Van Beers E H, Rings E H, Taminiau J A, Heymans H S, Einerhand A W, Dekker J, Büller H A
Laboratory for Pediatric Gastroenterology and Nutrition, Academic Medical Center, University of Amsterdam, The Netherlands.
J Pediatr Gastroenterol Nutr. 1998 Jul;27(1):37-46. doi: 10.1097/00005176-199807000-00007.
In children, lactase and sucrase-isomaltase are essential intestinal glycohydrolases, and insufficiency of either enzyme causes diarrhea and malnutrition. Little is known about the regulation of lactase and sucrase-isomaltase expression in the duodenum during childhood. In this study, the mechanisms of regulation of duodenal expression of both enzymes were examined in a study population with ages ranging from 1 to 18 years.
Duodenal biopsy specimens from 60 white children were used to analyze tissue morphology and to quantify lactase and sucrase-isomaltase mRNA and protein.
Among healthy subjects, high interindividual variability was noted in both mRNA and protein levels for lactase and sucrase-isomaltase. Lactase mRNA level per subject did not correlate with sucrase-isomaltase mRNA level and thus appeared independent. Both lactase and sucrase-isomaltase protein levels correlated significantly with their respective mRNA levels. For each enzyme, a significant inverse correlation was observed between the degree of villus atrophy and mRNA levels. Aging from 1 to 18 years did not result in significant changes in mRNA or protein levels of either enzyme. Immunostaining patterns within the duodenal epithelium for lactase differed from sucrase-isomaltase in adjacent sections, illustrating independent regulation at the cellular level.
In the duodenum of white children, lactase and sucrase-isomaltase seem primarily regulated at the transcriptional level. The expression of each enzyme in the intestinal epithelium is regulated by an independent mechanism. Lactase and sucrase-isomaltase exhibit stable mRNA and protein levels in healthy children as they grow to adulthood. Mucosal damage affected levels of both enzymes negatively.
在儿童中,乳糖酶和蔗糖酶 - 异麦芽糖酶是肠道必需的糖苷水解酶,任何一种酶的不足都会导致腹泻和营养不良。关于儿童期十二指肠中乳糖酶和蔗糖酶 - 异麦芽糖酶表达的调控知之甚少。在本研究中,在年龄范围为1至18岁的研究人群中研究了这两种酶十二指肠表达的调控机制。
使用60名白人儿童的十二指肠活检标本分析组织形态,并对乳糖酶和蔗糖酶 - 异麦芽糖酶的mRNA和蛋白质进行定量。
在健康受试者中,乳糖酶和蔗糖酶 - 异麦芽糖酶的mRNA和蛋白质水平均存在较高的个体间变异性。每个受试者的乳糖酶mRNA水平与蔗糖酶 - 异麦芽糖酶mRNA水平不相关,因此表现为独立。乳糖酶和蔗糖酶 - 异麦芽糖酶的蛋白质水平均与其各自的mRNA水平显著相关。对于每种酶,观察到绒毛萎缩程度与mRNA水平之间存在显著的负相关。从1岁到18岁的年龄增长并未导致任何一种酶的mRNA或蛋白质水平发生显著变化。十二指肠上皮内乳糖酶的免疫染色模式与相邻切片中蔗糖酶 - 异麦芽糖酶的不同,说明了细胞水平的独立调控。
在白人儿童的十二指肠中,乳糖酶和蔗糖酶 - 异麦芽糖酶似乎主要在转录水平上受到调控。肠道上皮中每种酶的表达由独立的机制调控。随着健康儿童成长至成年,乳糖酶和蔗糖酶 - 异麦芽糖酶的mRNA和蛋白质水平保持稳定。黏膜损伤对两种酶的水平均有负面影响。