Faijerson J, Tinsley R B, Apricó K, Thorsell A, Nodin C, Nilsson M, Blomstrand F, Eriksson P S
Institute of Neuroscience and Physiology at Sahlgrenska Academy, Göteborg University, Göteborg, Sweden.
J Neurosci Res. 2006 Nov 15;84(7):1415-24. doi: 10.1002/jnr.21044.
Neural stem cells reside in defined areas of the adult mammalian brain, including the dentate gyrus of the hippocampus. Rat neural stem/progenitor cells (NSPCs) isolated from this region retain their multipotency in vitro and in vivo after grafting into the adult brain. Recent studies have shown that endogenous or grafted NSPCs are activated after an injury and migrate toward lesioned areas. In these areas, reactive astrocytes are present and secrete numerous molecules and growth factors; however, it is not currently known whether reactive astrocytes can influence the lineage selection of NSPCs. We investigated whether reactive astrocytes could affect the differentiation, proliferation, and survival of adult NSPCs by modelling astrogliosis in vitro, using mechanical lesion of primary astrocytes. Initially, it was found that conditioned medium from lesioned astrocytes induced astrocytic differentiation of NSPCs without affecting neuronal or oligodendrocytic differentiation. In addition, NSPCs in coculture with lesioned astrocytes also displayed increased astrocytic differentiation and some of these NSPC-derived astrocytes participated in glial scar formation in vitro. When proliferation and survival of NSPCs were analyzed, no differential effects were observed between lesioned and nonlesioned astrocytes. To investigate the molecular mechanisms of the astrocyte-inducing activity, the expression of two potent inducers of astroglial differentiation, ciliary neurotrophic factor and leukemia inhibitory factor, was analyzed by Western blot and shown to be up-regulated in conditioned medium from lesioned astrocytes. These results demonstrate that lesioned astrocytes can induce astroglial differentiation of NSPCs and provide a mechanism for astroglial differentiation of these cells following brain injury.
神经干细胞存在于成年哺乳动物大脑的特定区域,包括海马体的齿状回。从该区域分离出的大鼠神经干细胞/祖细胞(NSPCs)在体外和移植到成年大脑后在体内都保留了它们的多能性。最近的研究表明,内源性或移植的NSPCs在损伤后被激活并向损伤区域迁移。在这些区域,存在反应性星形胶质细胞并分泌多种分子和生长因子;然而,目前尚不清楚反应性星形胶质细胞是否能影响NSPCs的谱系选择。我们通过对原代星形胶质细胞进行机械损伤,在体外模拟星形胶质细胞增生,研究反应性星形胶质细胞是否会影响成年NSPCs的分化、增殖和存活。最初,发现损伤星形胶质细胞的条件培养基可诱导NSPCs向星形胶质细胞分化,而不影响神经元或少突胶质细胞的分化。此外,与损伤星形胶质细胞共培养的NSPCs也表现出星形胶质细胞分化增加,并且这些NSPC衍生的星形胶质细胞中的一些在体外参与了胶质瘢痕的形成。当分析NSPCs的增殖和存活情况时,未观察到损伤星形胶质细胞和未损伤星形胶质细胞之间的差异效应。为了研究星形胶质细胞诱导活性的分子机制,通过蛋白质免疫印迹分析了两种强效的星形胶质细胞分化诱导剂睫状神经营养因子和白血病抑制因子的表达,结果显示在损伤星形胶质细胞的条件培养基中它们的表达上调。这些结果表明,损伤的星形胶质细胞可以诱导NSPCs向星形胶质细胞分化,并为脑损伤后这些细胞的星形胶质细胞分化提供了一种机制。