Gentle A, McBrien N A
Department of Optometry and Vision Sciences, The University of Melbourne, Parkville, Victoria, 3052, Australia.
Exp Eye Res. 1999 Feb;68(2):155-63. doi: 10.1006/exer.1998.0587.
Visually modulated scleral extracellular matrix remodelling is associated with the development of, and recovery from, induced axial myopia in the tree shrew, a commonly used mammalian model of refractive error development. The involvement of scleral cell proliferation in this process was investigated using [3H] thymidine. Tree shrews were monocularly deprived of pattern vision, using translucent occluders, or the retinal image was optically defocused, using negative lenses, over a period of 5 days. A further group was monocularly deprived for 5 days, then allowed 3 days of binocular recovery. A control group of binocularly open animals was employed to establish normal parameters. On the final day of the experimental period, [3H] thymidine was administered by intraperitoneal injection, then optical and biometric measures were taken and tissue samples collected for assay. Incorporation of [3H] thymidine into cellular DNA was measured in proteinase K digests, following precipitation with trichloroacetic acid. After 5 days, significant amounts of myopia were present in the treated eyes of both form-deprived [-7. 0+/-0.7 Dioptres (D), group mean+/-s.e.m.; P<0.01] and lens-defocused animals (-6.2+/-0.9 D;P<0.01). After 3 days of recovery, 50% of the refractive error had been compensated for, predominantly through shortening of the vitreous chamber in the treated eye. Reduced levels of [3H] thymidine incorporation were observed in sclera from both groups of myopic animals (form-deprived, -34.3+/-9.9%;P<0.05 and lens-defocus, -32.8+/-4.5%;P<0.005). Increased levels of [3H] thymidine incorporation were found in the sclera of recovering animals (+144.0+/-43.2%;P<0.05). The results show that changes in regulation of cell proliferation, during the development of myopia, are visually mediated and inversely related to the direction of change in ocular size. This implies that alterations in the scleral fibroblast population are involved in the modulation of scleral matrix turnover during myopia development.
视觉调节的巩膜细胞外基质重塑与树鼩诱导性轴性近视的发生及恢复有关,树鼩是一种常用的屈光不正发展的哺乳动物模型。使用[3H]胸腺嘧啶核苷研究巩膜细胞增殖在此过程中的作用。树鼩单眼使用半透明眼罩剥夺模式视觉,或使用负透镜使视网膜图像光学散焦,持续5天。另一组单眼剥夺5天,然后双眼恢复3天。使用双眼开放的动物作为对照组来建立正常参数。在实验期的最后一天,通过腹腔注射给予[3H]胸腺嘧啶核苷,然后进行光学和生物测量并收集组织样本进行检测。在蛋白酶K消化物中,用三氯乙酸沉淀后测量[3H]胸腺嘧啶核苷掺入细胞DNA的情况。5天后,剥夺形觉组(-7.0±0.7屈光度(D),组均值±标准误;P<0.01)和透镜散焦组动物(-6.2±0.9 D;P<0.01)的处理眼均出现大量近视。恢复3天后,50%的屈光不正得到代偿,主要是通过处理眼玻璃体腔缩短。两组近视动物(剥夺形觉组,-34.3±9.9%;P<0.05和透镜散焦组,-32.8±4.5%;P<0.005)巩膜中[3H]胸腺嘧啶核苷掺入水平降低。恢复动物的巩膜中[3H]胸腺嘧啶核苷掺入水平升高(+144.0±43.2%;P<0.05)。结果表明,近视发展过程中细胞增殖调节的变化是由视觉介导的,并且与眼大小变化方向呈负相关。这意味着巩膜成纤维细胞群体的改变参与了近视发展过程中巩膜基质更新的调节。