Kirchner G, Harbers M, Bünsch A, Seitz H J, Höppner W
Abteilung für Biochemische Endokrinologie, Universitäts-Krankenhaus Eppendorf, Hamburg, Germany.
FEBS Lett. 1993 Aug 9;328(1-2):119-24. doi: 10.1016/0014-5793(93)80978-4.
In the liver many metabolic pathways are preferentially localized in different zones of the acinus. It is assumed that this zonation allows an efficient adaptation to different states of nutrition, because alternative pathways can be regulated independently. It is reported that the rate limiting enzyme for the glycolytic pathway, glucokinase (EC 2.7.1.2), is predominantly located in the pericentral zone. The gene expression of glucokinase is induced to a maximum level after a carbohydrate-rich diet. In starved or diabetic rats glucokinase gene expression is barely detectable. In postnatal development glucokinase is induced to significant levels only from day 14 onwards. The distribution of the glucokinase protein in the rat liver lobule in the first 4 weeks of postnatal life was investigated by immunohistochemistry and compared to the distribution observed in adult rats. In adult rats considerably high levels of glucokinase are measureable as shown by immunoblotting utilizing a monospecific antibody and a photometric assay of glucokinase enzyme activity, respectively. Immunohistochemically the hepatic glucokinase protein is detected in the perivenous area. During postnatal development, the quantities of hepatic glucokinase protein and glucokinase enzyme activity start to increase significantly from day 15 onwards. Subsequently, glucokinase levels rise further until day 29. In contrast to the results obtained by immunoblotting, glucokinase is already detectable in some liver cells in sections from 6-day-old rats by immunohistochemistry. The liver lobule structure at this age is not completely developed, therefore it is not possible to definitely assign these cells to periportal or pericentral areas. At day 10 post partum the number of glucokinase expressing cells, which appear to be localized preferentially in the periportal zone, increases. In agreement with the immunoblotting, an immense increase in glucokinase activity was observed at day 14. The periportal zonation, clearly detectable at this time, remains stable until day 24. In sections from 29-day-old rats the periportal zonation begins to change into a more homogeneous pattern with a slight preference for periportal areas. The observed appearance of the periportal zonation of glucokinase during neonatal development is obviously in contrast to the perivenous expression of glucokinase in adult rats.
在肝脏中,许多代谢途径优先定位于腺泡的不同区域。据推测,这种分区有助于有效适应不同的营养状态,因为替代途径可以独立调节。据报道,糖酵解途径的限速酶葡萄糖激酶(EC 2.7.1.2)主要位于中央周围区域。富含碳水化合物的饮食后,葡萄糖激酶的基因表达被诱导至最高水平。在饥饿或糖尿病大鼠中,几乎检测不到葡萄糖激酶基因表达。在出生后发育过程中,葡萄糖激酶仅从第14天开始被诱导至显著水平。通过免疫组织化学研究了出生后前4周大鼠肝小叶中葡萄糖激酶蛋白的分布,并与成年大鼠中观察到的分布进行了比较。在成年大鼠中,通过使用单特异性抗体的免疫印迹和葡萄糖激酶酶活性的光度测定法分别显示,可测量到相当高水平的葡萄糖激酶。免疫组织化学检测显示,肝葡萄糖激酶蛋白在静脉周围区域被检测到。在出生后发育过程中,肝葡萄糖激酶蛋白的量和葡萄糖激酶酶活性从第15天开始显著增加。随后,葡萄糖激酶水平进一步上升直至第29天。与免疫印迹结果相反,通过免疫组织化学在6日龄大鼠切片的一些肝细胞中已经可以检测到葡萄糖激酶。这个年龄段的肝小叶结构尚未完全发育,因此不可能明确将这些细胞归为门静脉周围或中央周围区域。产后第10天,表达葡萄糖激酶的细胞数量增加,这些细胞似乎优先定位于门静脉周围区域。与免疫印迹一致,在第14天观察到葡萄糖激酶活性大幅增加。此时明显可检测到的门静脉周围分区一直保持稳定直到第24天。在29日龄大鼠的切片中,门静脉周围分区开始转变为更均匀的模式,对门静脉周围区域略有偏好。在新生儿发育过程中观察到的葡萄糖激酶门静脉周围分区的出现显然与成年大鼠中葡萄糖激酶的静脉周围表达形成对比。