Hydrogen Promotes the Effectiveness of Bone Mesenchymal Stem Cell Transplantation in Rats with Spinal Cord Injury

被引:9
作者
Luo, Shengchang [1 ]
Wu, Jianxin [2 ]
Qiu, Yuanyuan [3 ]
Xiao, Bing [4 ]
Xi, Yanhai [4 ]
Yang, Chengwei [5 ]
Shi, Zhicai [2 ]
Wang, Weiheng [4 ]
机构
[1] First Peoples Hosp Huzhou, Dept Orthopaed, 158 Plaza Back Rd, Huzhou 313099, Zhejiang, Peoples R China
[2] Naval Med Univ, Affiliated Hosp 1, Dept Orthopaed, 168 Changhai Rd, Shanghai 200433, Peoples R China
[3] Shanghai Univ Sport, Sch Hosp, 399 Changhai Rd, Shanghai 200433, Peoples R China
[4] Naval Med Univ, Affiliated Hosp 2, Dept Orthopaed, 415 Fengyang Rd, Shanghai 200003, Peoples R China
[5] 940th Hosp Joint Logist Support Force Peoples Libe, Dept Spinal Surg, 333 South Binhe Rd, Lanzhou 730050, Gansu, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
MARROW STROMAL CELLS; RICH SALINE; MODEL; APOPTOSIS; IMPROVES; OUTCOMES; NEURONS; PROTEIN; MICE; GAS;
D O I
10.1155/2023/8227382
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Although bone mesenchymal stem cell (BMSC) transplantation has been applied to the treatment of spinal cord injury (SCI), the effect is unsatisfactory due to the specific microenvironment (inflammation and oxidative stress) in the SCI area, which leads to the low survival rate of transplanted cells. Thus, additional strategies are required to improve the efficacy of transplanted cells in the treatment of SCI. Hydrogen possesses antioxidant and anti-inflammatory properties. However, whether hydrogen can enhance the effect of BMSC transplantation in the treatment of SCI has not yet been reported. This study was aimed at investigating whether hydrogen promotes the therapeutic effect of BMSC transplantation in the treatment of SCI in rats. In vitro, BMSCs were cultured in a normal medium and a hydrogen-rich medium to study the effect of hydrogen on the proliferation and migration of BMSCs. BMSCs were treated with a serum-deprived medium (SDM), and the effects of hydrogen on the apoptosis of BMSCs were studied. In vivo, BMSCs were injected into the rat model of SCI. Hydrogen-rich saline (5 ml/kg) and saline (5 ml/kg) were given once a day via intraperitoneal injection. Neurological function was evaluated using the Basso, Beattie, and Bresnahan (BBB) and CatWalk gait analyses. Histopathological analysis, oxidative stress, inflammatory factors (TNF-alpha, IL-1 beta, and IL-6), and transplanted cell viability were detected at 3 and 28 days after SCI. Hydrogen can significantly enhance BMSC proliferation and migration and tolerance to SDM. Hydrogen and BMSC codelivery can significantly enhance neurological function recovery by improving the transplant cell survival rate and migration. Hydrogen can enhance the migration and proliferation capacity of BMSCs to repair SCI by reducing the inflammatory response and oxidative stress in the injured area. Hydrogen and BMSC codelivery is an effective method to improve BMSC transplantation in the treatment of SCI.
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收藏
页数:14
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