Torii Tomohiro, Ohno Nobuhiko, Miyamoto Yuki, Kawahara Kazuko, Saitoh Yurika, Nakamura Kazuaki, Takashima Shou, Sakagami Hiroyuki, Tanoue Akito, Yamauchi Junji
Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA.
Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo, Yamanashi 409-3898, Japan; School of Life Science, The Graduate University for Advanced Studies and The National Institute for Physiological Sciences, Okazaki, Aichi 444-8585, Japan.
Biochem Biophys Res Commun. 2015 May 8;460(3):819-25. doi: 10.1016/j.bbrc.2015.03.113. Epub 2015 Mar 28.
In postnatal development of the peripheral nervous system (PNS), Schwann cells differentiate to insulate neuronal axons with myelin sheaths, increasing the nerve conduction velocity. To produce the mature myelin sheath with its multiple layers, Schwann cells undergo dynamic morphological changes. While extracellular molecules such as growth factors and cell adhesion ligands are known to regulate the myelination process, the intracellular molecular mechanism underlying myelination remains unclear. In this study, we have produced Schwann cell-specific conditional knockout mice for cytohesin-2, a guanine-nucleotide exchange factor (GEF) specifically activating Arf6. Arf6, a member of the Ras-like protein family, participates in various cellular functions including cell morphological changes. Cytohesin-2 knockout mice exhibit decreased Arf6 activity and reduced myelin thickness in the sciatic nerves, with decreased expression levels of myelin protein zero (MPZ), the major myelin marker protein. These results are consistent with those of experiments in which Schwann cell-neuronal cultures were treated with pan-cytohesin inhibitor SecinH3. On the other hand, the numbers of Ki67-positive cells in knockout mice and controls are comparable, indicating that cytohesin-2 does not have a positive effect on cell numbers. Thus, signaling through cytohesin-2 is required for myelination by Schwann cells, and cytohesin-2 is added to the list of molecules known to underlie PNS myelination.
在周围神经系统(PNS)的出生后发育过程中,施万细胞分化以用髓鞘包裹神经元轴突,从而提高神经传导速度。为了产生具有多层结构的成熟髓鞘,施万细胞会经历动态的形态变化。虽然已知细胞外分子如生长因子和细胞粘附配体可调节髓鞘形成过程,但髓鞘形成背后的细胞内分子机制仍不清楚。在本研究中,我们制备了施万细胞特异性条件性敲除细胞粘附蛋白2(cytohesin-2)的小鼠,细胞粘附蛋白2是一种特异性激活Arf6的鸟嘌呤核苷酸交换因子(GEF)。Arf6是Ras样蛋白家族的成员,参与包括细胞形态变化在内的各种细胞功能。细胞粘附蛋白2敲除小鼠的坐骨神经中Arf6活性降低,髓鞘厚度减小,髓鞘主要标记蛋白髓鞘蛋白零(MPZ)的表达水平也降低。这些结果与用泛细胞粘附蛋白抑制剂SecinH3处理施万细胞-神经元共培养物的实验结果一致。另一方面,敲除小鼠和对照组中Ki67阳性细胞的数量相当,这表明细胞粘附蛋白2对细胞数量没有积极影响。因此,施万细胞进行髓鞘形成需要通过细胞粘附蛋白2进行信号传导,并且细胞粘附蛋白2被添加到已知的PNS髓鞘形成相关分子列表中。