Kim Joo Yeon, Choi Kyuhyun, Shaker Mohammed R, Lee Ju-Hyun, Lee Boram, Lee Eunsoo, Park Jae-Yong, Lim Mi-Sun, Park Chang-Hwan, Shin Ki Soon, Kim Hyun, Geum Dongho, Sun Woong
Department of Anatomy and Division of Brain Korea 21 Plus Biomedical Science, Korea University College of Medicine, Seoul, Korea.
Department of Biology, Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, Republic of Korea.
Stem Cells. 2016 Apr;34(4):888-901. doi: 10.1002/stem.2276. Epub 2016 Jan 19.
Neurogenesis occurs spontaneously in the subventricular zone (SVZ) of the lateral ventricle in adult rodent brain, but it has long been debated whether there is sufficient adult neurogenesis in human SVZ. Subcallosal zone (SCZ), a posterior continuum of SVZ closely associated with posterior regions of cortical white matter, has also been reported to contain adult neural stem cells (aNSCs) in both rodents and humans. However, little is known whether SCZ-derived aNSC (SCZ-aNSCs) can produce cortical neurons following brain injury. We found that SCZ-aNSCs exhibited limited neuronal differentiation potential in culture and after transplantation in mice. Neuroblasts derived from SCZ initially migrated toward injured cortex regions following brain injury, but later exhibited apoptosis. Overexpression of anti-apoptotic bcl-xL in the SCZ by retroviral infection rescued neuroblasts from cell death in the injured cortex, but neuronal maturation was still limited, resulting in atrophy. In combination with Bcl-xL, infusion of brain-derived neurotropic factor rescued atrophy, and importantly, a subset of such SCZ-aNSCs differentiated and attained morphological and physiological characteristics of mature, excitatory neurons. These results suggest that the combination of anti-apoptotic and neurotrophic factors might enable the use of aNSCs derived from the SCZ in cortical neurogenesis for neural replacement therapy.
神经发生在成年啮齿动物大脑侧脑室的室下区(SVZ)自发发生,但人类SVZ中是否存在足够的成年神经发生长期以来一直存在争议。胼胝体下区(SCZ)是SVZ的后连续区域,与皮质白质的后部区域密切相关,据报道在啮齿动物和人类中都含有成年神经干细胞(aNSCs)。然而,关于SCZ来源的aNSC(SCZ-aNSCs)在脑损伤后是否能产生皮质神经元知之甚少。我们发现,SCZ-aNSCs在培养和移植到小鼠体内后表现出有限的神经元分化潜能。脑损伤后,源自SCZ的神经母细胞最初向损伤的皮质区域迁移,但后来出现凋亡。通过逆转录病毒感染在SCZ中过表达抗凋亡蛋白bcl-xL可挽救神经母细胞在损伤皮质中的细胞死亡,但神经元成熟仍然有限,导致萎缩。与Bcl-xL联合使用,注入脑源性神经营养因子可挽救萎缩,重要的是,这类SCZ-aNSCs的一个子集分化并获得了成熟兴奋性神经元的形态和生理特征。这些结果表明,抗凋亡和神经营养因子的组合可能使源自SCZ的aNSCs用于皮质神经发生的神经替代治疗成为可能。