Citeroni Maria Rita, Mauro Annunziata, Ciardulli Maria Camilla, Di Mattia Miriam, El Khatib Mohammad, Russo Valentina, Turriani Maura, Santer Michael, Della Porta Giovanna, Maffulli Nicola, Forsyth Nicholas R, Barboni Barbara
Unit of Basic and Applied Biosciences, Faculty of Bioscience and Agro-Food and Environmental Technology, University of Teramo, Teramo, Italy.
Department of Medicine, Surgery and Dentistry, University of Salerno, Salerno, Italy.
Front Bioeng Biotechnol. 2021 Mar 11;9:649288. doi: 10.3389/fbioe.2021.649288. eCollection 2021.
Regenerative medicine has greatly progressed, but tendon regeneration mechanisms and robust tendon differentiation protocols remain to be elucidated. Recently, tendon explant co-culture (CO) has been proposed as an model to recapitulate the microenvironment driving tendon development and regeneration. Here, we explored standardized protocols for production and storage of bioactive tendon-derived secretomes with an evaluation of their teno-inductive effects on ovine amniotic epithelial cells (AECs). Teno-inductive soluble factors were released in culture-conditioned media (CM) only in response to active communication between tendon explants and stem cells (CM). Unsuccessful tenogenic differentiation in AECs was noted when exposed to CM collected from tendon explants (CM) only, whereas CM upregulated and transcripts, in AECs, alongside stimulation of the development of mature 3D tendon-like structures enriched in TNMD and COL I extracellular matrix proteins. Furthermore, although the tenogenic effect on AECs was partially inhibited by freezing CM, this effect could be recovered by application of an -like physiological oxygen (2% O) environment during AECs tenogenesis. Therefore, CM can be considered as a waste tissue product with the potential to be used for the development of regenerative bio-inspired devices to innovate tissue engineering application to tendon differentiation and healing.
再生医学已经取得了巨大进展,但肌腱再生机制和强大的肌腱分化方案仍有待阐明。最近,肌腱外植体共培养(CO)已被提议作为一种模型,以重现驱动肌腱发育和再生的微环境。在这里,我们探索了生物活性肌腱衍生分泌组的生产和储存的标准化方案,并评估了它们对绵羊羊膜上皮细胞(AECs)的腱诱导作用。腱诱导可溶性因子仅在肌腱外植体与干细胞(CM)之间的活跃通讯时才在条件培养基(CM)中释放。当仅暴露于从肌腱外植体收集的CM(CM)时,在AECs中未观察到成功的腱分化,而CM上调了AECs中的 和 转录本,同时刺激了富含TNMD和COL I细胞外基质蛋白的成熟3D肌腱样结构的发育。此外,尽管冷冻CM会部分抑制对AECs的腱诱导作用,但在AECs腱形成过程中应用类似生理氧气(2% O)的环境可以恢复这种作用。因此,CM可以被认为是一种废弃组织产物,有潜力用于开发再生生物启发装置,以创新组织工程在肌腱分化和愈合方面的应用。