Wang Wen, Qin Shengnan, He Peiliang, Mao Wei, Chen Liang, Hua Xing, Zhang Jinli, Xiong Xifeng, Liu Zhihe, Wang Pengzhen, Meng Qingqi, Dong Fei, Li Aiguo, Chen Honghui, Xu Jiake
Department of Orthopedics, Guangzhou Institute of Traumatic Surgery, Guangzhou Red Cross Hospital, Medical College, Jinan University, Guangzhou, China.
Department of Clinical Medicine, Guizhou Medical University, Guiyang, China.
Front Cell Dev Biol. 2021 Jul 16;9:682719. doi: 10.3389/fcell.2021.682719. eCollection 2021.
Fibrocartilage transition zone (FC) is difficult to regenerate after surgical re-attachment of tendon to bone. Here, we investigated whether type II collagen-sponges (CII-sponges) facilitated tendon stem/progenitor cells (TSPCs) to adopt chondrogenic phenotypes and further observed if this material could increase the FC areas in bone-tendon junction (BTJ) injury model.
CII-sponges were made as we previously described. The appearance and pore structure of CII-sponges were photographed by camera and microscopies. The viability, proliferation, and differentiation of TSPCs were examined by LIVE/DEAD assay, alamarBlue, and PKH67 tracking. Subsequently, TSPCs were seeded in CII-sponges, Matrigel or monolayer, and induced under chondrogenic medium for 7 or 14 days before being harvested for qPCR or being transplanted into nude mice to examine the chondrogenesis of TSPCs. Lastly, partial patellectomy (PP) was applied to establish the BTJ injury model. CII-sponges were interposed between the patellar fragment and tendon, and histological examination was used to assess the FC regeneration at BTJ after surgery at 8 weeks.
CII-sponges were like sponges with interconnected pores. TSPCs could adhere, proliferate, and differentiate in this CII-sponge up to 14 days at least. Both qPCR and immunostaining data showed that compared with TSPCs cultured in monolayer or Matrigel, cells in CII-sponges group adopted more chondrogenic phenotypes with an overall increase of chondrocyte-related genes and proteins. Furthermore, in PP injured model, much more new formed cartilage-like tissues could be observed in CII-sponges group, evidenced by a large amount of positive proteoglycan expression and typical oval or round chondrocytes in this area.
Our study showed that CII-sponges facilitated the TSPCs to differentiate toward chondrocytes and increased the area of FCs, which suggests that CII-sponges are meaningful for the reconstruction of FC at bone tendon junction. However, the link between the two phenomena requires further research and validation.
在肌腱与骨手术重新附着后,纤维软骨过渡区(FC)难以再生。在此,我们研究了II型胶原海绵(CII海绵)是否促进肌腱干/祖细胞(TSPCs)呈现软骨生成表型,并进一步观察该材料是否能增加骨 - 肌腱结合处(BTJ)损伤模型中的FC面积。
按照我们之前描述的方法制备CII海绵。用相机和显微镜拍摄CII海绵的外观和孔隙结构。通过活/死检测、alamarBlue和PKH67追踪来检测TSPCs的活力、增殖和分化。随后,将TSPCs接种到CII海绵、基质胶或单层培养中,并在软骨生成培养基中诱导7或14天,然后收获用于qPCR或移植到裸鼠中以检查TSPCs的软骨生成情况。最后,采用部分髌骨切除术(PP)建立BTJ损伤模型。将CII海绵置于髌骨碎片和肌腱之间,并在术后8周通过组织学检查评估BTJ处FC的再生情况。
CII海绵呈具有相互连通孔隙的海绵状。TSPCs至少在该CII海绵中可附着、增殖并分化达14天。qPCR和免疫染色数据均显示,与单层培养或在基质胶中培养的TSPCs相比,CII海绵组的细胞呈现更多软骨生成表型,软骨细胞相关基因和蛋白总体增加。此外,在PP损伤模型中,CII海绵组可观察到更多新形成的软骨样组织,该区域大量蛋白聚糖阳性表达以及典型的椭圆形或圆形软骨细胞可作为证据。
我们的研究表明,CII海绵促进TSPCs向软骨细胞分化并增加FC面积,这表明CII海绵对于骨 - 肌腱结合处FC的重建具有意义。然而,这两种现象之间的联系需要进一步研究和验证。