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首页> 外文期刊>Experimental Eye Research >The function of VEGF-A in lens development: formation of the hyaloid capillary network and protection against transient nuclear cataracts.
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The function of VEGF-A in lens development: formation of the hyaloid capillary network and protection against transient nuclear cataracts.

机译:VEGF-A在晶状体发育中的功能:形成透明的玻璃状毛细血管网并防止短暂性核性白内障。

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A network of capillaries branches from the hyaloid vascular system and surrounds the mammalian lens throughout much of its embryonic development. These vessels are presumed to be important for the growth and maturation of the lens, although the lenses of non-mammalian vertebrates have no comparable vessels. Over expression of VEGF-A in the lens increases the extent of these capillaries, but it is not known whether VEGF-A from the lens is necessary for their formation or survival. To address this question, we deleted Vegfa in the lens. This prevented the formation of the capillary networks adjacent to the lens capsule, but did not alter nearby hyaloid vessels at the surface of the retina. Postnatal lenses lacking Vegfa were smaller than wild type and, by 1 month of age, many had mild nuclear opacities. These opacities regressed with age. The lens is hypoxic throughout most of life and VEGF-A expression is often regulated by the transcription factor, hypoxia inducible factor-1. Lenses lacking Hif1a were of apparently normal size, had markedly reduced levels of mRNA for VEGF-A and glyceraldehyde-3-phosphate dehydrogenase, but had normal-appearing capillaries covering their surface. We conclude that VEGF-A from the lens is necessary for the formation of the normal hyaloid vascular system and that lack of these capillaries was the most likely cause of growth retardation during fetal and early postnatal lens development. In the absence of HIF-1 function, sufficient VEGF-A is produced by the lens to promote capillary formation. Further study is needed to explain the formation of the mild opacities seen in some lenses lacking Vegfa and their regression later in life.
机译:毛细血管网络从玻璃状血管系统分支出来,并在整个胚胎发育过程中围绕着哺乳动物晶状体。尽管非哺乳动物脊椎动物的晶状体没有可比的脉管,但这些脉管被认为对晶状体的生长和成熟很重要。晶状体中VEGF-A的过度表达增加了这些毛细血管的程度,但是尚不清楚晶状体中的VEGF-A对于其形成或存活是否必要。为了解决这个问题,我们删除了镜头中的Vegfa。这阻止了与晶状体囊相邻的毛细血管网络的形成,但是并没有改变视网膜表面附近的透明玻璃状血管。缺乏Vegfa的产后晶状体比野生型小,到1个月大时,许多晶状体混浊程度较轻。这些不透明度随着年龄的增长而退化。晶状体在整个生命的大部分时间内都是低氧的,而VEGF-A的表达通常受转录因子低氧诱导因子-1的调节。缺少Hif1a的晶状体大小正常,明显降低了VEGF-A和3-磷酸甘油醛脱氢酶的mRNA水平,但表面覆盖了正常的毛细血管。我们得出的结论是,晶状体中的VEGF-A对于正常的透明玻璃体血管系统的形成是必不可少的,而这些毛细血管的缺乏是胎儿和出生后早期晶状体发育过程中生长迟缓的最可能原因。在没有HIF-1功能的情况下,晶状体会产生足够的VEGF-A以促进毛细血管形成。需要进一步的研究来解释在一些缺乏Vegfa的镜片中看到的轻度混浊的形成及其在以后的生活中的消退。

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