Factors Influencing the Retrograde Labeling of Retinal Ganglion Cells with Fluorogold in an Animal Optic Nerve Crush Model

被引:15
|
作者
Huang, Tzu-Lun [1 ,2 ,7 ]
Huang, Sun-Ping [1 ,2 ,3 ]
Chang, Chung-Hsing [5 ]
Lin, Kung-Hung [6 ]
Sheu, Min-Muh [2 ]
Tsai, Rong-Kung [1 ,2 ,4 ]
机构
[1] Tzu Chi Univ, Buddhist Tzu Chi Gen Hosp, Eye Res Inst, Hualien 97002, Taiwan
[2] Tzu Chi Univ, Dept Ophthalmol & Visual Sci, Hualien 97002, Taiwan
[3] Tzu Chi Univ, Dept Mol & Human Genet, Hualien 97002, Taiwan
[4] Tzu Chi Univ, Inst Med Sci, Hualien 97002, Taiwan
[5] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Dermatol, Kaohsiung, Taiwan
[6] Taiwan Adventist Hosp, Dept Neurol, New Taipei City, Taiwan
[7] Far Eastern Mem Hosp, Dept Ophthalmol, New Taipei City, Taiwan
关键词
Optic nerve crush; Retinal ganglion cell; Fluorogold; Microglia; FACTOR G-CSF; IN-VIVO; SECONDARY DEGENERATION; ADULT MICE; RATS; DAMAGE; DEATH; SURVIVAL; QUANTIFICATION; PRESSURE;
D O I
10.1159/000357736
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To investigate whether different crush durations or a different fluorogold (FG) injection timing can affect the efficiency of FG retrograde labeling of retinal ganglion cells (RGCs) in the optic nerve (ON) crush model. Methods: We performed the ON crush in rats with a clip at different durations or a jewel forceps to compare the effects of different crush methods with FG staining. RGC density was compared between the FG injection 1 week before the sacrifice of the animals (group A) and the injection before the crush experiment (group B). Double staining with CD1 1b and FG in the retinal sections was conducted to investigate the relationship between the overcounting of RGCs and microglia. Results: The FG-stained particles were significantly decreased at the distal part of the crush site compared to the proximal site of the ON with a crush duration of over 30 s or when crushed with the jewel forceps. Two weeks after ON crush, the RGC count was higher both in the central and mid-peripheral retinas in group B. The percentage of CD1 1b-stained cells among the FG-stained cells in the RGC layer of retinas in group B was higher than that of group A (34% in group B vs. 4% in group A, p = 0.0001). Overcounting of RGC density in group B was due to additional microglia with FG engulfing. Conclusions: Our results suggest that each laboratory should test its setting conditions to avoid factors influencing the RGC density measurement before conducting ON crush experiments. (c) 2014 S. Karger AG, Basel
引用
收藏
页码:173 / 178
页数:6
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