Lü Yu-ming, Cheng Li-ming, Pei Guo-xian, Cai Zhe, Pan Lin, Su Jun, Zhang Ke-hua, Guo Li-li, Yu Qing-sheng, Guo Yan-ru
Department of Orthopedics, Affiliated Hospital, Guangzhou Medical College, Guangzhou 510150, China.
Zhonghua Yi Xue Za Zhi. 2013 May 7;93(17):1335-40.
To explore whether a tissue-engineered construct composed of autogenous endothelial cells, osteoblasts and a new bioresorbable nano-hydroxyapatite/recombinant human-like collagen/polylactic acid (nHA/RHLC/PLA) would enhance bone regeneration and repair femoral head defects in canine models.
The bone marrow stem cells (BMSCs) were isolated from bone marrow of canine ilium and cultured in Dulbecco's modified eagle medium:nutrient mixture F-12 culture media for 1 week and the second-generation BMSCs were further induced by osteogenic medium (1×10(-8) mol/L dexamethasone, 10 mmol/L B-sodium glycerophosphate and 50 µg/ml vitamin C) and by endothelial cell grow medium (vascular endothelial growth factor and basic fibroblast growth factor) for 14 days in vitro. Thus BMSCs were induced into ECs and OBs. After the second passage, cells were digested and collected.And cell density was adjusted to 1.0×10(6)/ml.The cells and nHA/RHLC/PLA scaffold were co-cultured for 2-4 hours then nHA/RHLC/PLA scaffold composites prepared. Cavity defects of 8 mm in diameter and 10 mm in height were made in femoral heads.The nHA/RHLC/PLA scaffold composited with ECs and osteoblasts (OBs) (group A) and composited with OBs (group B) were inserted into different defects while cell-free nHA/RHLC/PLA scaffold served as controls (group C). New bone formation and defect repair were evaluated at 3 and 6 months by radiographic examination, histology and bone histomorphometry.
New bone formation was evident as early as 3 months in groups A, B and C.At 6 months, abundant bone tissue within defects was observed in group A. The control animals with cell-free scaffold showed less bone formation at both timepoints.The scaffold of nHA/RHLC/PLA was degraded and absorbed gradually with the formation of new bone tissues.Histology and bone histomorphometry further revealed significantly increased trabecular bones in group A compared with groups B and C at 6 months postimplantation (P < 0.01).
More abundant new bone tissue may be found in the bone defect areas implanted with osteoblast-endotheliocyte composite than osteoblasts composite and scaffold materials only.ECs and osteoblasts derived from BMSC are ideal seed cells for repairing femoral head defects.
探讨由自体内皮细胞、成骨细胞和新型可生物吸收的纳米羟基磷灰石/重组类人胶原蛋白/聚乳酸(nHA/RHLC/PLA)组成的组织工程构建体是否能增强骨再生并修复犬模型中的股骨头缺损。
从犬髂骨骨髓中分离骨髓间充质干细胞(BMSCs),在杜氏改良伊格尔培养基:营养混合物F-12培养基中培养1周,第二代BMSCs再分别用成骨培养基(1×10⁻⁸mol/L地塞米松、10mmol/Lβ-甘油磷酸钠和50μg/ml维生素C)和内皮细胞生长培养基(血管内皮生长因子和碱性成纤维细胞生长因子)在体外诱导14天。由此将BMSCs诱导为内皮细胞(ECs)和成骨细胞(OBs)。传代后,消化收集细胞,将细胞密度调整至1.0×10⁶/ml。将细胞与nHA/RHLC/PLA支架共培养2 - 4小时,制备nHA/RHLC/PLA支架复合材料。在犬股骨头制作直径8mm、高10mm的腔隙性缺损。将复合有内皮细胞和成骨细胞(OBs)的nHA/RHLC/PLA支架(A组)和复合有成骨细胞(OBs)的nHA/RHLC/PLA支架(B组)分别植入不同缺损处,而无细胞的nHA/RHLC/PLA支架作为对照(C组)。在3个月和6个月时通过影像学检查、组织学和骨组织形态计量学评估新骨形成和缺损修复情况。
A、B、C组早在3个月时就可见新骨形成。6个月时,A组缺损内可见大量骨组织。植入无细胞支架的对照动物在两个时间点的骨形成均较少。nHA/RHLC/PLA支架随着新骨组织的形成逐渐降解吸收。组织学和骨组织形态计量学进一步显示,植入后6个月时,A组的小梁骨明显多于B组和C组(P < 0.01)。
与仅植入成骨细胞复合材料和支架材料相比,植入成骨细胞 - 内皮细胞复合材料的骨缺损区域可能会发现更丰富的新骨组织。源自BMSC的内皮细胞和成骨细胞是修复股骨头缺损的理想种子细胞。