Department of Surgical, Medical, Dental and Morphological Sciences with Interest in Transplants, Oncology and Regenerative Medicine, University of Modena and Reggio Emilia, Modena, Italy.
Department of Surgical, Medical, Dental and Morphological Sciences with Interest in Transplants, Oncology and Regenerative Medicine, University of Modena and Reggio Emilia, Modena, Italy.
Life Sci. 2015 Jan 15;121:174-83. doi: 10.1016/j.lfs.2014.10.020. Epub 2014 Nov 5.
This study aims to evaluate the bone regeneration in a rat calvarias critical size bone defect treated with a construct consisting of collagen type I and human amniotic fluid stem cells (AFSCs) after oral administration of phytoestrogen ferutinin.
In 12 week old male rats (n=10), we performed two symmetric full-thickness cranial defects on each parietal region, and a scaffold was implanted into each cranial defect. The rats were divided into four groups: 1) collagen scaffold, 2) collagen scaffold+ferutinin at a dose of 2mg/kg/5 mL, 3) collagen scaffold + AFSCs, and 4) collagen scaffold + AFSCs + ferutinin. The rats were sacrificed after 4 weeks, and the calvariae were removed, fixed, embedded in paraffin and cut into 7 μm thick sections. Histomorphometric measures, immunohistochemical and immunofluorescence analyses were performed on the paraffin sections.
The histomorphometric analysis on H&E stained sections showed a significant increase in the regenerated area of the 4th group compared with the other groups. Immunohistochemistry performed with a human anti-mitochondrial antibody showed the presence of AFSCs 4 weeks after the transplant. Immunofluorescence analysis revealed the presence of osteocalcin and estrogen receptors (ERα and GPR30) in all groups, with a greater expression of all markers in samples where the scaffold was treated with AFSCs and the rats were orally administered ferutinin.
Our results demonstrated that the oral administration of ferutinin is able to improve the bone regeneration of critical-size bone defects in vivo that is obtained with collagen-AFSCs constructs.
本研究旨在评估经植物雌激素 ferutinin 口服给药后,由 I 型胶原蛋白和人羊膜间充质干细胞(AFSCs)组成的构建体在大鼠颅骨临界尺寸骨缺损中的骨再生情况。
在 12 周龄雄性大鼠(n=10)中,我们在每个顶骨区域上进行了两个对称的全层颅骨缺损,并将支架植入每个颅骨缺损中。大鼠分为四组:1)胶原蛋白支架,2)胶原蛋白支架+ferutinin 剂量为 2mg/kg/5mL,3)胶原蛋白支架+AFSCs,4)胶原蛋白支架+AFSCs+ferutinin。4 周后处死大鼠,取出颅骨,固定、包埋在石蜡中并切成 7μm 厚的切片。对石蜡切片进行组织形态计量学测量、免疫组织化学和免疫荧光分析。
H&E 染色切片的组织形态计量学分析显示,第 4 组的再生面积与其他组相比显著增加。移植后 4 周,用人抗线粒体抗体进行的免疫组织化学显示存在 AFSCs。免疫荧光分析显示所有组均存在骨钙素和雌激素受体(ERα和 GPR30),在支架用 AFSCs 处理且大鼠口服 ferutinin 的样本中,所有标志物的表达均更高。
我们的结果表明,ferutinin 的口服给药能够改善体内胶原蛋白-AFSCs 构建体获得的临界尺寸骨缺损的骨再生。