Zeng Mingbing, Wang Ningli, Wu Heping, Chen Jingchang, Fan Zhigang
Zhongshan Ophthalmic Center, Sun Yet-sen University. Guangzhou 510060, China.
Zhonghua Yan Ke Za Zhi. 2002 May;38(5):308-10.
To investigate the damage of the cells of the lateral geniculate bodies (LGB) of Sprague-Dawley (SD) rats after partial optic nerve injury.
The optic nerve was pressed by a forceps (40 g) for 30 seconds to set up the animal model with optic nerve injury. LGB was chopped in serial coronal slices (10 microm thickness) by a cryomicrotome. The apoptosis of LGB cells was detected with terminal deoxynucleotidyl transferase (TDT)-mediated dUTP nick end-labeling (TUNEL) technique after one week. After retrograde labeling with Granular Blue (GB) through injecting GB into optic center, the average density of the LGB cells was counted under the fluorescent microscope. Using monoclonal rabbit anti-rat neurofilament (NF) antibody, the neurons of LGB were detected by immunochemistry stains, and the standard avidin-biotin complex immunoperoxidase technique was used for immunostaining.
The results of TUNEL analysis showed that the mechanism of the LGB cells pathogenesis was apoptosis. The LGB cells appeared clear striation in the control group, and the cells in experimental group decreased obviously after immunohistrochemical staining. The average density of LGB cells was (5 172 +/- 248) cells/mm(2) in control group, and (4 144 +/- 61) cells/mm(2) in experimental group.
After partial optic nerve injury, the LGB cells are obviously damaged, which may be related to apoptosis of LGB cells.
探讨部分视神经损伤后对Sprague-Dawley(SD)大鼠外侧膝状体(LGB)细胞的损伤情况。
用镊子(40 g)对视神经施压30秒,建立视神经损伤动物模型。用冷冻切片机将LGB切成连续冠状切片(10微米厚)。一周后,采用末端脱氧核苷酸转移酶(TDT)介导的dUTP缺口末端标记(TUNEL)技术检测LGB细胞的凋亡情况。通过向视中枢注射颗粒蓝(GB)进行逆行标记后,在荧光显微镜下计数LGB细胞的平均密度。使用兔抗大鼠神经丝(NF)单克隆抗体,通过免疫化学染色检测LGB的神经元,采用标准抗生物素蛋白-生物素复合物免疫过氧化物酶技术进行免疫染色。
TUNEL分析结果显示,LGB细胞发病机制为凋亡。对照组LGB细胞出现清晰的条纹,免疫组织化学染色后实验组细胞明显减少。对照组LGB细胞平均密度为(5 172±248)个细胞/mm²,实验组为(4 144±61)个细胞/mm²。
部分视神经损伤后,LGB细胞明显受损,这可能与LGB细胞凋亡有关。