Cen Ling-Ping, Luo Jian-Min, Zhang Cheng-Wu, Fan You-Ming, Song Yue, So Kwok-Fai, van Rooijen Nico, Pang Chi Pui, Lam Dennis S C, Cui Qi
Joint Shantou International Eye Center of Shantou University and The Chinese University of Hong Kong, Shantou University Medical College, Shantou, Peoples Republic of China.
Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4257-66. doi: 10.1167/iovs.06-0791.
To examine whether ciliary neurotrophic factor (CNTF) has a chemotactic effect on macrophages and whether macrophages are involved in CNTF-induced retinal ganglion cell (RGC) survival and axonal regeneration after optic nerve (ON) injury.
Adult Fischer 344 rats received an autologous peripheral nerve graft onto transected ON for injured axons to grow. CNTF was applied intravitreally. When needed, clodronate liposomes were applied intravitreally or intravenously to deplete macrophages in the eye. A chemotaxis microchamber system was used to examine whether CNTF has a chemotactic effect on macrophages in vitro, whereas immunohistochemistry was used to identify the location of macrophages/microglia in the retina. The effects of CNTF on RGC neurite outgrowth and macrophage/microglia proliferation were tested in retinal explants.
Intravitreal CNTF significantly enhanced RGC survival and axonal regeneration as well as the number of macrophages in the eye. Removal of macrophages significantly reduced CNTF-induced RGC survival and axon regeneration. A chemotaxis assay showed a clear chemotactic effect of CNTF on blood-derived but not peritoneal macrophages. Immunohistochemistry revealed that local microglia was located in a region from the nerve fiber layer (NFL) to the inner nuclear layer, whereas blood-derived macrophages were in the NFL. In vitro experiments revealed that CNTF did not enhance neurite outgrowth or macrophage/microglia proliferation in retinal explants.
CNTF is a chemoattractant but not a proliferation enhancer for blood-derived macrophages, and blood-borne macrophages recruited into the eye by CNTF participate in RGC protection. This finding thus adds an important category to the existing understanding of the biological actions of CNTF.
研究睫状神经营养因子(CNTF)对巨噬细胞是否具有趋化作用,以及巨噬细胞是否参与CNTF诱导的视神经(ON)损伤后视网膜神经节细胞(RGC)存活和轴突再生。
成年Fischer 344大鼠接受自体周围神经移植到横断的视神经上,以使损伤的轴突生长。玻璃体内注射CNTF。必要时,玻璃体内或静脉内注射氯膦酸盐脂质体以清除眼中的巨噬细胞。使用趋化性微室系统检测CNTF在体外对巨噬细胞是否具有趋化作用,而免疫组织化学用于鉴定视网膜中巨噬细胞/小胶质细胞的位置。在视网膜外植体中测试CNTF对RGC神经突生长和巨噬细胞/小胶质细胞增殖的影响。
玻璃体内注射CNTF可显著提高RGC存活、轴突再生以及眼内巨噬细胞数量。清除巨噬细胞可显著降低CNTF诱导的RGC存活和轴突再生。趋化性试验显示CNTF对血液来源的巨噬细胞有明显趋化作用,但对腹腔巨噬细胞无趋化作用。免疫组织化学显示,局部小胶质细胞位于从神经纤维层(NFL)到内核层的区域,而血液来源的巨噬细胞位于NFL。体外实验显示,CNTF未增强视网膜外植体中的神经突生长或巨噬细胞/小胶质细胞增殖。
CNTF是血液来源巨噬细胞的趋化因子而非增殖增强剂,并且由CNTF募集到眼内的血源性巨噬细胞参与RGC保护。因此,这一发现为对CNTF生物学作用的现有认识增添了重要内容。