Xiang Yang, Li Xin, Huang Yuye, Gao Suyue, Wei Peng, Wu Lijun, Dong Jun
Department of Neurosurgery, The Second Affiliated Hospital of Soochow University, Soochow, China.
Department of Plastic Surgery, The First Affiliated Hospital of Ningbo University, Ningbo, China.
Regen Ther. 2024 Aug 30;26:671-682. doi: 10.1016/j.reth.2024.08.018. eCollection 2024 Jun.
Peripheral nerve injury is a prevalent disease but the spontaneous recovery of nerve function is protracted and incomplete. Given the damaging of stem cells and fragile of intra-neural structures in the course of stem cell transplantation, our study tried to investigate whether encapsulating adipose derived mesenchymal stem cells (ADSCs) with GelMA could achieve better repair in peripheral nerve injury. PC-12 cells were cultured on the surface of GelMA encapsulating ADSCs and 3D co-culture system was constructed. CCK-8, Real-Time PCR, ELISA, Immunofluorescent Assay and Western Blot were used to evaluate the functionality of this system. Ultimately, nerve conduit containing the 3D co-culture system was linked between the two ends of an injured nerve. ADSCs encapsulated in 5% GeIMA had a better activity than 10% GeIMA. Furthermore, the viability of PC-12 cells was also better in this 3D co-culture system than in co-culture system with ADSCs without GeIMA. The expression of SIRT6 and PGC-1α in PC-12 cells were prominently promoted, and the entry to nuclear of PGC-1α was more obvious in this 3D co-culture system. After silencing of SIRT6, the protein expression level of PGC-1α was inhibited, and the activity of PC-12 cells was significantly reduced, suggesting that ADSCs encapsulated in GelMA upregulated the expression of SIRT6 to induce the level of PGC-1α protein, thereby achieving an impact on the activity of PC-12 cells. , nerve conduit containing the 3D co-culture system significantly promoted the repair of damaged peripheral nerves. In conclusion, our study demonstrated that 5% GelMA enhanced ADSCs activity, thereby promoting the activity of nerve cells and repair of damaged peripheral nerves by SIRT6/PGC-1α pathway.
周围神经损伤是一种常见疾病,但神经功能的自发恢复过程漫长且不完全。鉴于干细胞移植过程中干细胞的损伤以及神经内结构的脆弱性,我们的研究试图探究用甲基丙烯酰化明胶(GelMA)包裹脂肪来源间充质干细胞(ADSCs)是否能在周围神经损伤中实现更好的修复。将PC-12细胞培养在包裹有ADSCs的GelMA表面,并构建三维共培养体系。采用CCK-8、实时荧光定量PCR、酶联免疫吸附测定、免疫荧光分析和蛋白质免疫印迹法来评估该体系的功能。最终,将含有三维共培养体系的神经导管连接在受损神经的两端。包裹在5% GelMA中的ADSCs比包裹在10% GelMA中的具有更好的活性。此外,在这种三维共培养体系中,PC-12细胞的活力也比在不含GelMA的ADSCs共培养体系中更好。PC-12细胞中SIRT6和PGC-1α的表达显著上调,并且在这种三维共培养体系中PGC-1α进入细胞核的情况更明显。在沉默SIRT6后,PGC-1α的蛋白表达水平受到抑制,PC-12细胞的活性显著降低,这表明包裹在GelMA中的ADSCs上调SIRT6的表达以诱导PGC-1α蛋白水平,从而对PC-12细胞的活性产生影响。含有三维共培养体系的神经导管显著促进了受损周围神经的修复。总之,我们的研究表明5% GelMA增强了ADSCs的活性,从而通过SIRT6/PGC-1α途径促进神经细胞的活性和受损周围神经的修复。