Ozaki M, Tohyama K, Kishida H, Buonanno A, Yano R, Hashikawa T
Laboratory for Cellular Information Processing, BSI, The Institute of Physical and Chemical Research (RIKEN), Saitama, Japan.
J Neurosci Res. 2000 Mar 1;59(5):612-23. doi: 10.1002/(SICI)1097-4547(20000301)59:5<612::AID-JNR4>3.0.CO;2-V.
Neuregulins (NRGs), a large group of structurally related signaling proteins, are likely to have important roles in the development, maintenance and repair of the nervous system and other selected tissues. We have demonstrated, by using the major form of NRG cloned from the mouse cerebellum that both the soluble form and the membrane anchored form of NRG may serve different functions in synaptogenesis. The soluble form of NRG was produced by proteolytic cleavage of the membrane anchored form of NRG. The proteolytic cleavage was promoted by protein kinase activation. The cleaved form of NRG trans-synaptically regulated the expression of the NMDA (N-methyl-D-aspartate) receptor subunit NR2C as neurally-derived factors, whereas the membrane anchored form of NRG showed a homophilic binding activity between NRGbeta1s. In adult mice the membrane anchored form of NRG was concentrated in neuro-terminals of both granule cells and pontocerebellar mossy fibers. The fact that NRG can be functionally viewed as cell recognition molecules as well as neurotrophic agents suggests new possibilities for the important class of molecules.
神经调节蛋白(NRGs)是一大类结构相关的信号蛋白,可能在神经系统及其他特定组织的发育、维持和修复中发挥重要作用。我们通过使用从小鼠小脑克隆的主要形式的NRG证明,NRG的可溶性形式和膜锚定形式在突触形成中可能发挥不同的功能。NRG的可溶性形式是由NRG的膜锚定形式经蛋白水解切割产生的。蛋白水解切割由蛋白激酶激活促进。切割后的NRG作为神经源性因子跨突触调节NMDA(N-甲基-D-天冬氨酸)受体亚基NR2C的表达,而NRG的膜锚定形式在NRGβ1s之间表现出嗜同性结合活性。在成年小鼠中,NRG的膜锚定形式集中在颗粒细胞和脑桥小脑苔藓纤维的神经末梢。NRG在功能上可被视为细胞识别分子以及神经营养因子这一事实为这一重要类别的分子带来了新的可能性。