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A potential role for beta- and gamma-crystallins in the vascular remodeling of the eye.

机译:β和γ晶状体蛋白在眼睛血管重塑中的潜在作用。

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摘要

We demonstrate that expression of beta- and gamma-crystallins is associated with intraocular vessels during normal vascular development of the eye and also in the Nuc1 rat, a mutant in which the hyaloid vascular system fails to regress normally. Real-Time RT PCR, Western blot and metabolic labeling studies indicate an increased expression of beta- and gamma-crystallins in Nuc1 retina. The increased expression of crystallins was localized to the astrocytes surrounding the intraocular vessels. A similar pattern of crystallin expression was also observed in the retinal vessels during normal development. Cultured human astrocytes exposed to 3-nitropropionic acid, an established model of neuronal hypoxia, increased VEGF expression, as expected, but also increased expression of crystallins. Our data suggest that crystallins may function together with VEGF during vascular remodeling. Interestingly, in human PFV (persistent fetal vasculature) disease, where the hyaloid vasculature abnormally persists after birth, we show that astrocytes express both VEGF and crystallins.
机译:我们证明,在正常血管的眼睛发育过程中,以及在Nuc1大鼠中,β-和γ-晶状体蛋白的表达与眼内血管相关,在该突变体中,玻璃样血管系统无法正常退化。实时RT PCR,蛋白质印迹和代谢标记研究表明,Nuc1视网膜中β和γ晶状体蛋白的表达增加。结晶蛋白的表达增加定位于眼内血管周围的星形胶质细胞。在正常发育期间,在视网膜血管中也观察到了类似的结晶蛋白表达模式。培养的人星形胶质细胞暴露于3-硝基丙酸(神经元缺氧的既定模型),与预期的一样,VEGF的表达增加,但结晶蛋白的表达也增加。我们的数据表明,在血管重塑期间,晶状体蛋白可能与VEGF一起起作用。有趣的是,在人类PFV(持续性胎儿脉管系统)疾病中,玻璃状脉管系统在出生后异常持续存在,我们显示了星形胶质细胞同时表达VEGF和结晶蛋白。

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