{"title":"骨髓间充质干细胞联合骨转运改善大鼠骨缺损","authors":"Ting Qiu, Chenhuan Wu, Ying Cai","doi":"10.1166/jbt.2023.3242","DOIUrl":null,"url":null,"abstract":"This study assessed the mechanism of BMSC combined with bone transport in improving bone defect. Fifty rats were divided into five sets randomly including NC set, DEX set, BMSC set and BT set. There were ten rats in each set. The BMSC was isolated using whole bone marrow adherent method\n and then cultivated. The general condition of rats in each set was observed and morphological parameter, pathological change in bone defect tissue was detected along with analysis of the expression of MCP-1, p53, TNF-α and STAT1 in bone tissue. The primary BMSC was cultivated\n for seven days and the fusiform BMSC was enlarged and the quantity of binucleate or multinucleate cells was increased after passage. The bone defect model was prepared successfully when the degree of fusion reached 100%. The mental condition was good. DEX set showed significantly reduced TBV\n and increased TRS compared with NC set. However, TBV was increased and TRS was reduced in BMSC set, BT set and BMSC+BT set significantly compared with DEX set. MCP-1 mRNA level in DEX set was lower and increased in the treatment group. In addition, p53, TNF-α and STAT1 was increased\n in DEX set but reduced in BMSC set, BT set and BMSC+BT set. In conclusion, MCP-1 in rats’ bone defect tissue is upregulated and the p53/TNF-α/STAT1 signal activity is restrained by BMSC combined with bone transport so as to treat the bone defect.","PeriodicalId":15300,"journal":{"name":"Journal of Biomaterials and Tissue Engineering","volume":" ","pages":""},"PeriodicalIF":0.1000,"publicationDate":"2023-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bone Marrow Mesenchymal Stem Cells Combined with Bone Transport Improves Bone Defect in Rats\",\"authors\":\"Ting Qiu, Chenhuan Wu, Ying Cai\",\"doi\":\"10.1166/jbt.2023.3242\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study assessed the mechanism of BMSC combined with bone transport in improving bone defect. Fifty rats were divided into five sets randomly including NC set, DEX set, BMSC set and BT set. There were ten rats in each set. The BMSC was isolated using whole bone marrow adherent method\\n and then cultivated. The general condition of rats in each set was observed and morphological parameter, pathological change in bone defect tissue was detected along with analysis of the expression of MCP-1, p53, TNF-α and STAT1 in bone tissue. The primary BMSC was cultivated\\n for seven days and the fusiform BMSC was enlarged and the quantity of binucleate or multinucleate cells was increased after passage. The bone defect model was prepared successfully when the degree of fusion reached 100%. The mental condition was good. DEX set showed significantly reduced TBV\\n and increased TRS compared with NC set. However, TBV was increased and TRS was reduced in BMSC set, BT set and BMSC+BT set significantly compared with DEX set. MCP-1 mRNA level in DEX set was lower and increased in the treatment group. In addition, p53, TNF-α and STAT1 was increased\\n in DEX set but reduced in BMSC set, BT set and BMSC+BT set. In conclusion, MCP-1 in rats’ bone defect tissue is upregulated and the p53/TNF-α/STAT1 signal activity is restrained by BMSC combined with bone transport so as to treat the bone defect.\",\"PeriodicalId\":15300,\"journal\":{\"name\":\"Journal of Biomaterials and Tissue Engineering\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.1000,\"publicationDate\":\"2023-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Biomaterials and Tissue Engineering\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1166/jbt.2023.3242\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biomaterials and Tissue Engineering","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1166/jbt.2023.3242","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Bone Marrow Mesenchymal Stem Cells Combined with Bone Transport Improves Bone Defect in Rats
This study assessed the mechanism of BMSC combined with bone transport in improving bone defect. Fifty rats were divided into five sets randomly including NC set, DEX set, BMSC set and BT set. There were ten rats in each set. The BMSC was isolated using whole bone marrow adherent method
and then cultivated. The general condition of rats in each set was observed and morphological parameter, pathological change in bone defect tissue was detected along with analysis of the expression of MCP-1, p53, TNF-α and STAT1 in bone tissue. The primary BMSC was cultivated
for seven days and the fusiform BMSC was enlarged and the quantity of binucleate or multinucleate cells was increased after passage. The bone defect model was prepared successfully when the degree of fusion reached 100%. The mental condition was good. DEX set showed significantly reduced TBV
and increased TRS compared with NC set. However, TBV was increased and TRS was reduced in BMSC set, BT set and BMSC+BT set significantly compared with DEX set. MCP-1 mRNA level in DEX set was lower and increased in the treatment group. In addition, p53, TNF-α and STAT1 was increased
in DEX set but reduced in BMSC set, BT set and BMSC+BT set. In conclusion, MCP-1 in rats’ bone defect tissue is upregulated and the p53/TNF-α/STAT1 signal activity is restrained by BMSC combined with bone transport so as to treat the bone defect.