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The treatment efficacy of bone tissue engineering strategy for repairing segmental bone defects under diabetic condition

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单位: [1]Huazhong Univ Sci & Technol, Jingshan Union Hosp, Union Hosp, Dept Plast Surg, Wuhan, Hubei, Peoples R China [2]Zhejiang Univ, Sch Med, Affiliated Hangzhou Peoples Hosp 1, Dept Plast Surg, Hangzhou, Zhejiang, Peoples R China [3]Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Res, Wuhan, Hubei, Peoples R China [4]Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Geriatr, Wuhan, Hubei, Peoples R China
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关键词: diabetes mellitus bone tissue engineering mesenchymal stem cells decalcified bone matrix bone regeneration

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Background: Diabetes mellitus is a systematic disease which exert detrimental effect on bone tissue. The repair and reconstruction of bone defects in diabetic patients still remain a major clinical challenge. This study aims to investigate the potential of bone tissue engineering approach to improve bone regeneration under diabetic condition. Methods: In the present study, decalcified bone matrix (DBM) scaffolds were seeded with allogenic fetal bone marrow-derived mesenchymal stem cells (BMSCs) and cultured in osteogenic induction medium to fabricate BMSC/DBM constructs. Then the BMSC/DBM constructs were implanted in both subcutaneous pouches and large femoral bone defects in diabetic (BMSC/DBM in DM group) and non-diabetic rats (BMSC/DBM in non-DM group), cell-free DBM scaffolds were implanted in diabetic rats to serve as the control group (DBM in DM group). X-ray, micro-CT and histological analyses were carried out to evaluate the bone regenerative potential of BMSC/DBM constructs under diabetic condition. Results: In the rat subcutaneous implantation model, quantitative micro-CT analysis demonstrated that BMSC/DBM in DM group showed impaired bone regeneration activity compared with the BMSC/DBM in non-DM group (bone volume: 46 +/- 4.4 mm(3) vs 58.9 +/- 7.15 mm(3), *p < 0.05). In the rat femoral defect model, X-ray examination demonstrated that bone union was delayed in BMSC/DBM in DM group compared with BMSC/DBM in non-DM group. However, quantitative micro-CT analysis showed that after 6 months of implantation, there was no significant difference in bone volume and bone density between the BMSC/DBM in DM group (199 +/- 63 mm(3) and 593 +/- 65 mg HA/ccm) and the BMSC/DBM in non-DM group (211 +/- 39 mm(3) and 608 +/- 53 mg HA/ccm). Our data suggested that BMSC/DBM constructs could repair large bone defects in diabetic rats, but with delayed healing process compared with non-diabetic rats. Conclusion: Our study suggest that biomaterial sacffolds seeded with allogenic fetal BMSCs represent a promising strategy to induce and improve bone regeneration under diabetic condition.

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出版当年[2023]版:
大类 | 3 区 工程技术
小类 | 3 区 综合性期刊
最新[2025]版:
大类 | 3 区 生物学
小类 | 3 区 生物工程与应用微生物 4 区 工程:生物医学
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出版当年[2022]版:
Q1 MULTIDISCIPLINARY SCIENCES
最新[2023]版:
Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Q2 ENGINEERING, BIOMEDICAL

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第一作者单位: [1]Huazhong Univ Sci & Technol, Jingshan Union Hosp, Union Hosp, Dept Plast Surg, Wuhan, Hubei, Peoples R China [2]Zhejiang Univ, Sch Med, Affiliated Hangzhou Peoples Hosp 1, Dept Plast Surg, Hangzhou, Zhejiang, Peoples R China
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