Huang Yuzhao, He Yuchen, Makarcyzk Meagan J, Lin Hang
Department of Orthopaedic Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.
Department of Orthopaedics, The Third Xiangya Hospital, Central South University, Changsha, China.
Front Bioeng Biotechnol. 2021 Apr 29;9:677576. doi: 10.3389/fbioe.2021.677576. eCollection 2021.
Autologous chondrocyte implantation (ACI) is a procedure used to treat articular cartilage injuries and prevent the onset of post-traumatic osteoarthritis. expansion of chondrocytes, a necessary step in ACI, results in the generation of senescent cells that adversely affect the quality and quantity of newly formed cartilage. Recently, a senolytic peptide, fork head box O transcription factor 4-D-Retro-Inverso (FOXO4-DRI), was reported to selectively kill the senescent fibroblasts. In this study, we hypothesized that FOXO4-DRI treatment could remove the senescent cells in the expanded chondrocytes, thus enhancing their potential in generating high-quality cartilage. To simulate the expansion for ACI, chondrocytes isolated from healthy donors were expanded to population doubling level (PDL) 9, representing chondrocytes ready for implantation. Cells at PDL3 were also used to serve as the minimally expanded control. Results showed that the treatment of FOXO4-DRI removed more than half of the cells in PDL9 but did not significantly affect the cell number of PDL3 chondrocytes. Compared to the untreated control, the senescence level in FOXO4-DRI treated PDL9 chondrocytes was significantly reduced. Based on the result from standard pellet culture, FOXO4-DRI pre-treatment did not enhance the chondrogenic potential of PDL9 chondrocytes. However, the cartilage tissue generated from FOXO4-DRI pretreated PDL9 cells displayed lower expression of senescence-relevant secretory factors than that from the untreated control group. Taken together, FOXO4-DRI is able to remove the senescent cells in PDL9 chondrocytes, but its utility in promoting cartilage formation from the expanded chondrocytes needs further investigation.
自体软骨细胞植入术(ACI)是一种用于治疗关节软骨损伤和预防创伤后骨关节炎发病的手术。软骨细胞的扩增是ACI中的一个必要步骤,这会导致衰老细胞的产生,而这些衰老细胞会对新形成软骨的质量和数量产生不利影响。最近,一种衰老细胞溶解肽,叉头框O转录因子4-D-反向-内翻肽(FOXO4-DRI),被报道可选择性杀死衰老的成纤维细胞。在本研究中,我们假设FOXO4-DRI治疗可以去除扩增软骨细胞中的衰老细胞,从而增强它们生成高质量软骨的潜力。为了模拟ACI的扩增过程,从健康供体分离的软骨细胞被扩增至群体倍增水平(PDL)9,代表准备植入的软骨细胞。PDL3的细胞也用作最小扩增对照。结果显示,FOXO4-DRI处理去除了PDL9中一半以上的细胞,但对PDL3软骨细胞的数量没有显著影响。与未处理的对照相比,FOXO4-DRI处理的PDL9软骨细胞中的衰老水平显著降低。基于标准微团培养的结果,FOXO4-DRI预处理并未增强PDL9软骨细胞的软骨生成潜力。然而,FOXO4-DRI预处理的PDL9细胞生成的软骨组织与未处理对照组相比,衰老相关分泌因子的表达较低。综上所述,FOXO4-DRI能够去除PDL9软骨细胞中的衰老细胞,但其在促进扩增软骨细胞形成软骨方面的效用仍需进一步研究。