信号通路。可以开发使用排列纳米纤维导管的新疗法来治疗创伤性神经瘤。