Institute of Pathology and Forensic Veterinary Medicine, Working Group Histology and Embryology, University of Veterinary Medicine Vienna, Vienna, Austria.
VetCORE, Facility for Research, University of Veterinary Medicine, Vienna, Austria.
J Gene Med. 2018 May;20(5):e3021. doi: 10.1002/jgm.3021. Epub 2018 Apr 22.
A combination of tissue engineering methods employing mesenchymal stem cells (MSCs) together with gene transfer takes advantage of innovative strategies and highlights a new approach for targeting osteoarthritis (OA) and other cartilage defects. Furthermore, the development of systems allowing tunable transgene expression as regulated by natural disease-induced substances is highly desirable.
Bone marrow-derived equine MSCs were transduced with a lentiviral vector expressing interleukin-1 receptor antagonist (IL-1Ra) gene under the control of an inducible nuclear factor-kappa B-responsive promoter and IL-1Ra production upon pro-inflammatory cytokine stimulation [tumor necrosis factor (TNF)α, interleukin (IL)-1β] was analysed. To assess the biological activity of the IL-1Ra protein that was produced and the therapeutic effect of IL-1Ra-expressing MSCs (MSC/IL-1Ra), cytokine-based two- and three-dimensional in vitro models of osteoarthritis using equine chondrocytes were established and quantitative real-time polymerase chain reaction (PCR) analysis was used to measure the gene expression of aggrecan, collagen IIA1, interleukin-1β, interleukin-6, interleukin-8, matrix metalloproteinase-1 and matrix metalloproteinase-13.
A dose-dependent increase in IL-1Ra expression was found in MSC/IL-1Ra cells upon TNFα administration, whereas stimulation using IL-1β did not lead to IL-1Ra production above the basal level observed in nonstimulated cells as a result of the existing feedback loop. Repeated cycles of induction allowed on/off modulation of transgene expression. In vitro analyses revealed that IL-1Ra protein present in the conditioned medium from MSC/IL-1Ra cells blocks OA onset in cytokine-treated equine chondrocytes and co-cultivation of MSC/IL-1Ra cells with osteoarthritic spheroids alleviates the severity of the osteoarthritic changes.
Thus, pro-inflammatory cytokine induced IL-1Ra protein expression from genetically modified MSCs might represent a promising strategy for osteoarthritis treatment.
将组织工程方法与基因转移相结合,利用间充质干细胞(MSCs),利用创新策略,突出了针对骨关节炎(OA)和其他软骨缺陷的新方法。此外,开发允许通过天然疾病诱导物质调节的可调节转基因表达的系统是非常可取的。
骨髓来源的马间充质干细胞被转导了一种慢病毒载体,该载体在诱导型核因子-kappa B 反应性启动子的控制下表达白细胞介素-1 受体拮抗剂(IL-1Ra)基因,并在促炎细胞因子刺激(肿瘤坏死因子(TNF)α,白细胞介素(IL)-1β)下分析 IL-1Ra 基因的表达。为了评估所产生的 IL-1Ra 蛋白的生物学活性和表达 IL-1Ra 的间充质干细胞(MSC/IL-1Ra)的治疗效果,建立了基于细胞因子的二维和三维体外马软骨细胞骨关节炎模型,并使用定量实时聚合酶链反应(PCR)分析来测量聚集蛋白聚糖,胶原 IIA1,白细胞介素-1β,白细胞介素-6,白细胞介素-8,基质金属蛋白酶-1 和基质金属蛋白酶-13 的基因表达。
在 TNFα 给药时,MSC/IL-1Ra 细胞中观察到 IL-1Ra 表达呈剂量依赖性增加,而用 IL-1β 刺激不会导致 IL-1Ra 产生高于非刺激细胞中存在的反馈环导致的基础水平。重复诱导循环允许对转基因表达进行开/关调节。体外分析表明,MSC/IL-1Ra 细胞条件培养基中存在的 IL-1Ra 蛋白可阻断细胞因子处理的马软骨细胞中 OA 的发生,并且与骨关节炎球体共培养 MSC/IL-1Ra 细胞可减轻骨关节炎变化的严重程度。
因此,从基因修饰的 MSC 中诱导产生的促炎细胞因子诱导的 IL-1Ra 蛋白表达可能代表一种有前途的骨关节炎治疗策略。