Department of Neurology and Neuroscience, Nagoya City University Graduate School of Medical Sciences, 1 Kawashumi, Mizuho-cho, Mizuho-ku, Nagoya, Aichi, Japan.
Brain Res. 2010 Apr 23;1327:107-17. doi: 10.1016/j.brainres.2010.02.071. Epub 2010 Mar 3.
Hippocampal cholinergic neurostimulating peptide (HCNP), originally purified from young rat hippocampus, has been known to promote the differentiation of septo-hippocampal cholinergic neurons. Recently, the precursor protein of HCNP (HCNP-pp) has also received attention as a multifunctional protein with roles, in addition to serving as the HCNP precursor, such as acting as an ATP-binding protein, a Raf kinase inhibitor protein (RKIP), and phosphatidylethanolamine-binding protein (PEBP). In particular, the function of RKIP has attracted attention over several years for its role in controlling cellular proliferation and metastasis in cancer cells. HCNP-pp is also thought to be important in regulating the proliferation and differentiation of neuronal cells in vitro and in vivo by modification of the MAPK cascade. In the present study, we used cultured adult rat hippocampal progenitor cells (AHPs), which are thought to be important for memory formation, and focused on the role of HCNP-pp in adult neurogenesis, namely, the production of new neurons from neural stem/progenitor cells. We found that HCNP-pp expression in AHPs was closely associated with differentiation into MAP2ab-positive neurons and RIP-positive oligodendrocytes, but not into GFAP-positive astrocytes. By contrast, a down-regulated HCNP-pp expression in AHPs accompanied differentiation into GFAP-positive astrocytes. Direct manipulations of HCNP-pp via viral over-expression or siRNA downregulation further confirmed the HCNP-pp contribution to specific neural lineage commitment of AHPs. Our results show that the expression level of HCNP-pp acts as a key regulator for differentiation of cultured AHPs into specific neural lineages, indicating that the control of neural stem cell fate can be achieved via the HCNP-pp pathway.
海马胆碱能神经刺激肽(HCNP)最初从幼年大鼠海马中纯化出来,已知能促进隔海马胆碱能神经元的分化。最近,HCNP 的前体蛋白(HCNP-pp)也因其除了作为 HCNP 前体的作用外,还具有作为 ATP 结合蛋白、Raf 激酶抑制剂蛋白(RKIP)和磷脂酰乙醇胺结合蛋白(PEBP)的多功能蛋白而受到关注。特别是,RKIP 的功能因其在控制癌细胞中细胞增殖和转移方面的作用而在几年内引起了关注。HCNP-pp 也被认为通过对 MAPK 级联的修饰在体外和体内调节神经元细胞的增殖和分化中起重要作用。在本研究中,我们使用了培养的成年大鼠海马祖细胞(AHPs),这些细胞被认为对记忆形成很重要,并且集中研究了 HCNP-pp 在成年神经发生中的作用,即从神经干细胞/祖细胞中产生新的神经元。我们发现,AHPs 中的 HCNP-pp 表达与分化为 MAP2ab 阳性神经元和 RIP 阳性少突胶质细胞密切相关,但与分化为 GFAP 阳性星形胶质细胞无关。相比之下,AHPs 中 HCNP-pp 表达下调伴随着分化为 GFAP 阳性星形胶质细胞。通过病毒过表达或 siRNA 下调对 HCNP-pp 的直接操作进一步证实了 HCNP-pp 对 AHPs 特定神经谱系定向分化的贡献。我们的结果表明,HCNP-pp 的表达水平是培养的 AHPs 分化为特定神经谱系的关键调节因子,表明可以通过 HCNP-pp 途径来控制神经干细胞命运。