不同光谱成分的人工光对幼年豚鼠硬骨中屈光发育、基质金属蛋白酶 2 和组织金属蛋白酶 2 抑制剂表达的影响

IF 2.1 4区 生物学 Q4 CELL BIOLOGY European Journal of Histochemistry Pub Date : 2024-06-27 DOI:10.4081/ejh.2024.3982
Jianbao Yuan, Linfang Li, Yi Fan, Xinyu Xu, Xiaoqiong Huang, Jiayu Shi, Chuanwei Zhang, Lixin Shi, Yuliang Wang
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引用次数: 0

摘要

人造光会影响眼球发育,增加近视率。基质金属蛋白酶 2(MMP-2)能降解细胞外基质并诱导其重塑,而基质金属蛋白酶 2 的组织抑制剂(TIMP-2)能抑制活跃的 MMP-2。本研究旨在探讨不同光谱成分的人造光如何影响豚鼠的屈光发育以及重塑巩膜中 MMP-2 和 TIMP-2 的表达。三周大的豚鼠被随机分配到暴露于五种不同光线的组别中:自然光、低色温的 LED 光、三种全光谱人造光,即 E 光(波长在 ~390-780 nm 范围内的连续光谱)、G 光(波长为 450 nm 的蓝色峰值和波长为 480 nm 的小波谷)和 F 光(连续光谱和波长为 400 nm 以下的过滤光)。在整个实验过程中,每两周用 A 型超声波扫描仪测量一次小白鼠的眼轴长度。光照十二周后,用光学显微镜和透射电子显微镜观察巩膜。免疫组化、Western 印迹和 RT-qPCR 被用来检测硬膜中 MMP-2 和 TIMP-2 蛋白及 mRNA 的表达水平。经过4、6、8、10和12周的光照后,LED和G光照组豚鼠的轴长明显长于自然光照组,而E和F光照组豚鼠的轴长明显短于LED组。光照12周后,巩膜MMP-2蛋白和mRNA的表达量由低到高依次为N组、E组、F组、G组、LED组;而巩膜TIMP-2蛋白和mRNA的表达量由高到低依次为N组、E组、F组、G组、LED组。组间比较有统计学意义(p
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Effects of artificial light with different spectral compositions on refractive development and matrix metalloproteinase 2 and tissue inhibitor of metalloproteinases 2 expression in the sclerae of juvenile guinea pigs.

Artificial light can affect eyeball development and increase myopia rate. Matrix metalloproteinase 2 (MMP-2) degrades the extracellular matrix, and induces its remodeling, while tissue inhibitor of matrix MMP-2 (TIMP-2) inhibits active MMP-2. The present study aimed to look into how refractive development and the expression of MMP-2 and TIMP-2 in the guinea pigs' remodeled sclerae are affected by artificial light with varying spectral compositions. Three weeks old guinea pigs were randomly assigned to groups exposed to five different types of light: natural light, LED light with a low color temperature, three full spectrum artificial lights, i.e. E light (continuous spectrum in the range of ~390-780 nm), G light (a blue peak at 450 nm and a small valley 480 nm) and F light (continuous spectrum and wavelength of 400 nm below filtered). A-scan ultrasonography was used to measure the axial lengths of their eyes, every two weeks throughout the experiment. Following twelve weeks of exposure to light, the sclerae were observed by optical and transmission electron microscopy. Immunohistochemistry, Western blot and RT-qPCR were used to detect the MMP-2 and TIMP-2 protein and mRNA expression levels in the sclerae. After four, six, eight, ten, and twelve weeks of illumination, the guinea pigs in the LED and G light groups had axial lengths that were considerably longer than the animals in the natural light group while the guinea pigs in the E and F light groups had considerably shorter axial lengths than those in the LED group. Following twelve weeks of exposure to light, the expression of the scleral MMP-2 protein and mRNA were, from low to high, N group, E group, F group, G group, LED group; however, the expression of the scleral TIMP-2 protein and mRNA were, from high to low, N group, E group, F group, G group, LED group. The comparison between groups was statistically significant (p<0.01). Continuous, peaks-free or valleys-free artificial light with full-spectrum preserves remodeling of scleral extracellular matrix in guinea pigs by downregulating MMP-2 and upregulating TIMP-2, controlling eye axis elongation, and inhibiting the onset and progression of myopia.

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来源期刊
European Journal of Histochemistry
European Journal of Histochemistry 生物-细胞生物学
CiteScore
3.70
自引率
5.00%
发文量
47
审稿时长
3 months
期刊介绍: The Journal publishes original papers concerning investigations by histochemical and immunohistochemical methods, and performed with the aid of light, super-resolution and electron microscopy, cytometry and imaging techniques. Coverage extends to: functional cell and tissue biology in animals and plants; cell differentiation and death; cell-cell interaction and molecular trafficking; biology of cell development and senescence; nerve and muscle cell biology; cellular basis of diseases. The histochemical approach is nowadays essentially aimed at locating molecules in the very place where they exert their biological roles, and at describing dynamically specific chemical activities in living cells. Basic research on cell functional organization is essential for understanding the mechanisms underlying major biological processes such as differentiation, the control of tissue homeostasis, and the regulation of normal and tumor cell growth. Even more than in the past, the European Journal of Histochemistry, as a journal of functional cytology, represents the venue where cell scientists may present and discuss their original results, technical improvements and theories.
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