Anerillas Luis Oliveros, Wiberg Mikael, Kingham Paul J, Kelk Peyman
Department of Integrative Medical Biology, Umeå University, 901 87 Umeå, Sweden.
Department of Surgical & Perioperative Sciences, Section for Hand and Plastic Surgery, Umeå University, 901 87 Umeå, Sweden.
Regen Ther. 2023 Aug 11;24:298-310. doi: 10.1016/j.reth.2023.07.011. eCollection 2023 Dec.
The use of mesenchymal stem cells (MSCs) for the development of tissue-engineered constructs has advanced in recent years. However, future clinically approved products require following good manufacturing practice (GMP) guidelines. This includes using alternatives to xenogeneic-derived cell culture supplements to avoid rejection of the transplants. Consequently, human platelet lysate (PLT) has been adopted as an affordable and effective alternative to foetal bovine serum (FBS) in traditional 2D cultures. However, little is known about its effect in more advanced 3D culture systems.
We evaluated bone marrow MSCs (BMSCs) proliferation and CD marker expression in cells expanded in FBS or PLT-supplemented media. Differentiation capacity of the BMSCs expanded in the presence of the different supplements was evaluated in 3D type I collagen hydrogels. Furthermore, the effects of the supplements on the process of differentiation were analyzed by using qPCR and histological staining.
Cell proliferation was greater in PLT-supplemented media versus FBS. BMSCs expanded in PLT showed similar osteogenic differentiation capacity in 3D compared with FBS expanded cells. In contrast, when cells were 3D differentiated in PLT they showed lower osteogenesis versus the traditional FBS protocol. This was also the case for adipogenic differentiation, in which FBS supplementation was superior to PLT.
PLT is a superior alternative to FBS for the expansion of MSCs without compromising their subsequent differentiation capacity in 3D. However, differentiation in PLT is impaired. Thus, PLT can be used to reduce the time required to expand the necessary cell numbers for development of 3D tissue engineered MSC constructs.
近年来,间充质干细胞(MSCs)在组织工程构建体开发中的应用取得了进展。然而,未来临床批准的产品需要遵循良好生产规范(GMP)指南。这包括使用异源细胞培养补充剂的替代品以避免移植排斥。因此,人血小板裂解物(PLT)已被用作传统二维培养中胎牛血清(FBS)的一种经济有效的替代品。然而,其在更先进的三维培养系统中的作用却鲜为人知。
我们评估了在补充有FBS或PLT的培养基中扩增的细胞中骨髓间充质干细胞(BMSCs)的增殖和CD标志物表达。在三维I型胶原水凝胶中评估了在不同补充剂存在下扩增的BMSCs的分化能力。此外,通过qPCR和组织学染色分析了补充剂对分化过程的影响。
与FBS相比,补充PLT的培养基中细胞增殖更强。与FBS扩增的细胞相比,在PLT中扩增的BMSCs在三维环境中显示出相似的成骨分化能力。相反,当细胞在PLT中进行三维分化时,与传统的FBS方案相比,它们的成骨作用较低。脂肪生成分化也是如此,其中补充FBS优于PLT。
PLT是FBS的一种优质替代品,可用于扩增MSCs,且不影响其随后在三维环境中的分化能力。然而,在PLT中的分化会受到损害。因此,PLT可用于减少扩增用于开发三维组织工程化MSCs构建体所需细胞数量的时间。