Wen Y, Bekhor I
Laboratory for Molecular Genetics, Doheny Eye Institute, Los Angeles, CA.
Curr Eye Res. 1993 Apr;12(4):323-32. doi: 10.3109/02713689308999456.
The level of expression of the genes for hexokinase, aldose reductase and sorbitol dehydrogenase was investigated in lenses of mice and rats. These genes represent two separate but interrelated pathways for the metabolism of glucose in the cell. It is hypothesized that the extent of expression of the hexokinase gene may play an important role in the regulation of the levels of glucose in the lens. It is known that if there occurs a build up of intracellular glucose, such as in diabetes mellitus, activation of the aldose reductase/sorbitol dehydrogenase pathway may lead to various diabetic complications, including a lessening of lens clarity. We have therefore determined the levels of expression of the genes for these three enzymes in the lens of both mice and rats. Mice are known to be more resistant than rats to the development of lens opacification during hyperglycemia. By Northern blot hybridization analysis, and by quantitation of the resulting hexokinase, aldose reductase and sorbitol dehydrogenase mRNA hybrids, we found that in the mouse lens the expression of the hexokinase gene exceeded that of the aldose reductase gene by a factor of three, while in the rat it only approached about 1/4 that of the aldose reductase gene. The extent of expression of the SDH gene, however, was equal between the mouse and rat lenses. These results were calculated relative to the level of expression of the alpha A-crystallin gene in those two types of lenses, in order to account for the generally higher genetic expression found in the rat relative to the mouse lens due to its higher content of DNA, henceforth larger mass. The presence of high levels of hexokinase mRNAs relative to aldose reductase mRNAs in the lens would be expected to favor metabolism of glucose via the glycolytic pathway rather than the sorbitol pathway, leading to retardation of development of sugar cataracts in the mouse lens; while the opposite is true for the rat lens.
研究了小鼠和大鼠晶状体中己糖激酶、醛糖还原酶和山梨醇脱氢酶基因的表达水平。这些基因代表了细胞内葡萄糖代谢的两条独立但相互关联的途径。据推测,己糖激酶基因的表达程度可能在晶状体中葡萄糖水平的调节中起重要作用。已知如果细胞内葡萄糖积累,如在糖尿病中,醛糖还原酶/山梨醇脱氢酶途径的激活可能导致各种糖尿病并发症,包括晶状体透明度降低。因此,我们测定了这三种酶在小鼠和大鼠晶状体中的基因表达水平。已知在高血糖期间,小鼠比大鼠更不易发生晶状体混浊。通过Northern印迹杂交分析以及对所得己糖激酶、醛糖还原酶和山梨醇脱氢酶mRNA杂交体的定量分析,我们发现,在小鼠晶状体中,己糖激酶基因的表达比醛糖还原酶基因高出三倍,而在大鼠中,其表达仅约为醛糖还原酶基因的1/4。然而,SDH基因在小鼠和大鼠晶状体中的表达程度相等。这些结果是相对于这两种晶状体中αA-晶状体蛋白基因的表达水平计算得出的,以便考虑到由于大鼠晶状体中DNA含量较高(因此质量较大),相对于小鼠晶状体,其基因表达普遍较高。相对于醛糖还原酶mRNA,晶状体中高水平的己糖激酶mRNA的存在预计有利于通过糖酵解途径而非山梨醇途径进行葡萄糖代谢,从而延缓小鼠晶状体中糖性白内障的发展;而大鼠晶状体则相反。