Siegwart John T, Norton Thomas T
Department of Vision Sciences, School of Optometry, University of Alabama at Birmingham, 35294, USA.
Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3484-92. doi: 10.1167/iovs.05-0194.
In juvenile tree shrews, a minus-power lens placed in front of the eye produces increased axial elongation and a myopic shift in refractive state that compensates for the power of the lens. Scleral tissue remodeling and modulation of the mechanical properties of the sclera occur during lens compensation. In this study, the time course of changes in scleral mRNA levels of three MMPs and three TIMPs during compensation for a minus lens and during recovery was investigated, to determine which, if any, are temporally associated with changes in the mechanical properties of the sclera and the axial elongation rate.
Competitive RT-PCR was used to measure the levels of mRNA for MT1-MMP, MMP-2, MMP-3, TIMP-1, TIMP-2, and TIMP-3 in the scleras of tree shrews that had received either 1, 2, 4, or 11 days of monocular -5-D lens treatment, or 11 days of -5-D lens treatment followed by 2 or 4 days of recovery.
Relative to their control eyes, treated eye MT1-MMP and MMP-2 mRNA levels were significantly higher, and TIMP-3 levels were lower by 1 to 4 days of minus lens treatment. These differential effects were absent by 11 days of treatment when the treated eyes had compensated for the lens. The levels of all three TIMPs spiked upward in both eyes after 2 days of recovery. The differential changes in MT1-MMP, MMP-2, and TIMP-3 mRNA levels were all restricted to the treated eye and were temporally associated with the differential changes in axial elongation, refractive state, and the previously measured changes in creep rate.
The observed changes in MT1-MMP, MMP-2, TIMP-2, and TIMP-3 mRNA are consistent with visually modulated MT1-MMP activation of MMP-2 and with MT1-MMP degradation of scleral extracellular matrix components. These data constitute further evidence that visual signals modulate gene expression of selected MMPs and TIMPs to control scleral remodeling, the mechanical properties of the sclera, axial elongation, and refractive state.
在幼年树鼩中,置于眼前的负屈光度镜片会导致眼轴延长增加以及屈光状态向近视偏移,从而抵消镜片的屈光度。在镜片补偿过程中会发生巩膜组织重塑以及巩膜力学性能的调节。在本研究中,研究了在负镜片补偿期间及恢复过程中三种基质金属蛋白酶(MMPs)和三种金属蛋白酶组织抑制剂(TIMPs)的巩膜mRNA水平的变化时间进程,以确定哪些(如果有的话)与巩膜力学性能和眼轴伸长率的变化在时间上相关联。
采用竞争性逆转录聚合酶链反应(RT-PCR)来测量接受单眼-5D镜片治疗1、2、4或11天,或接受11天-�D镜片治疗后再恢复2或4天的树鼩巩膜中MT1-MMP、MMP-2、MMP-3、TIMP-1、TIMP-2和TIMP-3的mRNA水平。
与对照眼相比,在负镜片治疗1至4天时,治疗眼的MT1-MMP和MMP-2 mRNA水平显著升高,而TIMP-3水平降低。当治疗眼对镜片进行了补偿时,在治疗11天时这些差异效应消失。恢复2天后,两只眼睛中所有三种TIMPs的水平均急剧上升。MT1-MMP、MMP-2和TIMP-3 mRNA水平的差异变化均局限于治疗眼,并且在时间上与眼轴伸长、屈光状态的差异变化以及先前测量的蠕变率变化相关联。
观察到的MT1-MMP、MMP-2、TIMP-2和TIMP-3 mRNA的变化与视觉调节的MT1-MMP对MMP-2的激活以及MT1-MMP对巩膜细胞外基质成分的降解相一致。这些数据进一步证明视觉信号调节选定的MMPs和TIMPs的基因表达,以控制巩膜重塑、巩膜力学性能、眼轴伸长和屈光状态。