Cui Qi, Cho Kin-Sang, So Kwok-Fai, Yip Henry K
Laboratory for Neural Repair, Shantou University Medical College, Shantou, China.
J Neurotrauma. 2004 May;21(5):617-25. doi: 10.1089/089771504774129946.
The presence of Nogo axon regeneration inhibitory molecules in the central nervous system (CNS) and the counteracting effect of IN-1 antibodies have been widely reported. In this study, we examined the effect of IN-1-producing hybridoma cells on axon regeneration in adult rodent retinal ganglion cells (RGCs) after various types of optic nerve (ON) injury, evaluating therein whether ciliary neurotrophic factor (CNTF) potentiated the effect of IN-1. We found that application of IN-1 alone failed to enhance regeneration of intracranially or intraorbitally transected RGC axons in a peripheral nerve (PN) graft. IN-1 hybridoma cells also failed to significantly promote intraorbitally crushed ON axons to reenter the distal part of the ON. However, a combined application of IN-1 and CNTF had a synergistic effect in both intracranial PN and intraorbital ON crush paradigms. This study suggests that the action of IN-1 antibodies in promoting axon regeneration in the CNS could be more effective when coupled with other appropriate factors.
中枢神经系统(CNS)中存在Nogo轴突再生抑制分子以及IN-1抗体的抵消作用已被广泛报道。在本研究中,我们检测了产生IN-1的杂交瘤细胞对成年啮齿动物视网膜神经节细胞(RGCs)在各种类型视神经(ON)损伤后轴突再生的影响,并评估睫状神经营养因子(CNTF)是否增强了IN-1的作用。我们发现单独应用IN-1未能增强颅内或眶内横断的RGC轴突在周围神经(PN)移植物中的再生。IN-1杂交瘤细胞也未能显著促进眶内挤压的ON轴突重新进入ON的远端部分。然而,IN-1和CNTF的联合应用在颅内PN和眶内ON挤压模型中均具有协同作用。本研究表明,当与其他合适的因子联合使用时,IN-1抗体在促进CNS轴突再生中的作用可能更有效。