Lorenzsonn V, Lloyd M, Olsen W A
Gastroenterology Research Laboratory, William S. Middleton Memorial Veterans Hospital, Madison, Wisconsin.
Gastroenterology. 1993 Jul;105(1):51-9. doi: 10.1016/0016-5085(93)90009-2.
Adult lactase deficiency may result either from diminished synthesis of precursor lactase-phlorizin hydrolase (phenotype I deficiency) or from altered posttranslational processing of the precursor protein (phenotype II). The aim of this study was to compare the location of lactase-phlorizin hydrolase along the crypt-villus axis in control with adult lactase-deficient subjects.
The immunocytochemical distribution of lactase-phlorizin hydrolase was studied in subjects with adult hypolactasia and in controls with persistent high lactase expression.
Duodenal biopsy samples from controls showed increasing intensity of brush border staining from upper crypt to midvillus. Subjects with phenotype I deficiency showed reduced and more patchy reaction product over brush borders. In some, maximal staining was localized over the upper half of the villi. The subject with phenotype II deficiency showed patchy staining but also intracellular accumulations of immunoreactivity within the apex of enterocytes mainly on the upper half of villi. Subsequent immunoelectronmicroscopy showed nearly a fourfold increase in label over the endoplasmic reticulum.
These findings support prior observations of diminished enzyme synthesis in phenotype I lactase deficiency and suggest that the alterations in posttranslational processing in phenotype II deficiency involve a partial block in transport from endoplasmic reticulum to Golgi apparatus.
成人乳糖酶缺乏可能是由于前体乳糖酶 - 根皮苷水解酶合成减少(I型表型缺乏)或前体蛋白翻译后加工改变(II型表型)所致。本研究的目的是比较成人乳糖酶缺乏受试者与对照组中乳糖酶 - 根皮苷水解酶沿隐窝 - 绒毛轴的定位。
研究了成人低乳糖血症受试者和持续高乳糖酶表达对照组中乳糖酶 - 根皮苷水解酶的免疫细胞化学分布。
对照组十二指肠活检样本显示,从隐窝上部到绒毛中部,刷状缘染色强度增加。I型表型缺乏的受试者刷状缘反应产物减少且更呈斑片状。在一些受试者中,最大染色位于绒毛上半部分。II型表型缺乏的受试者显示斑片状染色,但在肠上皮细胞顶端主要是绒毛上半部分也有免疫反应性的细胞内积聚。随后的免疫电子显微镜检查显示内质网上的标记物增加了近四倍。
这些发现支持了先前关于I型乳糖酶缺乏中酶合成减少的观察结果,并表明II型缺乏中翻译后加工的改变涉及从内质网到高尔基体转运的部分阻滞。