Bentz Kristine, Molcanyi Marek, Riess Peter, Elbers Andrea, Pohl Esther, Sachinidis Agapios, Hescheler Jürgen, Neugebauer Edmund, Schäfer Ute
Institute of Developmental Genetics, GSF-National Research Centre for Environment and Health, Munich, Germany.
J Neurosci Res. 2007 Apr;85(5):1057-64. doi: 10.1002/jnr.21219.
In the present study, we compare the capacity of two different embryonic stem (ES) cell lines to secrete neurotrophins in response to cerebral tissue extract derived from healthy or injured rat brains. The intrinsic capacity of the embryonic cell lines BAC7 (feeder cell-dependent cultivation) to release brain-derived neurotrophic factor (BDNF) or neurotrophin-3 (NT-3) exceeded the release of these factors by CGR8 cells (feeder cell-free growth) by factors of 10 and 4, respectively. Nerve growth factor (NGF) was secreted only by BAC7 cells. Conditioning of cell lines with cerebral tissue extract derived from healthy or fluid percussion-injured rat brains resulted in a significant time-dependent increase in BDNF release in both cell lines. The increase in BDNF release by BAC7 cells was more pronounced when cells were incubated with brain extract derived from injured brain. However, differences in neurotrophin release associated with the origin of brain extract were at no time statistically significant. Neutrophin-3 and NGF release was inhibited when cell lines were exposed to cerebral tissue extract. The magnitude of the response to cerebral tissue extract was dependent on the intrinsic capacity of the cell lines to release neurotrophins. Our results clearly demonstrate significant variations in the intrinsic capability of different stem cell lines to produce neurotrophic factors. Furthermore, a significant modulation of neurotrophic factor release was observed following conditioning of cell lines with tissue extract derived from rat brains. A significant modulation of neurotrophin release dependent on the source of cerebral tissue extract used was not observed.
在本研究中,我们比较了两种不同胚胎干细胞(ES)系响应源自健康或受伤大鼠脑的脑组织提取物分泌神经营养因子的能力。胚胎细胞系BAC7(依赖饲养层细胞培养)释放脑源性神经营养因子(BDNF)或神经营养因子-3(NT-3)的内在能力分别比CGR8细胞(无饲养层细胞生长)释放这些因子的能力高出10倍和4倍。神经生长因子(NGF)仅由BAC7细胞分泌。用源自健康或液压冲击损伤大鼠脑的脑组织提取物处理细胞系,导致两种细胞系中BDNF释放均随时间显著增加。当BAC7细胞与源自受伤脑的脑提取物孵育时,BDNF释放的增加更为明显。然而,与脑提取物来源相关的神经营养因子释放差异在任何时候都无统计学意义。当细胞系暴露于脑组织提取物时,神经营养因子-3和NGF的释放受到抑制。对脑组织提取物的反应程度取决于细胞系释放神经营养因子的内在能力。我们的结果清楚地表明不同干细胞系产生神经营养因子的内在能力存在显著差异。此外,在用源自大鼠脑的组织提取物处理细胞系后,观察到神经营养因子释放有显著调节。未观察到神经营养因子释放因所用脑组织提取物来源不同而有显著调节。