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A design-based method for estimating glomerular number in the developing kidney

机译:基于设计的估计发育中肾小球数目的方法

摘要

Low glomerular (nephron) endowment has been associated with an increased risk of cardiovascular and renal disease in adulthood. Nephron endowment in humans is determined by 36 wk of gestation, while in rats and mice nephrogenesis ends several days after birth. Specific genes and environmental perturbations have been shown to regulate nephron endowment. Until now, design-based method for estimating nephron number in developing kidneys was unavailable. This was due in part to the difficulty associated with unambiguously identifying developing glomeruli in histological sections. Here, we describe a method that uses lectin histochemistry to identify developing glomeruli and the physical disector/fractionator principle to provide unbiased estimates of total glomerular number (Nglom). We have characterized Nglom throughout development in kidneys from 76 rats and model this development with a 5-parameter logistic equation to predict Nglom from embryonic day 17.25 to adulthood (r2 = 0.98). This approach represents the first design-based method with which to estimate Nglom in the developing kidney.
机译:低肾小球(肾单位)end赋与成年后罹患心血管疾病和肾脏疾病的风险增加有关。人的肾单位天赋是由妊娠36周决定的,而在大鼠和小鼠中,肾生成在出生后几天就结束了。特定基因和环境扰动已被证明可以调节肾单位的end赋。到目前为止,尚无基于设计的估算肾脏发育中肾单位数目的方法。这部分是由于与组织切片中明确鉴定正在发展的肾小球相关的困难。在这里,我们描述了一种使用凝集素组织化学方法来鉴定正在发展的肾小球的方法,以及使用物理偏转器/分离器原理来提供总肾小球数目(Nglom)的无偏估计的方法。我们已经从76只大鼠的肾脏整个发育过程中表征了Nglom,并使用5参数对数方程对该发育进行建模,以预测Nglom从胚胎第17.25天到成年(r2 = 0.98)。该方法代表了第一个基于设计的方法,可用来估计发育中的肾脏中的Nglom。

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