首页> 外文期刊>Experimental Eye Research >Diabetes induces expression of aquaporin-0 in the retinal nerve fibers of spontaneously diabetic Torii rats.
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Diabetes induces expression of aquaporin-0 in the retinal nerve fibers of spontaneously diabetic Torii rats.

机译:糖尿病诱导自发性糖尿病Torii大鼠视网膜神经纤维中水通道蛋白0的表达。

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摘要

Diabetes redistributes the expression of glial aquaporin (AQP) water channels in the retina. However, it is not known whether diabetes also affects retinal AQP-0 expression. This study examined the effects of the development of diabetes on the expression of retinal AQP-0 in spontaneously diabetic Torii (SDT) rats. Male SDT rats at 10 and 40 weeks of age and age-matched male Sprague-Dawley (SD) rats were used. The localization of AQP-0 was assessed immunohistochemically using sagittal cryosections of the rats' retinas and optic nerves. Fold changes in AQP-0 gene expression relative to controls were assessed by real-time RT-PCR. All SDT rats spontaneously developed diabetes by 40 weeks of age (the mean hemoglobin (Hb) A1c levels were 2.8+/-0.2% and 11.2+/-1.0% at 10 and 40 weeks, respectively). SD rats did not develop diabetes (the HbA1c levels were 2.7+/-0.2% and 2.6+/-0.3% at 10 and 40 weeks, respectively). In the retinas of SD rats and in those of SDT rats at 10 weeks of age, immunoreactivity for AQP-0 was confined predominantly to the inner nuclear layer and to the border between the inner plexiform layer and the ganglion cell layer (GCL), where AQP-0 colocalized with protein kinase C-alpha. AQP-0 immunoreactivity was also observed in the GCL to a lesser degree, which colocalized with the neuronal nuclei. In the 40-week-old SDT rat retinas, additional AQP-0 immunoreactivity was observed in the GCL and colocalized with neurofilaments, indicating expression of AQP-0 in ganglion cell axons. However, the axonal AQP-0 immunoreactivity was restricted to the retinal nerve fibers, whereas the optic nerve axons were devoid of AQP-0. Retinal blood vessels did not express AQP-0. AQP-0 gene expression was 3.4-fold higher in SDT rat retinas than in SD rat retinas at 40 weeks of age. AQP-0 was predominantly expressed in the bipolar cells of the non-diabetic rat retinas, whereas it was also expressed in the retinal nerve fibers of diabetic rat retinas. The disrupted water transport between astrocytes and retinal nerve fibers may be associated with the known accelerated apoptosis of retinal ganglion cells induced by diabetes.
机译:糖尿病会在视网膜中重新分布神经胶质水通道蛋白(AQP)水通道的表达。然而,尚不清楚糖尿病是否也影响视网膜AQP-0表达。这项研究检查了糖尿病的发展对自发性糖尿病鸟(SDT)大鼠视网膜AQP-0表达的影响。使用10和40周龄的雄性SDT大鼠和年龄匹配的雄性Sprague-Dawley(SD)大鼠。使用大鼠视网膜和视神经的矢状冰冻切片,通过免疫组织化学方法评估了AQP-0的定位。通过实时RT-PCR评估相对于对照的AQP-0基因表达的倍数变化。所有SDT大鼠在40周龄时自发发展为糖尿病(在10周和40周时,平均血红蛋白(Hb)A1c水平分别为2.8 +/- 0.2%和11.2 +/- 1.0%)。 SD大鼠没有患上糖尿病(第10和40周时HbA1c水平分别为2.7 +/- 0.2%和2.6 +/- 0.3%)。在10周龄的SD大鼠和SDT大鼠的视网膜中,对AQP-0的免疫反应主要限于内部核层以及内部丛状层与神经节细胞层(GCL)之间的边界。 AQP-0与蛋白激酶C-alpha共定位。在GCL中也观察到了较小程度的AQP-0免疫反应性,其与神经元核共定位。在40周龄的SDT大鼠视网膜中,在GCL中观察到了另外的AQP-0免疫反应性,并与神经丝共定位,表明AQP-0在神经节细胞轴突中表达。然而,轴突AQP-0免疫反应仅限于视网膜神经纤维,而视神经轴突缺乏AQP-0。视网膜血管不表达AQP-0。在40周龄时,SDT大鼠视网膜的AQP-0基因表达比SD大鼠视网膜高3.4倍。 AQP-0主要在非糖尿病大鼠视网膜的双极细胞中表达,而在糖尿病大鼠视网膜的视网膜神经纤维中也表达。星形胶质细胞和视网膜神经纤维之间的水运输中断可能与糖尿病诱导的视网膜神经节细胞的已知加速凋亡有关。

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