Complex Structure of Surgical Sciences and Technologies, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Applied and Translational Research Center, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Cartilage. 2021 Dec;13(2_suppl):225S-237S. doi: 10.1177/1947603521993217. Epub 2021 Feb 15.
Osteoarthritis (OA) is an inflammatory and degenerative disease, and the numerous treatments currently used are not fully effective. Mesenchymal stem cells (MSCs) and platelet-rich plasma (PRP) are proposed for OA treatment as biologic therapies. The aim of the study was to observe the role of autologous protein solution (APS), a type of PRP, on chondrogenic differentiation of 2 types of MSCs, from bone marrow (BMSCs) and adipose tissue (ADSCs), in an osteoarthritic microenvironment.
Inflammatory culture conditions, mimicking OA, were obtained by adding interleukin-1β (IL-1β) and tumor necrosis factor α (TNFα), or synovial fluid from patient osteoarthritic knees (OSF), to the culture medium. MSCs were then treated with APS.
After 1 month of culture, both cell types formed mature micromasses, partially altered in the presence of IL-1β and TNFα but quite preserved with OSF. Inflammatory conditions hindered differentiation in terms of gene expression, not counterbalanced by APS. APS triggered type I collagen deposition and above all contributed to decrease the expression of metalloproteinases in the most aggressive conditions (IL-1β and TNFα in the culture medium). ADSCs originated micromasses more mature and less prone toward osteogenic lineage than BMSCs, thus showing to better adapt in an aggressive environment than BMSC.
APS seems to act better on inflammation front and, between cell types, ADSCs respond better to the inflammatory microenvironment of OA and to the treatment with APS than BMSCs.
骨关节炎(OA)是一种炎症性和退行性疾病,目前使用的许多治疗方法并不完全有效。间充质干细胞(MSCs)和富含血小板的血浆(PRP)被提议作为生物疗法用于 OA 治疗。本研究的目的是观察自体蛋白溶液(APS)在 OA 微环境中对骨髓(BMSCs)和脂肪组织(ADSCs)来源的 2 种 MSC 向软骨分化的作用。
通过向培养基中添加白细胞介素 1β(IL-1β)和肿瘤坏死因子 α(TNFα)或来自患者 OA 膝关节的滑液(OSF),模拟 OA 获得炎症培养条件。然后用 APS 处理 MSC。
在培养 1 个月后,两种细胞类型均形成成熟的微团,在存在 IL-1β和 TNFα的情况下部分改变,但在 OSF 中相当保留。炎症条件在基因表达方面阻碍了分化,APS 没有起到平衡作用。APS 触发 I 型胶原沉积,尤其是在最具侵袭性的条件下(培养基中的 IL-1β和 TNFα),有助于降低金属蛋白酶的表达。与 BMSCs 相比,ADSCs 来源的微团更成熟,向成骨谱系分化的倾向更小,因此在侵袭性环境中比 BMSCs 更能适应。
APS 似乎在炎症方面表现更好,并且在细胞类型之间,ADSCs 对 OA 的炎症微环境和 APS 的治疗反应比 BMSCs 更好。