Department of Orthopedic Surgery, Honghui Hospital, College of Medicine, Xi'an Jiaotong University, Xi'an, 710049, People's Republic of China.
Institute of Orthopedic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, People's Republic of China.
Stem Cell Res Ther. 2020 Feb 21;11(1):77. doi: 10.1186/s13287-020-01606-w.
Induced pluripotent stem cells (iPSCs) exhibit limitless pluripotent plasticity and proliferation capability to provide an abundant cell source for tissue regenerative medicine. Thus, inducing iPSCs toward a specific differentiation direction is an important scientific question. Traditionally, iPSCs have been induced to chondrocytes with the help of some small molecules within 21-36 days. To speed up the differentiation of iPSCs, we supposed to utilize bioactive ceramics to assist chondrogenic-induction process.
In this study, we applied ionic products (3.12512.5 mg/mL) of the lithium-containing bioceramic (LiCaSiO, L2C4S4) and individual Li (5.7823.73 mg/L) in the direct chondrogenic differentiation of human iPSCs.
Compared to pure chondrogenic medium and extracts of tricalcium phosphate (TCP), the extracts of L2C4S4 at a certain concentration range (3.12512.5 mg/mL) significantly enhanced chondrogenic proteins Type II Collagen (COL II)/Aggrecan/ SRY-Box 9 (SOX9) synthesis and reduced hypertrophic protein type X collagen (COL X)/matrix metallopeptidase 13 (MMP13) production in iPSCs-derived chondrocytes within 14 days, suggesting that these newly generated chondrocytes exhibited favorable chondrocytes characteristics and maintained a low-hypertrophy state. Further studies demonstrated that the individual Li ions at the concentration range of 5.7823.73 mg/L also accelerated the chondrogenic differentiation of iPSCs, indicating that Li ions played a pivotal role in chondrogenic differentiation process.
These findings indicated that lithium-containing bioceramic with bioactive specific ionic components may be used for a promising platform for inducing iPSCs toward chondrogenic differentiation and cartilage regeneration.
诱导多能干细胞(iPSCs)表现出无限的多能可塑性和增殖能力,为组织再生医学提供了丰富的细胞来源。因此,将 iPSCs 诱导到特定的分化方向是一个重要的科学问题。传统上,iPSCs 在一些小分子的帮助下,需要 21-36 天才能被诱导为软骨细胞。为了加速 iPSCs 的分化,我们假设利用生物活性陶瓷来辅助软骨诱导过程。
在这项研究中,我们应用了含锂生物陶瓷(LiCaSiO,L2C4S4)的离子产物(3.125-12.5mg/mL)和单独的 Li(5.78-23.73mg/L),在人 iPSCs 的直接软骨分化中。
与纯软骨形成培养基和磷酸三钙(TCP)提取物相比,一定浓度范围内(3.125-12.5mg/mL)的 L2C4S4 提取物显著增强了 iPSCs 来源的软骨细胞中的软骨蛋白 II 型胶原(COL II)/聚集蛋白/性别决定区 Y 框 9(SOX9)的合成,并降低了肥大蛋白 X 型胶原(COL X)/基质金属蛋白酶 13(MMP13)的产生在 14 天内,表明这些新生成的软骨细胞表现出良好的软骨细胞特征,并保持低肥大状态。进一步的研究表明,浓度范围为 5.78-23.73mg/L 的单个 Li 离子也加速了 iPSCs 的软骨分化,表明 Li 离子在软骨分化过程中起着关键作用。
这些发现表明,含有生物活性特定离子成分的含锂生物陶瓷可能被用作诱导 iPSCs 向软骨分化和软骨再生的有前途的平台。