Department of Neuropsychiatry and Laboratory of Molecular Psychiatry, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Cell Mol Neurobiol. 2012 May;32(4):567-76. doi: 10.1007/s10571-012-9798-2.
Cell therapy with mesenchymal stromal cells (MSCs) was found to protect neurons from damage after experimental stroke and is currently under investigation in clinical stroke trials. In order to elucidate the mechanisms of MSC-induced neuroprotection, we used the in vitro oxygen–glucose deprivation (OGD) model of cerebral ischemia. Co-culture of primary cortical neurons with MSCs in a transwell co-culture system for 48 h prior to OGD-reduced neuronal cell death by 30-35%. Similar protection from apoptosis was observed with MSC-conditioned media when added 48 h or 30 min prior to OGD, or even after OGD. Western blot analysis revealed increased phosphorylation of STAT3 and Akt in neuronal cultures after treatment with MSC-conditioned media. Inhibition of the PI3K/Akt pathway completely abolished the neuroprotective potential of MSC-conditioned media, suggesting that MSCs can improve neuronal survival by an Akt-dependent anti-apoptotic signaling cascade. Using mass spectrometry, we identified plasminogen activator inhibitor-1 as an active compound in MSC-conditioned media. Thus, paracrine factors secreted by MSCs protect neurons from apoptotic cell death in the OGD model of cerebral ischemia.
间充质基质细胞 (MSCs) 的细胞治疗被发现可保护实验性中风后的神经元免受损伤,目前正在临床试验中进行研究。为了阐明 MSC 诱导的神经保护机制,我们使用了体外氧葡萄糖剥夺 (OGD) 脑缺血模型。在 OGD 之前,将原代皮质神经元与 MSC 共培养 48 小时,在 Transwell 共培养系统中,神经元细胞死亡减少了 30-35%。当在 OGD 之前 48 小时或 30 分钟添加 MSC 条件培养基,甚至在 OGD 之后添加 MSC 条件培养基时,也观察到类似的抗细胞凋亡保护作用。Western blot 分析显示,MSC 条件培养基处理后的神经元培养物中 STAT3 和 Akt 的磷酸化增加。PI3K/Akt 通路的抑制完全消除了 MSC 条件培养基的神经保护潜力,表明 MSC 可以通过 Akt 依赖性抗细胞凋亡信号级联反应改善神经元的存活。使用质谱分析,我们鉴定出纤溶酶原激活物抑制剂-1 是 MSC 条件培养基中的一种活性化合物。因此,MSC 分泌的旁分泌因子可保护神经元免受脑缺血 OGD 模型中的细胞凋亡。