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首页> 外文期刊>Micron: The international research and review journal for microscopy >DNA content, chromatin supraorganization, nuclear glycoproteins and RNA amounts in hepatocytes of mice expressing insulin-dependent diabetes
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DNA content, chromatin supraorganization, nuclear glycoproteins and RNA amounts in hepatocytes of mice expressing insulin-dependent diabetes

机译:表达胰岛素依赖型糖尿病的小鼠肝细胞的DNA含量,染色质超组织,核糖蛋白和RNA含量

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Chromatin supraorganization and extensibility and nuclear glycoprotein content have been reported to change in hepatocytes from mice during development and aging, as well as under starvation and refeeding conditions. In non-obese diabetic (NOD) mice, the expression of insulin-dependent diabetes may be accompanied by metabolic changes in the liver. These changes are likely to be similar to those involved in the aging processes of non-diabetic animals. Therefore, we hypothesized that the chromatin organization, as well as the physical properties and compositions of hepatocyte nuclei would also be affected in NOD mice in the same way as those in aged non-diabetic mice. Nuclear image parameters were evaluated by image analysis of Feulgen-stained preparations. Chromatin extensibility in response to gravity was observed with polarized light after lysis and toluidine blue staining. The Con-A response of nuclear glycoproteins was evaluated with scanning microspectrophotometry. These charateristics were assessed using hepatocyte imprints from female NOD mice after a 28-day period of diabetes expression. Observations and measurements were made in comparison to healthy BALB/c mice. Total RNA amounts were determined for livers of NOD and BALB/c mice. Enhanced polyploidy levels, a decrease in chromatin higher-order packing states, an increased frequency of extended chromatin fiber formation, and deeper Con-A-responsive chromatin areas were observed in the hepatocytes of the NOD mice expressing insulin-dependent diabetes. Reduced amounts of total RNA were also found in the livers of these mice. Our findings for NOD mice expressing insulin-dependent diabetes are consistent with previously reported data for old-aged mice of the inbred strain A/Uni and may reflect changes in transcriptional activities associated with the stressful physiological demands on the liver during the expression of diabetes.
机译:据报道,在发育和衰老期间以及在饥饿和再喂养条件下,小鼠肝细胞中的染色质超组织和可扩展性以及核糖蛋白含量发生变化。在非肥胖糖尿病(NOD)小鼠中,胰岛素依赖型糖尿病的表达可能伴随肝脏代谢的改变。这些变化可能类似于非糖尿病动物衰老过程中的变化。因此,我们假设NOD小鼠中的染色质组织以及肝细胞核的物理性质和组成也将以与老年非糖尿病小鼠相同的方式受到影响。通过Feulgen染色制剂的图像分析评估核图像参数。裂解和甲苯胺蓝染色后,用偏振光观察到染色质响应重力的可扩展性。核糖蛋白的Con-A反应用扫描显微分光光度法进行了评估。在糖尿病表达28天后,使用雌性NOD小鼠的肝细胞印记评估了这些特征。与健康的BALB / c小鼠相比进行观察和测量。确定了NOD和BALB / c小鼠肝脏的总RNA量。在表达胰岛素依赖型糖尿病的NOD小鼠的肝细胞中观察到多倍体水平增强,染色质高阶堆积状态减少,染色质纤维形成延长频率增加,Con-A响应染色质区域更深。在这些小鼠的肝脏中还发现总RNA量减少。我们对表达胰岛素依赖型糖尿病的NOD小鼠的发现与自交系A / Uni的老年小鼠的先前报道的数据一致,并且可能反映了与糖尿病表达过程中肝脏对生理压力的需求相关的转录活性的变化。

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