Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS One. 2010 Feb 26;5(2):e9414. doi: 10.1371/journal.pone.0009414.
The ability to grow a uniform cell type from the adult central nervous system (CNS) is valuable for developing cell therapies and new strategies for drug discovery. The adult mammalian brain is a source of neural stem cells (NSC) found in both neurogenic and non-neurogenic zones but difficulties in culturing these hinders their use as research tools.
METHODOLOGY/PRINCIPAL FINDINGS: Here we show that NSCs can be efficiently grown in adherent cell cultures when angiogenic signals are included in the medium. These signals include both anti-angiogenic factors (the soluble form of the Notch receptor ligand, Dll4) and pro-angiogenic factors (the Tie-2 receptor ligand, Angiopoietin 2). These treatments support the self renewal state of cultured NSCs and expression of the transcription factor Hes3, which also identifies the cancer stem cell population in human tumors. In an organotypic slice model, angiogenic factors maintain vascular structure and increase the density of dopamine neuron processes.
CONCLUSIONS/SIGNIFICANCE: We demonstrate new properties of adult NSCs and a method to generate efficient adult NSC cultures from various central nervous system areas. These findings will help establish cellular models relevant to cancer and regeneration.
从成年中枢神经系统(CNS)中培养出均匀的细胞类型的能力对于开发细胞疗法和新药发现策略具有重要价值。成年哺乳动物大脑是神经干细胞(NSC)的来源,这些 NSC 存在于神经生成区和非神经生成区,但培养这些细胞的困难阻碍了它们作为研究工具的应用。
方法/主要发现:在这里,我们展示了当培养基中包含血管生成信号时,可以有效地在贴壁细胞培养物中培养 NSC。这些信号包括抗血管生成因子(Notch 受体配体可溶性形式 Dll4)和促血管生成因子(Tie-2 受体配体 Angiopoietin 2)。这些处理支持培养的 NSC 的自我更新状态和转录因子 Hes3 的表达,Hes3 也可以识别人类肿瘤中的癌症干细胞群体。在器官型切片模型中,血管生成因子维持血管结构并增加多巴胺神经元过程的密度。
结论/意义:我们证明了成年 NSC 的新特性,以及一种从各种中枢神经系统区域生成高效成年 NSC 培养物的方法。这些发现将有助于建立与癌症和再生相关的细胞模型。