Lustig M, Sakurai T, Grumet M
Department of Pharmacology, NYU Medical Center, 550 First Avenue, New York, New York, 10016, USA.
Dev Biol. 1999 May 15;209(2):340-51. doi: 10.1006/dbio.1999.9250.
Nr-CAM is a neuronal cell adhesion molecule (CAM) belonging to the immunoglobulin superfamily that has been implicated as a ligand for another CAM, axonin-1, in guidance of commissural axons across the floor plate in the spinal cord. Nr-CAM also serves as a neuronal receptor for several other cell surface molecules, but its role as a ligand in neurite outgrowth is poorly understood. We studied this problem using a chimeric Fc-fusion protein of the extracellular region of Nr-CAM (Nr-Fc) and investigated potential neuronal receptors in the developing peripheral nervous system. A recombinant Nr-CAM-Fc fusion protein, containing all six Ig domains and the first two fibronectin type III repeats of the extracellular region of Nr-CAM, retains cellular and molecular binding activities of the native protein. Injection of Nr-Fc into the central canal of the developing chick spinal cord in ovo resulted in guidance errors for commissural axons in the vicinity of the floor plate. This effect is similar to that resulting from treatment with antibodies against axonin-1, confirming that axonin-1/Nr-CAM interactions are important for guidance of commissural axons through a spatially and temporally restricted Nr-CAM positive domain in the ventral spinal cord. When tested as a substrate, Nr-Fc induced robust neurite outgrowth from dorsal root ganglion and sympathetic ganglion neurons, but it was not effective for tectal and forebrain neurons. The peripheral but not the central neurons expressed high levels of axonin-1 both in vitro and in vivo. Moreover, antibodies against axonin-1 inhibited Nr-Fc-induced neurite outgrowth, indicating that axonin-1 is a neuronal receptor for Nr-CAM on these peripheral ganglion neurons. The results demonstrate a role for Nr-CAM as a ligand in axon growth by a mechanism involving axonin-1 as a neuronal receptor and suggest that dynamic changes in Nr-CAM expression can modulate axonal growth and guidance during development.
Nr-CAM是一种属于免疫球蛋白超家族的神经元细胞粘附分子(CAM),在脊髓中连合轴突穿过底板的导向过程中,它被认为是另一种细胞粘附分子轴突素-1的配体。Nr-CAM还是其他几种细胞表面分子的神经元受体,但其作为配体在神经突生长中的作用却知之甚少。我们使用Nr-CAM细胞外区域的嵌合Fc融合蛋白(Nr-Fc)研究了这个问题,并研究了发育中的外周神经系统中潜在的神经元受体。一种重组Nr-CAM-Fc融合蛋白,包含Nr-CAM细胞外区域的所有六个免疫球蛋白结构域和前两个纤连蛋白III型重复序列,保留了天然蛋白的细胞和分子结合活性。将Nr-Fc注射到鸡胚发育中的脊髓中央管内,导致底板附近的连合轴突出现导向错误。这种效应与用抗轴突素-1抗体处理所产生的效应相似,证实了轴突素-1/Nr-CAM相互作用对于连合轴突通过脊髓腹侧空间和时间受限的Nr-CAM阳性区域的导向很重要。当作为底物进行测试时,Nr-Fc诱导背根神经节和交感神经节神经元强烈的神经突生长,但对顶盖和前脑神经元无效。外周神经元而非中枢神经元在体外和体内均表达高水平的轴突素-1。此外,抗轴突素-1抗体抑制了Nr-Fc诱导的神经突生长,表示轴突素-1是这些外周神经节神经元上Nr-CAM的神经元受体。结果表明Nr-CAM作为配体在轴突生长中具有作用,其机制涉及轴突素-1作为神经元受体,并表明Nr-CAM表达的动态变化可以在发育过程中调节轴突生长和导向。