Improved healing of critical-size femoral defect in osteoporosis rat models using 3D elastin/polycaprolactone/nHA scaffold in combination with mesenchymal stem cells.
Improved healing of critical-size femoral defect in osteoporosis rat models using 3D elastin/polycaprolactone/nHA scaffold in combination with mesenchymal stem cells.
复制标题
DOI:
10.1007/s10856-021-06495-w
复制
发表时间:
2021-03-08
期刊:
影响因子:
--
通讯作者:
Abdollahifar MA
中科院分区:
文献类型:
--
作者:
Hejazi F;Ebrahimi V;Asgary M;Piryaei A;Fridoni MJ;Kermani AA;Zare F;Abdollahifar MA
Osteoporosis is a common bone disease that results in elevated risk of fracture, and delayed bone healing and impaired bone regeneration are implicated by this disease. In this study, Elastin/Polycaprolactone/nHA nanofibrous scaffold in combination with mesenchymal stem cells were used to regenerate bone defects. Cytotoxicity, cytocompatibility and cellular morphology were evaluated in vitro and observations revealed that an appropriate environment for cellular attachment, growth, migration, and proliferation is provided by this scaffold. At 3 months following ovariectomy (OVX), the rats were used as animal models with an induced critical size defect in the femur to evaluate the therapeutic potential of osteogenic differentiation of bone marrow mesenchymal stem cells (BM-MSCs) seeded on 3 dimension (3D) scaffolds. In this experimental study, 24 female Wistar rats were equally divided into three groups: Control, scaffold (non-seeded BM-MSC), and scaffold + cell (seeded BM-MSC) groups. 30 days after surgery, the right femur was removed, and underwent a stereological analysis and RNA extraction in order to examine the expression of Bmp-2 and Vegf genes. The results showed a significant increase in stereological parameters and expression of Bmp-2 and Vegf in scaffold and scaffold + cell groups compared to the control rats. The present study suggests that the use of the 3D Elastin/Polycaprolactone (PCL)/Nano hydroxyapatite (nHA) scaffold in combination with MSCs may improve the fracture regeneration and accelerates bone healing at the osteotomy site in rats.
登录
查看更多内容
影响因子:
5
作者:
Stastna E;Castkova K;Rahel J
通讯作者:
Rahel J
影响因子:
5.3
作者:
Shen M;Wu R;Jin R;Pan J;Guo F;Li Z;Lin X;Xu S
通讯作者:
Xu S
影响因子:
--
作者:
Sefati N;Norouzian M;Abbaszadeh HA;Abdollahifar MA;Amini A;Bagheri M;Aryan A;Fadaei Fathabady F
通讯作者:
Fadaei Fathabady F
影响因子:
4.6
作者:
Leuning DG;Beijer NRM;du Fossé NA;Vermeulen S;Lievers E;van Kooten C;Rabelink TJ;Boer J
通讯作者:
Boer J
影响因子:
12.4
作者:
Kumar, Sanjay;Wan, Chao;Ponnazhagan, Selvarangan
通讯作者:
Ponnazhagan, Selvarangan