Gu Weidong, Zhang Fujun, Xue Qingsheng, Ma Zhengwen, Lu Peihua, Yu Buwei
Shanghai Minhang Central Hospital, Shanghai, China.
Neurol Res. 2012 Mar;34(2):172-80. doi: 10.1179/1743132811Y.0000000068. Epub 2012 Feb 2.
It has been demonstrated that bone mesenchymal stromal cells (BMSCs) stimulate neurite outgrowth from dorsal root ganglion (DRG) neurons. The present in vitro study tested the hypothesis that BMSCs stimulate the neurite outgrowth from spinal neurons by secreting neurotrophic factors. Spinal neurons were cocultured with BMSCs, fibroblasts and control medium in a non-contact system. Neurite outgrowth of spinal neurons cocultured with BMSCs was significantly greater than the neurite outgrowth observed in neurons cultured with control medium or with fibroblasts. In addition, BMSC-conditioned medium increased the length of neurites from spinal neurons compared to those of neurons cultured in the control medium or in the fibroblasts-conditioned medium. BMSCs expressed brain-derived neurotrophic factor (BDNF) and glial cell line-derived neurotrophic factor (GDNF). The concentrations of BDNF and GDNF in BMSC-conditioned medium were 132±12 and 70±6 pg ml(-1), respectively. The addition of anti-BDNF and anti-GDNF antibodies to BMSC-conditioned medium partially blocked the neurite-promoting effect of the BMSC-conditioned medium. In conclusion, our results demonstrate that BMSCs promote neurite outgrowth in spinal neurons by secreting soluble factors. The neurite-promoting effect of BMSCs is partially mediated by BDNF and GDNF.
已经证明,骨间充质基质细胞(BMSCs)可刺激背根神经节(DRG)神经元的神经突生长。本体外研究检验了以下假设:BMSCs通过分泌神经营养因子来刺激脊髓神经元的神经突生长。在非接触系统中将脊髓神经元与BMSCs、成纤维细胞和对照培养基共培养。与BMSCs共培养的脊髓神经元的神经突生长明显大于在对照培养基或成纤维细胞中培养的神经元所观察到的神经突生长。此外,与在对照培养基或成纤维细胞条件培养基中培养的神经元相比,BMSC条件培养基增加了脊髓神经元神经突的长度。BMSCs表达脑源性神经营养因子(BDNF)和胶质细胞系源性神经营养因子(GDNF)。BMSC条件培养基中BDNF和GDNF的浓度分别为132±12和70±6 pg ml(-1)。向BMSC条件培养基中添加抗BDNF和抗GDNF抗体可部分阻断BMSC条件培养基的促神经突作用。总之,我们的结果表明,BMSCs通过分泌可溶性因子促进脊髓神经元的神经突生长。BMSCs的促神经突作用部分由BDNF和GDNF介导。