Penolazzi Letizia, Pozzobon Michela, Bergamin Leticia Scussel, D'Agostino Stefania, Francescato Riccardo, Bonaccorsi Gloria, De Bonis Pasquale, Cavallo Michele, Lambertini Elisabetta, Piva Roberta
Department of Biomedical and Specialty Surgical Sciences, University of Ferrara, Ferrara, Italy.
Stem Cells and Regenerative Medicine Lab, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, Padua, Italy.
Front Bioeng Biotechnol. 2020 Mar 27;8:262. doi: 10.3389/fbioe.2020.00262. eCollection 2020.
Regenerative therapies for intervertebral disc (IVD) injuries are currently a major challenge that is addressed in different ways by scientists working in this field. Extracellular matrix (ECM) deriving from decellularized non-autologous tissues has been established as a biomaterial with remarkable regenerative capacity and its potential as a therapeutic agent is rising. In the present study, we investigated the potential of decellularized Wharton's jelly matrix (DWJM) from human umbilical cord to act as an ECM-based scaffold for IVD cell culturing. An efficient detergent-enzymatic treatment (DET) was used to produce DWJM maintaining its native microarchitecture. Afterward, immunofluorescence, biochemical assays and electron microscopy analysis showed that DWJM was able to produce sizeable 3D cell aggregates, when combined with human mesenchymal stromal cells isolated from WJ (MSCs) and IVD cells. These latter cells are characterized by the loss of their chondrocyte-like phenotype since they have been isolated from degenerated IVD and expanded to further de-differentiate. While the effect exerted by DWJM on MSCs was essentially the induction of proliferation, conversely, on IVD cells the DWJM promoted cell differentiation toward a discogenic phenotype. Notably, for the first time, the ability of DWJM to improve the degenerated phenotype of human IVD cells was demonstrated, showing that the mere presence of the matrix maintained the viability of the cells, and positively affected the expression of critical regulators of IVD homeostasis, such as SOX2, SOX9, and TRPS1 transcription factors at specific culture time. Our data are in line with the hypothesis that the strengthening of cell properties in terms of viability and expression of specific proteins at precise times represents an important condition in the perspective of guiding the recovery of cellular functionality and triggering regenerative potential. Currently, there are no definitive surgical or pharmacological treatments for IVD degeneration (IDD) able to restore the disc structure and function. Therefore, the potential of DWJM to revert degenerated IVD cells could be exploited in the next future an ECM-based intradiscal injectable therapeutic.
椎间盘(IVD)损伤的再生疗法目前是一个重大挑战,该领域的科学家正在以不同方式应对这一挑战。源自脱细胞非自体组织的细胞外基质(ECM)已被确立为具有显著再生能力的生物材料,其作为治疗剂的潜力正在不断提升。在本研究中,我们研究了来自人脐带的脱细胞华通氏胶基质(DWJM)作为基于ECM的支架用于IVD细胞培养的潜力。采用高效的去污剂 - 酶处理(DET)来制备保持其天然微结构的DWJM。随后,免疫荧光、生化分析和电子显微镜分析表明,当DWJM与从华通氏胶分离的人间充质基质细胞(MSCs)和IVD细胞结合时,它能够产生相当大的三维细胞聚集体。这些IVD细胞由于是从退化的IVD中分离并扩增以进一步去分化,其软骨样表型已经丧失。虽然DWJM对MSCs的作用主要是诱导增殖,但相反,对IVD细胞而言,DWJM促进细胞向椎间盘源性表型分化。值得注意的是,首次证明了DWJM改善人IVD细胞退化表型的能力,表明基质的存在本身就能维持细胞的活力,并在特定培养时间对IVD稳态的关键调节因子如SOX2、SOX9和TRPS1转录因子的表达产生积极影响。我们的数据符合这样的假设,即从在特定时间增强细胞活力和特定蛋白质表达的角度来看,加强细胞特性是指导细胞功能恢复和触发再生潜力的重要条件。目前,对于能够恢复椎间盘结构和功能的IVD退变(IDD),尚无明确的手术或药物治疗方法。因此,DWJM恢复退变IVD细胞的潜力在未来可能被用于基于ECM的椎间盘内可注射治疗。