Murao Naoya, Matsuda Taito, Noguchi Hirofumi, Koseki Haruhiko, Namihira Masakazu, Nakashima Kinichi
Department of Stem Cell Biology and Medicine; Graduate School of Medical Sciences; Kyushu University; Fukuoka, Japan; Laboratory of Gene Regulation Research; Graduate School of Biological Sciences; Nara Institute of Science and Technology; Nara, Japan.
Department of Stem Cell Biology and Medicine; Graduate School of Medical Sciences; Kyushu University ; Fukuoka, Japan.
Neurogenesis (Austin). 2014 Nov 17;1(1):e976026. doi: 10.4161/23262133.2014.976026. eCollection 2014.
Nuclear protein 95 KDa (Np95, also known as UHRF1 or ICBP90) plays an important role in maintaining DNA methylation of newly synthesized DNA strands by recruiting DNA methyltransferase 1 (DNMT1) during cell division. In addition, Np95 participates in chromatin remodeling by interacting with histone modification enzymes such as histone deacetylases. However, its expression pattern and function in the brain have not been analyzed extensively. We here investigated the expression pattern of Np95 in the mouse brain, from developmental to adult stages. In the fetal brain, Np95 is abundantly expressed at the midgestational stage, when a large number of neural stem/precursor cells (NS/PCs) exist. Interestingly, Np95 is expressed specifically in NS/PCs but not in differentiated cells such as neurons or glial cells. Furthermore, we demonstrate that Np95 is preferentially expressed in type 2a cells, which are highly proliferative NS/PCs in the dentate gyrus of the adult hippocampus. Moreover, the number of Np95-expressing cells increases in response to kainic acid administration or to voluntary running, which are known to enhance the proliferation of adult NS/PCs. These results suggest that Np95 participates in the process of proliferation and differentiation of NS/PCs, and that it should be a useful novel marker for proliferating NS/PCs, facilitating the analysis of the complex behavior of NS/PCs in the brain.
核蛋白95千道尔顿(Np95,也称为UHRF1或ICBP90)在细胞分裂过程中通过招募DNA甲基转移酶1(DNMT1)来维持新合成DNA链的DNA甲基化,发挥着重要作用。此外,Np95通过与组蛋白修饰酶如组蛋白脱乙酰酶相互作用,参与染色质重塑。然而,其在大脑中的表达模式和功能尚未得到广泛分析。我们在此研究了Np95在小鼠大脑从发育到成年阶段的表达模式。在胎儿大脑中,Np95在妊娠中期大量表达,此时存在大量神经干细胞/前体细胞(NS/PCs)。有趣的是,Np95特异性地在NS/PCs中表达,而在神经元或神经胶质细胞等分化细胞中不表达。此外,我们证明Np95优先在2a型细胞中表达,2a型细胞是成年海马齿状回中高度增殖的NS/PCs。而且,给予 kainic 酸或自愿跑步后,表达Np95的细胞数量增加,已知这两种情况会增强成年NS/PCs的增殖。这些结果表明Np95参与NS/PCs的增殖和分化过程,并且它应该是增殖性NS/PCs的一个有用的新型标记物,有助于分析大脑中NS/PCs的复杂行为。